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    {"id":"48916","name":"Ayvakyt : Orphan maintenance assessment report (initial authorisation)","type":"orphan-maintenance-report","status":"Adopted","consultation_date":"","first_published_date":"2020-09-30T09:27:00Z","last_updated_date":"2020-09-30T09:27:00Z","reference_number":"EMADOC-1700519818-499131","document_url":"https://www.ema.europa.eu/en/documents/orphan-maintenance-report/ayvakyt-orphan-maintenance-assessment-report-initial-authorisation_en.pdf"},
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    {"id":"49358","name":"Oxlumo : Orphan maintenance assessment report (initial authorisation)","type":"orphan-maintenance-report","status":"Adopted","consultation_date":"","first_published_date":"2020-11-25T14:16:00Z","last_updated_date":"2020-11-25T14:16:00Z","reference_number":"EMA/OD/0000034914","document_url":"https://www.ema.europa.eu/en/documents/orphan-maintenance-report/oxlumo-orphan-maintenance-assessment-report-initial-authorisation_en.pdf"},
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    {"id":"49756","name":"Fintepla : Orphan maintenance assessment report (initial authorisation)","type":"orphan-maintenance-report","status":"Adopted","consultation_date":"","first_published_date":"2021-01-08T10:51:00Z","last_updated_date":"2021-01-08T10:51:00Z","reference_number":"EMADOC-1700519818-578199","document_url":"https://www.ema.europa.eu/en/documents/orphan-maintenance-report/fintepla-orphan-maintenance-assessment-report-initial-authorisation_en.pdf"},
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    {"id":"51059","name":"Evrysdi : Orphan maintenance assessment report (initial authorisation)","type":"orphan-maintenance-report","status":"Adopted","consultation_date":"","first_published_date":"2021-05-04T13:10:00Z","last_updated_date":"2023-09-12T16:06:00Z","reference_number":"EMA/OD/0000039037","document_url":"https://www.ema.europa.eu/en/documents/orphan-maintenance-report/evrysdi-orphan-maintenance-assessment-report-initial-authorisation_en.pdf"},
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    {"id":"51327","name":"Orladeyo : Orphan designation withdrawal assessment report (initial authorisation)","type":"orphan-maintenance-report","status":"Adopted","consultation_date":"","first_published_date":"2021-06-01T13:35:00Z","last_updated_date":"2021-06-01T13:35:00Z","reference_number":"EMA/OD/0000045564","document_url":"https://www.ema.europa.eu/en/documents/orphan-maintenance-report/orladeyo-orphan-designation-withdrawal-assessment-report-initial-authorisation_en.pdf"},
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    {"id":"51676","name":"Enspryng : Orphan maintenance assessment report (initial authorisation)","type":"orphan-maintenance-report","status":"Adopted","consultation_date":"","first_published_date":"2021-06-30T10:51:00Z","last_updated_date":"2021-06-30T10:51:00Z","reference_number":"EMADOC-1700519818-673949","document_url":"https://www.ema.europa.eu/en/documents/orphan-maintenance-report/enspryng-orphan-maintenance-assessment-report-initial-authorisation_en.pdf"},
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    {"id":"3040","name":"Icandra (previously vildagliptin / metformin hydrochloride Novartis)-H-C-1050-WS-0257 : EPAR - Assessment Report - Variation","type":"variation-report","status":"Adopted","consultation_date":"","first_published_date":"2013-02-20T01:00:00Z","last_updated_date":"2013-02-20T01:00:00Z","reference_number":"EMA/CHMP/565928/2012","document_url":"https://www.ema.europa.eu/en/documents/variation-report/icandra-previously-vildagliptin-metformin-hydrochloride-novartis-h-c-1050-ws-0257-epar-assessment-report-variation_en.pdf"},
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    {"id":"19691","name":"Kinzalmono (previously Telmisartan Boehringer Ingelheim Pharma KG)-H-C-211-A31-0094 : EPAR - Assessment Report - Article 31","type":"variation-report","status":"Adopted","consultation_date":"","first_published_date":"2014-10-03T02:00:00Z","last_updated_date":"2014-10-03T02:00:00Z","reference_number":"EMA/PRAC/294920/2014","document_url":"https://www.ema.europa.eu/en/documents/variation-report/kinzalmono-previously-telmisartan-boehringer-ingelheim-pharma-kg-h-c-211-a31-0094-epar-assessment-report-article-31_en.pdf"},
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    {"id":"29990","name":"Cerenia-V-C-106-X-0023 : EPAR - Assessment Report - Extension","type":"variation-report","status":"Adopted","consultation_date":"","first_published_date":"2015-07-08T03:00:00Z","last_updated_date":"2024-06-28T17:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/variation-report/cerenia-v-c-106-x-0023-epar-assessment-report-extension_en.pdf"},
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    {"id":"30112","name":"BTVPUR AlSap 2-4-V-C-139-S-0004 : EPAR - Assessment Report - Annual re-assessment","type":"variation-report","status":"Adopted","consultation_date":"","first_published_date":"2014-06-13T02:00:00Z","last_updated_date":"2018-11-13T02:00:00Z","reference_number":"EMA/132659/2014","document_url":"https://www.ema.europa.eu/en/documents/variation-report/btvpur-alsap-2-4-v-c-139-s-0004-epar-assessment-report-annual-re-assessment_en.pdf"},
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    {"id":"41713","name":"ellaOne-H-C-1027-II-0021 : EPAR - Assessment Report - Variation","type":"variation-report","status":"Adopted","consultation_date":"","first_published_date":"2015-02-06T16:45:00Z","last_updated_date":"2015-02-06T16:45:00Z","reference_number":"EMA/73099/2015","document_url":"https://www.ema.europa.eu/en/documents/variation-report/ellaone-h-c-1027-ii-0021-epar-assessment-report-variation_en.pdf"},
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    {"id":"41742","name":"Sovaldi-H-C-2798-II-0036 : EPAR - Assessment Report - Variation","type":"variation-report","status":"Adopted","consultation_date":"","first_published_date":"2017-10-18T02:00:00Z","last_updated_date":"2017-10-18T02:00:00Z","reference_number":"EMA/508676/2017","document_url":"https://www.ema.europa.eu/en/documents/variation-report/sovaldi-h-c-2798-ii-0036-epar-assessment-report-variation_en.pdf"},
    {"id":"41776","name":"Micardis-H-C-209-A31-0099 : EPAR - Assessment Report - Article 31","type":"variation-report","status":"Adopted","consultation_date":"","first_published_date":"2014-09-25T02:00:00Z","last_updated_date":"2014-09-25T02:00:00Z","reference_number":"EMA/PRAC/294920/2014","document_url":"https://www.ema.europa.eu/en/documents/variation-report/micardis-h-c-209-a31-0099-epar-assessment-report-article-31_en.pdf"},
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    {"id":"43356","name":"Humira-H-C-481-P46-103 : EPAR - Assessment Report","type":"variation-report","status":"Adopted","consultation_date":"","first_published_date":"2019-01-14T16:33:00Z","last_updated_date":"2019-01-14T16:33:00Z","reference_number":"EMA/CHMP/428944/2018","document_url":"https://www.ema.europa.eu/en/documents/variation-report/humira-h-c-481-p46-103-epar-assessment-report_en.pdf"},
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    {"id":"43362","name":"Elocta-H-C-3964-X-0021 : EPAR - Assessment Report -  Extension","type":"variation-report","status":"Adopted","consultation_date":"","first_published_date":"2019-01-15T12:59:00Z","last_updated_date":"2019-01-15T12:59:00Z","reference_number":"EMA/CHMP/697649/2018","document_url":"https://www.ema.europa.eu/en/documents/variation-report/elocta-h-c-3964-x-0021-epar-assessment-report-extension_en.pdf"},
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    {"id":"43433","name":"Ecalta-H-C-788-P46-046 : EPAR - Assessment Report","type":"variation-report","status":"Adopted","consultation_date":"","first_published_date":"2019-01-22T12:39:00Z","last_updated_date":"2019-01-22T12:39:00Z","reference_number":"EMA/916359/2019","document_url":"https://www.ema.europa.eu/en/documents/variation-report/ecalta-h-c-788-p46-046-epar-assessment-report_en.pdf"},
    {"id":"43473","name":"Cabometyx-H-C-004163-II-0005 : EPAR - Assessment report - Variation","type":"variation-report","status":"Adopted","consultation_date":"","first_published_date":"2019-01-24T15:32:00Z","last_updated_date":"2019-01-24T15:32:00Z","reference_number":"EMA/704052/2018","document_url":"https://www.ema.europa.eu/en/documents/variation-report/cabometyx-h-c-004163-ii-0005-epar-assessment-report-variation_en.pdf"},
    {"id":"43480","name":"Sutent-H-C-687-II-0070 : EPAR - Assessment Report - Variation","type":"variation-report","status":"Adopted","consultation_date":"","first_published_date":"2019-01-24T17:00:00Z","last_updated_date":"2019-01-24T17:00:00Z","reference_number":"EMA/CHMP/28241/2019","document_url":"https://www.ema.europa.eu/en/documents/variation-report/sutent-h-c-687-ii-0070-epar-assessment-report-variation_en.pdf"},
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    {"id":"43542","name":"Ravicti-H-C-3822-II-0019 : EPAR - Assessment report - Variation","type":"variation-report","status":"Adopted","consultation_date":"","first_published_date":"2019-01-29T11:49:00Z","last_updated_date":"2019-01-29T11:49:00Z","reference_number":"EMA/CHMP/831384/2018","document_url":"https://www.ema.europa.eu/en/documents/variation-report/ravicti-h-c-3822-ii-0019-epar-assessment-report-variation_en.pdf"},
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    {"id":"43786","name":"Gilenya-H-C-2202-X-0044-G : EPAR - Assessment Report - Variation","type":"variation-report","status":"Adopted","consultation_date":"","first_published_date":"2019-02-19T08:11:00Z","last_updated_date":"2019-02-19T08:11:00Z","reference_number":"EMA/779102/2018","document_url":"https://www.ema.europa.eu/en/documents/variation-report/gilenya-h-c-2202-x-0044-g-epar-assessment-report-variation_en.pdf"},
    {"id":"43793","name":"Cinqaero-H-C-3912-P46-0008 : EPAR - Assessment Report","type":"variation-report","status":"Adopted","consultation_date":"","first_published_date":"2019-02-19T12:38:00Z","last_updated_date":"2019-02-19T12:38:00Z","reference_number":"EMA/847608/2018","document_url":"https://www.ema.europa.eu/en/documents/variation-report/cinqaero-h-c-3912-p46-0008-epar-assessment-report_en.pdf"},
    {"id":"43796","name":"Rubraca-H-C-4272-II-0001 : EPAR - Assessment report - Variation","type":"variation-report","status":"Adopted","consultation_date":"","first_published_date":"2019-02-19T13:15:00Z","last_updated_date":"2019-02-19T13:15:00Z","reference_number":"EMA/902679/2019","document_url":"https://www.ema.europa.eu/en/documents/variation-report/rubraca-h-c-4272-ii-0001-epar-assessment-report-variation_en.pdf"},
    {"id":"43876","name":"Humira-H-C-481-P46-110 : EPAR - Assessment Report","type":"variation-report","status":"unknown","consultation_date":"","first_published_date":"2019-02-22T15:32:00Z","last_updated_date":"2019-02-22T15:32:00Z","reference_number":"EMA/907573/2019","document_url":"https://www.ema.europa.eu/en/documents/variation-report/humira-h-c-481-p46-110-epar-assessment-report_en.pdf"},
    {"id":"43900","name":"Fiasp-H-C-4046-P46-002 : EPAR - Assessment report","type":"variation-report","status":"Adopted","consultation_date":"","first_published_date":"2019-02-26T09:18:00Z","last_updated_date":"2019-02-26T09:18:00Z","reference_number":"EMA/142332/2019","document_url":"https://www.ema.europa.eu/en/documents/variation-report/fiasp-h-c-4046-p46-002-epar-assessment-report_en.pdf"},
    {"id":"43901","name":"Tresiba-H-C-2498-P46-012 : EPAR - Assessment report","type":"variation-report","status":"Adopted","consultation_date":"","first_published_date":"2019-02-26T09:22:00Z","last_updated_date":"2019-02-26T09:22:00Z","reference_number":"EMA/142406/2019","document_url":"https://www.ema.europa.eu/en/documents/variation-report/tresiba-h-c-2498-p46-012-epar-assessment-report_en.pdf"},
    {"id":"43902","name":"NovoRapid-H-C-258-P46-0048 : EPAR - Assessment Report","type":"variation-report","status":"Adopted","consultation_date":"","first_published_date":"2019-02-26T09:27:00Z","last_updated_date":"2019-02-26T09:27:00Z","reference_number":"EMA/142348/2019","document_url":"https://www.ema.europa.eu/en/documents/variation-report/novorapid-h-c-258-p46-0048-epar-assessment-report_en.pdf"},
    {"id":"43910","name":"Mircera-H-C-739-II-0067 : EPAR - Assessment Report - Variation","type":"variation-report","status":"unknown","consultation_date":"","first_published_date":"2019-02-26T11:10:00Z","last_updated_date":"2019-02-26T11:10:00Z","reference_number":"EMA/131222/2019","document_url":"https://www.ema.europa.eu/en/documents/variation-report/mircera-h-c-739-ii-0067-epar-assessment-report-variation_en.pdf"},
    {"id":"43913","name":"Blincyto-H-C-3731-II-0011 : EPAR - Assessment report - Variation","type":"variation-report","status":"Adopted","consultation_date":"","first_published_date":"2019-02-26T15:36:00Z","last_updated_date":"2019-02-26T15:36:00Z","reference_number":"EMA/847661/2018","document_url":"https://www.ema.europa.eu/en/documents/variation-report/blincyto-h-c-3731-ii-0011-epar-assessment-report-variation_en.pdf"},
    {"id":"43925","name":"Nucala-H-C-3860-P046-003 : EPAR - Assessment Report","type":"variation-report","status":"unknown","consultation_date":"","first_published_date":"2019-02-27T17:53:00Z","last_updated_date":"2019-02-27T17:53:00Z","reference_number":"EMA/731252/2018","document_url":"https://www.ema.europa.eu/en/documents/variation-report/nucala-h-c-3860-p046-003-epar-assessment-report_en.pdf"},
    {"id":"43975","name":"Nimenrix-H-C-2226-P46-0052 : EPAR - Assessment Report","type":"variation-report","status":"Adopted","consultation_date":"","first_published_date":"2019-03-04T17:29:00Z","last_updated_date":"2019-03-04T17:29:00Z","reference_number":"EMA/148825/2019","document_url":"https://www.ema.europa.eu/en/documents/variation-report/nimenrix-h-c-2226-p46-0052-epar-assessment-report_en.pdf"},
    {"id":"43980","name":"Humira-H-C-481-P46-112 : EPAR - Assessment Report","type":"variation-report","status":"Adopted","consultation_date":"","first_published_date":"2019-03-06T11:39:00Z","last_updated_date":"2019-03-06T11:39:00Z","reference_number":"EMA/145491/2019","document_url":"https://www.ema.europa.eu/en/documents/variation-report/humira-h-c-481-p46-112-epar-assessment-report_en.pdf"},
    {"id":"43989","name":"Translarna-H-C-2720-II-0049 : EPAR - Assessment Report - Variation","type":"variation-report","status":"Adopted","consultation_date":"","first_published_date":"2019-03-07T16:19:00Z","last_updated_date":"2025-04-16T11:11:11Z","reference_number":"EMA/CHMP/159564/2019","document_url":"https://www.ema.europa.eu/en/documents/variation-report/translarna-h-c-2720-ii-0049-epar-assessment-report-variation_en.pdf"},
    {"id":"44006","name":"Aftovaxpur DOE-V-C-2292-II-0009 : EPAR - Assessment Report - Variation","type":"variation-report","status":"Adopted","consultation_date":"","first_published_date":"2019-03-11T12:11:00Z","last_updated_date":"2023-07-04T13:58:00Z","reference_number":"EMA/807571/2018","document_url":"https://www.ema.europa.eu/en/documents/variation-report/aftovaxpur-doe-v-c-2292-ii-0009-epar-assessment-report-variation_en.pdf"},
    {"id":"44016","name":"Bexsero-H-C-2333-P46-0027 : EPAR - Assessment Report","type":"variation-report","status":"Adopted","consultation_date":"","first_published_date":"2019-03-12T17:50:00Z","last_updated_date":"2019-03-12T17:50:00Z","reference_number":"EMA/CHMP/100778/2018","document_url":"https://www.ema.europa.eu/en/documents/variation-report/bexsero-h-c-2333-p46-0027-epar-assessment-report_en.pdf"},
    {"id":"44019","name":"Adcetris-H-C-002455-II-0055 : EPAR - Assessment Report - Variation","type":"variation-report","status":"Adopted","consultation_date":"","first_published_date":"2019-03-13T10:45:00Z","last_updated_date":"2019-03-13T10:45:00Z","reference_number":"EMA/6661/2019","document_url":"https://www.ema.europa.eu/en/documents/variation-report/adcetris-h-c-002455-ii-0055-epar-assessment-report-variation_en.pdf"},
    {"id":"44023","name":"Simponi-H-C-992-X-0083-G: EPAR - Assessment Report - Extension","type":"variation-report","status":"Adopted","consultation_date":"","first_published_date":"2019-03-13T16:25:00Z","last_updated_date":"2019-03-13T16:25:00Z","reference_number":"EMA/898638/2018","document_url":"https://www.ema.europa.eu/en/documents/variation-report/simponi-h-c-992-x-0083-g-epar-assessment-report-extension_en.pdf"},
    {"id":"44050","name":"Zulvac BTV-V-C-4185-X-0001 : Assessment report - Variation","type":"variation-report","status":"Adopted","consultation_date":"","first_published_date":"2019-03-19T10:59:00Z","last_updated_date":"2025-10-15T15:00:00Z","reference_number":"EMA/870927/2018","document_url":"https://www.ema.europa.eu/en/documents/variation-report/zulvac-btv-v-c-4185-x-0001-assessment-report-variation_en.pdf"},
    {"id":"44076","name":"Trimbow-H-C-4257-II-0002 : EPAR - Assessment Report - Variation","type":"variation-report","status":"Adopted","consultation_date":"","first_published_date":"2019-03-20T14:57:00Z","last_updated_date":"2019-03-20T14:57:00Z","reference_number":"EMA/910019/2019","document_url":"https://www.ema.europa.eu/en/documents/variation-report/trimbow-h-c-4257-ii-0002-epar-assessment-report-variation_en.pdf"},
    {"id":"44138","name":"Quinsair-H-A-31-1452 : EPAR - Assessment report","type":"variation-report","status":"Adopted","consultation_date":"","first_published_date":"2019-03-29T08:52:00Z","last_updated_date":"2019-03-29T08:52:00Z","reference_number":"EMA/818158/2018","document_url":"https://www.ema.europa.eu/en/documents/variation-report/quinsair-h-31-1452-epar-assessment-report_en.pdf"},
    {"id":"44141","name":"Sprycel-H-C-709-II-0059 : EPAR - Assessment report - Variation","type":"variation-report","status":"Adopted","consultation_date":"","first_published_date":"2019-03-29T09:29:00Z","last_updated_date":"2019-03-29T09:29:00Z","reference_number":"EMA/CHMP/3851/2019","document_url":"https://www.ema.europa.eu/en/documents/variation-report/sprycel-h-c-709-ii-0059-epar-assessment-report-variation_en.pdf"},
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    {"id":"49377","name":"Velphoro-H-C-2705-X-20-G: EPAR - Assessment report - Variation","type":"variation-report","status":"Adopted","consultation_date":"","first_published_date":"2020-11-26T15:38:00Z","last_updated_date":"2021-02-03T11:27:00Z","reference_number":"EMA/522604/2020 Corr.","document_url":"https://www.ema.europa.eu/en/documents/variation-report/velphoro-h-c-2705-x-20-g-epar-assessment-report-variation_en.pdf"},
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    {"id":"49410","name":"Kanuma-H-C-004004-II-0026-G : EPAR - Assessment report - Variation","type":"variation-report","status":"Adopted","consultation_date":"","first_published_date":"2020-12-01T10:49:00Z","last_updated_date":"2020-12-01T10:49:00Z","reference_number":"EMA/CHMP/637875/2020","document_url":"https://www.ema.europa.eu/en/documents/variation-report/kanuma-h-c-004004-ii-0026-g-epar-assessment-report-variation_en.pdf"},
    {"id":"49454","name":"Desloratadine ratiopharm-H-C-2404-II-0023-G : EPAR - Assessment report - Variation","type":"variation-report","status":"Adopted","consultation_date":"","first_published_date":"2020-12-03T17:10:00Z","last_updated_date":"2020-12-03T17:10:00Z","reference_number":"EMA/592592/2020","document_url":"https://www.ema.europa.eu/en/documents/variation-report/desloratadine-ratiopharm-h-c-2404-ii-0023-g-epar-assessment-report-variation_en.pdf"},
    {"id":"49483","name":"Ristfor-H-C-1235-WS-1898: EPAR - Assessment Report - Variation","type":"variation-report","status":"Adopted","consultation_date":"","first_published_date":"2020-12-08T15:21:00Z","last_updated_date":"2020-12-08T15:21:00Z","reference_number":"EMA/603247/2020","document_url":"https://www.ema.europa.eu/en/documents/variation-report/ristfor-h-c-1235-ws-1898-epar-assessment-report-variation_en.pdf"},
    {"id":"49484","name":"Kalydeco-H-C-2494-II-0086 : EPAR - Assessment Report - Variation","type":"variation-report","status":"Adopted","consultation_date":"","first_published_date":"2020-12-09T09:43:00Z","last_updated_date":"2020-12-09T09:43:00Z","reference_number":"EMA/530990/2020","document_url":"https://www.ema.europa.eu/en/documents/variation-report/kalydeco-h-c-2494-ii-0086-epar-assessment-report-variation_en.pdf"},
    {"id":"49496","name":"Velmetia-H-C-862-WS-1898 : EPAR - Assessment Report - Variation","type":"variation-report","status":"Adopted","consultation_date":"","first_published_date":"2020-12-09T16:48:00Z","last_updated_date":"2020-12-09T16:48:00Z","reference_number":"EMA/603247/2020","document_url":"https://www.ema.europa.eu/en/documents/variation-report/velmetia-h-c-862-ws-1898-epar-assessment-report-variation_en.pdf"},
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    {"id":"49534","name":"Epclusa-H-C-4210-X-43-G : EPAR - Assessment report - Variation","type":"variation-report","status":"Adopted","consultation_date":"","first_published_date":"2020-12-11T10:09:00Z","last_updated_date":"2020-12-11T10:09:00Z","reference_number":"EMA/379603/2020","document_url":"https://www.ema.europa.eu/en/documents/variation-report/epclusa-h-c-4210-x-43-g-epar-assessment-report-variation_en.pdf"},
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    {"id":"49600","name":"Efficib-H-C-896-WS-1898 : EPAR - Assessment Report - Variation","type":"variation-report","status":"Adopted","consultation_date":"","first_published_date":"2020-12-17T01:00:00Z","last_updated_date":"2020-12-17T01:00:00Z","reference_number":"EMA/603247/2020","document_url":"https://www.ema.europa.eu/en/documents/variation-report/efficib-h-c-896-ws-1898-epar-assessment-report-variation_en.pdf"},
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    {"id":"50236","name":"Vimpat-H-C-863-P46-039 : EPAR - Assessment Report","type":"variation-report","status":"Adopted","consultation_date":"","first_published_date":"2021-02-18T15:35:00Z","last_updated_date":"2021-02-18T15:35:00Z","reference_number":"EMA/101296/2021","document_url":"https://www.ema.europa.eu/en/documents/variation-report/vimpat-h-c-863-p46-039-epar-assessment-report_en.pdf"},
    {"id":"50249","name":"Symkevi-H-C-4682-X-0015-G : EPAR - Assessment Report - Variation","type":"variation-report","status":"Adopted","consultation_date":"","first_published_date":"2021-02-22T09:36:00Z","last_updated_date":"2021-02-22T09:36:00Z","reference_number":"EMA/48399/2021","document_url":"https://www.ema.europa.eu/en/documents/variation-report/symkevi-h-c-4682-x-0015-g-epar-assessment-report-variation_en.pdf"},
    {"id":"50260","name":"Tecentriq-H-C-004143-II-0039 : EPAR - Assessment report - Variation","type":"variation-report","status":"Adopted","consultation_date":"","first_published_date":"2021-02-23T15:24:00Z","last_updated_date":"2021-02-23T15:24:00Z","reference_number":"EMA/584169/2020","document_url":"https://www.ema.europa.eu/en/documents/variation-report/tecentriq-h-c-004143-ii-0039-epar-assessment-report-variation_en.pdf"},
    {"id":"50314","name":"Trimbow-H-C-4257-X-0008-G : EPAR - Assessment Report - Extension","type":"variation-report","status":"Adopted","consultation_date":"","first_published_date":"2021-02-26T17:31:00Z","last_updated_date":"2021-02-26T17:31:00Z","reference_number":"EMA/667393/2020","document_url":"https://www.ema.europa.eu/en/documents/variation-report/trimbow-h-c-4257-x-0008-g-epar-assessment-report-extension_en.pdf"},
    {"id":"50316","name":"Bydureon-H-C-2020-P46-028 : EPAR - Assessment report","type":"variation-report","status":"Adopted","consultation_date":"","first_published_date":"2021-03-01T10:22:00Z","last_updated_date":"2021-03-01T10:22:00Z","reference_number":"EMA/94820/2021","document_url":"https://www.ema.europa.eu/en/documents/variation-report/bydureon-h-c-2020-p46-028-epar-assessment-report_en.pdf"},
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    {"id":"50354","name":"Angiotensin-II-receptor antagonists (sartans) Article 31 referral - CHMP assessment report - Impact of the Article 5(3) scientific opinion on nitrosamines","type":"variation-report","status":"Adopted","consultation_date":"","first_published_date":"2021-03-02T09:33:00Z","last_updated_date":"2021-03-02T09:33:00Z","reference_number":"EMA/47245/2021","document_url":"https://www.ema.europa.eu/en/documents/variation-report/angiotensin-ii-receptor-antagonists-sartans-article-31-referral-chmp-assessment-report-impact-article-53-scientific-opinion-nitrosamines_en.pdf"},
    {"id":"50475","name":"Spravato-H-C-4535-II-0001-G : EPAR - Assessment report - Variation","type":"variation-report","status":"Adopted","consultation_date":"","first_published_date":"2021-03-08T12:04:00Z","last_updated_date":"2021-03-08T12:04:00Z","reference_number":"EMA/141382/2021","document_url":"https://www.ema.europa.eu/en/documents/variation-report/spravato-h-c-4535-ii-0001-g-epar-assessment-report-variation_en.pdf"},
    {"id":"50498","name":"Innovax-ND-IBD-V-C-4422-II-0004 : EPAR - Assessment report - Variation","type":"variation-report","status":"Adopted","consultation_date":"","first_published_date":"2021-03-09T12:05:00Z","last_updated_date":"2021-03-09T12:05:00Z","reference_number":"EMA/193705/2019","document_url":"https://www.ema.europa.eu/en/documents/variation-report/innovax-nd-ibd-v-c-4422-ii-0004-epar-assessment-report-variation_en.pdf"},
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    {"id":"52117","name":"Orkambi-H-C-3954-P46-016.1 : EPAR - Assessment Report","type":"variation-report","status":"unknown","consultation_date":"","first_published_date":"2021-07-28T11:10:00Z","last_updated_date":"2021-07-28T11:10:00Z","reference_number":"EMA/278069/2021","document_url":"https://www.ema.europa.eu/en/documents/variation-report/orkambi-h-c-3954-p46-0161-epar-assessment-report_en.pdf"},
    {"id":"52123","name":"Maviret-H-C-004430-X-0033-G : EPAR - Assessment report - Variation","type":"variation-report","status":"Adopted","consultation_date":"","first_published_date":"2021-07-28T14:40:00Z","last_updated_date":"2021-07-28T14:42:00Z","reference_number":"EMA/372473/2021","document_url":"https://www.ema.europa.eu/en/documents/variation-report/maviret-h-c-004430-x-0033-g-epar-assessment-report-variation_en.pdf"},
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    {"id":"52208","name":"Aakynzeo-H-C-003728-P46-004.1 : EPAR - Assessment report","type":"variation-report","status":"Adopted","consultation_date":"","first_published_date":"2021-08-10T11:31:00Z","last_updated_date":"2021-08-10T11:31:00Z","reference_number":"EMA/300397/2021","document_url":"https://www.ema.europa.eu/en/documents/variation-report/aakynzeo-h-c-003728-p46-0041-epar-assessment-report_en.pdf"},
    {"id":"52248","name":"Xalkori-H-C-002489-P46-025 : EPAR - Assessment Report","type":"variation-report","status":"Adopted","consultation_date":"","first_published_date":"2021-08-20T10:11:00Z","last_updated_date":"2021-08-20T10:11:00Z","reference_number":"EMA/CHMP/443216/2021","document_url":"https://www.ema.europa.eu/en/documents/variation-report/xalkori-h-c-002489-p46-025-epar-assessment-report_en.pdf"},
    {"id":"52260","name":"Galvus-H-C-771-WS-1938-G: EPAR - Assessment Report - Variation","type":"variation-report","status":"Adopted","consultation_date":"","first_published_date":"2021-08-24T02:00:00Z","last_updated_date":"2021-08-24T02:00:00Z","reference_number":"EMA/413658/2021","document_url":"https://www.ema.europa.eu/en/documents/variation-report/galvus-h-c-771-ws-1938-g-epar-assessment-report-variation_en.pdf"},
    {"id":"52267","name":"Eucreas-H-C-807-WS-1937-G: EPAR - Assessment Report - Variation","type":"variation-report","status":"Adopted","consultation_date":"","first_published_date":"2021-08-25T01:00:00Z","last_updated_date":"2021-08-25T01:00:00Z","reference_number":"EMA/402373/2021","document_url":"https://www.ema.europa.eu/en/documents/variation-report/eucreas-h-c-807-ws-1937-g-epar-assessment-report-variation_en.pdf"},
    {"id":"52268","name":"Zavicefta-H-C-4027-II-0019 : EPAR - Assessment Report - Variation","type":"variation-report","status":"Adopted","consultation_date":"","first_published_date":"2021-08-25T09:12:00Z","last_updated_date":"2021-08-25T09:12:00Z","reference_number":"EMA/437085/2020","document_url":"https://www.ema.europa.eu/en/documents/variation-report/zavicefta-h-c-4027-ii-0019-epar-assessment-report-variation_en.pdf"},
    {"id":"52292","name":"Galafold-H-C-004059-II-0029 : EPAR - Assessment report variation","type":"variation-report","status":"Adopted","consultation_date":"","first_published_date":"2021-08-27T14:38:00Z","last_updated_date":"2021-08-27T14:38:00Z","reference_number":"EMA/CHMP/412211/2021","document_url":"https://www.ema.europa.eu/en/documents/variation-report/galafold-h-c-004059-ii-0029-epar-assessment-report-variation_en.pdf"},
    {"id":"52296","name":"Intelence-H-C-900-P46-0054 : EPAR - Assessment Report","type":"variation-report","status":"Adopted","consultation_date":"","first_published_date":"2021-08-30T12:26:00Z","last_updated_date":"2021-08-30T12:26:00Z","reference_number":"EMA/475740/2021","document_url":"https://www.ema.europa.eu/en/documents/variation-report/intelence-h-c-900-p46-0054-epar-assessment-report_en.pdf"},
    {"id":"52297","name":"Exviera-H-C-3837-P46-0019 : EPAR - Assessment report","type":"variation-report","status":"Adopted","consultation_date":"","first_published_date":"2021-08-30T15:10:00Z","last_updated_date":"2024-10-01T16:10:00Z","reference_number":"EMA/CHMP/105448/2019","document_url":"https://www.ema.europa.eu/en/documents/variation-report/exviera-h-c-3837-p46-0019-epar-assessment-report_en.pdf"},
    {"id":"52298","name":"Viekirax-H-C-3839-P46-0021 : EPAR - Assessment report","type":"variation-report","status":"Adopted","consultation_date":"","first_published_date":"2021-08-30T15:16:00Z","last_updated_date":"2024-10-02T09:40:00Z","reference_number":"EMA/CHMP/105448/2019","document_url":"https://www.ema.europa.eu/en/documents/variation-report/viekirax-h-c-3839-p46-0021-epar-assessment-report_en.pdf"},
    {"id":"52312","name":"Exviera-H-C-3837-P46-0021 : EPAR - Assessment report","type":"variation-report","status":"Adopted","consultation_date":"","first_published_date":"2021-09-01T11:18:00Z","last_updated_date":"2024-10-01T16:11:00Z","reference_number":"EMA/92477/2021","document_url":"https://www.ema.europa.eu/en/documents/variation-report/exviera-h-c-3837-p46-0021-epar-assessment-report_en.pdf"},
    {"id":"52313","name":"Viekirax-H-C-3839-P46-023 : EPAR - Assessment report","type":"variation-report","status":"Adopted","consultation_date":"","first_published_date":"2021-09-01T11:30:00Z","last_updated_date":"2024-10-02T09:41:00Z","reference_number":"EMA/92477/2021","document_url":"https://www.ema.europa.eu/en/documents/variation-report/viekirax-h-c-3839-p46-023-epar-assessment-report_en.pdf"},
    {"id":"52317","name":"Zulvac BTV-V-C-4185-II-0004 : Assessment report - Variation","type":"variation-report","status":"Adopted","consultation_date":"","first_published_date":"2021-09-01T17:30:00Z","last_updated_date":"2025-10-15T15:00:00Z","reference_number":"EMA/519278/2019","document_url":"https://www.ema.europa.eu/en/documents/variation-report/zulvac-btv-v-c-4185-ii-0004-assessment-report-variation_en.pdf"},
    {"id":"52320","name":"Edistride-H-C-WS-1941 : EPAR - Assessment report - Variation","type":"variation-report","status":"Adopted","consultation_date":"","first_published_date":"2021-09-02T14:03:00Z","last_updated_date":"2021-09-02T14:03:00Z","reference_number":"EMA/431093/2021","document_url":"https://www.ema.europa.eu/en/documents/variation-report/edistride-h-c-ws-1941-epar-assessment-report-variation_en.pdf"},
    {"id":"52322","name":"Forxiga-H-C-WS-1941 : EPAR - Assessment report - Variation","type":"variation-report","status":"Adopted","consultation_date":"","first_published_date":"2021-09-02T14:52:00Z","last_updated_date":"2021-09-02T14:52:00Z","reference_number":"EMA/431093/2021","document_url":"https://www.ema.europa.eu/en/documents/variation-report/forxiga-h-c-ws-1941-epar-assessment-report-variation_en.pdf"},
    {"id":"52332","name":"Cosentyx-H-C-003729-II-0073 : EPAR - Assessment Report - Variation","type":"variation-report","status":"Adopted","consultation_date":"","first_published_date":"2021-09-03T10:52:00Z","last_updated_date":"2021-09-03T10:52:00Z","reference_number":"EMA/422077/2021","document_url":"https://www.ema.europa.eu/en/documents/variation-report/cosentyx-h-c-003729-ii-0073-epar-assessment-report-variation_en.pdf"},
    {"id":"52338","name":"Cosentyx-H-C-3729-P46-012 : EPAR - Assessment report","type":"variation-report","status":"Adopted","consultation_date":"","first_published_date":"2021-09-06T11:04:00Z","last_updated_date":"2021-09-06T11:04:00Z","reference_number":"EMA/471835/2021","document_url":"https://www.ema.europa.eu/en/documents/variation-report/cosentyx-h-c-3729-p46-012-epar-assessment-report_en.pdf"},
    {"id":"52355","name":"Jalra-H-C-1048-WS-1938 : EPAR - Assessment Report - Variation","type":"variation-report","status":"Adopted","consultation_date":"","first_published_date":"2021-09-07T11:54:00Z","last_updated_date":"2021-09-07T11:54:00Z","reference_number":"EMA/413658/2021","document_url":"https://www.ema.europa.eu/en/documents/variation-report/jalra-h-c-1048-ws-1938-epar-assessment-report-variation_en.pdf"},
    {"id":"52359","name":"Xiliarx-H-C-1051-WS-1938-G : EPAR - Assessment Report - Variation","type":"variation-report","status":"Adopted","consultation_date":"","first_published_date":"2021-09-07T15:11:00Z","last_updated_date":"2021-09-07T15:11:00Z","reference_number":"EMA/413658/2021","document_url":"https://www.ema.europa.eu/en/documents/variation-report/xiliarx-h-c-1051-ws-1938-g-epar-assessment-report-variation_en.pdf"},
    {"id":"52360","name":"Zomarist-H-C-1049-WS-1937-G : EPAR - Assessment Report - Variation","type":"variation-report","status":"Adopted","consultation_date":"","first_published_date":"2021-09-07T16:53:00Z","last_updated_date":"2021-09-07T16:53:00Z","reference_number":"EMA/402373/2021","document_url":"https://www.ema.europa.eu/en/documents/variation-report/zomarist-h-c-1049-ws-1937-g-epar-assessment-report-variation_en.pdf"},
    {"id":"52361","name":"Icandra-H-C-1050-WS-1937-G : EPAR - Assessment Report - Variation","type":"variation-report","status":"Adopted","consultation_date":"","first_published_date":"2021-09-08T09:52:00Z","last_updated_date":"2021-09-08T09:52:00Z","reference_number":"EMA/402373/2021","document_url":"https://www.ema.europa.eu/en/documents/variation-report/icandra-h-c-1050-ws-1937-g-epar-assessment-report-variation_en.pdf"},
    {"id":"52364","name":"Rinvoq-H-C-004760-X-0006-G : EPAR - Assessment report - Variation","type":"variation-report","status":"Adopted","consultation_date":"","first_published_date":"2021-09-08T14:00:00Z","last_updated_date":"2021-09-08T14:00:00Z","reference_number":"EMA/396759/2021","document_url":"https://www.ema.europa.eu/en/documents/variation-report/rinvoq-h-c-004760-x-0006-g-epar-assessment-report-variation_en.pdf"},
    {"id":"52390","name":"Venclyxto-H-C-004106-P46-01: EPAR - Assessment report","type":"variation-report","status":"Adopted","consultation_date":"","first_published_date":"2021-09-09T11:58:00Z","last_updated_date":"2021-09-09T11:58:00Z","reference_number":"EMA/425184/2021","document_url":"https://www.ema.europa.eu/en/documents/variation-report/venclyxto-h-c-004106-p46-01-epar-assessment-report_en.pdf"},
    {"id":"52407","name":"RotaTeq-H-C-000669-P46-046 : EPAR - Assessment Report","type":"variation-report","status":"Adopted","consultation_date":"","first_published_date":"2021-09-09T16:45:00Z","last_updated_date":"2021-09-09T16:45:00Z","reference_number":"EMA/CHMP/367688/2021","document_url":"https://www.ema.europa.eu/en/documents/variation-report/rotateq-h-c-000669-p46-046-epar-assessment-report_en.pdf"},
    {"id":"52409","name":"HBVaxPro-H-C-000373-P46-060 : EPAR - Assessment Report","type":"variation-report","status":"Adopted","consultation_date":"","first_published_date":"2021-09-09T16:54:00Z","last_updated_date":"2021-09-09T16:54:00Z","reference_number":"EMA/500196/2021","document_url":"https://www.ema.europa.eu/en/documents/variation-report/hbvaxpro-h-c-000373-p46-060-epar-assessment-report_en.pdf"},
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    {"id":"52457","name":"Cytopoint-V-C-003939-II-0009 : EPAR - Assessment report - Variation","type":"variation-report","status":"Adopted","consultation_date":"","first_published_date":"2021-09-15T17:29:00Z","last_updated_date":"2025-03-17T12:35:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/variation-report/cytopoint-v-c-003939-ii-0009-epar-assessment-report-variation_en.pdf"},
    {"id":"52458","name":"Stelara-H-C-958-P46-051 : EPAR - Assessment Report","type":"variation-report","status":"Adopted","consultation_date":"","first_published_date":"2021-09-16T08:58:00Z","last_updated_date":"2021-09-16T08:58:00Z","reference_number":"EMA/294893/2021","document_url":"https://www.ema.europa.eu/en/documents/variation-report/stelara-h-c-958-p46-051-epar-assessment-report_en.pdf"},
    {"id":"52552","name":"Fycompa-H-C-002434-P46-020: EPAR - Assessment report","type":"variation-report","status":"Adopted","consultation_date":"","first_published_date":"2021-09-22T14:48:00Z","last_updated_date":"2021-09-22T14:48:00Z","reference_number":"EMA/437972/2021","document_url":"https://www.ema.europa.eu/en/documents/variation-report/fycompa-h-c-002434-p46-020-epar-assessment-report_en.pdf"},
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    {"id":"52652","name":"Volibris-H-C-839-X-0061-G: EPAR - Assessment Report - Variation","type":"variation-report","status":"Adopted","consultation_date":"","first_published_date":"2021-09-28T15:02:00Z","last_updated_date":"2021-09-28T15:02:00Z","reference_number":"EMA/CHMP/476747/2021","document_url":"https://www.ema.europa.eu/en/documents/variation-report/volibris-h-c-839-x-0061-g-epar-assessment-report-variation_en.pdf"},
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    {"id":"53122","name":"Comirnaty-H-C-5735-R-0046 : EPAR - Assessment report - Renewal","type":"variation-report","status":"Adopted","consultation_date":"","first_published_date":"2021-11-15T15:48:00Z","last_updated_date":"2021-11-15T15:48:00Z","reference_number":"EMA/596333/2021","document_url":"https://www.ema.europa.eu/en/documents/variation-report/comirnaty-h-c-5735-r-0046-epar-assessment-report-renewal_en.pdf"},
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    {"id":"53164","name":"Vaxzevria (previously COVID-19 Vaccine AstraZeneca)-H-C-5675-R-0037 : EPAR - Assessment report - Renewal","type":"variation-report","status":"Adopted","consultation_date":"","first_published_date":"2021-11-18T17:14:00Z","last_updated_date":"2024-05-07T11:00:00Z","reference_number":"EMA/622071/2021","document_url":"https://www.ema.europa.eu/en/documents/variation-report/vaxzevria-previously-covid-19-vaccine-astrazeneca-h-c-5675-r-0037-epar-assessment-report-renewal_en.pdf"},
    {"id":"53250","name":"Keytruda-H-C-003820-II-0105 : EPAR - Assessment report - Variation","type":"variation-report","status":"Adopted","consultation_date":"","first_published_date":"2021-11-24T09:44:00Z","last_updated_date":"2021-11-24T09:44:00Z","reference_number":"EMA/617606/2021","document_url":"https://www.ema.europa.eu/en/documents/variation-report/keytruda-h-c-003820-ii-0105-epar-assessment-report-variation_en.pdf"},
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    {"id":"53278","name":"Jyseleca-H-C-005113-II-0001 : EPAR - Assessment report - Variation","type":"variation-report","status":"Adopted","consultation_date":"","first_published_date":"2021-11-25T17:11:00Z","last_updated_date":"2021-11-25T17:11:00Z","reference_number":"EMA/553754/2021","document_url":"https://www.ema.europa.eu/en/documents/variation-report/jyseleca-h-c-005113-ii-0001-epar-assessment-report-variation_en.pdf"},
    {"id":"53284","name":"Adempas-H-C-002737-II-0032-G : EPAR - Assessment report - Variation","type":"variation-report","status":"Adopted","consultation_date":"","first_published_date":"2021-11-26T08:09:00Z","last_updated_date":"2021-11-26T08:09:00Z","reference_number":"EMA/621814/2021","document_url":"https://www.ema.europa.eu/en/documents/variation-report/adempas-h-c-002737-ii-0032-g-epar-assessment-report-variation_en.pdf"},
    {"id":"53286","name":"Eylea-H-C-002392-P46-020 : EPAR - Assessment report","type":"variation-report","status":"Adopted","consultation_date":"","first_published_date":"2021-11-26T09:02:00Z","last_updated_date":"2021-11-26T09:02:00Z","reference_number":"EMA/605744/2021","document_url":"https://www.ema.europa.eu/en/documents/variation-report/eylea-h-c-002392-p46-020-epar-assessment-report_en.pdf"},
    {"id":"53298","name":"Spikevax (previously COVID-19 Vaccine Moderna)-H-C-5791-II-34 : EPAR - Assessment Report - Variation","type":"variation-report","status":"Adopted","consultation_date":"","first_published_date":"2021-11-26T15:37:00Z","last_updated_date":"2021-11-26T15:37:00Z","reference_number":"EMA/618924/2021","document_url":"https://www.ema.europa.eu/en/documents/variation-report/spikevax-previously-covid-19-vaccine-moderna-h-c-5791-ii-34-epar-assessment-report-variation_en.pdf"},
    {"id":"53333","name":"Kisplyx-H-C-004224-II-0045 : EPAR - Assessment report","type":"variation-report","status":"Adopted","consultation_date":"","first_published_date":"2021-11-29T17:39:00Z","last_updated_date":"2021-11-29T17:39:00Z","reference_number":"EMA/621560/2021","document_url":"https://www.ema.europa.eu/en/documents/variation-report/kisplyx-h-c-004224-ii-0045-epar-assessment-report_en.pdf"},
    {"id":"53340","name":"Ultomiris-H-C-004954-II-0010 : EPAR - Assessment report - Variation","type":"variation-report","status":"Adopted","consultation_date":"","first_published_date":"2021-11-30T14:39:00Z","last_updated_date":"2021-11-30T14:39:00Z","reference_number":"EMA/552844/2021","document_url":"https://www.ema.europa.eu/en/documents/variation-report/ultomiris-h-c-004954-ii-0010-epar-assessment-report-variation_en.pdf"},
    {"id":"53342","name":"Rotarix-H-C-639-P46-102 : EPAR - Assessment Report","type":"variation-report","status":"Adopted","consultation_date":"","first_published_date":"2021-12-01T10:30:00Z","last_updated_date":"2021-12-01T10:30:00Z","reference_number":"EMA/469887/2021","document_url":"https://www.ema.europa.eu/en/documents/variation-report/rotarix-h-c-639-p46-102-epar-assessment-report_en.pdf"},
    {"id":"53343","name":"Lenvima-H-C-003727-II-0042 : EPAR - Assessment report - Variation","type":"variation-report","status":"Adopted","consultation_date":"","first_published_date":"2021-12-01T13:25:00Z","last_updated_date":"2021-12-01T13:25:00Z","reference_number":"EMA/CHMP/618201/2021","document_url":"https://www.ema.europa.eu/en/documents/variation-report/lenvima-h-c-003727-ii-0042-epar-assessment-report-variation_en.pdf"},
    {"id":"53344","name":"Skyrizi-H-C-004759-P46-006 : EPAR - Assessment report","type":"variation-report","status":"Adopted","consultation_date":"","first_published_date":"2021-12-01T14:39:00Z","last_updated_date":"2021-12-01T14:39:00Z","reference_number":"EMA/712018/2021","document_url":"https://www.ema.europa.eu/en/documents/variation-report/skyrizi-h-c-004759-p46-006-epar-assessment-report_en.pdf"},
    {"id":"53362","name":"Suvaxyn CSF Marker-V-C-002757-II-0009 : EPAR - Assessment report - Variation","type":"variation-report","status":"Adopted","consultation_date":"","first_published_date":"2021-12-03T15:35:00Z","last_updated_date":"2025-09-02T11:11:01Z","reference_number":"EMA/472597/2021","document_url":"https://www.ema.europa.eu/en/documents/variation-report/suvaxyn-csf-marker-v-c-002757-ii-0009-epar-assessment-report-variation_en.pdf"},
    {"id":"53370","name":"Gilenya-H-C-2202-P46-039 : EPAR - Assessment Report","type":"variation-report","status":"Adopted","consultation_date":"","first_published_date":"2021-12-06T13:44:00Z","last_updated_date":"2021-12-06T13:44:00Z","reference_number":"EMA/CHMP/716292/2021","document_url":"https://www.ema.europa.eu/en/documents/variation-report/gilenya-h-c-2202-p46-039-epar-assessment-report_en.pdf"},
    {"id":"53381","name":"Noxafil-H-C-610-II-0062 : EPAR - Assessment Report - Variation","type":"variation-report","status":"Adopted","consultation_date":"","first_published_date":"2021-12-07T10:32:00Z","last_updated_date":"2021-12-07T10:32:00Z","reference_number":"EMA/590500/2021","document_url":"https://www.ema.europa.eu/en/documents/variation-report/noxafil-h-c-610-ii-0062-epar-assessment-report-variation_en.pdf"},
    {"id":"53412","name":"Halaven-H-C-002084-P46-025 : EPAR - Assessment Report","type":"variation-report","status":"Adopted","consultation_date":"","first_published_date":"2021-12-08T11:46:00Z","last_updated_date":"2021-12-08T11:46:00Z","reference_number":"EMA/545362/2021","document_url":"https://www.ema.europa.eu/en/documents/variation-report/halaven-h-c-002084-p46-025-epar-assessment-report_en.pdf"},
    {"id":"53418","name":"Circovac-V-C-000114-WS1945-0018 : EPAR - Assessment report - Variation","type":"variation-report","status":"Adopted","consultation_date":"","first_published_date":"2021-12-08T12:33:00Z","last_updated_date":"2024-06-03T14:14:00Z","reference_number":"EMA/564312/2021","document_url":"https://www.ema.europa.eu/en/documents/variation-report/circovac-v-c-000114-ws1945-0018-epar-assessment-report-variation_en.pdf"},
    {"id":"53438","name":"RoActemra-H-C-955-II-0101 : EPAR - Assessment Report - Variation","type":"variation-report","status":"Adopted","consultation_date":"","first_published_date":"2021-12-10T13:58:00Z","last_updated_date":"2021-12-10T13:58:00Z","reference_number":"EMA/733881/2021","document_url":"https://www.ema.europa.eu/en/documents/variation-report/roactemra-h-c-955-ii-0101-epar-assessment-report-variation_en.pdf"},
    {"id":"53451","name":"Nucala-H-C-003860-II-0035 : EPAR - Assessment Report - Variation","type":"variation-report","status":"Adopted","consultation_date":"","first_published_date":"2021-12-13T15:28:00Z","last_updated_date":"2021-12-13T15:28:00Z","reference_number":"EMA/560926/2021","document_url":"https://www.ema.europa.eu/en/documents/variation-report/nucala-h-c-003860-ii-0035-epar-assessment-report-variation_en.pdf"},
    {"id":"53452","name":"Nucala-H-C-003860-II-0036-G : EPAR - Assessment Report - Variation","type":"variation-report","status":"Adopted","consultation_date":"","first_published_date":"2021-12-13T15:31:00Z","last_updated_date":"2022-03-29T10:33:00Z","reference_number":"EMA/560927/2021 Corr. 1","document_url":"https://www.ema.europa.eu/en/documents/variation-report/nucala-h-c-003860-ii-0036-g-epar-assessment-report-variation_en.pdf"},
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    {"id":"54514","name":"Briviact-H-C-3898-II-0032-G : EPAR - Assessment Report - Extension","type":"variation-report","status":"Adopted","consultation_date":"","first_published_date":"2022-03-17T16:49:00Z","last_updated_date":"2022-03-17T16:49:00Z","reference_number":"EMA/99325/2022","document_url":"https://www.ema.europa.eu/en/documents/variation-report/briviact-h-c-3898-ii-0032-g-epar-assessment-report-extension_en.pdf"},
    {"id":"54517","name":"Relvar Ellipta-H-C-2673-P46-015 : EPAR - Assessment Report","type":"variation-report","status":"Adopted","consultation_date":"","first_published_date":"2022-03-18T12:06:00Z","last_updated_date":"2022-03-18T12:06:00Z","reference_number":"EMA/168280/2022","document_url":"https://www.ema.europa.eu/en/documents/variation-report/relvar-ellipta-h-c-2673-p46-015-epar-assessment-report_en.pdf"},
    {"id":"54519","name":"Dupixent-H-C-4390-P46-006 : EPAR - Assessment Report","type":"variation-report","status":"Adopted","consultation_date":"","first_published_date":"2022-03-18T14:29:00Z","last_updated_date":"2022-03-18T14:29:00Z","reference_number":"EMA/148767/2022","document_url":"https://www.ema.europa.eu/en/documents/variation-report/dupixent-h-c-4390-p46-006-epar-assessment-report_en.pdf"},
    {"id":"54526","name":"NovoThirteen-H-C-002284-II-0026-G : EPAR - Assessment Report - Variation","type":"variation-report","status":"Adopted","consultation_date":"","first_published_date":"2022-03-21T10:48:00Z","last_updated_date":"2022-03-21T10:48:00Z","reference_number":"EMA/539227/2020","document_url":"https://www.ema.europa.eu/en/documents/variation-report/novothirteen-h-c-002284-ii-0026-g-epar-assessment-report-variation_en.pdf"},
    {"id":"54530","name":"Bravecto-V-C-2526-II-0051 : EPAR - Assessment Report - Variation","type":"variation-report","status":"Adopted","consultation_date":"","first_published_date":"2022-03-21T14:52:00Z","last_updated_date":"2024-06-03T11:26:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/variation-report/bravecto-v-c-2526-ii-0051-epar-assessment-report-variation_en.pdf"},
    {"id":"54589","name":"Spikevax (previously COVID-19 Vaccine Moderna)-H-C-5791-II-42 : EPAR - Assessment Report - Variation","type":"variation-report","status":"Adopted","consultation_date":"","first_published_date":"2022-03-25T15:37:00Z","last_updated_date":"2022-03-25T15:37:00Z","reference_number":"EMA/137482/2022","document_url":"https://www.ema.europa.eu/en/documents/variation-report/spikevax-previously-covid-19-vaccine-moderna-h-c-5791-ii-42-epar-assessment-report-variation_en.pdf"},
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    {"id":"54624","name":"Jardiance-H-C-002677-II-0060 : EPAR - Assessment report - Variation","type":"variation-report","status":"Adopted","consultation_date":"","first_published_date":"2022-03-30T13:49:00Z","last_updated_date":"2022-03-30T13:49:00Z","reference_number":"EMA/102340/2022","document_url":"https://www.ema.europa.eu/en/documents/variation-report/jardiance-h-c-002677-ii-0060-epar-assessment-report-variation_en.pdf"},
    {"id":"54627","name":"Lacosamide UCB-H-C-WS2049-G : EPAR - Assessment report - Variation","type":"variation-report","status":"Adopted","consultation_date":"","first_published_date":"2022-03-30T15:14:00Z","last_updated_date":"2022-03-30T15:14:00Z","reference_number":"EMA/99116/2022","document_url":"https://www.ema.europa.eu/en/documents/variation-report/lacosamide-ucb-h-c-ws2049-g-epar-assessment-report-variation_en.pdf"},
    {"id":"54636","name":"Afstyla-H-C-004075-P46-003 : EPAR - Assessment report","type":"variation-report","status":"Adopted","consultation_date":"","first_published_date":"2022-03-31T11:50:00Z","last_updated_date":"2022-03-31T11:50:00Z","reference_number":"EMA/456459/2021","document_url":"https://www.ema.europa.eu/en/documents/variation-report/afstyla-h-c-004075-p46-003-epar-assessment-report_en.pdf"},
    {"id":"54668","name":"Teysuno-H-C-001242-II-0045 : EPAR - Assessment Report - Variation","type":"variation-report","status":"Adopted","consultation_date":"","first_published_date":"2022-04-04T16:51:00Z","last_updated_date":"2022-04-04T16:51:00Z","reference_number":"EMA/CHMP/2190/2022","document_url":"https://www.ema.europa.eu/en/documents/variation-report/teysuno-h-c-001242-ii-0045-epar-assessment-report-variation_en.pdf"},
    {"id":"54670","name":"Improvac-V-C-136-II-0036 : EPAR - Assessment Report - Variation","type":"variation-report","status":"Adopted","consultation_date":"","first_published_date":"2022-04-05T09:45:00Z","last_updated_date":"2024-06-11T11:45:00Z","reference_number":"EMA/746574/2021","document_url":"https://www.ema.europa.eu/en/documents/variation-report/improvac-v-c-136-ii-0036-epar-assessment-report-variation_en.pdf"},
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    {"id":"54685","name":"Kengrexal-H-C-003773-P46-003.1 : EPAR - Assessment Report","type":"variation-report","status":"Adopted","consultation_date":"","first_published_date":"2022-04-06T12:17:00Z","last_updated_date":"2022-04-06T12:17:00Z","reference_number":"EMA/105362/2022","document_url":"https://www.ema.europa.eu/en/documents/variation-report/kengrexal-h-c-003773-p46-0031-epar-assessment-report_en.pdf"},
    {"id":"54704","name":"Nulojix-H-C-002098-II-0065-G : EPAR - Assessment report","type":"variation-report","status":"Adopted","consultation_date":"","first_published_date":"2022-04-08T13:49:00Z","last_updated_date":"2022-04-08T13:49:00Z","reference_number":"EMA/708312/2021","document_url":"https://www.ema.europa.eu/en/documents/variation-report/nulojix-h-c-002098-ii-0065-g-epar-assessment-report_en.pdf"},
    {"id":"54712","name":"Dupixent-H-C-004390-X-0045-G : EPAR - Assessment Report","type":"variation-report","status":"Adopted","consultation_date":"","first_published_date":"2022-04-08T16:39:00Z","last_updated_date":"2022-04-08T16:39:00Z","reference_number":"EMA/98744/2022","document_url":"https://www.ema.europa.eu/en/documents/variation-report/dupixent-h-c-004390-x-0045-g-epar-assessment-report_en.pdf"},
    {"id":"54741","name":"Pifeltro-H-C-WS2065 : EPAR - Assessment Report - Variation","type":"variation-report","status":"Adopted","consultation_date":"","first_published_date":"2022-04-12T17:08:00Z","last_updated_date":"2022-04-12T17:08:00Z","reference_number":"EMA/CHMP/PRAC/104864/2022","document_url":"https://www.ema.europa.eu/en/documents/variation-report/pifeltro-h-c-ws2065-epar-assessment-report-variation_en.pdf"},
    {"id":"54745","name":"Delstrigo-H-C-WS2065 : EPAR - Assessment Report - Variation","type":"variation-report","status":"Adopted","consultation_date":"","first_published_date":"2022-04-12T17:36:00Z","last_updated_date":"2022-04-12T17:36:00Z","reference_number":"EMA/CHMP/PRAC/104864/2022","document_url":"https://www.ema.europa.eu/en/documents/variation-report/delstrigo-h-c-ws2065-epar-assessment-report-variation_en.pdf"},
    {"id":"54759","name":"Spikevax (previously COVID-19 Vaccine Moderna)-H-C-5791-II-41 : EPAR - Assessment Report - Variation","type":"variation-report","status":"Adopted","consultation_date":"","first_published_date":"2022-04-19T17:54:00Z","last_updated_date":"2022-04-19T17:54:00Z","reference_number":"EMA/137337/2022 – Rev.1","document_url":"https://www.ema.europa.eu/en/documents/variation-report/spikevax-previously-covid-19-vaccine-moderna-h-c-5791-ii-41-epar-assessment-report-variation_en.pdf"},
    {"id":"54769","name":"Yervoy-H-C-WS2113 : EPAR - Assessment Report - Variation","type":"variation-report","status":"Adopted","consultation_date":"","first_published_date":"2022-04-20T15:50:00Z","last_updated_date":"2022-04-20T15:50:00Z","reference_number":"EMA/155438/2022","document_url":"https://www.ema.europa.eu/en/documents/variation-report/yervoy-h-c-ws2113-epar-assessment-report-variation_en.pdf"},
    {"id":"54770","name":"Opdivo-H-C-WS-2113 : EPAR - Assessment Report - Variation","type":"variation-report","status":"Adopted","consultation_date":"","first_published_date":"2022-04-20T16:22:00Z","last_updated_date":"2022-04-20T16:22:00Z","reference_number":"EMA/155438/2022","document_url":"https://www.ema.europa.eu/en/documents/variation-report/opdivo-h-c-ws-2113-epar-assessment-report-variation_en.pdf"},
    {"id":"54771","name":"Opdivo-H-C-003985-II-0100 : EPAR - Assessment Report - Variation","type":"variation-report","status":"Adopted","consultation_date":"","first_published_date":"2022-04-20T16:24:00Z","last_updated_date":"2022-04-20T16:24:00Z","reference_number":"EMA/155845/2022","document_url":"https://www.ema.europa.eu/en/documents/variation-report/opdivo-h-c-003985-ii-0100-epar-assessment-report-variation_en.pdf"},
    {"id":"54772","name":"Opdivo-H-C-003985-II-0107 : EPAR - Assessment Report - Variation","type":"variation-report","status":"Adopted","consultation_date":"","first_published_date":"2022-04-20T16:27:00Z","last_updated_date":"2022-04-20T16:27:00Z","reference_number":"EMA/155595/2022","document_url":"https://www.ema.europa.eu/en/documents/variation-report/opdivo-h-c-003985-ii-0107-epar-assessment-report-variation_en.pdf"},
    {"id":"54774","name":"Verzenios-H-C-004302-II-0013: EPAR - Assessment report - Variation","type":"variation-report","status":"Adopted","consultation_date":"","first_published_date":"2022-04-21T10:16:00Z","last_updated_date":"2022-04-21T10:16:00Z","reference_number":"EMA/156033/2022","document_url":"https://www.ema.europa.eu/en/documents/variation-report/verzenios-h-c-004302-ii-0013-epar-assessment-report-variation_en.pdf"},
    {"id":"54775","name":"Maviret-H-C-004430-P46-011 : EPAR - Assessment report","type":"variation-report","status":"Adopted","consultation_date":"","first_published_date":"2022-04-21T10:59:00Z","last_updated_date":"2022-04-21T10:59:00Z","reference_number":"EMA/CHMP/121612/2022","document_url":"https://www.ema.europa.eu/en/documents/variation-report/maviret-h-c-004430-p46-011-epar-assessment-report_en.pdf"},
    {"id":"54821","name":"Simbrinza-H-C-003698-P46-002  : EPAR - Assessment Report","type":"variation-report","status":"Adopted","consultation_date":"","first_published_date":"2022-04-25T13:07:00Z","last_updated_date":"2022-04-25T13:07:00Z","reference_number":"EMA/CHMP/66626/2022","document_url":"https://www.ema.europa.eu/en/documents/variation-report/simbrinza-h-c-003698-p46-002-epar-assessment-report_en.pdf"},
    {"id":"54884","name":"Bosulif-H-C-002373-II-0050-G:EPAR - Assessment report - Variation","type":"variation-report","status":"Adopted","consultation_date":"","first_published_date":"2022-05-03T16:28:00Z","last_updated_date":"2022-05-03T16:28:00Z","reference_number":"EMA/126509/2022","document_url":"https://www.ema.europa.eu/en/documents/variation-report/bosulif-h-c-002373-ii-0050-gepar-assessment-report-variation_en.pdf"},
    {"id":"54972","name":"Vimpat-H-C-863-P46-042 : EPAR - Assessment Report","type":"variation-report","status":"Adopted","consultation_date":"","first_published_date":"2022-05-17T12:34:00Z","last_updated_date":"2022-05-17T12:34:00Z","reference_number":"EMA/254431/2022","document_url":"https://www.ema.europa.eu/en/documents/variation-report/vimpat-h-c-863-p46-042-epar-assessment-report_en.pdf"},
    {"id":"54975","name":"Keytruda-H-C-003820-II-0109 : EPAR - Assessment report - Variation","type":"variation-report","status":"Adopted","consultation_date":"","first_published_date":"2022-05-17T14:30:00Z","last_updated_date":"2022-05-17T14:30:00Z","reference_number":"EMA/224161/2022","document_url":"https://www.ema.europa.eu/en/documents/variation-report/keytruda-h-c-003820-ii-0109-epar-assessment-report-variation_en.pdf"},
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    {"id":"55762","name":"Enhertu-H-C-005124-II-0014 : EPAR - Assessment Report - Variation","type":"variation-report","status":"Adopted","consultation_date":"","first_published_date":"2022-08-02T14:21:00Z","last_updated_date":"2022-08-02T14:21:00Z","reference_number":"EMA/CHMP/636117/2022","document_url":"https://www.ema.europa.eu/en/documents/variation-report/enhertu-h-c-005124-ii-0014-epar-assessment-report-variation_en.pdf"},
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    {"id":"56610","name":"Exparel liposomal-H-C-4586-II-0005: EPAR - Assessment report - Variation","type":"variation-report","status":"Adopted","consultation_date":"","first_published_date":"2022-11-14T12:03:00Z","last_updated_date":"2022-11-14T12:03:00Z","reference_number":"EMA/CHMP/794139/2022","document_url":"https://www.ema.europa.eu/en/documents/variation-report/exparel-liposomal-h-c-4586-ii-0005-epar-assessment-report-variation_en.pdf"},
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    {"id":"56714","name":"Sunosi-H-C-4893-P46-005 : EPAR - Assessment report","type":"variation-report","status":"Adopted","consultation_date":"","first_published_date":"2022-11-18T14:54:00Z","last_updated_date":"2022-11-18T14:54:00Z","reference_number":"EMA/CHMP/894270/2022","document_url":"https://www.ema.europa.eu/en/documents/variation-report/sunosi-h-c-4893-p46-005-epar-assessment-report_en.pdf"},
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    {"id":"57503","name":"Lynparza-H-C-3726-II-0053 : EPAR - Assessment Report - Variation","type":"variation-report","status":"Adopted","consultation_date":"","first_published_date":"2023-02-02T11:38:00Z","last_updated_date":"2023-02-02T11:38:00Z","reference_number":"EMA/941572/2022","document_url":"https://www.ema.europa.eu/en/documents/variation-report/lynparza-h-c-3726-ii-0053-epar-assessment-report-variation_en.pdf"},
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    {"id":"58091","name":"Elocta-H-C-3964-P46-007 : EPAR - Assessment Report","type":"variation-report","status":"Adopted","consultation_date":"","first_published_date":"2023-03-21T14:56:00Z","last_updated_date":"2023-03-21T14:56:00Z","reference_number":"EMA/CHMP/753870/2021","document_url":"https://www.ema.europa.eu/en/documents/variation-report/elocta-h-c-3964-p46-007-epar-assessment-report_en.pdf"},
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    {"id":"58131","name":"Dupixent-H-C-4390-II-0060 : EPAR - Assessment Report - Variation","type":"variation-report","status":"Adopted","consultation_date":"","first_published_date":"2023-03-23T11:07:00Z","last_updated_date":"2023-03-23T11:07:00Z","reference_number":"EMA/66726/2023","document_url":"https://www.ema.europa.eu/en/documents/variation-report/dupixent-h-c-4390-ii-0060-epar-assessment-report-variation_en.pdf"},
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    {"id":"58289","name":"Cometriq-H-C-002640-P46 : EPAR - Assessment report","type":"variation-report","status":"Adopted","consultation_date":"","first_published_date":"2023-04-05T13:36:00Z","last_updated_date":"2023-04-05T13:36:00Z","reference_number":"EMA/CHMP/68009/2023","document_url":"https://www.ema.europa.eu/en/documents/variation-report/cometriq-h-c-002640-p46-epar-assessment-report_en.pdf"},
    {"id":"58290","name":"Cabometyx-H-C-004163-P46 : EPAR - Assessment report","type":"variation-report","status":"Adopted","consultation_date":"","first_published_date":"2023-04-05T13:41:00Z","last_updated_date":"2023-04-05T13:41:00Z","reference_number":"EMA/CHMP/68009/2023","document_url":"https://www.ema.europa.eu/en/documents/variation-report/cabometyx-h-c-004163-p46-epar-assessment-report_en.pdf"},
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    {"id":"58979","name":"Opdivo-H-C-003985-II-0125-G : EPAR - Assessment Report - Variation","type":"variation-report","status":"Adopted","consultation_date":"","first_published_date":"2023-06-16T11:55:00Z","last_updated_date":"2023-06-16T11:55:00Z","reference_number":"EMA/221123/2023","document_url":"https://www.ema.europa.eu/en/documents/variation-report/opdivo-h-c-003985-ii-0125-g-epar-assessment-report-variation_en.pdf"},
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    {"id":"59929","name":"Lonsurf-H-C-003897-II-0026 : EPAR - Assessment report - Variation","type":"variation-report","status":"Adopted","consultation_date":"","first_published_date":"2023-09-11T13:48:00Z","last_updated_date":"2023-09-11T13:48:00Z","reference_number":"EMA/CHMP/221594/2023","document_url":"https://www.ema.europa.eu/en/documents/variation-report/lonsurf-h-c-003897-ii-0026-epar-assessment-report-variation_en.pdf"},
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    {"id":"60040","name":"Jinarc-H-C-002788-P46-010 : EPAR - Assessment Report","type":"variation-report","status":"Adopted","consultation_date":"","first_published_date":"2023-09-18T13:22:00Z","last_updated_date":"2023-09-18T13:22:00Z","reference_number":"EMA/CHMP/158910/2023","document_url":"https://www.ema.europa.eu/en/documents/variation-report/jinarc-h-c-002788-p46-010-epar-assessment-report_en.pdf"},
    {"id":"60082","name":"Olumiant-H-C-4085-X-0035-G : EPAR - Assessment report - Variation","type":"variation-report","status":"Adopted","consultation_date":"","first_published_date":"2023-09-21T09:18:00Z","last_updated_date":"2023-09-21T09:18:00Z","reference_number":"EMA/365746/2023","document_url":"https://www.ema.europa.eu/en/documents/variation-report/olumiant-h-c-4085-x-0035-g-epar-assessment-report-variation_en.pdf"},
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    {"id":"60107","name":"Tenkasi-H-C-003785-X-0036 : EPAR - Assessment report - Variation","type":"variation-report","status":"Adopted","consultation_date":"","first_published_date":"2023-09-22T09:20:00Z","last_updated_date":"2023-09-22T09:20:00Z","reference_number":"EMA/323178/2023","document_url":"https://www.ema.europa.eu/en/documents/variation-report/tenkasi-h-c-003785-x-0036-epar-assessment-report-variation_en.pdf"},
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    {"id":"60113","name":"Vaxneuvance-H-C-005477-P46-003 : EPAR - Assessment report","type":"variation-report","status":"unknown","consultation_date":"","first_published_date":"2023-09-22T13:26:00Z","last_updated_date":"2023-09-22T13:26:00Z","reference_number":"EMA/429416/2023","document_url":"https://www.ema.europa.eu/en/documents/variation-report/vaxneuvance-h-c-005477-p46-003-epar-assessment-report_en.pdf"},
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    {"id":"63134","name":"Volibris-H-C-000839-II-0067 : EPAR - Assessment Report - Variation","type":"variation-report","status":"Adopted","consultation_date":"","first_published_date":"2024-05-02T09:45:00Z","last_updated_date":"2024-05-02T09:45:00Z","reference_number":"EMA/120148/2024","document_url":"https://www.ema.europa.eu/en/documents/variation-report/volibris-h-c-000839-ii-0067-epar-assessment-report-variation_en.pdf"},
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    {"id":"63199","name":"Reblozyl-H-C-4444-II-0021 : EPAR - Assessment report - Variation","type":"variation-report","status":"Adopted","consultation_date":"","first_published_date":"2024-05-13T11:16:00Z","last_updated_date":"2024-05-13T11:16:00Z","reference_number":"EMA/112157/2024","document_url":"https://www.ema.europa.eu/en/documents/variation-report/reblozyl-h-c-4444-ii-0021-epar-assessment-report-variation_en.pdf"},
    {"id":"63207","name":"Aspaveli-H-C-005553-II-0011 : EPAR - Assessment report - Variation","type":"variation-report","status":"Adopted","consultation_date":"","first_published_date":"2024-05-14T09:14:00Z","last_updated_date":"2024-05-14T09:14:00Z","reference_number":"EMA/62863/2024","document_url":"https://www.ema.europa.eu/en/documents/variation-report/aspaveli-h-c-005553-ii-0011-epar-assessment-report-variation_en.pdf"},
    {"id":"63211","name":"Uptravi-EMEA-H-C-003774-X-0038 : EPAR - Assessment report - Extension","type":"variation-report","status":"unknown","consultation_date":"","first_published_date":"2024-05-15T10:28:51Z","last_updated_date":"2024-05-15T10:28:51Z","reference_number":"EMA/91623/2024","document_url":"https://www.ema.europa.eu/en/documents/variation-report/uptravi-emea-h-c-003774-x-0038-epar-assessment-report-extension_en.pdf"},
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    {"id":"63215","name":"Zoonotic Influenza Vaccine Seqirus-H-C-006375-II-0001 : EPAR - Assessment report - Variation","type":"variation-report","status":"Adopted","consultation_date":"","first_published_date":"2024-05-16T10:41:00Z","last_updated_date":"2024-05-16T10:41:00Z","reference_number":"EMA/128110/2024","document_url":"https://www.ema.europa.eu/en/documents/variation-report/zoonotic-influenza-vaccine-seqirus-h-c-006375-ii-0001-epar-assessment-report-variation_en.pdf"},
    {"id":"63232","name":"Kalydeco-H-C-002494-X-0115-G : EPAR - Assessment report - Variation","type":"variation-report","status":"Adopted","consultation_date":"","first_published_date":"2024-05-16T12:08:00Z","last_updated_date":"2024-05-16T12:08:00Z","reference_number":"EMA/110324/2024","document_url":"https://www.ema.europa.eu/en/documents/variation-report/kalydeco-h-c-002494-x-0115-g-epar-assessment-report-variation_en.pdf"},
    {"id":"63252","name":"Onivyde pegylated liposomal-H-C-004125-II-0034 : EPAR - Assessment report - Variation","type":"variation-report","status":"Adopted","consultation_date":"","first_published_date":"2024-05-17T13:00:00Z","last_updated_date":"2024-05-17T13:00:00Z","reference_number":"EMA/162308/2024","document_url":"https://www.ema.europa.eu/en/documents/variation-report/onivyde-pegylated-liposomal-h-c-004125-ii-0034-epar-assessment-report-variation_en.pdf"},
    {"id":"63270","name":"Evenity-H-C-004465-P46-007: EPAR - Assessment report","type":"variation-report","status":"Adopted","consultation_date":"","first_published_date":"2024-05-21T08:47:00Z","last_updated_date":"2024-05-21T08:47:00Z","reference_number":"EMA/39377/2024","document_url":"https://www.ema.europa.eu/en/documents/variation-report/evenity-h-c-004465-p46-007-epar-assessment-report_en.pdf"},
    {"id":"63300","name":"Amgevita-H-C-004212-X-0036-G : EPAR - Assessment report","type":"variation-report","status":"Adopted","consultation_date":"","first_published_date":"2024-05-22T12:23:00Z","last_updated_date":"2024-05-22T12:23:00Z","reference_number":"EMA/146658/2024","document_url":"https://www.ema.europa.eu/en/documents/variation-report/amgevita-h-c-004212-x-0036-g-epar-assessment-report_en.pdf"},
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    {"id":"63341","name":"Xromi-H-C-004837-II-0019 : EPAR - Assessment report - Variation","type":"variation-report","status":"Adopted","consultation_date":"","first_published_date":"2024-05-28T14:48:00Z","last_updated_date":"2024-05-28T14:48:00Z","reference_number":"EMA/153487/2024","document_url":"https://www.ema.europa.eu/en/documents/variation-report/xromi-h-c-004837-ii-0019-epar-assessment-report-variation_en.pdf"},
    {"id":"63356","name":"Rixubis-H-C-003771-P46-007 : EPAR - Assessment report","type":"variation-report","status":"unknown","consultation_date":"","first_published_date":"2024-05-29T09:00:00Z","last_updated_date":"2024-05-29T09:00:00Z","reference_number":"EMA/101747/2024","document_url":"https://www.ema.europa.eu/en/documents/variation-report/rixubis-h-c-003771-p46-007-epar-assessment-report_en.pdf"},
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    {"id":"63406","name":"Kapruvia : EPAR - Assessment report for paediatric studies submitted according to Article 46 of the Regulation (EC) No 1901/2006","type":"variation-report","status":"unknown","consultation_date":"","first_published_date":"2024-05-30T15:05:00Z","last_updated_date":"2024-05-30T15:05:00Z","reference_number":"EMA/224087/2024","document_url":"https://www.ema.europa.eu/en/documents/variation-report/kapruvia-epar-assessment-report-paediatric-studies-submitted-according-article-46-regulation-ec-no-1901-2006_en.pdf"},
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    {"id":"64304","name":"Tevimbra-H-C-005919-II-0008 : EPAR - Assessment report - Variation","type":"variation-report","status":"Adopted","consultation_date":"","first_published_date":"2024-07-25T11:17:00Z","last_updated_date":"2024-07-25T11:17:00Z","reference_number":"EMA/294229/2024","document_url":"https://www.ema.europa.eu/en/documents/variation-report/tevimbra-h-c-005919-ii-0008-epar-assessment-report-variation_en.pdf"},
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    {"id":"64566","name":"Spikevax (previously COVID-19 Vaccine Moderna)-H-C-005791-P46-136 : EPAR - Assessment Report ","type":"variation-report","status":"unknown","consultation_date":"","first_published_date":"2024-08-14T10:50:34Z","last_updated_date":"2024-08-14T10:50:34Z","reference_number":"EMA/372442/2024","document_url":"https://www.ema.europa.eu/en/documents/variation-report/spikevax-previously-covid-19-vaccine-moderna-h-c-005791-p46-136-epar-assessment-report_en.pdf"},
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    {"id":"64584","name":"Cosentyx-H-C-3729-P46-016 : EPAR - Assessment report","type":"variation-report","status":"Adopted","consultation_date":"","first_published_date":"2024-08-16T13:13:10Z","last_updated_date":"2024-08-16T13:13:10Z","reference_number":"EMA/282777/2024","document_url":"https://www.ema.europa.eu/en/documents/variation-report/cosentyx-h-c-3729-p46-016-epar-assessment-report_en.pdf"},
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    {"id":"64596","name":"Eliquis-H-C-2148-X-0089-G : EPAR - Assessment Report - Variation","type":"variation-report","status":"unknown","consultation_date":"","first_published_date":"2024-08-19T16:25:09Z","last_updated_date":"2024-08-19T16:25:09Z","reference_number":"EMA/281735/2024","document_url":"https://www.ema.europa.eu/en/documents/variation-report/eliquis-h-c-2148-x-0089-g-epar-assessment-report-variation_en.pdf"},
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    {"id":"66353","name":"Pravafenix-H-C-001243-II-0037 : EPAR - Assessment Report - Variation","type":"variation-report","status":"Adopted","consultation_date":"","first_published_date":"2025-01-17T13:51:21Z","last_updated_date":"2025-01-17T13:51:21Z","reference_number":"EMA/569435/2024","document_url":"https://www.ema.europa.eu/en/documents/variation-report/pravafenix-h-c-001243-ii-0037-epar-assessment-report-variation_en.pdf"},
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    {"id":"67367","name":"Prevenar 13-H-C-001104-P46-073 : EPAR - Assessment Report","type":"variation-report","status":"Adopted","consultation_date":"","first_published_date":"2025-03-20T12:41:40Z","last_updated_date":"2025-03-20T12:41:40Z","reference_number":"EMA/101185/2025","document_url":"https://www.ema.europa.eu/en/documents/variation-report/prevenar-13-h-c-001104-p46-073-epar-assessment-report_en.pdf"},
    {"id":"67370","name":"Sivextro-H-C-002846-II-0054 : EPAR - Assessment report - Variation","type":"variation-report","status":"Adopted","consultation_date":"","first_published_date":"2025-03-20T14:04:42Z","last_updated_date":"2025-03-20T14:04:42Z","reference_number":"EMA/63803/2025","document_url":"https://www.ema.europa.eu/en/documents/variation-report/sivextro-h-c-002846-ii-0054-epar-assessment-report-variation_en.pdf"},
    {"id":"67375","name":"Darzalex-H-C-004077-II-0030 : EPAR - Assessment report - Variation","type":"variation-report","status":"Adopted","consultation_date":"","first_published_date":"2025-03-20T16:59:58Z","last_updated_date":"2025-03-20T16:59:58Z","reference_number":"EMA/CHMP/22749/2020","document_url":"https://www.ema.europa.eu/en/documents/variation-report/darzalex-h-c-004077-ii-0030-epar-assessment-report-variation_en.pdf"},
    {"id":"67395","name":"Dupixent-H-C-4390-P46-017 : EPAR - Assessment Report","type":"variation-report","status":"Adopted","consultation_date":"","first_published_date":"2025-03-21T14:39:04Z","last_updated_date":"2025-03-21T14:39:04Z","reference_number":"EMA/58890/2025","document_url":"https://www.ema.europa.eu/en/documents/variation-report/dupixent-h-c-4390-p46-017-epar-assessment-report_en.pdf"},
    {"id":"67448","name":"Comirnaty-VR-0000231586 : EPAR - Assessment report - Variation","type":"variation-report","status":"Adopted","consultation_date":"","first_published_date":"2025-03-25T17:11:06Z","last_updated_date":"2025-03-25T17:11:06Z","reference_number":"EMADOC-1700519818-1717428","document_url":"https://www.ema.europa.eu/en/documents/variation-report/comirnaty-vr-0000231586-epar-assessment-report-variation_en.pdf"},
    {"id":"67456","name":"Alofisel-H-C-004258-II-0051-G : EPAR - Assessment report - Variation","type":"variation-report","status":"unknown","consultation_date":"","first_published_date":"2025-03-26T12:09:56Z","last_updated_date":"2025-03-26T12:09:56Z","reference_number":"EMA/598555/2024","document_url":"https://www.ema.europa.eu/en/documents/variation-report/alofisel-h-c-004258-ii-0051-g-epar-assessment-report-variation_en.pdf"},
    {"id":"67457","name":"Cyramza-H-C-2829-P46-0010 : EPAR - Assessment report","type":"variation-report","status":"Adopted","consultation_date":"","first_published_date":"2025-03-26T12:23:10Z","last_updated_date":"2025-03-26T12:23:10Z","reference_number":"EMA/46449/2025","document_url":"https://www.ema.europa.eu/en/documents/variation-report/cyramza-h-c-2829-p46-0010-epar-assessment-report_en.pdf"},
    {"id":"67577","name":"Slenyto-H-C-004425-II-0028 : EPAR - Assessment report - Variation","type":"variation-report","status":"Adopted","consultation_date":"","first_published_date":"2025-04-01T14:56:53Z","last_updated_date":"2025-04-04T13:32:28Z","reference_number":"EMA/119604/2025","document_url":"https://www.ema.europa.eu/en/documents/variation-report/slenyto-h-c-004425-ii-0028-epar-assessment-report-variation_en.pdf"},
    {"id":"67580","name":"Opdivo-H-C-003985-P46-061 : EPAR - Assessment Report - Variation","type":"variation-report","status":"Adopted","consultation_date":"","first_published_date":"2025-04-01T15:27:21Z","last_updated_date":"2025-04-01T15:27:21Z","reference_number":"EMA/44963/2025","document_url":"https://www.ema.europa.eu/en/documents/variation-report/opdivo-h-c-003985-p46-061-epar-assessment-report-variation_en.pdf"},
    {"id":"67581","name":"Dupixent-H-C-4390-P46-018 : EPAR - Assessment Report","type":"variation-report","status":"unknown","consultation_date":"","first_published_date":"2025-04-01T15:35:49Z","last_updated_date":"2025-04-01T15:35:49Z","reference_number":"EMA/58920/2025","document_url":"https://www.ema.europa.eu/en/documents/variation-report/dupixent-h-c-4390-p46-018-epar-assessment-report_en.pdf"},
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    {"id":"52182","name":"Polystyrene sulfonate - List of nationally authorised medicinal products - PSUSA-00002472-202010","type":"pip-compliance","status":"unknown","consultation_date":"","first_published_date":"2021-08-03T14:54:00Z","last_updated_date":"2021-08-03T14:54:00Z","reference_number":"EMA/420759/2021","document_url":"https://www.ema.europa.eu/en/documents/pip-compliance/polystyrene-sulfonate-list-nationally-authorised-medicinal-products-psusa-00002472-202010_en.pdf"},
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    {"id":"55098","name":"Tecfidera : EPAR - Paediatric investigation plan compliance statement","type":"pip-compliance","status":"unknown","consultation_date":"","first_published_date":"2022-05-25T09:22:00Z","last_updated_date":"2022-05-25T09:22:00Z","reference_number":"EMA/CHMP/45040/2022","document_url":"https://www.ema.europa.eu/en/documents/pip-compliance/tecfidera-epar-paediatric-investigation-plan-compliance-statement_en.pdf"},
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    {"id":"55386","name":"Edistride : EPAR - Paediatric investigation plan compliance statement","type":"pip-compliance","status":"unknown","consultation_date":"","first_published_date":"2022-06-27T15:15:00Z","last_updated_date":"2022-06-27T15:15:00Z","reference_number":"EMA/CHMP/592350/2022","document_url":"https://www.ema.europa.eu/en/documents/pip-compliance/edistride-epar-paediatric-investigation-plan-compliance-statement_en.pdf"},
    {"id":"55388","name":"Forxiga : EPAR - Statement indicating compliance with the agreed completed paediatric investigation plan","type":"pip-compliance","status":"unknown","consultation_date":"","first_published_date":"2022-06-27T15:33:00Z","last_updated_date":"2022-06-27T15:33:00Z","reference_number":"EMA/CHMP/592350/2022","document_url":"https://www.ema.europa.eu/en/documents/pip-compliance/forxiga-epar-statement-indicating-compliance-agreed-completed-paediatric-investigation-plan_en.pdf"},
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    {"id":"56163","name":"Imbruvica : EPAR - Statement indicating compliance with the agreed completed paediatric investigation plan","type":"pip-compliance","status":"unknown","consultation_date":"","first_published_date":"2022-09-22T09:58:00Z","last_updated_date":"2022-09-22T09:58:00Z","reference_number":"EMA/630579/2022","document_url":"https://www.ema.europa.eu/en/documents/pip-compliance/imbruvica-epar-statement-indicating-compliance-agreed-completed-paediatric-investigation-plan_en.pdf"},
    {"id":"56539","name":"Nuwiq : EPAR - Paediatric investigation plan compliance statement","type":"pip-compliance","status":"unknown","consultation_date":"","first_published_date":"2022-11-07T12:13:00Z","last_updated_date":"2022-11-07T12:13:00Z","reference_number":"EMA/828539/2022","document_url":"https://www.ema.europa.eu/en/documents/pip-compliance/nuwiq-epar-paediatric-investigation-plan-compliance-statement_en.pdf"},
    {"id":"56540","name":"Vihuma : EPAR - Paediatric investigation plan compliance statement","type":"pip-compliance","status":"unknown","consultation_date":"","first_published_date":"2022-11-07T12:49:00Z","last_updated_date":"2022-11-07T12:49:00Z","reference_number":"EMA/828539/2022","document_url":"https://www.ema.europa.eu/en/documents/pip-compliance/vihuma-epar-paediatric-investigation-plan-compliance-statement_en.pdf"},
    {"id":"57360","name":"Repatha: EPAR - Paediatric investigation plan compliance statement","type":"pip-compliance","status":"unknown","consultation_date":"","first_published_date":"2023-01-23T17:00:00Z","last_updated_date":"2023-01-23T17:00:00Z","reference_number":"EMA/690314/2022","document_url":"https://www.ema.europa.eu/en/documents/pip-compliance/repatha-epar-paediatric-investigation-plan-compliance-statement_en.pdf"},
    {"id":"57900","name":"Tivicay : EPAR - Paediatric investigation plan compliance statement","type":"pip-compliance","status":"unknown","consultation_date":"","first_published_date":"2023-03-07T11:27:00Z","last_updated_date":"2023-03-07T11:27:00Z","reference_number":"EMA/CHMP/106165/2023","document_url":"https://www.ema.europa.eu/en/documents/pip-compliance/tivicay-epar-paediatric-investigation-plan-compliance-statement_en.pdf"},
    {"id":"58132","name":"Dupixent : EPAR - Paediatric investigation plan compliance statement","type":"pip-compliance","status":"unknown","consultation_date":"","first_published_date":"2023-03-23T11:40:00Z","last_updated_date":"2023-03-23T11:40:00Z","reference_number":"EMA/CHMP/15748/2023","document_url":"https://www.ema.europa.eu/en/documents/pip-compliance/dupixent-epar-paediatric-investigation-plan-compliance-statement_en.pdf"},
    {"id":"58478","name":"Wakix : EPAR - Statement indicating compliance with the agreed completed paediatric investigation plan","type":"pip-compliance","status":"unknown","consultation_date":"","first_published_date":"2023-04-20T12:20:00Z","last_updated_date":"2023-04-20T12:20:00Z","reference_number":"EMA/CHMP/37982/2023","document_url":"https://www.ema.europa.eu/en/documents/pip-compliance/wakix-epar-statement-indicating-compliance-agreed-completed-paediatric-investigation-plan_en.pdf"},
    {"id":"58603","name":"Trajenta - EPAR - Paediatric investigation plan compliance statement","type":"pip-compliance","status":"unknown","consultation_date":"","first_published_date":"2023-05-10T10:38:00Z","last_updated_date":"2023-05-10T10:38:00Z","reference_number":"EMA/CHMP/141255/2023","document_url":"https://www.ema.europa.eu/en/documents/pip-compliance/trajenta-epar-paediatric-investigation-plan-compliance-statement_en.pdf"},
    {"id":"58850","name":"Pedmarqsi : EPAR - Paediatric investigation plan compliance statement","type":"pip-compliance","status":"unknown","consultation_date":"","first_published_date":"2023-06-02T09:05:00Z","last_updated_date":"2023-06-02T09:05:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/pip-compliance/pedmarqsi-epar-paediatric-investigation-plan-compliance-statement_en.pdf"},
    {"id":"58980","name":"Opdivo : EPAR - Paediatric investigation plan compliance statement","type":"pip-compliance","status":"unknown","consultation_date":"","first_published_date":"2023-06-16T12:11:00Z","last_updated_date":"2023-06-16T12:11:00Z","reference_number":"EMA/190289/2023","document_url":"https://www.ema.europa.eu/en/documents/pip-compliance/opdivo-epar-paediatric-investigation-plan-compliance-statement_en.pdf"},
    {"id":"59031","name":"Neparvis : EPAR - Paediatric investigation plan compliance statement","type":"pip-compliance","status":"unknown","consultation_date":"","first_published_date":"2023-06-22T10:39:00Z","last_updated_date":"2023-06-22T10:39:00Z","reference_number":"EMA/286177/2023","document_url":"https://www.ema.europa.eu/en/documents/pip-compliance/neparvis-epar-paediatric-investigation-plan-compliance-statement_en.pdf"},
    {"id":"59034","name":"Entresto : EPAR - Paediatric investigation plan compliance statement","type":"pip-compliance","status":"unknown","consultation_date":"","first_published_date":"2023-06-22T11:15:00Z","last_updated_date":"2023-06-22T11:15:00Z","reference_number":"EMA/286179/2023","document_url":"https://www.ema.europa.eu/en/documents/pip-compliance/entresto-epar-paediatric-investigation-plan-compliance-statement_en.pdf"},
    {"id":"59286","name":"Esperoct: EPAR - Statement indicating compliance with the agreed completed paediatric investigation plan","type":"pip-compliance","status":"unknown","consultation_date":"","first_published_date":"2023-07-06T16:22:00Z","last_updated_date":"2023-07-06T16:22:00Z","reference_number":"EMA/82756/2023","document_url":"https://www.ema.europa.eu/en/documents/pip-compliance/esperoct-epar-statement-indicating-compliance-agreed-completed-paediatric-investigation-plan_en.pdf"},
    {"id":"59464","name":"Vipidia : EPAR - Paediatric investigation plan compliance statement","type":"pip-compliance","status":"unknown","consultation_date":"","first_published_date":"2023-07-21T17:17:00Z","last_updated_date":"2023-07-21T17:17:00Z","reference_number":"EMA/CHMP/232792/2023","document_url":"https://www.ema.europa.eu/en/documents/pip-compliance/vipidia-epar-paediatric-investigation-plan-compliance-statement_en.pdf"},
    {"id":"59533","name":"Ofev : EPAR - Paediatric investigation plan compliance statement","type":"pip-compliance","status":"unknown","consultation_date":"","first_published_date":"2023-08-01T09:06:00Z","last_updated_date":"2023-08-01T09:06:00Z","reference_number":"EMA/CHMP/269668/2023","document_url":"https://www.ema.europa.eu/en/documents/pip-compliance/ofev-epar-paediatric-investigation-plan-compliance-statement_en.pdf"},
    {"id":"59572","name":"Soliris : EPAR - Paediatric investigation plan compliance statement","type":"pip-compliance","status":"unknown","consultation_date":"","first_published_date":"2023-08-08T17:50:00Z","last_updated_date":"2023-08-08T17:50:00Z","reference_number":"EMA/319068/2023","document_url":"https://www.ema.europa.eu/en/documents/pip-compliance/soliris-epar-paediatric-investigation-plan-compliance-statement_en.pdf"},
    {"id":"59590","name":"Mircera : EPAR - Paediatric investigation plan compliance statement","type":"pip-compliance","status":"Adopted","consultation_date":"","first_published_date":"2023-08-11T15:52:00Z","last_updated_date":"2023-08-11T15:52:00Z","reference_number":"EMA/CHMP/286711/2023","document_url":"https://www.ema.europa.eu/en/documents/pip-compliance/mircera-epar-paediatric-investigation-plan-compliance-statement_en.pdf"},
    {"id":"60699","name":"Briviact : EPAR - Paediatric investigation plan compliance statement","type":"pip-compliance","status":"unknown","consultation_date":"","first_published_date":"2023-04-04T15:52:00Z","last_updated_date":"2023-04-04T15:52:00Z","reference_number":"EMA/CHMP/119919/2023","document_url":"https://www.ema.europa.eu/en/documents/pip-compliance/briviact-epar-paediatric-investigation-plan-compliance-statement_en.pdf"},
    {"id":"60701","name":"Artesunate Amivas : EPAR - Statement indicating compliance with the agreed completed paediatric investigation plan","type":"pip-compliance","status":"unknown","consultation_date":"","first_published_date":"2023-04-24T14:07:00Z","last_updated_date":"2023-04-24T14:07:00Z","reference_number":"EMA/97317/2023","document_url":"https://www.ema.europa.eu/en/documents/pip-compliance/artesunate-amivas-epar-statement-indicating-compliance-agreed-completed-paediatric-investigation-plan_en.pdf"},
    {"id":"60718","name":"Eliquis : EPAR - Paediatric investigation plan compliance statement","type":"pip-compliance","status":"unknown","consultation_date":"","first_published_date":"2023-06-23T09:31:00Z","last_updated_date":"2023-06-23T09:31:00Z","reference_number":"EMA/CHMP/231524/2023","document_url":"https://www.ema.europa.eu/en/documents/pip-compliance/eliquis-epar-paediatric-investigation-plan-compliance-statement_en.pdf"},
    {"id":"60731","name":"Kovaltry : EPAR - Paediatric investigation plan compliance statement","type":"pip-compliance","status":"unknown","consultation_date":"","first_published_date":"2023-07-26T11:38:00Z","last_updated_date":"2023-07-26T11:38:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/pip-compliance/kovaltry-epar-paediatric-investigation-plan-compliance-statement_en.pdf"},
    {"id":"60779","name":"Refixia : EPAR - Paediatric investigation plan compliance statement","type":"pip-compliance","status":"unknown","consultation_date":"","first_published_date":"2023-11-06T16:10:00Z","last_updated_date":"2023-11-06T16:10:00Z","reference_number":"EMA/CHMP/278050/2023","document_url":"https://www.ema.europa.eu/en/documents/pip-compliance/refixia-epar-paediatric-investigation-plan-compliance-statement_en.pdf"},
    {"id":"60977","name":"Vimizim : EPAR - Statement indicating compliance with the agreed completed paediatric investigation plan","type":"pip-compliance","status":"unknown","consultation_date":"","first_published_date":"2023-11-20T12:17:25Z","last_updated_date":"2023-11-20T12:17:25Z","reference_number":"EMA/CHMP/372980/2023","document_url":"https://www.ema.europa.eu/en/documents/pip-compliance/vimizim-epar-statement-indicating-compliance-agreed-completed-paediatric-investigation-plan_en.pdf"},
    {"id":"61251","name":"Finlee: EPAR - Paediatric investigation plan compliance statement","type":"pip-compliance","status":"unknown","consultation_date":"","first_published_date":"2023-12-05T14:33:03Z","last_updated_date":"2023-12-05T14:33:03Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/pip-compliance/finlee-epar-paediatric-investigation-plan-compliance-statement_en.pdf"},
    {"id":"61683","name":"Roteas : EPAR - Statement indicating compliance with the agreed completed paediatric investigation plan (WS2409)","type":"pip-compliance","status":"unknown","consultation_date":"","first_published_date":"2024-01-10T12:10:15Z","last_updated_date":"2024-01-10T12:10:15Z","reference_number":"EMA/CHMP/446134/2023","document_url":"https://www.ema.europa.eu/en/documents/pip-compliance/roteas-epar-statement-indicating-compliance-agreed-completed-paediatric-investigation-plan-ws2409_en.pdf"},
    {"id":"61692","name":"Lixiana : EPAR - Paediatric investigation plan compliance statement","type":"pip-compliance","status":"unknown","consultation_date":"","first_published_date":"2024-01-10T13:17:26Z","last_updated_date":"2024-01-10T13:17:26Z","reference_number":"EMA/10588/2024","document_url":"https://www.ema.europa.eu/en/documents/pip-compliance/lixiana-epar-paediatric-investigation-plan-compliance-statement_en.pdf"},
    {"id":"61780","name":"Brintellix : EPAR - Statement indicating compliance with the agreed completed paediatric investigation plan (IB-40)","type":"pip-compliance","status":"unknown","consultation_date":"","first_published_date":"2024-01-16T13:17:40Z","last_updated_date":"2024-01-16T13:17:40Z","reference_number":"EMA/13649/2024","document_url":"https://www.ema.europa.eu/en/documents/pip-compliance/brintellix-epar-statement-indicating-compliance-agreed-completed-paediatric-investigation-plan-ib-40_en.pdf"},
    {"id":"61800","name":"Spexotras : EPAR - Statement indicating compliance with the agreed completed paediatric investigation plan","type":"pip-compliance","status":"unknown","consultation_date":"","first_published_date":"2024-01-17T14:36:11Z","last_updated_date":"2024-01-17T14:36:11Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/pip-compliance/spexotras-epar-statement-indicating-compliance-agreed-completed-paediatric-investigation-plan_en.pdf"},
    {"id":"61948","name":"Filsuvez : EPAR - Statement indicating compliance with the agreed completed paediatric investigation plan","type":"pip-compliance","status":"unknown","consultation_date":"","first_published_date":"2024-01-30T08:26:02Z","last_updated_date":"2024-01-30T08:26:02Z","reference_number":"EMA/CHMP/549864/2023","document_url":"https://www.ema.europa.eu/en/documents/pip-compliance/filsuvez-epar-statement-indicating-compliance-agreed-completed-paediatric-investigation-plan_en.pdf"},
    {"id":"63336","name":"Sarclisa : EPAR - Statement indicating compliance with the agreed completed paediatric investigation plan","type":"pip-compliance","status":"unknown","consultation_date":"","first_published_date":"2024-05-28T13:16:00Z","last_updated_date":"2024-05-28T13:16:00Z","reference_number":"EMA/CHMP/137460/2024","document_url":"https://www.ema.europa.eu/en/documents/pip-compliance/sarclisa-epar-statement-indicating-compliance-agreed-completed-paediatric-investigation-plan_en.pdf"},
    {"id":"63493","name":"Beyfortus : EPAR - Statement indicating compliance with the agreed completed paediatric investigation plan","type":"pip-compliance","status":"unknown","consultation_date":"","first_published_date":"2024-06-05T14:34:00Z","last_updated_date":"2024-06-05T14:34:00Z","reference_number":"EMA/182502/2024","document_url":"https://www.ema.europa.eu/en/documents/pip-compliance/beyfortus-epar-statement-indicating-compliance-agreed-completed-paediatric-investigation-plan_en.pdf"},
    {"id":"64787","name":"Cresemba : EPAR - Statement indicating compliance with the agreed completed paediatric investigation plan","type":"pip-compliance","status":"unknown","consultation_date":"","first_published_date":"2024-09-11T11:30:00Z","last_updated_date":"2024-09-11T11:30:00Z","reference_number":"EMA/CHMP/298354/2024","document_url":"https://www.ema.europa.eu/en/documents/pip-compliance/cresemba-epar-statement-indicating-compliance-agreed-completed-paediatric-investigation-plan_en.pdf"},
    {"id":"65266","name":"Spevigo : EPAR - Statement indicating compliance with the agreed completed paediatric investigation plan","type":"pip-compliance","status":"unknown","consultation_date":"","first_published_date":"2024-10-10T13:06:00Z","last_updated_date":"2024-10-10T13:06:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/pip-compliance/spevigo-epar-statement-indicating-compliance-agreed-completed-paediatric-investigation-plan_en.pdf"},
    {"id":"65297","name":"Takhzyro : EPAR - Statement indicating compliance with the agreed completed paediatric investigation plan","type":"pip-compliance","status":"unknown","consultation_date":"","first_published_date":"2024-10-15T15:20:00Z","last_updated_date":"2024-10-15T15:20:00Z","reference_number":"EMA/CHMP/424426/2023","document_url":"https://www.ema.europa.eu/en/documents/pip-compliance/takhzyro-epar-statement-indicating-compliance-agreed-completed-paediatric-investigation-plan_en.pdf"},
    {"id":"66857","name":"Prevenar 20 : EPAR - Statement indicating compliance with the agreed completed paediatric investigation plan","type":"pip-compliance","status":"unknown","consultation_date":"","first_published_date":"2025-02-19T08:47:54Z","last_updated_date":"2025-02-19T08:47:54Z","reference_number":"EMA/CHMP/58317/2025","document_url":"https://www.ema.europa.eu/en/documents/pip-compliance/prevenar-20-epar-statement-indicating-compliance-agreed-completed-paediatric-investigation-plan_en.pdf"},
    {"id":"67376","name":"Drovelis : EPAR - Statement indicating compliance with the agreed completed paediatric investigation plan","type":"pip-compliance","status":"unknown","consultation_date":"","first_published_date":"2025-03-21T11:13:16Z","last_updated_date":"2025-03-21T11:13:16Z","reference_number":"EMA/39693/2025","document_url":"https://www.ema.europa.eu/en/documents/pip-compliance/drovelis-epar-statement-indicating-compliance-agreed-completed-paediatric-investigation-plan_en.pdf"},
    {"id":"67547","name":"Lydisilka : EPAR - Statement indicating compliance with the agreed completed paediatric investigation plan","type":"pip-compliance","status":"unknown","consultation_date":"","first_published_date":"2025-03-28T16:42:06Z","last_updated_date":"2025-03-28T16:42:06Z","reference_number":"EMA/39706/2025","document_url":"https://www.ema.europa.eu/en/documents/pip-compliance/lydisilka-epar-statement-indicating-compliance-agreed-completed-paediatric-investigation-plan_en.pdf"},
    {"id":"68339","name":"Bylvay : EPAR - Statement indicating compliance with the agreed completed paediatric investigation plan","type":"pip-compliance","status":"unknown","consultation_date":"","first_published_date":"2025-05-19T11:10:26Z","last_updated_date":"2025-05-19T11:10:26Z","reference_number":"EMA/CHMP/89429/2025","document_url":"https://www.ema.europa.eu/en/documents/pip-compliance/bylvay-epar-statement-indicating-compliance-agreed-completed-paediatric-investigation-plan_en.pdf"},
    {"id":"69639","name":"Kalydeco : EPAR - Statement indicating compliance with the agreed completed paediatric investigation plan","type":"pip-compliance","status":"unknown","consultation_date":"","first_published_date":"2025-08-04T12:57:30Z","last_updated_date":"2025-08-04T12:57:30Z","reference_number":"EMADOC-1700519818-2240068","document_url":"https://www.ema.europa.eu/en/documents/pip-compliance/kalydeco-epar-statement-indicating-compliance-agreed-completed-paediatric-investigation-plan_en.pdf"},
    {"id":"70301","name":"Voranigo : EPAR - Statement indicating compliance with the agreed completed paediatric investigation plan","type":"pip-compliance","status":"unknown","consultation_date":"","first_published_date":"2025-09-26T14:47:34Z","last_updated_date":"2025-09-26T14:47:34Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/pip-compliance/voranigo-epar-statement-indicating-compliance-agreed-completed-paediatric-investigation-plan_en.pdf"},
    {"id":"70310","name":"Xalkori : EPAR - Statement indicating compliance with the agreed completed paediatric investigation plan","type":"pip-compliance","status":"unknown","consultation_date":"","first_published_date":"2025-09-29T08:38:17Z","last_updated_date":"2025-09-29T08:38:17Z","reference_number":"EMADOC-1700519818-2457012","document_url":"https://www.ema.europa.eu/en/documents/pip-compliance/xalkori-epar-statement-indicating-compliance-agreed-completed-paediatric-investigation-plan_en.pdf"},
    {"id":"71002","name":"Braftovi : EPAR - Statement indicating compliance with the agreed completed paediatric investigation plan","type":"pip-compliance","status":"unknown","consultation_date":"","first_published_date":"2025-11-05T10:37:10Z","last_updated_date":"2025-11-05T10:37:10Z","reference_number":"EMADOC-1700519818-2438413","document_url":"https://www.ema.europa.eu/en/documents/pip-compliance/braftovi-epar-statement-indicating-compliance-agreed-completed-paediatric-investigation-plan_en.pdf"},
    {"id":"71004","name":"Mektovi : EPAR - Statement indicating compliance with the agreed completed paediatric investigation plan","type":"pip-compliance","status":"unknown","consultation_date":"","first_published_date":"2025-11-05T10:44:59Z","last_updated_date":"2025-11-05T10:44:59Z","reference_number":"EMADOC-1700519818-2438413","document_url":"https://www.ema.europa.eu/en/documents/pip-compliance/mektovi-epar-statement-indicating-compliance-agreed-completed-paediatric-investigation-plan_en.pdf"},
    {"id":"71886","name":"Tremfya : EPAR - Statement indicating compliance with the agreed completed paediatric investigation plan","type":"pip-compliance","status":"unknown","consultation_date":"","first_published_date":"2025-12-19T15:12:46Z","last_updated_date":"2025-12-19T15:12:46Z","reference_number":"EMADOC-1700519818-2494684","document_url":"https://www.ema.europa.eu/en/documents/pip-compliance/tremfya-epar-statement-indicating-compliance-agreed-completed-paediatric-investigation-plan_en.pdf"},
    {"id":"72481","name":"Winlevi : EPAR - Statement indicating compliance with the agreed completed  paediatric investigation plan","type":"pip-compliance","status":"unknown","consultation_date":"","first_published_date":"2026-02-10T11:28:43Z","last_updated_date":"2026-02-10T11:28:43Z","reference_number":"EMA/CHMP/278079/2025","document_url":"https://www.ema.europa.eu/en/documents/pip-compliance/winlevi-epar-statement-indicating-compliance-agreed-completed-paediatric-investigation-plan_en.pdf"},
    {"id":"72498","name":"Plegridy : EPAR - Statement indicating compliance with the agreed completed paediatric investigation plan","type":"pip-compliance","status":"unknown","consultation_date":"","first_published_date":"2026-02-11T09:03:43Z","last_updated_date":"2026-02-11T09:03:43Z","reference_number":"EMADOC-1700519818-2712795","document_url":"https://www.ema.europa.eu/en/documents/pip-compliance/plegridy-epar-statement-indicating-compliance-agreed-completed-paediatric-investigation-plan_en.pdf"},
    {"id":"73144","name":"Rxulti : EPAR - Statement indicating compliance with the agreed completed paediatric investigation plan","type":"pip-compliance","status":"unknown","consultation_date":"","first_published_date":"2026-03-23T13:01:18Z","last_updated_date":"2026-03-23T13:01:18Z","reference_number":"EMADOC-1700519818-3014087","document_url":"https://www.ema.europa.eu/en/documents/pip-compliance/rxulti-epar-statement-indicating-compliance-agreed-completed-paediatric-investigation-plan_en.pdf"},
    {"id":"73170","name":"Stivarga : EPAR - Statement indicating compliance with the agreed completed paediatric investigation plan","type":"pip-compliance","status":"unknown","consultation_date":"","first_published_date":"2026-03-24T15:14:52Z","last_updated_date":"2026-03-24T15:14:52Z","reference_number":"EMADOC-1700519818-2940864","document_url":"https://www.ema.europa.eu/en/documents/pip-compliance/stivarga-epar-statement-indicating-compliance-agreed-completed-paediatric-investigation-plan_en.pdf"},
    {"id":"73351","name":"Doptelet : EPAR - Statement indicating compliance with the agreed completed paediatric investigation plan","type":"pip-compliance","status":"unknown","consultation_date":"","first_published_date":"2026-04-08T13:50:42Z","last_updated_date":"2026-04-08T13:50:42Z","reference_number":"EMADOC-1700519818-3014602","document_url":"https://www.ema.europa.eu/en/documents/pip-compliance/doptelet-epar-statement-indicating-compliance-agreed-completed-paediatric-investigation-plan_en.pdf"},
    {"id":"73476","name":"Livmarli : EPAR - Statement indicating compliance with the agreed completed paediatric investigation plan","type":"pip-compliance","status":"unknown","consultation_date":"","first_published_date":"2026-04-17T14:35:32Z","last_updated_date":"2026-04-17T14:35:32Z","reference_number":"EMA/354363/2025","document_url":"https://www.ema.europa.eu/en/documents/pip-compliance/livmarli-epar-statement-indicating-compliance-agreed-completed-paediatric-investigation-plan_en.pdf"},
    {"id":"73536","name":"Taltz : EPAR - Statement indicating compliance with the agreed completed paediatric investigation plan","type":"pip-compliance","status":"unknown","consultation_date":"","first_published_date":"2026-04-23T12:32:52Z","last_updated_date":"2026-04-23T12:32:52Z","reference_number":"EMADOC-1700519818-2999860","document_url":"https://www.ema.europa.eu/en/documents/pip-compliance/taltz-epar-statement-indicating-compliance-agreed-completed-paediatric-investigation-plan_en.pdf"},
    {"id":"73754","name":"Tafinlar : EPAR - Statement indicating compliance with the agreed completed paediatric investigation plan","type":"pip-compliance","status":"unknown","consultation_date":"","first_published_date":"2026-05-19T11:54:33Z","last_updated_date":"2026-05-19T11:54:33Z","reference_number":"EMADOC-1700519818-3039069","document_url":"https://www.ema.europa.eu/en/documents/pip-compliance/tafinlar-epar-statement-indicating-compliance-agreed-completed-paediatric-investigation-plan_en.pdf"},
    {"id":"73770","name":"Mekinist : EPAR - Statement indicating compliance with the agreed completed paediatric investigation plan","type":"pip-compliance","status":"unknown","consultation_date":"","first_published_date":"2026-05-19T16:37:18Z","last_updated_date":"2026-05-19T16:37:18Z","reference_number":"EMADOC-1700519818-3039069","document_url":"https://www.ema.europa.eu/en/documents/pip-compliance/mekinist-epar-statement-indicating-compliance-agreed-completed-paediatric-investigation-plan_en.pdf"},
    {"id":"73788","name":"Kisqali : EPAR - Statement indicating compliance with the agreed completed paediatric investigation plan","type":"pip-compliance","status":"unknown","consultation_date":"","first_published_date":"2026-05-21T10:52:57Z","last_updated_date":"2026-05-21T10:52:57Z","reference_number":"EMADOC-1700519818-3015561","document_url":"https://www.ema.europa.eu/en/documents/pip-compliance/kisqali-epar-statement-indicating-compliance-agreed-completed-paediatric-investigation-plan_en.pdf"},
    {"id":"73864","name":"Verzenios : EPAR - Statement indicating compliance with the agreed completed paediatric investigation plan","type":"pip-compliance","status":"unknown","consultation_date":"","first_published_date":"2026-05-27T14:29:33Z","last_updated_date":"2026-05-27T14:29:33Z","reference_number":"EMADOC-1700519818-3051385","document_url":"https://www.ema.europa.eu/en/documents/pip-compliance/verzenios-epar-statement-indicating-compliance-agreed-completed-paediatric-investigation-plan_en.pdf"},
    {"id":"73960","name":"Lynparza : EPAR - Statement indicating compliance with the agreed completed paediatric investigation plan","type":"pip-compliance","status":"unknown","consultation_date":"","first_published_date":"2026-06-03T15:37:20Z","last_updated_date":"2026-06-03T15:37:20Z","reference_number":"EMADOC-1700519818-3211686","document_url":"https://www.ema.europa.eu/en/documents/pip-compliance/lynparza-epar-statement-indicating-compliance-agreed-completed-paediatric-investigation-plan_en.pdf"},
    {"id":"2398","name":"Abseamed : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-10-13T02:00:00Z","last_updated_date":"2025-07-11T17:02:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/abseamed-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"2422","name":"NeuroBloc : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-08-25T02:09:00Z","last_updated_date":"2023-05-04T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/neurobloc-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"2509","name":"Ranexa : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-09-14T02:00:00Z","last_updated_date":"2022-08-11T13:08:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/ranexa-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"2557","name":"Kanuma : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2015-11-12T01:00:00Z","last_updated_date":"2026-03-24T15:52:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/kanuma-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"2595","name":"Prevenar : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-10-08T16:25:00Z","last_updated_date":"2017-11-24T15:25:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/prevenar-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"2619","name":"Karvea : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-05-06T02:00:00Z","last_updated_date":"2025-02-14T14:54:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/karvea-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"2655","name":"Zerene : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-07-08T03:09:00Z","last_updated_date":"2012-10-15T03:09:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/zerene-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"2672","name":"Alprolix : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2016-11-24T17:15:00Z","last_updated_date":"2025-05-02T14:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/alprolix-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"2676","name":"Suvaxyn CSF Marker : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2015-07-20T02:00:00Z","last_updated_date":"2025-09-02T15:55:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/suvaxyn-csf-marker-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf-0"},
    {"id":"2695","name":"Refludan : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-04-27T02:00:00Z","last_updated_date":"2012-07-27T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/refludan-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"2754","name":"Ketoconazole Esteve : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2015-04-22T02:00:00Z","last_updated_date":"2025-01-14T12:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/ketoconazole-esteve-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"2781","name":"Darunavir Mylan : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2017-07-05T02:00:00Z","last_updated_date":"2024-05-13T12:30:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/darunavir-mylan-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"2901","name":"Mycamine : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-12-16T00:09:00Z","last_updated_date":"2025-08-04T12:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/mycamine-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
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    {"id":"3627","name":"Sifrol : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-11-17T01:00:00Z","last_updated_date":"2018-03-22T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/sifrol-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
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    {"id":"3794","name":"RevitaCAM : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2012-09-28T02:00:00Z","last_updated_date":"2016-05-30T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/revitacam-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"3797","name":"Nespo : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-01-29T00:09:21Z","last_updated_date":"2009-01-29T00:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/nespo-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"3920","name":"Jinarc : EPAR - Procedural steps taken and scientific information after authorisation (archived)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2016-09-29T02:00:00Z","last_updated_date":"2025-04-03T14:37:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/jinarc-epar-procedural-steps-taken-scientific-information-after-authorisation-archived_en.pdf"},
    {"id":"3926","name":"Darzalex : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2017-06-02T15:55:00Z","last_updated_date":"2025-08-29T17:19:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/darzalex-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"3928","name":"Entresto : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2016-03-17T01:00:00Z","last_updated_date":"2025-05-14T16:49:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/entresto-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"3964","name":"Bosulif : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2014-04-10T02:00:00Z","last_updated_date":"2025-08-26T15:43:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/bosulif-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"4015","name":"ChondroCelect : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2011-10-21T02:00:00Z","last_updated_date":"2017-01-12T18:09:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/chondrocelect-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"4085","name":"Zonisamide Viatris : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2017-04-03T02:00:00Z","last_updated_date":"2025-10-22T11:26:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/zonisamide-viatris-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"4115","name":"Tadalafil Lilly : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2017-07-11T02:00:00Z","last_updated_date":"2026-01-28T13:35:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/tadalafil-lilly-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"4135","name":"Rapiscan : EPAR - Procedural steps taken and scientific information after authorisation (archived)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2011-03-31T02:00:00Z","last_updated_date":"2023-05-25T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/rapiscan-epar-procedural-steps-taken-scientific-information-after-authorisation-archived_en.pdf"},
    {"id":"4140","name":"Integrilin : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-12-01T01:00:00Z","last_updated_date":"2022-03-17T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/integrilin-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"4158","name":"Ribavirin Teva : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-11-16T01:00:00Z","last_updated_date":"2021-07-09T11:55:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/ribavirin-teva-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"4160","name":"Zalviso : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2016-05-19T02:00:00Z","last_updated_date":"2022-09-27T11:22:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/zalviso-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"4161","name":"Neuraceq : EPAR - Procedural steps taken and scientific information after authorisation (archived)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2014-04-10T02:00:00Z","last_updated_date":"2024-05-15T10:14:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/neuraceq-epar-procedural-steps-taken-scientific-information-after-authorisation-archived_en.pdf"},
    {"id":"4189","name":"Fasturtec : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-03-12T00:09:00Z","last_updated_date":"2024-08-12T16:39:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/fasturtec-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"4199","name":"Episalvan : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2017-03-16T01:00:00Z","last_updated_date":"2022-07-15T13:33:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/episalvan-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"4217","name":"Eravac : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2017-07-11T02:00:00Z","last_updated_date":"2025-09-02T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/eravac-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"4262","name":"Inflacam : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2016-11-14T10:43:00Z","last_updated_date":"2025-10-08T10:43:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/inflacam-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"4264","name":"Invanz : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-10-28T02:00:00Z","last_updated_date":"2024-06-26T12:38:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/invanz-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"4291","name":"Flebogamma DIF : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-08-18T02:00:00Z","last_updated_date":"2023-11-06T12:45:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/flebogamma-dif-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"4314","name":"Brinavess : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2011-07-21T02:00:00Z","last_updated_date":"2025-03-07T11:17:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/brinavess-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"4332","name":"Cialis : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2008-11-13T00:09:00Z","last_updated_date":"2026-01-28T14:23:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/cialis-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"4347","name":"Bovalto Ibraxion : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2008-04-04T02:00:00Z","last_updated_date":"2019-08-13T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/bovalto-ibraxion-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"4378","name":"Jentadueto : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2012-11-08T01:00:00Z","last_updated_date":"2025-05-08T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/jentadueto-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"4386","name":"Draxxin : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2008-10-03T02:09:00Z","last_updated_date":"2025-09-04T16:10:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/draxxin-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"4392","name":"Orencia : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2007-06-05T02:00:00Z","last_updated_date":"2026-05-11T12:30:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/orencia-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
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    {"id":"4770","name":"Combivir : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-04-28T02:09:00Z","last_updated_date":"2022-08-29T15:25:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/combivir-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
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    {"id":"4842","name":"Kevzara : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2017-09-26T02:00:00Z","last_updated_date":"2025-03-28T13:23:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/kevzara-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
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    {"id":"4925","name":"Eviplera : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2012-11-16T16:00:00Z","last_updated_date":"2025-12-09T11:55:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/eviplera-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"4932","name":"Erivedge : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2014-07-28T02:00:00Z","last_updated_date":"2025-11-05T17:19:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/erivedge-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"4956","name":"Capecitabine Accord : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2013-06-24T15:05:00Z","last_updated_date":"2025-05-05T14:05:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/capecitabine-accord-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"4993","name":"Xolair : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-08-26T13:00:00Z","last_updated_date":"2025-05-28T10:32:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/xolair-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"5021","name":"Relistor : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-08-04T02:00:00Z","last_updated_date":"2026-01-19T12:30:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/relistor-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"5041","name":"Actrapid : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-02-18T01:00:00Z","last_updated_date":"2020-10-21T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/actrapid-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"5050","name":"NovoMix : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2008-08-21T02:00:00Z","last_updated_date":"2023-08-29T13:33:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/novomix-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"5117","name":"Purevax RCPCh FeLV : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2010-01-26T01:00:00Z","last_updated_date":"2024-10-11T16:20:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/purevax-rcpch-felv-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"5128","name":"Galliprant : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2018-05-30T02:00:00Z","last_updated_date":"2025-10-07T11:30:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/galliprant-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"5129","name":"Silgard : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-09-25T02:00:00Z","last_updated_date":"2019-04-02T17:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/silgard-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"5187","name":"Urorec : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2010-06-22T13:16:00Z","last_updated_date":"2025-05-07T08:41:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/urorec-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"5200","name":"MabCampath : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-08-03T02:09:21Z","last_updated_date":"2012-08-15T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/mabcampath-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"5227","name":"Zulvac 1+8 Ovis : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2011-08-30T02:00:00Z","last_updated_date":"2025-10-15T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/zulvac-18-ovis-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"5264","name":"Xagrid : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-11-20T00:09:00Z","last_updated_date":"2023-02-20T12:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/xagrid-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"5270","name":"ReFacto AF : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-07-22T02:00:00Z","last_updated_date":"2025-03-05T15:13:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/refacto-af-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"5276","name":"Sprycel : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-08-18T03:00:00Z","last_updated_date":"2025-05-15T14:07:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/sprycel-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"5285","name":"Caprelsa : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2013-02-28T16:00:00Z","last_updated_date":"2024-09-23T15:48:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/caprelsa-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"5290","name":"Tenofovir disoproxil Mylan : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2017-05-10T16:05:00Z","last_updated_date":"2024-07-19T09:10:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/tenofovir-disoproxil-mylan-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"5303","name":"Venclyxto : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2017-07-17T16:16:00Z","last_updated_date":"2025-10-22T16:52:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/venclyxto-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"5352","name":"Eperzan : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2014-10-06T02:00:00Z","last_updated_date":"2019-02-20T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/eperzan-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"5361","name":"Sprimeo HCT : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2012-08-28T02:00:00Z","last_updated_date":"2012-08-28T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/sprimeo-hct-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"5388","name":"Komboglyze : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2012-06-12T15:30:00Z","last_updated_date":"2024-04-09T10:42:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/komboglyze-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"5402","name":"Ryzodeg : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2013-10-25T02:00:00Z","last_updated_date":"2024-05-30T12:31:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/ryzodeg-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"5426","name":"Neupro : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-12-21T01:00:00Z","last_updated_date":"2024-08-01T15:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/neupro-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"5514","name":"Simbrinza : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2015-03-13T01:00:00Z","last_updated_date":"2025-09-02T11:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/simbrinza-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"5525","name":"Beromun : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2007-10-10T02:09:00Z","last_updated_date":"2022-01-11T01:09:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/beromun-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"5660","name":"Tafinlar : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2013-09-18T02:00:00Z","last_updated_date":"2025-07-23T15:30:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/tafinlar-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"5679","name":"Controloc Control : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2011-06-23T02:00:00Z","last_updated_date":"2023-05-25T09:09:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/controloc-control-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"5705","name":"Helicobacter Test INFAI : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-07-14T02:09:00Z","last_updated_date":"2026-02-06T11:55:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/helicobacter-test-infai-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"5710","name":"Abraxane : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-08-10T03:00:00Z","last_updated_date":"2026-01-21T09:39:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/abraxane-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"5747","name":"Onsenal : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-11-09T01:00:00Z","last_updated_date":"2011-04-06T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/onsenal-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"5805","name":"Imvanex : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2014-08-14T02:00:00Z","last_updated_date":"2025-06-16T01:16:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/imvanex-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"5844","name":"Amlodipine  / Valsartan Mylan  : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2017-02-06T12:53:00Z","last_updated_date":"2025-07-24T12:43:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/amlodipine-valsartan-mylan-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
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    {"id":"5890","name":"Adasuve : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2013-12-10T02:00:00Z","last_updated_date":"2025-10-09T17:35:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/adasuve-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"5908","name":"Nuwiq : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2015-11-26T01:00:00Z","last_updated_date":"2026-05-21T16:45:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/nuwiq-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"5923","name":"Wilzin : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2007-10-11T02:00:00Z","last_updated_date":"2024-12-18T15:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/wilzin-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"5953","name":"Xaluprine : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2012-09-27T02:00:00Z","last_updated_date":"2025-08-20T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/xaluprine-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
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    {"id":"5988","name":"Raxone : EPAR - Procedural steps taken and scientific information after authorisation (archived)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2018-04-26T02:00:00Z","last_updated_date":"2024-08-21T15:24:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/raxone-epar-procedural-steps-taken-scientific-information-after-authorisation-archived_en.pdf"},
    {"id":"6055","name":"Credelio : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2018-07-26T02:00:00Z","last_updated_date":"2024-06-03T12:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/credelio-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"6069","name":"Clopidogrel Teva Pharma: EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2010-06-11T02:00:00Z","last_updated_date":"2016-02-26T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/clopidogrel-teva-pharma-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"6089","name":"Teysuno : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2011-11-08T01:00:00Z","last_updated_date":"2025-05-21T14:30:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/teysuno-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"6091","name":"Rotarix : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-10-05T02:00:00Z","last_updated_date":"2026-04-22T10:07:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/rotarix-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"6092","name":"Blitzima : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2017-10-26T17:27:00Z","last_updated_date":"2024-12-09T15:35:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/blitzima-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"6100","name":"Picato : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2014-01-17T01:00:00Z","last_updated_date":"2020-07-31T11:22:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/picato-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"6139","name":"Unituxin : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2016-08-04T12:41:00Z","last_updated_date":"2017-04-28T12:41:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/unituxin-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"6150","name":"Ibandronic acid Sandoz : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2014-07-11T02:00:00Z","last_updated_date":"2022-07-06T12:41:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/ibandronic-acid-sandoz-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"6158","name":"Imbruvica : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2015-04-23T02:00:00Z","last_updated_date":"2025-10-27T11:10:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/imbruvica-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"6210","name":"Levetiracetam Actavis : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2012-05-24T13:36:00Z","last_updated_date":"2025-06-30T13:25:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/levetiracetam-actavis-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"6224","name":"Odomzo : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2016-03-07T01:00:00Z","last_updated_date":"2025-11-17T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/odomzo-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"6246","name":"Wakix : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2016-11-30T18:25:00Z","last_updated_date":"2025-09-05T16:52:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/wakix-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"6248","name":"Darunavir Krka : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2018-07-06T02:00:00Z","last_updated_date":"2025-01-28T14:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/darunavir-krka-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"6256","name":"Olanzapine Apotex : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2011-02-25T01:00:00Z","last_updated_date":"2023-03-09T10:30:00Z","reference_number":"EMA/175903/2020","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/olanzapine-apotex-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"6277","name":"Pregabalin Zentiva : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2017-07-20T02:00:00Z","last_updated_date":"2026-02-16T15:40:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/pregabalin-zentiva-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"6291","name":"Kogenate Bayer : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-11-12T01:00:00Z","last_updated_date":"2018-05-04T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/kogenate-bayer-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"6346","name":"Bortezomib Accord : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2016-06-20T02:00:00Z","last_updated_date":"2025-04-01T10:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/bortezomib-accord-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"6427","name":"Izba : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2017-05-05T02:00:00Z","last_updated_date":"2025-01-27T14:30:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/izba-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"6462","name":"Tesavel : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-12-08T01:09:00Z","last_updated_date":"2025-12-01T12:08:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/tesavel-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"6537","name":"Porcilis PCV ID : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2018-04-24T02:00:00Z","last_updated_date":"2024-10-14T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/porcilis-pcv-id-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"6552","name":"Docetaxel Zentiva (previously Docetaxel Winthrop) : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-01-16T01:00:00Z","last_updated_date":"2022-05-20T15:57:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/docetaxel-zentiva-previously-docetaxel-winthrop-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"6572","name":"Cimalgex : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2016-01-14T01:00:00Z","last_updated_date":"2025-03-17T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/cimalgex-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"6582","name":"Topotecan Hospira : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2012-03-05T01:00:00Z","last_updated_date":"2025-09-04T11:52:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/topotecan-hospira-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"6616","name":"Dexdomitor : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-11-20T00:09:00Z","last_updated_date":"2024-09-17T19:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/dexdomitor-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"6686","name":"Symtuza : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2017-12-06T10:53:00Z","last_updated_date":"2024-07-25T13:13:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/symtuza-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"6701","name":"Actelsar HCT : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2014-07-23T02:00:00Z","last_updated_date":"2025-02-12T15:15:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/actelsar-hct-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"6746","name":"Cerezyme : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2003-08-28T19:00:00Z","last_updated_date":"2025-12-01T11:15:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/cerezyme-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"6763","name":"Twinrix Adult : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2008-07-09T03:09:00Z","last_updated_date":"2024-02-07T10:45:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/twinrix-adult-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"6842","name":"Plenadren : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2012-09-13T02:00:00Z","last_updated_date":"2023-10-11T10:40:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/plenadren-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"6884","name":"Zomarist : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-09-21T02:09:00Z","last_updated_date":"2025-02-05T17:43:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/zomarist-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"6947","name":"Ioa : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2012-04-24T02:00:00Z","last_updated_date":"2014-08-26T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/ioa-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"6955","name":"Simponi : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2010-04-19T12:00:00Z","last_updated_date":"2026-01-30T11:52:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/simponi-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"6961","name":"Tandemact : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-10-05T02:00:00Z","last_updated_date":"2023-09-13T13:31:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/tandemact-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"7007","name":"Repaglinide Teva : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2011-05-05T02:00:00Z","last_updated_date":"2025-02-11T17:40:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/repaglinide-teva-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"7061","name":"Clopidogrel ratiopharm : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-12-01T01:00:00Z","last_updated_date":"2013-12-12T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/clopidogrel-ratiopharm-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"7135","name":"Rasagiline Mylan : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2016-06-22T02:00:00Z","last_updated_date":"2024-05-13T10:57:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/rasagiline-mylan-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"7151","name":"Edurant : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2012-11-16T16:00:00Z","last_updated_date":"2025-04-11T14:56:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/edurant-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"7192","name":"NovoEight : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2015-04-16T02:00:00Z","last_updated_date":"2021-05-19T09:38:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/novoeight-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"7218","name":"Gazyvaro : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2015-08-17T02:00:00Z","last_updated_date":"2025-10-08T10:50:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/gazyvaro-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"7232","name":"Clopidogrel 1A Pharma : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-10-13T02:00:00Z","last_updated_date":"2011-02-28T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/clopidogrel-1a-pharma-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"7241","name":"Arepanrix : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2011-10-25T02:00:00Z","last_updated_date":"2011-10-25T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/arepanrix-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
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    {"id":"7517","name":"Advocate : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-07-28T01:09:00Z","last_updated_date":"2024-01-29T15:32:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/advocate-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
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    {"id":"7694","name":"Ibandronic acid Accord : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2014-07-11T02:00:00Z","last_updated_date":"2025-03-04T12:32:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/ibandronic-acid-accord-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"7755","name":"Votubia : EPAR - Procedural steps taken and scientific information after authorisation (Archived)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2012-02-23T01:00:00Z","last_updated_date":"2024-12-06T11:28:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/votubia-epar-procedural-steps-taken-scientific-information-after-authorisation-archived_en.pdf"},
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    {"id":"8087","name":"Protopy : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2008-10-29T01:00:00Z","last_updated_date":"2008-10-29T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/protopy-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"8118","name":"Lifmior : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2017-10-18T02:00:00Z","last_updated_date":"2020-02-20T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/lifmior-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
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    {"id":"8168","name":"ProMeris Duo : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-04-28T02:09:21Z","last_updated_date":"2015-07-13T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/promeris-duo-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
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    {"id":"8488","name":"Ammonaps : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-11-09T01:00:00Z","last_updated_date":"2022-12-16T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/ammonaps-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"8532","name":"Velosulin : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2008-07-15T02:09:21Z","last_updated_date":"2008-07-15T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/velosulin-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"8632","name":"Hycamtin : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-05-12T02:09:00Z","last_updated_date":"2026-01-20T15:27:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/hycamtin-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"8675","name":"Advagraf : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-05-19T02:00:00Z","last_updated_date":"2025-02-27T10:12:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/advagraf-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"8700","name":"Ecansya : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2012-09-10T02:00:00Z","last_updated_date":"2025-05-05T10:44:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/ecansya-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"8812","name":"Avonex : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-03-19T01:00:00Z","last_updated_date":"2025-10-16T09:46:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/avonex-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"8859","name":"Ultratard : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2008-02-15T00:09:21Z","last_updated_date":"2008-02-15T00:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/ultratard-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"8863","name":"Praxbind : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2016-09-07T02:00:00Z","last_updated_date":"2026-04-23T17:26:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/praxbind-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"8877","name":"Zulvac 8 Bovis : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2011-01-10T01:00:00Z","last_updated_date":"2017-04-11T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/zulvac-8-bovis-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"8889","name":"Tevagrastim : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-10-19T02:09:00Z","last_updated_date":"2024-08-30T16:37:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/tevagrastim-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"8930","name":"Entacapone Orion : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2012-08-15T13:10:00Z","last_updated_date":"2024-09-24T12:10:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/entacapone-orion-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"8954","name":"BeneFIX : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-11-26T01:00:00Z","last_updated_date":"2025-03-07T10:36:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/benefix-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"8961","name":"Nemdatine : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2013-10-28T17:00:00Z","last_updated_date":"2024-01-17T17:14:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/nemdatine-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"8976","name":"Nivestim : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2010-09-13T02:00:00Z","last_updated_date":"2026-03-02T17:56:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/nivestim-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"8980","name":"Edarbi : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2012-06-11T02:00:00Z","last_updated_date":"2025-01-29T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/edarbi-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"9015","name":"Kalydeco : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2013-04-22T12:40:00Z","last_updated_date":"2025-08-04T01:38:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/kalydeco-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"9023","name":"Prezista : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-11-05T01:00:00Z","last_updated_date":"2024-07-26T09:47:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/prezista-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"9041","name":"Zejula : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2018-02-01T01:00:00Z","last_updated_date":"2025-11-26T13:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/zejula-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"9066","name":"Vipidia : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2014-07-15T02:00:00Z","last_updated_date":"2023-07-21T15:47:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/vipidia-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"9157","name":"Busulfan Fresenius Kabi : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2015-04-21T02:00:00Z","last_updated_date":"2025-06-30T12:06:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/busulfan-fresenius-kabi-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"9186","name":"Iasibon : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2012-03-23T01:00:00Z","last_updated_date":"2024-08-29T17:40:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/iasibon-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"9206","name":"Rituzena (previously Tuxella) : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2017-09-26T02:00:00Z","last_updated_date":"2019-02-18T16:04:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/rituzena-previously-tuxella-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"9233","name":"Bovela : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2016-10-13T02:00:00Z","last_updated_date":"2024-11-07T15:18:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/bovela-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"9252","name":"Nuedexta : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2014-08-13T02:00:00Z","last_updated_date":"2014-11-26T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/nuedexta-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
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    {"id":"9342","name":"Comfortis : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2011-08-22T02:00:00Z","last_updated_date":"2023-06-26T12:43:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/comfortis-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"9376","name":"Lamivudine/Zidovudine Teva : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2012-08-08T15:30:00Z","last_updated_date":"2023-03-21T17:26:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/lamivudinezidovudine-teva-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"9409","name":"Avandamet : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-09-01T02:00:00Z","last_updated_date":"2016-06-08T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/avandamet-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"9462","name":"Dynastat : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2010-01-08T01:00:00Z","last_updated_date":"2024-06-20T09:30:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/dynastat-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"9539","name":"Glyxambi : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2017-06-27T02:00:00Z","last_updated_date":"2025-04-01T16:30:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/glyxambi-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"9608","name":"Irbesartan BMS : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-11-26T01:00:00Z","last_updated_date":"2009-11-26T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/irbesartan-bms-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"9615","name":"Cresemba : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2017-02-23T01:00:00Z","last_updated_date":"2025-03-27T16:41:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/cresemba-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"9619","name":"Eucreas : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-09-21T02:00:00Z","last_updated_date":"2025-02-04T16:30:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/eucreas-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"9661","name":"Tasmar : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-06-04T02:09:00Z","last_updated_date":"2025-09-10T10:48:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/tasmar-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"9678","name":"Aptivus : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-12-17T01:00:00Z","last_updated_date":"2026-04-23T09:36:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/aptivus-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"9726","name":"Adrovance : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-12-07T01:00:00Z","last_updated_date":"2026-02-12T12:56:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/adrovance-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"9744","name":"Lojuxta : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2014-03-11T01:00:00Z","last_updated_date":"2025-01-27T14:26:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/lojuxta-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
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    {"id":"9781","name":"Equilis Prequenza Te : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-04-01T02:09:00Z","last_updated_date":"2025-03-07T02:09:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/equilis-prequenza-te-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
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    {"id":"9924","name":"Prepandrix : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-12-21T01:00:00Z","last_updated_date":"2019-07-26T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/prepandrix-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"9973","name":"Trevaclyn : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-09-10T02:09:00Z","last_updated_date":"2013-03-22T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/trevaclyn-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"9981","name":"Panacur AquaSol : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2013-03-04T10:00:00Z","last_updated_date":"2024-06-28T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/panacur-aquasol-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"10026","name":"Exviera : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2015-09-30T02:00:00Z","last_updated_date":"2024-10-01T15:47:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/exviera-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"10060","name":"Nimvastid : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2010-07-16T02:00:00Z","last_updated_date":"2024-01-10T12:40:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/nimvastid-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"10081","name":"Zalasta : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-12-01T00:09:00Z","last_updated_date":"2024-03-08T17:19:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/zalasta-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"10100","name":"ProteqFlu-Te : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2008-06-03T02:00:00Z","last_updated_date":"2024-10-24T10:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/proteqflu-te-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"10143","name":"Ledaga : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2017-09-05T02:00:00Z","last_updated_date":"2024-12-12T15:58:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/ledaga-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"10147","name":"Nobilis Influenza H7N1 : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-08-24T02:00:00Z","last_updated_date":"2010-07-26T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/nobilis-influenza-h7n1-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"10177","name":"Mixtard : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-02-18T01:09:00Z","last_updated_date":"2024-01-24T02:09:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/mixtard-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"10276","name":"Twynsta : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2011-09-12T13:45:00Z","last_updated_date":"2025-04-28T16:05:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/twynsta-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"10278","name":"Cyanokit : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-04-20T02:00:00Z","last_updated_date":"2025-12-16T14:19:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/cyanokit-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"10299","name":"Certifect : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2013-01-22T17:00:00Z","last_updated_date":"2018-07-27T12:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/certifect-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"10308","name":"Kolbam : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2014-09-11T02:00:00Z","last_updated_date":"2020-07-15T10:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/kolbam-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"10319","name":"Prevomax : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2018-01-31T01:00:00Z","last_updated_date":"2025-10-14T12:33:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/prevomax-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"10350","name":"Herceptin : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2008-12-18T00:09:00Z","last_updated_date":"2024-08-20T17:47:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/herceptin-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"10361","name":"Twinrix Paediatric : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2008-07-09T03:09:00Z","last_updated_date":"2024-02-07T10:40:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/twinrix-paediatric-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"10365","name":"Rydapt : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2018-02-02T01:00:00Z","last_updated_date":"2026-01-14T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/rydapt-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"10389","name":"Vizamyl : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2014-12-16T11:27:00Z","last_updated_date":"2025-09-23T14:46:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/vizamyl-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"10410","name":"Afstyla : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2017-05-10T02:00:00Z","last_updated_date":"2025-12-11T16:42:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/afstyla-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"10422","name":"Grepid : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-10-13T02:09:00Z","last_updated_date":"2025-06-23T11:57:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/grepid-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"10683","name":"BindRen : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2014-01-03T01:00:00Z","last_updated_date":"2015-04-01T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/bindren-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"10699","name":"Mepact : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2010-02-26T01:00:00Z","last_updated_date":"2025-07-17T14:30:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/mepact-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"10773","name":"Entacapone Teva : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2013-02-07T01:00:00Z","last_updated_date":"2021-09-28T17:49:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/entacapone-teva-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"10816","name":"Vaniqa : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-09-28T03:00:00Z","last_updated_date":"2024-11-27T17:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/vaniqa-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"10854","name":"Elocta : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2016-04-11T02:00:00Z","last_updated_date":"2025-04-25T16:14:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/elocta-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"10858","name":"Clopidogrel Hexal : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-10-13T02:00:00Z","last_updated_date":"2012-07-26T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/clopidogrel-hexal-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"10859","name":"Rivastigmine Actavis : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2012-01-12T01:00:00Z","last_updated_date":"2025-03-19T13:09:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/rivastigmine-actavis-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"10898","name":"Atriance : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-04-16T02:00:00Z","last_updated_date":"2024-07-26T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/atriance-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"10900","name":"Gilenya : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2011-09-02T02:00:00Z","last_updated_date":"2025-09-23T13:43:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/gilenya-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"10901","name":"Mozobil : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2010-04-15T02:00:00Z","last_updated_date":"2024-07-31T14:08:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/mozobil-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
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    {"id":"11635","name":"Fortacin : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2014-12-08T01:00:00Z","last_updated_date":"2025-02-03T11:36:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/fortacin-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"11662","name":"Prandin : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-02-18T01:00:00Z","last_updated_date":"2018-05-14T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/prandin-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"11709","name":"Kiovig : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2007-10-23T02:00:00Z","last_updated_date":"2022-06-27T13:08:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/kiovig-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"11725","name":"Ingelvac PCV FLEX : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2017-09-07T02:00:00Z","last_updated_date":"2017-11-30T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/ingelvac-pcv-flex-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"11730","name":"Incruse Ellipta : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2015-02-13T01:00:00Z","last_updated_date":"2025-07-22T12:07:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/incruse-ellipta-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"11745","name":"Xenical : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-05-04T03:00:00Z","last_updated_date":"2023-05-10T12:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/xenical-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"11782","name":"Aranesp : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-12-15T01:00:00Z","last_updated_date":"2026-01-13T14:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/aranesp-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"11804","name":"Temozolomide Teva : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2010-05-17T02:00:00Z","last_updated_date":"2022-02-18T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/temozolomide-teva-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"11806","name":"Carbaglu : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-09-21T02:09:00Z","last_updated_date":"2025-12-09T12:15:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/carbaglu-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"11867","name":"Ocrevus : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2018-04-11T02:00:00Z","last_updated_date":"2025-03-25T16:35:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/ocrevus-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"11910","name":"Rixathon : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2017-11-23T11:55:00Z","last_updated_date":"2025-05-26T15:24:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/rixathon-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"11938","name":"Desloratadine ratiopharm : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2013-10-09T02:00:00Z","last_updated_date":"2022-06-24T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/desloratadine-ratiopharm-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
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    {"id":"11957","name":"Daliresp : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2011-06-15T02:00:00Z","last_updated_date":"2018-02-06T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/daliresp-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"11989","name":"Protaphane : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-12-09T01:00:00Z","last_updated_date":"2020-10-27T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/protaphane-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"12014","name":"DuoTrav : EPAR - Procedural steps taken and scientific information after authorisation (archived)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-02-12T01:00:00Z","last_updated_date":"2025-01-07T16:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/duotrav-epar-procedural-steps-taken-scientific-information-after-authorisation-archived_en.pdf"},
    {"id":"12028","name":"Leganto : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2012-04-02T02:00:00Z","last_updated_date":"2022-02-18T16:41:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/leganto-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"12043","name":"Equioxx : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-12-03T01:00:00Z","last_updated_date":"2025-09-09T11:29:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/equioxx-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"12055","name":"Cimzia : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2010-01-21T16:40:00Z","last_updated_date":"2025-04-29T12:43:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/cimzia-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"12088","name":"Skilarence : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2018-07-11T02:00:00Z","last_updated_date":"2025-03-17T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/skilarence-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"12165","name":"Maviret : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2018-02-06T01:00:00Z","last_updated_date":"2023-03-02T13:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/maviret-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"12169","name":"Tenkasi: EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2016-03-31T02:00:00Z","last_updated_date":"2024-11-20T14:43:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/tenkasi-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"12200","name":"Versican Plus L4 : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2016-09-26T02:00:00Z","last_updated_date":"2019-05-17T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/versican-plus-l4-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"12243","name":"Clynav : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2018-08-28T02:00:00Z","last_updated_date":"2025-09-04T13:06:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/clynav-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"12258","name":"Respiporc Flu3 : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2015-01-21T01:00:00Z","last_updated_date":"2025-10-14T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/respiporc-flu3-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"12260","name":"Alecensa : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2017-05-16T15:17:00Z","last_updated_date":"2026-02-27T17:10:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/alecensa-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"12300","name":"Ebilfumin : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2014-11-14T12:49:00Z","last_updated_date":"2025-09-02T13:49:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/ebilfumin-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"12312","name":"Rivastigmine Sandoz : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2010-12-16T01:00:00Z","last_updated_date":"2024-12-18T17:41:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/rivastigmine-sandoz-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"12328","name":"Veraflox : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2012-06-26T02:00:00Z","last_updated_date":"2025-10-15T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/veraflox-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
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    {"id":"12417","name":"Zoledronic acid Teva Generics : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2014-10-06T02:00:00Z","last_updated_date":"2016-08-08T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/zoledronic-acid-teva-generics-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
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    {"id":"12508","name":"Imnovid : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2013-10-10T02:00:00Z","last_updated_date":"2025-10-06T10:42:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/imnovid-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
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    {"id":"12680","name":"Portrazza : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2016-04-13T02:00:00Z","last_updated_date":"2021-07-27T12:12:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/portrazza-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
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    {"id":"12703","name":"Raptiva : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-08-04T02:00:00Z","last_updated_date":"2009-08-04T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/raptiva-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
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    {"id":"12720","name":"Xigduo : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2014-10-10T02:00:00Z","last_updated_date":"2024-11-25T15:46:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/xigduo-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
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    {"id":"12833","name":"Novaquin : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2016-02-12T01:00:00Z","last_updated_date":"2025-10-09T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/novaquin-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"12847","name":"Yondelis : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-07-15T02:09:00Z","last_updated_date":"2025-04-03T12:25:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/yondelis-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"12870","name":"Osurnia : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2015-08-04T02:00:00Z","last_updated_date":"2025-10-09T11:57:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/osurnia-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"12932","name":"Telmisartan Teva Pharma : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2012-08-09T17:35:00Z","last_updated_date":"2021-10-26T17:50:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/telmisartan-teva-pharma-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"12971","name":"Volibris : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2010-01-19T01:00:00Z","last_updated_date":"2025-07-25T14:56:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/volibris-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"13132","name":"Rivastigmine Teva : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-07-06T03:00:00Z","last_updated_date":"2012-09-27T03:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/rivastigmine-teva-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"13133","name":"Netvax : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2011-07-11T02:00:00Z","last_updated_date":"2014-06-11T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/netvax-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"13183","name":"Voriconazole Hikma (previously Voriconazole Hospira): EPAR - Procedural steps taken and scientific information after authorisation (archived)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2016-03-23T01:00:00Z","last_updated_date":"2025-01-20T13:33:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/voriconazole-hikma-previously-voriconazole-hospira-epar-procedural-steps-taken-scientific-information-after-authorisation-archived_en.pdf"},
    {"id":"13209","name":"Ovitrelle : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-08-11T02:09:00Z","last_updated_date":"2025-05-23T17:12:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/ovitrelle-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"13223","name":"Sabervel : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2014-05-15T02:00:00Z","last_updated_date":"2014-09-29T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/sabervel-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"13297","name":"Rekovelle : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2017-06-29T02:00:00Z","last_updated_date":"2023-10-03T16:52:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/rekovelle-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"13326","name":"Arzerra : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2011-04-08T02:00:00Z","last_updated_date":"2017-08-22T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/arzerra-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"13389","name":"Uptravi : EPAR - Procedural steps taken and scientific information after authorisation (archived)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2016-10-26T19:08:00Z","last_updated_date":"2025-03-17T09:57:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/uptravi-epar-procedural-steps-taken-scientific-information-after-authorisation-archived_en.pdf"},
    {"id":"13401","name":"Clopidogrel ratiopharm : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2015-09-28T02:00:00Z","last_updated_date":"2024-03-26T10:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/clopidogrel-ratiopharm-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"13418","name":"BTVPUR AlSap 1 : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2012-05-04T02:00:00Z","last_updated_date":"2018-05-17T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/btvpur-alsap-1-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"13523","name":"Exforge : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-05-05T13:20:00Z","last_updated_date":"2025-02-12T14:07:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/exforge-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"13560","name":"Hetlioz : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2017-03-02T01:00:00Z","last_updated_date":"2022-10-11T10:38:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/hetlioz-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"13580","name":"Vimizim : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2014-09-25T02:00:00Z","last_updated_date":"2023-11-20T17:21:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/vimizim-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"13595","name":"Porcilis PCV : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2010-01-21T00:09:00Z","last_updated_date":"2025-03-14T16:50:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/porcilis-pcv-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"13597","name":"Levetiracetam Accord : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2012-09-18T02:00:00Z","last_updated_date":"2025-01-09T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/levetiracetam-accord-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"13605","name":"HBVaxPro : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2008-02-20T00:09:00Z","last_updated_date":"2025-06-06T14:11:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/hbvaxpro-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"13619","name":"Tasermity : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2016-09-12T02:00:00Z","last_updated_date":"2018-03-27T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/tasermity-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"13635","name":"Pantoloc Control : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2010-03-05T01:00:00Z","last_updated_date":"2022-01-18T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/pantoloc-control-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"13667","name":"Ozempic : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2018-07-31T17:55:00Z","last_updated_date":"2025-02-13T14:19:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/ozempic-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"13668","name":"Temozolomide Sandoz : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2010-09-01T02:00:00Z","last_updated_date":"2023-02-27T16:51:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/temozolomide-sandoz-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"13675","name":"Clopidogrel DURA : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2010-03-30T02:00:00Z","last_updated_date":"2015-07-10T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/clopidogrel-dura-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"13681","name":"Adcetris : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2013-04-05T16:00:00Z","last_updated_date":"2026-03-20T16:51:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/adcetris-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"13686","name":"Trudexa : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2008-02-15T00:09:00Z","last_updated_date":"2008-02-15T00:09:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/trudexa-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"13700","name":"Porcilis PCV M Hyo : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2015-12-21T01:00:00Z","last_updated_date":"2020-06-18T11:51:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/porcilis-pcv-m-hyo-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"13709","name":"Brilique : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2012-06-29T02:00:00Z","last_updated_date":"2026-03-31T11:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/brilique-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"13780","name":"Biograstim : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-11-10T00:09:21Z","last_updated_date":"2017-01-19T11:42:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/biograstim-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
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    {"id":"14610","name":"PegIntron : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-09-17T02:00:00Z","last_updated_date":"2021-06-03T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/pegintron-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"14694","name":"Irbesartan Hydrochlorothiazide BMS : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-11-24T01:00:00Z","last_updated_date":"2009-11-24T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/irbesartan-hydrochlorothiazide-bms-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"14742","name":"Adjupanrix (previously Pandemic influenza vaccine (H5N1) (split virion, inactivated, adjuvanted) GlaxoSmithKline Biologicals): EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2011-12-21T01:00:00Z","last_updated_date":"2025-12-17T15:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/adjupanrix-previously-pandemic-influenza-vaccine-h5n1-split-virion-inactivated-adjuvanted-glaxosmithkline-biologicals-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"14773","name":"CoAprovel : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-10-26T00:09:00Z","last_updated_date":"2025-02-11T17:03:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/coaprovel-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"14785","name":"Lamivudine Teva Pharma B.V. : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2013-02-28T17:30:00Z","last_updated_date":"2023-04-21T15:49:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/lamivudine-teva-pharma-bv-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"14820","name":"Recuvyra : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2012-03-21T01:00:00Z","last_updated_date":"2017-07-12T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/recuvyra-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"14837","name":"Docefrez : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2011-02-16T01:00:00Z","last_updated_date":"2012-06-14T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/docefrez-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"14885","name":"Vokanamet : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2014-12-23T01:00:00Z","last_updated_date":"2025-06-10T14:08:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/vokanamet-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"14961","name":"Ribavirin Mylan : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2011-02-17T01:00:00Z","last_updated_date":"2019-07-31T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/ribavirin-mylan-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"15003","name":"Quixidar : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2008-05-16T02:00:00Z","last_updated_date":"2008-05-16T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/quixidar-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"15019","name":"Bluevac BTV : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2013-01-24T01:00:00Z","last_updated_date":"2024-06-13T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/bluevac-btv-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"15121","name":"Caelyx pegylated liposomal : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-03-10T00:09:00Z","last_updated_date":"2025-09-02T14:20:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/caelyx-pegylated-liposomal-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"15126","name":"Besponsa : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2017-12-01T01:00:00Z","last_updated_date":"2026-05-18T14:15:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/besponsa-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"15160","name":"Clopidogrel Teva Generics B.V. : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2011-12-20T01:00:00Z","last_updated_date":"2014-05-12T16:50:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/clopidogrel-teva-generics-bv-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"15193","name":"Synjardy : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2015-11-20T01:00:00Z","last_updated_date":"2025-07-01T14:09:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/synjardy-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"15196","name":"Stivarga : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2014-09-18T02:00:00Z","last_updated_date":"2025-07-02T12:27:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/stivarga-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"15228","name":"Nitisinone MDK (previously Nitisinone MendeliKABS) : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2017-10-05T02:00:00Z","last_updated_date":"2023-06-14T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/nitisinone-mdk-previously-nitisinone-mendelikabs-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"15229","name":"Simparica : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2016-01-26T01:00:00Z","last_updated_date":"2024-06-11T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/simparica-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"15230","name":"Emdocam : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2013-02-01T01:00:00Z","last_updated_date":"2025-09-05T14:37:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/emdocam-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"15286","name":"Savene : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2008-02-15T01:00:00Z","last_updated_date":"2024-09-06T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/savene-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"15292","name":"Nobilis OR inac : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2005-01-28T01:00:00Z","last_updated_date":"2022-10-03T14:34:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/nobilis-or-inac-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"15351","name":"Naxcel : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-10-20T02:00:00Z","last_updated_date":"2024-06-28T16:26:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/naxcel-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"15359","name":"Jardiance : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2015-02-04T01:00:00Z","last_updated_date":"2025-06-25T09:23:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/jardiance-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"15435","name":"Glustin : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-10-05T02:00:00Z","last_updated_date":"2022-10-17T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/glustin-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"15477","name":"Betaferon : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-11-20T00:09:00Z","last_updated_date":"2023-01-12T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/betaferon-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"15554","name":"Mircera : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-10-13T02:00:00Z","last_updated_date":"2025-04-15T15:40:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/mircera-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"15567","name":"Tepadina : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2011-09-29T02:00:00Z","last_updated_date":"2025-10-07T11:01:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/tepadina-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"15607","name":"Pravafenix  : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2013-08-29T02:00:00Z","last_updated_date":"2025-01-17T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/pravafenix-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"15649","name":"Purevax RCPCh : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2010-01-22T01:00:00Z","last_updated_date":"2024-10-11T16:10:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/purevax-rcpch-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"15737","name":"Cerdelga : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2015-04-21T02:00:00Z","last_updated_date":"2025-05-16T15:23:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/cerdelga-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"15824","name":"Aftovaxpur DOE : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2014-10-07T02:00:00Z","last_updated_date":"2023-07-04T10:56:00Z","reference_number":"EMA/573851/2014 ","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/aftovaxpur-doe-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"15862","name":"Adcirca : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2010-01-22T01:00:00Z","last_updated_date":"2026-01-27T15:19:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/adcirca-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"15863","name":"Viekirax : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2015-09-28T02:00:00Z","last_updated_date":"2024-10-02T16:43:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/viekirax-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"15902","name":"Pregabalin Mylan : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2016-02-04T01:00:00Z","last_updated_date":"2024-05-16T12:25:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/pregabalin-mylan-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"15952","name":"Zimulti : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2010-01-30T02:09:21Z","last_updated_date":"2010-01-30T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/zimulti-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"15999","name":"Victoza : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2010-02-22T00:09:00Z","last_updated_date":"2025-02-20T09:42:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/victoza-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"16004","name":"Votrient : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2011-02-17T01:00:00Z","last_updated_date":"2025-10-28T11:28:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/votrient-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"16086","name":"Rebif : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-10-23T02:00:00Z","last_updated_date":"2026-04-08T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/rebif-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"16106","name":"Procysbi : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2014-09-04T02:00:00Z","last_updated_date":"2025-09-08T17:11:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/procysbi-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"16190","name":"Sylvant : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2014-08-14T02:00:00Z","last_updated_date":"2025-10-24T18:44:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/sylvant-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"16210","name":"Rolufta Ellipta (previously Rolufta) : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2017-09-05T14:01:00Z","last_updated_date":"2025-03-28T14:05:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/rolufta-ellipta-previously-rolufta-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"16218","name":"Advasure : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2008-03-18T00:09:21Z","last_updated_date":"2008-03-18T00:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/advasure-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"16234","name":"Varuby : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2017-11-06T01:00:00Z","last_updated_date":"2020-03-02T15:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/varuby-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"16293","name":"Adenuric : EPAR - Procedural steps taken and scientific information after authorisation (archived)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-09-08T15:00:00Z","last_updated_date":"2024-09-13T17:35:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/adenuric-epar-procedural-steps-taken-scientific-information-after-authorisation-archived_en.pdf"},
    {"id":"16301","name":"Efavirenz/Emtricitabine/Tenofovir disoproxil Mylan : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2018-07-03T02:00:00Z","last_updated_date":"2024-10-28T11:37:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/efavirenz-emtricitabine-tenofovir-disoproxil-mylan-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"16350","name":"Bovilis Blue-8 : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2018-07-26T02:00:00Z","last_updated_date":"2024-06-17T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/bovilis-blue-8-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"16355","name":"Zarzio : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-11-09T01:00:00Z","last_updated_date":"2025-07-08T12:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/zarzio-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"16382","name":"Xadago : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2015-11-06T01:00:00Z","last_updated_date":"2026-02-09T17:26:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/xadago-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"16400","name":"Xofigo : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2014-05-07T02:00:00Z","last_updated_date":"2025-07-28T15:01:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/xofigo-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"16404","name":"Cancidas : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-08-05T02:09:00Z","last_updated_date":"2025-04-24T16:42:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/cancidas-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"16415","name":"Edistride : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2016-04-14T02:00:00Z","last_updated_date":"2026-03-13T12:42:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/edistride-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"16418","name":"Foscan : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-04-30T02:09:21Z","last_updated_date":"2026-02-12T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/foscan-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
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    {"id":"16968","name":"Leucogen : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2014-06-23T02:00:00Z","last_updated_date":"2025-09-02T13:10:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/leucogen-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"16971","name":"Bronchitol : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2012-08-06T18:16:00Z","last_updated_date":"2026-02-17T10:55:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/bronchitol-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
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    {"id":"17120","name":"Rabigen SAG2 : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2008-05-29T02:00:00Z","last_updated_date":"2025-10-14T16:40:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/rabigen-sag2-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"17142","name":"Canigen L4 : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2016-08-15T02:00:00Z","last_updated_date":"2024-11-07T15:40:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/canigen-l4-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"17149","name":"Exelon : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2018-02-21T11:41:00Z","last_updated_date":"2025-04-11T11:36:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/exelon-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"17177","name":"Daptomycin Hospira : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2018-02-26T11:09:00Z","last_updated_date":"2025-02-17T12:09:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/daptomycin-hospira-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"17180","name":"Pheburane : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2014-10-06T02:00:00Z","last_updated_date":"2025-01-14T12:28:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/pheburane-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"17209","name":"Rebetol : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-10-22T02:00:00Z","last_updated_date":"2023-11-07T16:05:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/rebetol-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"17217","name":"Hemangiol : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2014-09-22T02:00:00Z","last_updated_date":"2023-02-09T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/hemangiol-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"17262","name":"Trisenox : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-10-08T02:09:00Z","last_updated_date":"2026-01-30T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/trisenox-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"17317","name":"Hiprabovis IBR Marker Live : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2013-08-29T02:00:00Z","last_updated_date":"2024-11-05T15:33:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/hiprabovis-ibr-marker-live-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"17376","name":"NeoRecormon : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2008-11-04T00:09:00Z","last_updated_date":"2025-05-02T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/neorecormon-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"17415","name":"Yargesa : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2017-07-03T02:00:00Z","last_updated_date":"2025-06-16T09:12:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/yargesa-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"17422","name":"Olazax : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2010-05-27T02:00:00Z","last_updated_date":"2026-05-11T13:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/olazax-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"17463","name":"Zuprevo : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2012-09-24T02:00:00Z","last_updated_date":"2024-06-28T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/zuprevo-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"17507","name":"Imprida HCT : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2010-11-04T01:00:00Z","last_updated_date":"2012-10-29T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/imprida-hct-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"17544","name":"NovoRapid : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-12-17T01:00:00Z","last_updated_date":"2025-05-28T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/novorapid-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"17574","name":"Advate : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-07-14T02:00:00Z","last_updated_date":"2025-05-23T12:22:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/advate-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"17599","name":"Insulin lispro Sanofi : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2017-11-06T01:00:00Z","last_updated_date":"2026-01-29T14:43:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/insulin-lispro-sanofi-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"17612","name":"Aripiprazole Accord : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2016-02-24T01:00:00Z","last_updated_date":"2022-07-13T13:49:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/aripiprazole-accord-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"17633","name":"Colobreathe : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2012-09-10T18:40:00Z","last_updated_date":"2025-06-20T16:56:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/colobreathe-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"17643","name":"Neoclarityn : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-04-02T01:09:00Z","last_updated_date":"2026-03-02T12:07:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/neoclarityn-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"17697","name":"Trelegy Ellipta : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2018-06-12T02:00:00Z","last_updated_date":"2025-05-05T12:01:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/trelegy-ellipta-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"17750","name":"Potactasol : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2015-02-06T01:00:00Z","last_updated_date":"2025-01-20T15:35:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/potactasol-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"17817","name":"Visudyne : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2008-12-15T01:00:00Z","last_updated_date":"2020-09-16T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/visudyne-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"17839","name":"Clopidogrel Taw Pharma (previously Clopidogrel Mylan) : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-12-15T01:00:00Z","last_updated_date":"2023-12-19T13:50:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/clopidogrel-taw-pharma-previously-clopidogrel-mylan-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"17846","name":"Infanrix Hexa : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2008-11-26T01:00:00Z","last_updated_date":"2026-02-12T16:15:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/infanrix-hexa-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"17856","name":"ATryn : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-08-21T02:00:00Z","last_updated_date":"2019-07-02T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/atryn-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"17899","name":"NovoThirteen : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2014-03-25T01:00:00Z","last_updated_date":"2022-03-21T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/novothirteen-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"17909","name":"Vosevi : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2018-06-14T02:00:00Z","last_updated_date":"2023-08-14T16:33:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/vosevi-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"17911","name":"Fevaxyn Pentofel : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-10-15T02:00:00Z","last_updated_date":"2024-11-21T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/fevaxyn-pentofel-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"17987","name":"MicardisPlus : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-02-26T02:09:00Z","last_updated_date":"2026-04-28T10:34:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/micardisplus-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"18003","name":"Vylaer Spiromax : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2015-03-10T01:00:00Z","last_updated_date":"2016-07-15T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/vylaer-spiromax-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"18030","name":"Multaq : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2011-07-20T02:00:00Z","last_updated_date":"2025-10-28T12:33:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/multaq-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"18032","name":"Memantine ratiopharm : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2014-09-17T02:00:00Z","last_updated_date":"2022-06-30T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/memantine-ratiopharm-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"18091","name":"Taltz : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2016-12-15T17:06:00Z","last_updated_date":"2025-09-11T12:17:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/taltz-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"18098","name":"Tobi Podhaler : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2012-05-03T02:00:00Z","last_updated_date":"2025-12-11T17:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/tobi-podhaler-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"18119","name":"Clopidogrel/Acetylsalicylic acid Zentiva (previously DuoCover) : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2010-09-28T15:30:00Z","last_updated_date":"2019-11-13T14:30:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/clopidogrelacetylsalicylic-acid-zentiva-previously-duocover-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"18151","name":"Imatinib medac : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2015-06-26T02:00:00Z","last_updated_date":"2018-05-14T18:37:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/imatinib-medac-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"18156","name":"Emtricitabine/Tenofovir disoproxil Mylan : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2017-06-27T02:00:00Z","last_updated_date":"2023-12-05T14:26:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/emtricitabine-tenofovir-disoproxil-mylan-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"18172","name":"Monotard : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2008-02-15T00:09:21Z","last_updated_date":"2008-02-15T00:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/monotard-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"18206","name":"Sycrest : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2011-03-14T01:00:00Z","last_updated_date":"2026-02-25T11:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/sycrest-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"18254","name":"BTVPUR Alsap 8 : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2010-01-26T00:09:21Z","last_updated_date":"2018-05-17T01:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/btvpur-alsap-8-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"18266","name":"Incurin : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2006-08-07T02:00:00Z","last_updated_date":"2025-10-08T14:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/incurin-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"18293","name":"Taxespira (previously Docetaxel Hospira UK Limited) : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2016-02-02T01:00:00Z","last_updated_date":"2019-10-15T12:32:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/taxespira-previously-docetaxel-hospira-uk-limited-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"18314","name":"Thorinane : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2017-08-10T13:57:00Z","last_updated_date":"2019-10-24T11:58:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/thorinane-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"18359","name":"Rapilysin : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2008-08-13T03:00:00Z","last_updated_date":"2023-06-01T03:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/rapilysin-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"18362","name":"Startvac : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2014-02-25T01:00:00Z","last_updated_date":"2025-09-02T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/startvac-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"18430","name":"Mekinist : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2015-02-04T01:00:00Z","last_updated_date":"2025-11-03T14:46:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/mekinist-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"18479","name":"Zoledronic acid medac : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2014-03-12T01:00:00Z","last_updated_date":"2026-05-19T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/zoledronic-acid-medac-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"18507","name":"Efient : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-12-02T01:00:00Z","last_updated_date":"2024-09-04T14:18:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/efient-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"18510","name":"Vaxelis : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2016-06-14T02:00:00Z","last_updated_date":"2025-10-14T16:09:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/vaxelis-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"18519","name":"Intrinsa : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2008-09-26T02:00:00Z","last_updated_date":"2012-06-18T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/intrinsa-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"18525","name":"M-M-RVaxPro : EPAR - Procedural steps taken and scientific information after authorisation (archived)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2008-08-04T02:09:00Z","last_updated_date":"2025-01-21T16:36:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/m-m-rvaxpro-epar-procedural-steps-taken-scientific-information-after-authorisation-archived_en.pdf"},
    {"id":"18528","name":"Ritonavir Mylan : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2018-06-12T13:08:00Z","last_updated_date":"2024-01-10T10:29:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/ritonavir-mylan-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"18534","name":"Spectrila : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2017-08-22T19:10:00Z","last_updated_date":"2023-11-20T12:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/spectrila-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"18562","name":"Vivanza : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-08-25T03:00:00Z","last_updated_date":"2022-02-28T03:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/vivanza-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"18591","name":"Clopidogrel HCS : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2011-12-20T01:00:00Z","last_updated_date":"2018-08-01T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/clopidogrel-hcs-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"18606","name":"Somatropin Biopartners : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2014-07-30T02:00:00Z","last_updated_date":"2017-04-27T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/somatropin-biopartners-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"18624","name":"Evotaz : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2016-03-31T17:51:00Z","last_updated_date":"2025-07-10T17:51:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/evotaz-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"18628","name":"Viread : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-07-31T02:00:00Z","last_updated_date":"2025-11-18T16:48:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/viread-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"18657","name":"Olanzapine Cipla : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-11-24T01:00:00Z","last_updated_date":"2014-07-24T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/olanzapine-cipla-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"18703","name":"Velmetia : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-12-08T01:00:00Z","last_updated_date":"2025-05-23T15:56:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/velmetia-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"18712","name":"Cosentyx : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2015-05-11T11:29:00Z","last_updated_date":"2025-03-26T09:37:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/cosentyx-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"18715","name":"Nplate : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-03-13T00:09:00Z","last_updated_date":"2025-03-31T10:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/nplate-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"18738","name":"Docetaxel Teva : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2010-09-23T02:00:00Z","last_updated_date":"2021-12-14T11:42:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/docetaxel-teva-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"18760","name":"Emtricitabine/Tenofovir disoproxil Krka d.d. : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2017-07-12T10:57:00Z","last_updated_date":"2024-07-02T15:04:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/emtricitabine-tenofovir-disoproxil-krka-dd-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"18765","name":"Fluenz Tetra : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2014-04-10T02:00:00Z","last_updated_date":"2025-08-14T16:01:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/fluenz-tetra-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"18791","name":"Jylamvo : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2018-06-01T02:00:00Z","last_updated_date":"2024-10-24T11:42:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/jylamvo-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"18820","name":"Suboxone : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-06-25T02:00:00Z","last_updated_date":"2024-07-29T15:38:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/suboxone-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"18828","name":"Anoro Ellipta : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2015-05-13T02:00:00Z","last_updated_date":"2025-07-31T09:30:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/anoro-ellipta-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"18845","name":"SonoVue : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2008-02-21T01:00:00Z","last_updated_date":"2025-11-24T15:43:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/sonovue-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"18854","name":"BTVPUR AlSap 2-4 : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2013-03-14T01:00:00Z","last_updated_date":"2018-11-13T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/btvpur-alsap-2-4-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
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    {"id":"19703","name":"Zoledronic acid Mylan : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2013-08-28T02:00:00Z","last_updated_date":"2025-11-07T10:47:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/zoledronic-acid-mylan-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
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    {"id":"19808","name":"Kinzalkomb : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-11-26T01:00:00Z","last_updated_date":"2025-01-17T16:59:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/kinzalkomb-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
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    {"id":"19862","name":"Comtan : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2008-11-14T01:00:00Z","last_updated_date":"2026-05-07T16:37:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/comtan-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"19875","name":"Reconcile : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2010-01-20T01:00:00Z","last_updated_date":"2025-10-14T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/reconcile-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"19892","name":"Viagra : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-03-04T01:00:00Z","last_updated_date":"2024-05-22T10:51:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/viagra-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"19919","name":"Siklos : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2008-08-11T03:00:00Z","last_updated_date":"2025-09-30T12:24:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/siklos-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"19963","name":"Zytiga : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2012-06-13T02:00:00Z","last_updated_date":"2024-10-18T14:34:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/zytiga-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"19987","name":"Ecoporc Shiga : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2014-05-21T02:00:00Z","last_updated_date":"2020-09-18T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/ecoporc-shiga-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
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    {"id":"20084","name":"PhotoBarr : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-04-21T02:00:00Z","last_updated_date":"2012-05-07T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/photobarr-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"20095","name":"Sevelamer carbonate Winthrop : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2015-05-28T02:00:00Z","last_updated_date":"2024-12-18T12:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/sevelamer-carbonate-winthrop-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"20098","name":"Methylthioninium chloride Proveblue : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2012-02-28T01:00:00Z","last_updated_date":"2025-12-19T17:21:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/methylthioninium-chloride-proveblue-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"20101","name":"Vantobra : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2015-12-15T01:00:00Z","last_updated_date":"2019-03-29T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/vantobra-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
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    {"id":"20178","name":"Ganfort : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2010-05-03T02:00:00Z","last_updated_date":"2024-11-18T16:13:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/ganfort-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
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    {"id":"21051","name":"Olazax Disperzi : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2010-06-09T02:00:00Z","last_updated_date":"2026-05-12T13:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/olazax-disperzi-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
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    {"id":"21143","name":"Nobivac L4 : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2015-08-13T02:00:00Z","last_updated_date":"2024-12-19T14:30:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/nobivac-l4-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"21189","name":"Suvaxyn Aujeszky 783 + O/W : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2008-11-13T01:00:00Z","last_updated_date":"2024-10-28T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/suvaxyn-aujeszky-783-o-w-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"21219","name":"Kovaltry : EPAR - Procedural steps taken and scientific information after authorisation (archived)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2016-08-02T02:00:00Z","last_updated_date":"2023-07-26T10:30:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/kovaltry-epar-procedural-steps-taken-scientific-information-after-authorisation-archived_en.pdf"},
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    {"id":"21239","name":"BiResp Spiromax : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2015-10-30T01:00:00Z","last_updated_date":"2024-07-24T16:25:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/biresp-spiromax-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
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    {"id":"21289","name":"Slentrol : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2010-01-26T01:00:00Z","last_updated_date":"2015-02-24T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/slentrol-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"21306","name":"Cholib : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2014-04-09T02:00:00Z","last_updated_date":"2025-12-16T10:29:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/cholib-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"21327","name":"Enzepi : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2016-09-16T11:28:00Z","last_updated_date":"2016-09-16T11:28:00Z","reference_number":"EMA/609014/2016 ","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/enzepi-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"21328","name":"Ameluz : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2012-08-17T16:06:00Z","last_updated_date":"2024-03-05T15:22:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/ameluz-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
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    {"id":"21432","name":"Tybost : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2014-07-29T13:19:00Z","last_updated_date":"2023-02-14T16:51:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/tybost-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"21443","name":"Levetiracetam ratiopharm : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2012-01-25T01:00:00Z","last_updated_date":"2025-06-30T17:59:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/levetiracetam-ratiopharm-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"21480","name":"Lopinavir/Ritonavir Mylan : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2016-07-08T02:00:00Z","last_updated_date":"2024-01-30T01:18:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/lopinavir-ritonavir-mylan-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"21550","name":"Equilis West Nile : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2018-04-18T16:06:00Z","last_updated_date":"2025-09-09T16:06:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/equilis-west-nile-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"21577","name":"Zostavax : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-12-04T01:00:00Z","last_updated_date":"2025-06-11T14:58:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/zostavax-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"21597","name":"NeoSpect : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2008-04-23T02:09:21Z","last_updated_date":"2010-11-18T01:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/neospect-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"21598","name":"Recocam : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2013-02-19T18:00:00Z","last_updated_date":"2024-06-17T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/recocam-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"21599","name":"Bavencio : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2018-01-17T01:00:00Z","last_updated_date":"2026-01-22T16:58:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/bavencio-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
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    {"id":"23256","name":"Capecitabine Medac : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2013-05-03T02:00:00Z","last_updated_date":"2025-05-02T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/capecitabine-medac-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"23271","name":"Clopidogrel Teva (hydrogen sulphate) : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-10-14T02:09:00Z","last_updated_date":"2024-02-29T13:28:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/clopidogrel-teva-hydrogen-sulphate-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"23307","name":"Bortezomib Hospira : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2017-03-09T01:00:00Z","last_updated_date":"2026-04-15T14:05:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/bortezomib-hospira-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"23358","name":"Flexicam : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2008-12-16T01:00:00Z","last_updated_date":"2014-05-20T16:50:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/flexicam-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"23406","name":"Evicel : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-05-13T02:00:00Z","last_updated_date":"2024-08-02T10:59:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/evicel-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"23429","name":"Bovilis BTV8 : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2011-12-14T01:00:00Z","last_updated_date":"2022-07-27T11:22:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/bovilis-btv8-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"23463","name":"Clopidogrel ratiopharm GmbH : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-10-13T02:00:00Z","last_updated_date":"2019-10-02T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/clopidogrel-ratiopharm-gmbh-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"23469","name":"Benlysta : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2012-02-08T01:00:00Z","last_updated_date":"2025-10-07T14:53:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/benlysta-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"23472","name":"Ferriprox : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-10-28T00:09:00Z","last_updated_date":"2025-08-13T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/ferriprox-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"23504","name":"Dukoral : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2008-11-11T01:00:00Z","last_updated_date":"2022-04-06T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/dukoral-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"23505","name":"Xeplion : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2011-09-02T02:00:00Z","last_updated_date":"2024-07-22T17:50:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/xeplion-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"23556","name":"Acticam : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-11-18T01:00:00Z","last_updated_date":"2021-03-24T14:15:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/acticam-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"23600","name":"Aprovel : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-05-05T02:00:00Z","last_updated_date":"2025-02-11T16:28:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/aprovel-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"23611","name":"Lantus : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-05-08T02:00:00Z","last_updated_date":"2026-03-05T11:04:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/lantus-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"23618","name":"Nodetrip (previously Xeristar) : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-08-17T02:00:00Z","last_updated_date":"2021-06-22T14:42:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/nodetrip-previously-xeristar-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"23747","name":"Fungitraxx : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2016-06-20T02:00:00Z","last_updated_date":"2025-09-09T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/fungitraxx-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"23771","name":"Revestive : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2013-11-08T01:00:00Z","last_updated_date":"2025-05-23T08:58:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/revestive-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"23776","name":"Benepali : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2016-03-16T01:00:00Z","last_updated_date":"2025-03-05T11:53:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/benepali-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"23793","name":"Onsior : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2010-01-11T01:00:00Z","last_updated_date":"2024-06-28T11:30:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/onsior-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"23838","name":"Gripovac 3 : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2014-12-22T01:00:00Z","last_updated_date":"2018-09-04T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/gripovac-3-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"23936","name":"Proteq West Nile : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2013-01-22T17:00:00Z","last_updated_date":"2020-08-20T14:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/proteq-west-nile-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"23940","name":"Zebinix : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-05-27T02:09:00Z","last_updated_date":"2025-03-31T16:07:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/zebinix-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"23969","name":"Modigraf : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2010-01-21T01:00:00Z","last_updated_date":"2025-03-03T17:01:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/modigraf-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"24144","name":"Ablavar : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-07-30T03:00:00Z","last_updated_date":"2011-09-16T03:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/ablavar-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"24155","name":"Pramipexole Teva : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-08-28T02:00:00Z","last_updated_date":"2024-09-02T17:42:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/pramipexole-teva-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"24249","name":"Equip WNV : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-09-24T02:09:21Z","last_updated_date":"2024-10-14T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/equip-wnv-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"24254","name":"Optaflu : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-05-11T02:09:21Z","last_updated_date":"2017-02-13T16:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/optaflu-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"24268","name":"Clopidogrel Acino : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"Adopted","consultation_date":"","first_published_date":"2011-03-31T02:00:00Z","last_updated_date":"2016-08-11T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/clopidogrel-acino-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"24324","name":"Prolia : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2011-06-08T02:00:00Z","last_updated_date":"2025-10-22T11:37:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/prolia-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"24338","name":"Tolura : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2011-07-21T02:00:00Z","last_updated_date":"2025-03-19T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/tolura-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"24364","name":"Helixate NexGen : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-11-12T01:00:00Z","last_updated_date":"2020-06-02T12:38:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/helixate-nexgen-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"24429","name":"Fortekor Plus : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2016-03-23T01:00:00Z","last_updated_date":"2025-09-09T11:43:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/fortekor-plus-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"24430","name":"Pandemic influenza vaccine H5N1 AstraZeneca : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2017-02-10T01:00:00Z","last_updated_date":"2025-12-10T16:33:03Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/pandemic-influenza-vaccine-h5n1-astrazeneca-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"24442","name":"Exjade : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-08-20T02:00:00Z","last_updated_date":"2025-08-21T15:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/exjade-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"24466","name":"Quintanrix : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2008-09-10T02:00:00Z","last_updated_date":"2008-09-10T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/quintanrix-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"24510","name":"Eryseng Parvo : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2015-03-09T01:00:00Z","last_updated_date":"2025-09-09T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/eryseng-parvo-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"24533","name":"Memantine Merz : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2014-06-11T02:00:00Z","last_updated_date":"2025-06-20T16:31:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/memantine-merz-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"24550","name":"Coliprotec F4/F18 : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2017-05-24T16:39:00Z","last_updated_date":"2025-09-04T10:43:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/coliprotec-f4-f18-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"24593","name":"Stocrin : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2010-01-13T01:00:00Z","last_updated_date":"2023-04-25T12:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/stocrin-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"24599","name":"Palladia : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2010-06-03T02:00:00Z","last_updated_date":"2024-06-28T16:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/palladia-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"24683","name":"Melovem : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2010-06-07T02:00:00Z","last_updated_date":"2024-06-13T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/melovem-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"24691","name":"Sildenafil Actavis : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2011-04-13T02:00:00Z","last_updated_date":"2023-11-13T17:59:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/sildenafil-actavis-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"24698","name":"Emtricitabine/Tenofovir disoproxil Zentiva : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2018-01-23T01:00:00Z","last_updated_date":"2025-03-19T12:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/emtricitabine-tenofovir-disoproxil-zentiva-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"24707","name":"ProMeris : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-07-16T02:09:21Z","last_updated_date":"2015-07-13T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/promeris-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"24737","name":"Vyndaqel : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2013-04-22T02:00:00Z","last_updated_date":"2025-02-18T15:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/vyndaqel-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"24751","name":"Iclusig : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2013-08-22T02:00:00Z","last_updated_date":"2025-11-12T18:27:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/iclusig-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"24752","name":"Neulasta : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-11-09T01:00:00Z","last_updated_date":"2025-12-08T13:11:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/neulasta-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"24772","name":"Ciambra : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2017-03-20T15:22:00Z","last_updated_date":"2024-10-17T15:40:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/ciambra-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"24780","name":"Cerenia : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2010-02-23T01:00:00Z","last_updated_date":"2024-06-28T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/cerenia-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"24831","name":"MS-H Vaccine : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2014-04-16T14:00:00Z","last_updated_date":"2025-10-09T15:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/ms-h-vaccine-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
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    {"id":"25696","name":"Acomplia : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2010-01-30T01:00:00Z","last_updated_date":"2010-01-30T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/acomplia-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
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    {"id":"25724","name":"Letifend : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2016-09-07T02:00:00Z","last_updated_date":"2025-10-09T11:10:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/letifend-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
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    {"id":"25759","name":"Naglazyme : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-07-29T02:09:00Z","last_updated_date":"2024-12-16T15:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/naglazyme-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
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    {"id":"25819","name":"Brineura : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2018-01-12T01:00:00Z","last_updated_date":"2023-12-12T12:19:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/brineura-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"25852","name":"Pregabalin Pfizer : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2014-10-06T02:00:00Z","last_updated_date":"2025-07-03T15:38:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/pregabalin-pfizer-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"25899","name":"Voriconazole Accord : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2013-11-28T01:00:00Z","last_updated_date":"2025-05-12T17:01:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/voriconazole-accord-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
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    {"id":"26429","name":"Improvac : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-11-27T01:00:00Z","last_updated_date":"2024-06-11T15:15:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/improvac-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
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    {"id":"26484","name":"Pirsue : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2006-11-23T00:09:00Z","last_updated_date":"2025-05-02T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/pirsue-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
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    {"id":"26492","name":"Clopidogrel BMS : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-11-11T01:00:00Z","last_updated_date":"2009-11-11T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/clopidogrel-bms-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"26540","name":"Cinacalcet Mylan : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2017-02-10T11:54:00Z","last_updated_date":"2025-10-07T11:40:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/cinacalcet-mylan-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"26560","name":"Glivec : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-08-18T02:00:00Z","last_updated_date":"2025-11-12T09:28:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/glivec-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"26569","name":"Cystadane : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2008-02-13T00:09:00Z","last_updated_date":"2024-12-12T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/cystadane-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
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    {"id":"26638","name":"Clopidogrel/Acetylsalicylic acid Teva : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2016-04-11T02:00:00Z","last_updated_date":"2017-04-28T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/clopidogrelacetylsalicylic-acid-teva-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"26647","name":"Spironolactone Ceva : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-07-30T02:09:00Z","last_updated_date":"2016-11-30T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/spironolactone-ceva-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"26677","name":"Somavert : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-05-11T03:00:00Z","last_updated_date":"2023-11-27T12:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/somavert-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"26682","name":"Raplixa : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2016-01-14T01:00:00Z","last_updated_date":"2018-10-10T18:30:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/raplixa-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"26719","name":"MabThera : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-10-30T01:00:00Z","last_updated_date":"2025-04-03T15:08:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/mabthera-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"26739","name":"Zulvac 1 Ovis : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2012-01-17T16:00:00Z","last_updated_date":"2020-04-01T17:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/zulvac-1-ovis-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"26744","name":"Viraferon : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2008-05-27T03:09:21Z","last_updated_date":"2008-05-27T03:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/viraferon-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"26774","name":"Onduarp : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2012-08-10T15:50:00Z","last_updated_date":"2014-04-02T15:50:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/onduarp-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"26785","name":"Clopidogrel Acino Pharma GmbH : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2011-03-31T02:00:00Z","last_updated_date":"2012-07-26T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/clopidogrel-acino-pharma-gmbh-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"26789","name":"Cortavance : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2007-08-02T02:09:00Z","last_updated_date":"2025-09-04T02:09:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/cortavance-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"26819","name":"Nobivac Bb : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2007-10-01T02:00:00Z","last_updated_date":"2025-10-09T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/nobivac-bb-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"26825","name":"Kanjinti : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2018-08-24T02:00:00Z","last_updated_date":"2025-05-13T11:56:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/kanjinti-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"26831","name":"Kinzalmono : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-06-25T02:00:00Z","last_updated_date":"2025-04-23T11:35:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/kinzalmono-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"26861","name":"Firdapse : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2010-02-10T12:00:00Z","last_updated_date":"2022-02-24T11:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/firdapse-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"26889","name":"Ibrance : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2017-01-17T18:26:00Z","last_updated_date":"2025-03-07T16:38:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/ibrance-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"26931","name":"Cuprymina : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2015-04-28T02:00:00Z","last_updated_date":"2022-07-01T13:52:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/cuprymina-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"26934","name":"Trazec : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-08-24T02:00:00Z","last_updated_date":"2009-08-24T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/trazec-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"26970","name":"Novem : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-03-20T01:00:00Z","last_updated_date":"2025-10-09T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/novem-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"26978","name":"Provenge : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2015-05-20T02:00:00Z","last_updated_date":"2015-05-20T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/provenge-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"26989","name":"Meloxoral : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2011-05-16T18:43:00Z","last_updated_date":"2024-05-31T12:43:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/meloxoral-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"27018","name":"Byetta : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-06-25T02:00:00Z","last_updated_date":"2024-11-06T15:42:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/byetta-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"27022","name":"Amgevita : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2018-01-17T01:00:00Z","last_updated_date":"2025-03-31T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/amgevita-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"27091","name":"Somac Control : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2010-06-24T02:00:00Z","last_updated_date":"2023-05-24T09:32:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/somac-control-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"27108","name":"Keytruda : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2016-03-29T16:03:00Z","last_updated_date":"2025-08-14T16:06:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/keytruda-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"27128","name":"Ribavirin Teva Pharma B.V. : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2010-01-22T01:00:00Z","last_updated_date":"2021-07-09T13:30:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/ribavirin-teva-pharma-bv-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"27163","name":"Paxene : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-08-12T02:00:00Z","last_updated_date":"2010-03-22T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/paxene-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"27167","name":"Celsentri : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-08-11T02:09:00Z","last_updated_date":"2025-07-23T15:57:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/celsentri-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"27182","name":"Resolor : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2010-08-10T02:00:00Z","last_updated_date":"2024-09-12T13:41:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/resolor-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"27219","name":"Econor : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-07-02T02:09:00Z","last_updated_date":"2025-09-04T10:30:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/econor-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"27254","name":"Mimpara : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-11-20T00:09:00Z","last_updated_date":"2026-05-20T17:58:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/mimpara-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
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    {"id":"27301","name":"Pioglitazone Teva Pharma : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2014-07-14T02:00:00Z","last_updated_date":"2022-08-30T16:52:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/pioglitazone-teva-pharma-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"27307","name":"Zyclara : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2013-11-28T01:00:00Z","last_updated_date":"2025-07-22T14:51:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/zyclara-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
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    {"id":"27400","name":"NutropinAq : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-09-01T02:09:00Z","last_updated_date":"2023-07-20T14:30:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/nutropinaq-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
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    {"id":"27453","name":"Zoledronic acid Teva Pharma : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2013-08-20T02:00:00Z","last_updated_date":"2018-12-12T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/zoledronic-acid-teva-pharma-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
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    {"id":"27707","name":"Yentreve : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-09-15T03:09:00Z","last_updated_date":"2024-07-09T15:34:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/yentreve-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"27827","name":"Fendrix : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-04-07T02:09:00Z","last_updated_date":"2023-05-24T11:28:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/fendrix-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"27866","name":"Procoralan : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-05-15T02:00:00Z","last_updated_date":"2025-11-17T17:52:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/procoralan-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"27879","name":"Zoely : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2011-12-02T01:00:00Z","last_updated_date":"2025-02-19T17:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/zoely-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"27891","name":"Rivastigmine 1 A Pharma  : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2010-12-16T01:00:00Z","last_updated_date":"2025-01-29T11:57:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/rivastigmine-1-pharma-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"27910","name":"Copalia HCT : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2010-08-26T02:00:00Z","last_updated_date":"2025-02-12T11:20:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/copalia-hct-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"27943","name":"Renagel : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2005-10-21T02:00:00Z","last_updated_date":"2025-01-22T13:50:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/renagel-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"27976","name":"Hepsera : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-07-09T02:09:00Z","last_updated_date":"2023-03-01T14:29:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/hepsera-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"28005","name":"Pregabalin Sandoz GmbH : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2015-12-21T01:00:00Z","last_updated_date":"2023-10-12T14:31:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/pregabalin-sandoz-gmbh-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"28018","name":"Roteas : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2018-01-12T10:31:00Z","last_updated_date":"2025-08-27T10:31:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/roteas-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"28045","name":"Suvaxyn PCV : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2010-03-12T01:00:00Z","last_updated_date":"2020-04-15T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/suvaxyn-pcv-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"28082","name":"Emadine : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-01-30T01:00:00Z","last_updated_date":"2025-03-25T09:25:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/emadine-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"28088","name":"Angiox : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-09-02T02:00:00Z","last_updated_date":"2018-09-14T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/angiox-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"28102","name":"Isentress : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-09-18T02:00:00Z","last_updated_date":"2025-05-14T13:18:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/isentress-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"28128","name":"Effentora : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-07-27T16:40:00Z","last_updated_date":"2025-04-11T11:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/effentora-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"28133","name":"Lumark : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2016-09-07T02:00:00Z","last_updated_date":"2026-02-11T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/lumark-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"28164","name":"Ofev : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2016-02-24T01:00:00Z","last_updated_date":"2025-03-28T15:23:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/ofev-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"28168","name":"Ypozane : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2012-01-05T12:52:00Z","last_updated_date":"2024-06-28T12:52:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/ypozane-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"28193","name":"Scintimun : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2011-11-11T01:00:00Z","last_updated_date":"2025-03-20T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/scintimun-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"28230","name":"Numient : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2016-12-14T18:45:00Z","last_updated_date":"2018-08-09T18:22:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/numient-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"28320","name":"Levemir : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-06-15T17:41:00Z","last_updated_date":"2021-07-13T14:41:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/levemir-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"28326","name":"Kuvan : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-07-27T02:00:00Z","last_updated_date":"2025-04-22T11:16:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/kuvan-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"28343","name":"Valdoxan : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2010-05-21T02:00:00Z","last_updated_date":"2025-04-15T13:32:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/valdoxan-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"28367","name":"Replagal : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2008-11-03T01:00:00Z","last_updated_date":"2025-09-18T11:15:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/replagal-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"28372","name":"Sonata : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-07-13T03:00:00Z","last_updated_date":"2015-10-21T03:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/sonata-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"28385","name":"Ulunar Breezhaler : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2015-01-29T01:00:00Z","last_updated_date":"2025-03-06T14:10:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/ulunar-breezhaler-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"28415","name":"Nexgard Spectra : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2017-07-13T02:00:00Z","last_updated_date":"2024-06-13T10:30:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/nexgard-spectra-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
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    {"id":"29315","name":"Otezla : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2016-02-08T01:00:00Z","last_updated_date":"2026-01-14T11:09:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/otezla-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
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    {"id":"29467","name":"Ribavirin BioPartners : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2010-12-13T01:00:00Z","last_updated_date":"2013-05-06T12:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/ribavirin-biopartners-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
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    {"id":"29579","name":"Iblias : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2016-07-08T02:00:00Z","last_updated_date":"2018-04-27T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/iblias-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"29590","name":"Evoltra : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-07-01T02:00:00Z","last_updated_date":"2024-07-19T10:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/evoltra-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"29614","name":"Keppra : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-09-18T02:00:00Z","last_updated_date":"2025-06-30T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/keppra-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"29620","name":"Rasilez : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-06-18T02:00:00Z","last_updated_date":"2026-03-02T16:30:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/rasilez-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"29632","name":"Filgrastim Hexal : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-11-09T18:11:00Z","last_updated_date":"2025-07-08T12:11:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/filgrastim-hexal-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"29662","name":"Tysabri : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-06-18T02:09:00Z","last_updated_date":"2025-11-14T13:02:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/tysabri-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"29685","name":"Purevax RCP FeLV : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2010-01-26T01:00:00Z","last_updated_date":"2024-12-19T13:36:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/purevax-rcp-felv-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"29692","name":"Actos : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-10-05T02:00:00Z","last_updated_date":"2023-08-28T15:57:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/actos-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"29707","name":"Revinty Ellipta : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2015-02-04T01:00:00Z","last_updated_date":"2024-09-03T11:34:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/revinty-ellipta-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"29757","name":"Onivyde pegylated liposomal : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2017-07-12T02:00:00Z","last_updated_date":"2024-11-29T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/onivyde-pegylated-liposomal-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"29812","name":"Efavirenz/Emtricitabine/Tenofovir disoproxil Zentiva : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2018-02-06T01:00:00Z","last_updated_date":"2025-03-18T14:28:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/efavirenz-emtricitabine-tenofovir-disoproxil-zentiva-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"29854","name":"Nobilis Influenza H5N6 : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2008-08-19T02:00:00Z","last_updated_date":"2010-07-26T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/nobilis-influenza-h5n6-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"29934","name":"Irbesartan Zentiva : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-05-06T02:00:00Z","last_updated_date":"2024-10-15T15:14:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/irbesartan-zentiva-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"29960","name":"Pandemic Influenza Vaccine H5N1 Baxter : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2012-06-14T02:00:00Z","last_updated_date":"2023-09-13T12:20:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/pandemic-influenza-vaccine-h5n1-baxter-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"30003","name":"Desloratadine Actavis : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2014-03-19T01:00:00Z","last_updated_date":"2023-06-01T14:54:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/desloratadine-actavis-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"30005","name":"Stronghold Plus : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2017-04-05T15:29:00Z","last_updated_date":"2025-07-07T15:29:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/stronghold-plus-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"30038","name":"Meloxidolor : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2013-12-04T01:00:00Z","last_updated_date":"2025-10-09T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/meloxidolor-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"30088","name":"Movymia : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2017-05-05T02:00:00Z","last_updated_date":"2025-04-24T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/movymia-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"30114","name":"Pemetrexed Pfizer : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2018-02-06T12:25:00Z","last_updated_date":"2021-07-28T13:25:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/pemetrexed-pfizer-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"30159","name":"Neparvis : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2016-10-05T02:00:00Z","last_updated_date":"2025-05-14T16:34:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/neparvis-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"30182","name":"Imatinib Accord : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2013-11-13T01:00:00Z","last_updated_date":"2024-07-02T16:28:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/imatinib-accord-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"30185","name":"Procomvax : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-07-29T02:00:00Z","last_updated_date":"2009-07-29T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/procomvax-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"30231","name":"Aripiprazole Sandoz : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2016-04-13T02:00:00Z","last_updated_date":"2025-06-24T17:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/aripiprazole-sandoz-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"30241","name":"Procox : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2011-07-12T02:00:00Z","last_updated_date":"2025-10-14T09:40:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/procox-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"30267","name":"Liprolog : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-08-28T02:00:00Z","last_updated_date":"2026-01-21T18:37:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/liprolog-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"30290","name":"Rilonacept Regeneron : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2010-07-06T02:00:00Z","last_updated_date":"2012-09-24T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/rilonacept-regeneron-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"30338","name":"Tolucombi : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2014-07-23T02:00:00Z","last_updated_date":"2025-06-24T14:16:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/tolucombi-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"30365","name":"Zontivity : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2015-10-30T01:00:00Z","last_updated_date":"2017-09-20T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/zontivity-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"30408","name":"Synagis : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-12-04T01:00:00Z","last_updated_date":"2023-10-11T17:22:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/synagis-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"30418","name":"Iressa : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2010-02-01T01:00:00Z","last_updated_date":"2023-07-17T11:36:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/iressa-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"30481","name":"Budesonide/Formoterol Teva : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2015-10-09T15:28:00Z","last_updated_date":"2017-01-31T14:28:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/budesonideformoterol-teva-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"30496","name":"Epoetin Alfa Hexal : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-10-12T02:00:00Z","last_updated_date":"2025-07-11T12:56:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/epoetin-alfa-hexal-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"30498","name":"Kaletra : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-09-23T02:00:00Z","last_updated_date":"2025-04-10T15:50:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/kaletra-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"30504","name":"Onglyza : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2010-09-01T02:00:00Z","last_updated_date":"2024-05-13T16:50:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/onglyza-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"30549","name":"Elonva : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2010-05-07T02:00:00Z","last_updated_date":"2025-10-30T14:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/elonva-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"30568","name":"Levetiracetam Actavis Group : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2012-09-12T02:00:00Z","last_updated_date":"2025-06-30T11:08:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/levetiracetam-actavis-group-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"30581","name":"Axura : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-09-07T02:00:00Z","last_updated_date":"2025-06-20T16:49:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/axura-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"30619","name":"Duloxetine Boehringer Ingelheim : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-08-17T02:00:00Z","last_updated_date":"2010-01-28T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/duloxetine-boehringer-ingelheim-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"30637","name":"Lonquex : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2014-05-16T02:00:00Z","last_updated_date":"2024-02-19T11:44:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/lonquex-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"30661","name":"Seebri Breezhaler : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2013-08-09T18:00:00Z","last_updated_date":"2025-08-06T18:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/seebri-breezhaler-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"30673","name":"Trumenba : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2018-01-17T01:00:00Z","last_updated_date":"2025-02-25T15:38:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/trumenba-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"30742","name":"Obizur : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2016-05-17T02:00:00Z","last_updated_date":"2025-11-21T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/obizur-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"30792","name":"Celvapan : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-11-15T01:00:00Z","last_updated_date":"2016-12-21T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/celvapan-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"30812","name":"RoActemra : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2010-01-08T01:00:00Z","last_updated_date":"2025-04-03T15:40:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/roactemra-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"30818","name":"Thalidomide BMS (previously Thalidomide Celgene) : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2008-05-19T03:09:00Z","last_updated_date":"2025-01-22T16:43:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/thalidomide-bms-previously-thalidomide-celgene-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"30825","name":"Cepedex : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2017-05-16T11:36:00Z","last_updated_date":"2024-11-11T11:36:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/cepedex-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"30845","name":"Topotecan Eagle : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2014-11-10T01:00:00Z","last_updated_date":"2014-11-14T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/topotecan-eagle-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"30848","name":"Tenofovir disoproxil Zentiva : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2017-03-23T01:00:00Z","last_updated_date":"2024-05-24T14:28:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/tenofovir-disoproxil-zentiva-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"30855","name":"Zenapax : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2008-04-08T03:09:21Z","last_updated_date":"2008-04-08T03:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/zenapax-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"30931","name":"Lutathera : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2018-04-11T18:25:00Z","last_updated_date":"2025-11-12T11:54:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/lutathera-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"30932","name":"Cometriq : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2014-08-14T02:00:00Z","last_updated_date":"2026-02-27T11:26:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/cometriq-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"30981","name":"Pregabalin Accord : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2016-02-22T01:00:00Z","last_updated_date":"2024-08-29T17:55:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/pregabalin-accord-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
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    {"id":"31020","name":"Torisel : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-09-22T02:00:00Z","last_updated_date":"2025-03-03T15:47:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/torisel-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
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    {"id":"31058","name":"Descovy : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2016-12-01T13:15:00Z","last_updated_date":"2023-02-17T15:16:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/descovy-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
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    {"id":"31086","name":"Lysodren : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-04-29T02:00:00Z","last_updated_date":"2025-04-08T11:47:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/lysodren-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
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    {"id":"31252","name":"Lynparza : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2016-04-13T02:00:00Z","last_updated_date":"2025-07-18T13:55:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/lynparza-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"31281","name":"Irbesartan / Hydrochlorothiazide Teva : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2010-03-30T02:00:00Z","last_updated_date":"2025-01-29T17:50:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/irbesartan-hydrochlorothiazide-teva-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"31288","name":"Budesonide/Formoterol Teva Pharma B.V. : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2015-10-26T14:58:00Z","last_updated_date":"2017-01-30T14:58:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/budesonideformoterol-teva-pharma-bv-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"31308","name":"Macugen : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-08-03T02:00:00Z","last_updated_date":"2019-06-27T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/macugen-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"31404","name":"Fablyn : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-08-07T02:09:21Z","last_updated_date":"2012-06-21T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/fablyn-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
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    {"id":"31629","name":"Champix : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-12-21T01:09:00Z","last_updated_date":"2025-09-11T16:59:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/champix-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"31655","name":"Pramipexole Accord : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2013-02-26T01:00:00Z","last_updated_date":"2024-03-11T14:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/pramipexole-accord-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"31671","name":"Ambirix : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2007-09-24T02:00:00Z","last_updated_date":"2024-02-08T12:41:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/ambirix-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"31689","name":"Suvaxyn Circo+MH RTU : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2016-07-20T02:00:00Z","last_updated_date":"2025-10-14T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/suvaxyn-circomh-rtu-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"31770","name":"Vpriv : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2010-11-18T01:00:00Z","last_updated_date":"2026-01-28T13:41:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/vpriv-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
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    {"id":"31810","name":"Ruconest : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2011-10-14T02:00:00Z","last_updated_date":"2025-12-19T12:49:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/ruconest-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
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    {"id":"31888","name":"Aldurazyme : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-07-27T02:00:00Z","last_updated_date":"2024-10-17T17:02:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/aldurazyme-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"31891","name":"Zyprexa : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-08-20T02:00:00Z","last_updated_date":"2025-06-06T17:05:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/zyprexa-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"31978","name":"Xigris : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-12-21T01:00:00Z","last_updated_date":"2012-02-21T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/xigris-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"31979","name":"Eylea : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2013-09-04T13:20:00Z","last_updated_date":"2025-06-27T12:32:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/eylea-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"32057","name":"Adempas : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2014-11-07T01:00:00Z","last_updated_date":"2025-08-06T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/adempas-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"32171","name":"Exforge HCT : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2010-08-26T02:00:00Z","last_updated_date":"2025-02-12T15:35:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/exforge-hct-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"32205","name":"Nobivac Myxo-RHD : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2014-04-23T02:00:00Z","last_updated_date":"2023-09-12T13:31:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/nobivac-myxo-rhd-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"32215","name":"Orgalutran : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2008-02-29T01:00:00Z","last_updated_date":"2025-12-18T17:20:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/orgalutran-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"32273","name":"Zyprexa Velotab : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-08-20T02:00:00Z","last_updated_date":"2024-12-18T15:40:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/zyprexa-velotab-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"32279","name":"Xarelto : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-12-01T01:09:00Z","last_updated_date":"2024-09-12T13:29:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/xarelto-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"32286","name":"Zevalin : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-11-03T01:00:00Z","last_updated_date":"2021-06-29T17:06:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/zevalin-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"32304","name":"Meloxivet : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-12-14T01:00:00Z","last_updated_date":"2018-05-28T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/meloxivet-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"32314","name":"Buccolam : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2012-08-09T02:00:00Z","last_updated_date":"2024-11-13T08:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/buccolam-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"32327","name":"Cystadrops : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2017-03-09T01:00:00Z","last_updated_date":"2025-08-08T14:13:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/cystadrops-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"32336","name":"Cinryze : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2012-06-28T13:36:00Z","last_updated_date":"2025-06-18T13:19:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/cinryze-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"32341","name":"Exalief : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-05-27T02:00:00Z","last_updated_date":"2012-08-16T17:30:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/exalief-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"32369","name":"Vedrop : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2011-04-19T02:00:00Z","last_updated_date":"2024-12-16T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/vedrop-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"32373","name":"Pemetrexed Lilly : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2016-02-29T01:00:00Z","last_updated_date":"2021-11-26T17:02:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/pemetrexed-lilly-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"32378","name":"Zepatier : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2017-02-03T15:44:00Z","last_updated_date":"2025-05-07T16:46:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/zepatier-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"32387","name":"TruScient : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2012-02-23T01:00:00Z","last_updated_date":"2015-02-03T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/truscient-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"32487","name":"Myozyme : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-09-07T02:00:00Z","last_updated_date":"2024-08-16T15:09:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/myozyme-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"32493","name":"Ratiograstim : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-11-26T01:00:00Z","last_updated_date":"2024-08-30T10:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/ratiograstim-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"32503","name":"Sevohale : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2016-08-19T02:00:00Z","last_updated_date":"2025-10-14T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/sevohale-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
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    {"id":"32625","name":"Sileo : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2016-02-10T01:00:00Z","last_updated_date":"2024-06-21T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/sileo-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
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    {"id":"32729","name":"Clopidogrel Zentiva: EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-10-27T17:05:00Z","last_updated_date":"2026-02-05T16:45:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/clopidogrel-zentiva-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"32784","name":"Accofil : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2015-03-12T01:00:00Z","last_updated_date":"2025-11-25T13:57:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/accofil-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"32801","name":"Remsima : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2014-01-27T01:00:00Z","last_updated_date":"2025-11-19T11:22:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/remsima-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"32809","name":"Metacam : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-11-25T01:00:00Z","last_updated_date":"2024-12-02T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/metacam-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"32868","name":"Rienso : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2012-08-10T17:50:00Z","last_updated_date":"2015-07-13T13:03:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/rienso-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"32945","name":"Irbesartan Hydrochlorothiazide Zentiva: EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-10-26T01:00:00Z","last_updated_date":"2025-01-29T14:08:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/irbesartan-hydrochlorothiazide-zentiva-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
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    {"id":"32979","name":"Gonazon : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-08-18T02:00:00Z","last_updated_date":"2012-08-15T12:20:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/gonazon-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"33010","name":"Sprimeo : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-06-18T02:00:00Z","last_updated_date":"2012-08-20T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/sprimeo-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"33028","name":"Ikervis : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2015-07-23T16:10:00Z","last_updated_date":"2026-01-15T14:02:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/ikervis-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
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    {"id":"33069","name":"Pixuvri : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2012-07-25T02:00:00Z","last_updated_date":"2021-12-07T11:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/pixuvri-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"33158","name":"Alkindi : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2018-07-13T16:25:00Z","last_updated_date":"2025-10-24T17:40:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/alkindi-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"33189","name":"Neocolipor : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2008-04-04T02:00:00Z","last_updated_date":"2025-01-31T15:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/neocolipor-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"33218","name":"Locatim : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-08-07T02:00:00Z","last_updated_date":"2025-10-09T12:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/locatim-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"33246","name":"Olysio : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2015-03-02T01:00:00Z","last_updated_date":"2018-05-23T17:45:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/olysio-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"33285","name":"Aripiprazole Mylan Pharma : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2016-04-18T02:00:00Z","last_updated_date":"2026-01-23T09:35:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/aripiprazole-mylan-pharma-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"33315","name":"Cyramza : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2015-02-11T01:00:00Z","last_updated_date":"2024-10-21T16:28:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/cyramza-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"33340","name":"Prac-tic : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2008-10-02T02:09:21Z","last_updated_date":"2025-10-13T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/prac-tic-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"33358","name":"Ceprotin : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2007-10-12T02:09:00Z","last_updated_date":"2026-05-21T11:36:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/ceprotin-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"33373","name":"Filgrastim ratiopharm : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2011-03-07T01:00:00Z","last_updated_date":"2011-07-20T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/filgrastim-ratiopharm-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"33405","name":"Retacrit : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-02-06T01:00:00Z","last_updated_date":"2025-04-22T16:28:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/retacrit-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"33409","name":"Scenesse : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2015-10-28T01:00:00Z","last_updated_date":"2025-10-17T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/scenesse-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"33411","name":"Onbrez Breezhaler : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2010-04-09T02:00:00Z","last_updated_date":"2025-09-30T14:25:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/onbrez-breezhaler-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"33428","name":"Velphoro : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2015-01-28T01:00:00Z","last_updated_date":"2026-03-24T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/velphoro-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"33436","name":"ViraferonPeg : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-09-17T02:00:00Z","last_updated_date":"2021-01-22T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/viraferonpeg-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"33447","name":"DepoCyte : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-06-08T02:00:00Z","last_updated_date":"2017-08-07T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/depocyte-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"33477","name":"Ibaflin : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2008-08-01T02:00:00Z","last_updated_date":"2010-06-24T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/ibaflin-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"33487","name":"Ocaliva : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2017-06-13T02:00:00Z","last_updated_date":"2025-01-20T13:14:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/ocaliva-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"33527","name":"Emend : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-08-12T02:00:00Z","last_updated_date":"2025-04-23T11:25:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/emend-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"33572","name":"Plavix : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-10-13T02:00:00Z","last_updated_date":"2025-07-14T12:15:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/plavix-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"33605","name":"Activyl : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2012-02-23T01:00:00Z","last_updated_date":"2024-06-17T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/activyl-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"33741","name":"Zutectra : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2010-08-07T01:31:00Z","last_updated_date":"2025-10-15T12:10:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/zutectra-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"33744","name":"Constella : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2012-11-30T01:00:00Z","last_updated_date":"2026-01-27T17:31:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/constella-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"33750","name":"Translarna : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2014-11-28T01:00:00Z","last_updated_date":"2025-04-16T12:49:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/translarna-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"33768","name":"Duaklir Genuair : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2015-02-23T01:00:00Z","last_updated_date":"2025-07-29T17:45:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/duaklir-genuair-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"33823","name":"Fasenra : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2018-05-18T02:00:00Z","last_updated_date":"2025-02-27T12:32:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/fasenra-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"33828","name":"Pantecta Control : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2011-06-23T02:00:00Z","last_updated_date":"2016-11-15T16:20:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/pantecta-control-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"33843","name":"Zykadia : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2015-07-09T02:00:00Z","last_updated_date":"2025-01-29T12:27:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/zykadia-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"33990","name":"Suprelorin : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2008-01-14T01:00:00Z","last_updated_date":"2024-02-15T15:06:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/suprelorin-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"33997","name":"Zyllt : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2010-09-07T02:00:00Z","last_updated_date":"2025-05-14T12:07:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/zyllt-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"34031","name":"Pregabalin Sandoz : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2015-11-26T01:00:00Z","last_updated_date":"2024-05-16T15:57:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/pregabalin-sandoz-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"34036","name":"Alisade : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-07-09T02:00:00Z","last_updated_date":"2010-03-05T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/alisade-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"34047","name":"Faslodex : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-02-18T00:09:00Z","last_updated_date":"2025-05-15T11:25:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/faslodex-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"34061","name":"Zinbryta : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"Adopted","consultation_date":"","first_published_date":"2016-09-22T12:45:00Z","last_updated_date":"2018-06-28T17:13:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/zinbryta-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"34076","name":"Tecentriq : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2018-01-25T14:34:00Z","last_updated_date":"2025-06-17T14:02:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/tecentriq-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"34160","name":"Prometax : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-02-13T01:00:00Z","last_updated_date":"2025-04-15T14:06:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/prometax-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"34166","name":"Ifirmasta : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-11-26T01:00:00Z","last_updated_date":"2025-05-23T17:53:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/ifirmasta-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"34218","name":"Semglee : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2018-06-04T02:00:00Z","last_updated_date":"2023-12-01T14:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/semglee-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"34233","name":"Dicural : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2008-11-18T00:09:21Z","last_updated_date":"2015-10-30T00:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/dicural-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"34255","name":"Glybera : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2014-09-03T02:00:00Z","last_updated_date":"2017-07-10T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/glybera-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"34257","name":"Lenvima : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2016-10-11T13:48:00Z","last_updated_date":"2025-04-22T16:15:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/lenvima-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"34270","name":"Zactran : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-10-05T02:09:00Z","last_updated_date":"2024-06-28T18:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/zactran-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"34293","name":"Azopt : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-01-26T01:00:00Z","last_updated_date":"2026-02-09T11:35:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/azopt-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"34312","name":"NovoNorm : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-02-18T01:00:00Z","last_updated_date":"2017-09-28T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/novonorm-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"34403","name":"Pantozol Control : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2011-06-23T11:22:00Z","last_updated_date":"2023-05-25T09:41:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/pantozol-control-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"34425","name":"Tamiflu : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-12-01T01:00:00Z","last_updated_date":"2023-03-24T13:29:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/tamiflu-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"34433","name":"Clopidogrel Acino Pharma : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"Adopted","consultation_date":"","first_published_date":"2011-03-30T02:00:00Z","last_updated_date":"2012-07-26T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/clopidogrel-acino-pharma-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"34476","name":"Aloxi : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-08-04T02:00:00Z","last_updated_date":"2018-07-19T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/aloxi-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"34509","name":"Equilis Te : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2008-07-23T02:09:00Z","last_updated_date":"2025-03-07T02:09:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/equilis-te-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"34519","name":"Versican Plus DHPPi : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2015-04-13T02:00:00Z","last_updated_date":"2024-12-19T14:30:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/versican-plus-dhppi-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"34524","name":"Vectra 3D : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2015-03-16T01:00:00Z","last_updated_date":"2024-06-13T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/vectra-3d-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"34543","name":"Zoledronic acid Actavis : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2013-06-25T19:00:00Z","last_updated_date":"2026-05-12T18:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/zoledronic-acid-actavis-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"34547","name":"SomaKit TOC : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2017-05-04T02:00:00Z","last_updated_date":"2025-03-04T14:47:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/somakit-toc-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"34589","name":"Halagon : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2018-02-26T17:34:00Z","last_updated_date":"2025-10-07T13:45:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/halagon-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"34664","name":"Pioglitazone Krka : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2014-07-14T02:00:00Z","last_updated_date":"2014-09-26T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/pioglitazone-krka-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"34685","name":"Riprazo HCT  : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2012-09-20T02:00:00Z","last_updated_date":"2012-09-20T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/riprazo-hct-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"34687","name":"Cymbalta : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-08-12T02:00:00Z","last_updated_date":"2024-07-09T15:40:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/cymbalta-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"34691","name":"Jevtana : EPAR - Procedural steps taken and scientific information after authorisation (archived)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2011-11-25T14:16:00Z","last_updated_date":"2024-09-03T13:08:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/jevtana-epar-procedural-steps-taken-scientific-information-after-authorisation-archived_en.pdf"},
    {"id":"34692","name":"Nobivac Piro : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-07-23T02:00:00Z","last_updated_date":"2009-07-23T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/nobivac-piro-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"34757","name":"Tyverb : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-12-01T01:00:00Z","last_updated_date":"2025-08-25T15:30:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/tyverb-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"34769","name":"Trifexis : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2014-01-24T01:00:00Z","last_updated_date":"2018-10-08T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/trifexis-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"34770","name":"Poulvac Flufend H5N3 RG : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-11-04T00:09:21Z","last_updated_date":"2012-05-08T01:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/poulvac-flufend-h5n3-rg-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"34788","name":"Silapo : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2008-12-10T01:00:00Z","last_updated_date":"2020-11-25T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/silapo-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"34868","name":"Cyltezo : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2018-03-21T01:00:00Z","last_updated_date":"2018-11-12T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/cyltezo-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"34886","name":"Xeljanz : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2017-07-19T12:25:00Z","last_updated_date":"2025-10-20T11:40:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/xeljanz-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"34888","name":"Cardalis : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2013-06-17T12:00:00Z","last_updated_date":"2024-11-11T12:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/cardalis-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"34891","name":"Briviact : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2016-05-19T11:48:00Z","last_updated_date":"2025-05-19T13:40:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/briviact-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"34903","name":"Vargatef : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2015-05-27T02:00:00Z","last_updated_date":"2024-08-22T15:45:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/vargatef-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"34904","name":"Janumet : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-12-09T00:09:00Z","last_updated_date":"2025-05-23T09:28:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/janumet-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"34905","name":"Daklinza : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2014-11-10T01:00:00Z","last_updated_date":"2019-08-22T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/daklinza-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"35067","name":"Vectra Felis : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2015-03-03T01:00:00Z","last_updated_date":"2025-10-15T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/vectra-felis-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"35068","name":"Victrelis : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2011-09-29T02:00:00Z","last_updated_date":"2018-07-31T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/victrelis-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"35087","name":"Rasitrio : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2012-09-20T02:00:00Z","last_updated_date":"2012-09-20T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/rasitrio-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"35093","name":"Spinraza : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2018-01-11T01:00:00Z","last_updated_date":"2026-01-29T13:45:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/spinraza-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf-0"},
    {"id":"35094","name":"Dafiro HCT : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2010-08-26T02:00:00Z","last_updated_date":"2025-02-12T13:56:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/dafiro-hct-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"35097","name":"Inflectra : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2013-10-25T02:00:00Z","last_updated_date":"2024-09-17T10:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/inflectra-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"35116","name":"Cytopoint : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2018-02-19T01:00:00Z","last_updated_date":"2025-03-17T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/cytopoint-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"35141","name":"Versican Plus Pi/L4R : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2016-05-20T02:00:00Z","last_updated_date":"2024-10-14T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/versican-plus-pi-l4r-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"35160","name":"Eryseng : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2015-08-21T02:00:00Z","last_updated_date":"2025-09-09T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/eryseng-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"35168","name":"Olanzapine Glenmark Europe : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2010-06-23T02:00:00Z","last_updated_date":"2026-05-08T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/olanzapine-glenmark-europe-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"35210","name":"Viracept : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2008-10-06T02:00:00Z","last_updated_date":"2014-06-10T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/viracept-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"35251","name":"Ytracis : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-03-10T01:09:00Z","last_updated_date":"2022-01-17T02:09:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/ytracis-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"35275","name":"Xalkori : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2013-03-07T10:00:00Z","last_updated_date":"2024-11-25T11:43:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/xalkori-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"35307","name":"Evra : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-04-06T02:00:00Z","last_updated_date":"2025-04-22T17:30:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/evra-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"35310","name":"Amglidia : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2018-08-22T12:32:00Z","last_updated_date":"2026-05-11T13:42:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/amglidia-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
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    {"id":"35360","name":"Zoledronic Acid Accord : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2015-03-10T01:00:00Z","last_updated_date":"2024-11-13T11:50:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/zoledronic-acid-accord-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"35361","name":"Jalra : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-09-17T02:09:00Z","last_updated_date":"2025-02-05T09:27:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/jalra-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"35376","name":"Olumiant : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2017-10-20T13:08:00Z","last_updated_date":"2025-07-25T16:58:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/olumiant-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"35406","name":"Truberzi : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2017-01-05T01:00:00Z","last_updated_date":"2021-02-25T09:40:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/truberzi-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
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    {"id":"35450","name":"Farydak : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2016-04-13T02:00:00Z","last_updated_date":"2025-10-01T17:42:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/farydak-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"35476","name":"Emtricitabine/Tenofovir disoproxil Krka : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2017-05-23T02:00:00Z","last_updated_date":"2024-06-20T08:24:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/emtricitabine-tenofovir-disoproxil-krka-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"35542","name":"Erelzi : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2017-09-29T02:00:00Z","last_updated_date":"2025-11-25T16:24:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/erelzi-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"35571","name":"Entyvio : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2015-05-20T12:00:00Z","last_updated_date":"2025-04-11T17:05:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/entyvio-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
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    {"id":"35602","name":"Zalmoxis : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2018-08-31T02:00:00Z","last_updated_date":"2018-08-31T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/zalmoxis-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
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    {"id":"35766","name":"Docetaxel Teva Pharma : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2012-02-08T01:00:00Z","last_updated_date":"2014-01-29T17:05:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/docetaxel-teva-pharma-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"35814","name":"Ongentys : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2017-02-02T18:03:00Z","last_updated_date":"2025-05-07T18:03:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/ongentys-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"35819","name":"Purevax RCCh : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-03-13T00:09:21Z","last_updated_date":"2015-01-23T00:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/purevax-rcch-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
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    {"id":"35872","name":"Temomedac : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2010-05-17T02:00:00Z","last_updated_date":"2022-03-28T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/temomedac-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"35875","name":"Duavive : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2015-07-22T02:00:00Z","last_updated_date":"2025-05-20T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/duavive-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"35884","name":"Prialt : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-05-08T02:00:00Z","last_updated_date":"2025-12-12T13:33:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/prialt-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
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    {"id":"35967","name":"Fluenz  : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2012-11-27T01:00:00Z","last_updated_date":"2014-12-03T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/fluenz-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"36015","name":"Conbriza : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2010-05-17T02:00:00Z","last_updated_date":"2025-05-20T10:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/conbriza-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"36041","name":"Cubicin : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-09-09T02:00:00Z","last_updated_date":"2025-05-28T17:05:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/cubicin-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"36060","name":"Eliquis : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2012-12-20T01:00:00Z","last_updated_date":"2025-09-29T16:23:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/eliquis-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"36064","name":"Omidria : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2017-04-04T02:00:00Z","last_updated_date":"2024-11-08T14:17:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/omidria-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"36101","name":"Plegridy : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2014-10-06T02:00:00Z","last_updated_date":"2025-10-16T14:17:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/plegridy-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"36156","name":"Fuzeon : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2008-11-10T01:00:00Z","last_updated_date":"2024-02-23T14:24:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/fuzeon-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"36207","name":"Tagrisso : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2016-04-12T02:00:00Z","last_updated_date":"2025-12-04T17:35:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/tagrisso-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"36251","name":"Alofisel : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2018-05-30T02:00:00Z","last_updated_date":"2025-01-21T14:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/alofisel-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"36285","name":"Orkambi : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2016-03-15T01:00:00Z","last_updated_date":"2025-09-30T17:45:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/orkambi-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"36339","name":"Optimark : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-04-23T02:09:21Z","last_updated_date":"2017-05-08T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/optimark-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"36422","name":"Avastin : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-09-17T15:08:00Z","last_updated_date":"2025-12-19T17:08:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/avastin-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"36425","name":"Sialanar : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2017-05-11T02:00:00Z","last_updated_date":"2025-04-11T11:20:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/sialanar-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"36445","name":"Revasc : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2007-10-03T02:00:00Z","last_updated_date":"2014-07-29T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/revasc-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"36466","name":"Lymphoseek : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2016-10-19T02:00:00Z","last_updated_date":"2024-08-14T14:08:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/lymphoseek-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"36502","name":"Ivabradine Accord : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2018-05-08T02:00:00Z","last_updated_date":"2024-09-06T15:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/ivabradine-accord-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"36547","name":"Luveris : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-08-11T02:00:00Z","last_updated_date":"2024-07-22T12:10:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/luveris-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"36619","name":"TachoSil : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-06-25T03:00:00Z","last_updated_date":"2025-06-17T03:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/tachosil-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"36622","name":"Bortezomib Sun : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2017-01-12T01:00:00Z","last_updated_date":"2025-05-06T13:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/bortezomib-sun-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"36698","name":"Neofordex : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2016-08-02T02:00:00Z","last_updated_date":"2026-04-09T16:20:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/neofordex-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"36704","name":"Memantine Mylan : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2015-07-31T02:00:00Z","last_updated_date":"2024-06-18T09:34:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/memantine-mylan-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"36712","name":"Cayston : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-11-04T01:00:00Z","last_updated_date":"2026-03-09T14:46:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/cayston-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"36730","name":"Azarga : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2010-01-13T01:00:00Z","last_updated_date":"2025-09-02T11:22:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/azarga-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"36746","name":"Lixiana : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2015-11-18T01:00:00Z","last_updated_date":"2025-08-27T13:10:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/lixiana-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"36754","name":"Aclasta : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-07-08T02:00:00Z","last_updated_date":"2026-04-20T10:53:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/aclasta-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"36759","name":"Clopidogrel BGR (previously Zylagren) : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2010-09-07T02:00:00Z","last_updated_date":"2020-03-11T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/clopidogrel-bgr-previously-zylagren-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"36772","name":"Ebymect : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2016-05-26T02:00:00Z","last_updated_date":"2025-05-23T16:19:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/ebymect-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"36799","name":"Dexdor : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2012-05-08T18:00:00Z","last_updated_date":"2025-06-11T09:45:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/dexdor-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"36848","name":"Levviax : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2008-02-15T00:09:21Z","last_updated_date":"2008-02-15T00:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/levviax-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"36862","name":"Fampyra : EPAR - Procedural steps taken and scientific information after authorisation (archived)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2012-03-27T02:00:00Z","last_updated_date":"2025-01-14T16:57:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/fampyra-epar-procedural-steps-taken-scientific-information-after-authorisation-archived_en.pdf"},
    {"id":"36914","name":"Apoquel : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2014-01-08T01:00:00Z","last_updated_date":"2024-06-25T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/apoquel-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"36918","name":"Yarvitan : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2008-10-27T01:00:00Z","last_updated_date":"2008-10-27T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/yarvitan-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"36948","name":"Forcaltonin : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2008-11-21T00:09:21Z","last_updated_date":"2008-11-21T00:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/forcaltonin-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"36954","name":"Vfend : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-10-27T16:39:00Z","last_updated_date":"2026-02-20T15:10:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/vfend-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"36994","name":"Porcilis ColiClos : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2014-04-14T02:00:00Z","last_updated_date":"2024-11-05T17:49:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/porcilis-coliclos-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"37032","name":"Fertavid : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2010-03-05T01:00:00Z","last_updated_date":"2020-06-23T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/fertavid-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"37088","name":"Zelboraf : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2013-01-25T12:55:00Z","last_updated_date":"2025-06-19T10:17:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/zelboraf-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"37089","name":"Zerit : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-11-16T01:00:00Z","last_updated_date":"2019-03-27T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/zerit-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"37100","name":"Osigraft : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2008-04-21T02:09:21Z","last_updated_date":"2016-07-27T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/osigraft-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"37147","name":"Ketek : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-11-16T01:00:00Z","last_updated_date":"2019-06-19T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/ketek-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"37151","name":"Qtern : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2017-06-13T02:00:00Z","last_updated_date":"2026-03-13T09:46:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/qtern-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"37215","name":"Pelzont : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-09-14T02:00:00Z","last_updated_date":"2013-03-22T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/pelzont-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"37256","name":"Enbrel : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-09-11T19:10:00Z","last_updated_date":"2024-06-06T14:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/enbrel-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"37278","name":"Granpidam : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2017-02-08T11:47:00Z","last_updated_date":"2023-04-11T17:22:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/granpidam-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"37345","name":"INOmax : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-11-23T01:00:00Z","last_updated_date":"2025-03-27T13:55:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/inomax-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"37394","name":"Busilvex : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2008-09-19T02:09:00Z","last_updated_date":"2023-08-04T12:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/busilvex-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"37395","name":"Epclusa : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2017-02-02T16:17:00Z","last_updated_date":"2023-08-14T16:18:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/epclusa-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"37401","name":"Zaltrap : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2014-08-14T02:00:00Z","last_updated_date":"2024-08-29T14:26:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/zaltrap-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"37412","name":"Abilify Maintena : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2014-04-08T03:00:00Z","last_updated_date":"2025-10-28T15:18:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/abilify-maintena-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"37460","name":"Rilutek : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-08-25T02:09:00Z","last_updated_date":"2024-08-21T15:15:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/rilutek-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"37510","name":"Ristaben : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2010-09-07T02:00:00Z","last_updated_date":"2025-10-30T12:45:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/ristaben-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"37557","name":"Infanrix Penta : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2008-10-03T02:00:00Z","last_updated_date":"2013-07-10T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/infanrix-penta-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"37563","name":"Clopidogrel Qualimed : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2010-08-09T02:00:00Z","last_updated_date":"2014-09-08T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/clopidogrel-qualimed-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"37608","name":"Purevax Rabies : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2012-01-27T12:00:00Z","last_updated_date":"2024-10-17T10:28:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/purevax-rabies-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"37636","name":"Kexxtone : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2014-06-11T02:00:00Z","last_updated_date":"2021-06-25T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/kexxtone-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"37674","name":"Erbitux : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-07-14T02:00:00Z","last_updated_date":"2026-01-26T11:55:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/erbitux-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"37760","name":"Firazyr : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-07-14T02:00:00Z","last_updated_date":"2026-01-29T14:50:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/firazyr-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"37854","name":"Levetiracetam Hospira : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2014-04-29T02:00:00Z","last_updated_date":"2025-05-12T14:38:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/levetiracetam-hospira-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"37881","name":"Pergoveris : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-07-31T02:00:00Z","last_updated_date":"2025-06-18T17:34:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/pergoveris-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"37971","name":"Micardis : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-06-25T02:09:00Z","last_updated_date":"2025-04-23T11:50:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/micardis-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"38001","name":"Avamys : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2010-01-18T01:00:00Z","last_updated_date":"2025-06-27T14:49:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/avamys-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"38102","name":"Toviaz : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-08-25T03:00:00Z","last_updated_date":"2025-03-04T10:56:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/toviaz-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"38156","name":"NovoSeven : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-07-14T11:26:00Z","last_updated_date":"2023-02-27T13:51:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/novoseven-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"38188","name":"Epivir : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-12-02T01:00:00Z","last_updated_date":"2022-08-29T14:37:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/epivir-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"38262","name":"Sepioglin : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2013-07-18T12:00:00Z","last_updated_date":"2013-07-18T12:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/sepioglin-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"38306","name":"HyQvia : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2014-01-24T01:00:00Z","last_updated_date":"2025-05-27T11:41:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/hyqvia-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"38320","name":"Akynzeo : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2016-08-11T02:00:00Z","last_updated_date":"2025-12-01T11:54:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/akynzeo-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"38324","name":"Bemfola : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2014-08-22T02:00:00Z","last_updated_date":"2024-01-12T18:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/bemfola-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"38377","name":"Hirobriz Breezhaler : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2010-04-09T02:00:00Z","last_updated_date":"2025-09-30T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/hirobriz-breezhaler-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
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    {"id":"38802","name":"Solymbic : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2018-01-31T16:58:00Z","last_updated_date":"2018-07-10T15:43:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/solymbic-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
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    {"id":"38903","name":"Stronghold : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2010-01-22T01:00:00Z","last_updated_date":"2024-06-28T11:10:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/stronghold-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"38917","name":"ellaOne : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-11-13T01:00:00Z","last_updated_date":"2025-04-03T13:42:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/ellaone-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"38959","name":"Dacogen : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2013-02-04T01:00:00Z","last_updated_date":"2024-10-02T15:10:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/dacogen-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"38962","name":"Competact : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-10-05T02:09:00Z","last_updated_date":"2023-08-16T10:37:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/competact-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"39081","name":"Versican Plus Pi/L4 : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2016-09-26T02:00:00Z","last_updated_date":"2019-05-17T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/versican-plus-pi-l4-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"39124","name":"Coxevac : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2011-08-11T02:00:00Z","last_updated_date":"2024-06-13T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/coxevac-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"39160","name":"Zubsolv : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2018-03-06T01:00:00Z","last_updated_date":"2025-04-01T11:02:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/zubsolv-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"39171","name":"Tracleer : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-08-05T02:09:00Z","last_updated_date":"2024-10-25T15:04:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/tracleer-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"39188","name":"Mysimba : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2016-01-12T01:00:00Z","last_updated_date":"2025-11-06T14:59:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/mysimba-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"39242","name":"Clopidogrel Krka : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-12-15T01:00:00Z","last_updated_date":"2025-05-14T09:49:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/clopidogrel-krka-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"39262","name":"Pemetrexed medac : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2017-06-01T11:36:00Z","last_updated_date":"2025-05-28T15:59:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/pemetrexed-medac-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"39361","name":"Omnitrope : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2008-04-02T02:00:00Z","last_updated_date":"2025-08-05T09:52:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/omnitrope-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"39362","name":"Lyxumia  : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2013-11-28T01:00:00Z","last_updated_date":"2026-02-05T16:56:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/lyxumia-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"39373","name":"Qutenza : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-03-23T01:00:00Z","last_updated_date":"2026-05-05T14:49:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/qutenza-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"39393","name":"Pumarix : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2012-02-27T01:00:00Z","last_updated_date":"2015-03-17T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/pumarix-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"39401","name":"Cotellic : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2016-02-12T01:00:00Z","last_updated_date":"2025-06-24T18:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/cotellic-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"39402","name":"Kadcyla : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2014-12-03T11:00:00Z","last_updated_date":"2026-03-24T10:50:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/kadcyla-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"39438","name":"Voncento : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2014-05-26T02:00:00Z","last_updated_date":"2024-12-18T11:43:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/voncento-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"39445","name":"Baraclude : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-10-13T03:00:00Z","last_updated_date":"2025-12-03T16:40:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/baraclude-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"39516","name":"Clopidogrel Krka d.d.: EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2010-03-25T01:00:00Z","last_updated_date":"2025-05-13T12:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/clopidogrel-krka-dd-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"39550","name":"Vectibix : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-06-18T03:00:00Z","last_updated_date":"2025-05-07T10:44:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/vectibix-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"39557","name":"Ifirmacombi : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2012-11-14T17:00:00Z","last_updated_date":"2025-05-23T12:01:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/ifirmacombi-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"39561","name":"Tredaptive : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-09-10T02:09:21Z","last_updated_date":"2013-03-22T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/tredaptive-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"39575","name":"CaniLeish : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2013-01-21T01:00:00Z","last_updated_date":"2023-10-24T13:12:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/canileish-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"39592","name":"Hizentra : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2011-12-08T01:00:00Z","last_updated_date":"2025-09-26T15:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/hizentra-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"39674","name":"Fareston : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-04-03T01:09:00Z","last_updated_date":"2024-07-30T12:23:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/fareston-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"39675","name":"Tresiba : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2013-10-30T13:00:00Z","last_updated_date":"2025-06-27T15:30:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/tresiba-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"39689","name":"Neupopeg : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-01-26T00:09:21Z","last_updated_date":"2009-01-26T00:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/neupopeg-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"39696","name":"Leflunomide ratiopharm : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2011-03-21T01:00:00Z","last_updated_date":"2025-12-18T13:10:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/leflunomide-ratiopharm-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"39734","name":"Paglitaz : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2014-07-14T02:00:00Z","last_updated_date":"2014-07-14T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/paglitaz-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"39741","name":"Duloxetine Viatris : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2015-01-12T01:00:00Z","last_updated_date":"2025-10-15T14:15:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/duloxetine-viatris-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"39755","name":"Topotecan Teva : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2010-02-12T01:00:00Z","last_updated_date":"2018-07-13T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/topotecan-teva-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"39889","name":"Lemtrada : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2014-03-26T01:00:00Z","last_updated_date":"2025-10-21T16:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/lemtrada-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"39900","name":"Suvaxyn PRRS MLV : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2018-05-24T02:00:00Z","last_updated_date":"2024-10-17T09:47:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/suvaxyn-prrs-mlv-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"39923","name":"Empliciti : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2016-12-15T16:45:00Z","last_updated_date":"2025-09-29T11:30:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/empliciti-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"39925","name":"Litak : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2005-10-21T02:00:00Z","last_updated_date":"2025-04-03T14:12:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/litak-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
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    {"id":"39951","name":"Brimica Genuair : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2015-02-04T01:00:00Z","last_updated_date":"2025-02-25T11:51:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/brimica-genuair-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"39966","name":"LeukoScan : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2007-08-13T02:00:00Z","last_updated_date":"2018-02-09T18:02:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/leukoscan-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"39976","name":"Ebixa : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-09-07T02:00:00Z","last_updated_date":"2022-01-05T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/ebixa-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"40037","name":"Viramune : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-06-11T03:00:00Z","last_updated_date":"2026-04-07T09:26:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/viramune-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"40127","name":"Brintellix : EPAR - Procedural steps taken and scientific information after authorisation (archived)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2014-06-06T02:00:00Z","last_updated_date":"2024-01-16T09:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/brintellix-epar-procedural-steps-taken-scientific-information-after-authorisation-archived_en.pdf"},
    {"id":"40170","name":"Bondronat : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2007-10-09T02:09:00Z","last_updated_date":"2024-04-08T17:36:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/bondronat-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"40188","name":"Xydalba : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2015-05-13T02:00:00Z","last_updated_date":"2025-05-23T08:22:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/xydalba-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"40224","name":"Ozurdex : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2011-07-04T02:00:00Z","last_updated_date":"2025-10-24T15:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/ozurdex-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"40244","name":"Spherox : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2018-05-31T13:43:00Z","last_updated_date":"2023-02-20T11:54:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/spherox-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"40249","name":"Ristempa : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2015-11-17T01:00:00Z","last_updated_date":"2018-03-07T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/ristempa-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"40333","name":"Ceplene : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2010-05-17T02:00:00Z","last_updated_date":"2023-04-19T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/ceplene-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"40335","name":"Temozolomide Sun : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2012-09-12T02:00:00Z","last_updated_date":"2024-05-21T14:25:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/temozolomide-sun-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"40338","name":"Reyataz : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-12-15T01:00:00Z","last_updated_date":"2024-10-16T15:46:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/reyataz-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"40358","name":"Travatan : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-02-03T01:09:00Z","last_updated_date":"2026-01-23T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/travatan-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"40388","name":"GONAL-f : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-08-07T02:09:00Z","last_updated_date":"2025-01-09T12:14:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/gonal-f-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"40407","name":"Altargo : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-04-28T02:00:00Z","last_updated_date":"2019-03-15T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/altargo-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"40435","name":"Parvoduk : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2015-12-09T01:00:00Z","last_updated_date":"2019-04-15T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/parvoduk-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"40440","name":"Zoledronic acid Teva : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2013-08-20T02:00:00Z","last_updated_date":"2025-09-25T12:23:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/zoledronic-acid-teva-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"40443","name":"Mirapexin : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-11-18T00:09:00Z","last_updated_date":"2024-04-30T17:09:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/mirapexin-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"40455","name":"Purevax FeLV : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2008-11-19T01:00:00Z","last_updated_date":"2024-12-19T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/purevax-felv-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"40539","name":"Livensa : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2008-09-26T02:00:00Z","last_updated_date":"2012-04-16T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/livensa-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"40541","name":"Duloxetine Lilly : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2015-08-11T02:00:00Z","last_updated_date":"2024-07-09T15:26:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/duloxetine-lilly-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"40549","name":"Firmagon : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-08-11T02:00:00Z","last_updated_date":"2022-03-30T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/firmagon-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"40563","name":"Enyglid : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2010-05-04T02:00:00Z","last_updated_date":"2022-12-14T16:50:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/enyglid-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"40617","name":"Qarziba : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2017-08-01T02:00:00Z","last_updated_date":"2023-10-27T12:04:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/qarziba-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"40621","name":"Zolvix : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2010-11-16T01:00:00Z","last_updated_date":"2024-06-25T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/zolvix-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"40722","name":"Eklira Genuair : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2020-12-01T01:00:00Z","last_updated_date":"2025-07-29T17:05:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/eklira-genuair-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"40730","name":"Trocoxil : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2010-01-29T01:00:00Z","last_updated_date":"2024-06-25T15:48:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/trocoxil-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"40767","name":"Jakavi : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2013-04-10T02:00:00Z","last_updated_date":"2025-02-11T13:53:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/jakavi-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"40850","name":"Kyprolis : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2016-04-26T02:00:00Z","last_updated_date":"2024-04-10T09:46:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/kyprolis-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"40891","name":"Ariclaim : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-07-16T02:00:00Z","last_updated_date":"2018-08-07T12:40:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/ariclaim-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"40997","name":"Myocet liposomal (previously Myocet) : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-11-12T01:00:00Z","last_updated_date":"2024-06-06T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/myocet-liposomal-previously-myocet-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"40998","name":"Elebrato Ellipta : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2018-06-12T17:27:00Z","last_updated_date":"2025-05-06T12:10:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/elebrato-ellipta-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"41003","name":"Mycophenolate mofetil Teva : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-10-15T02:09:00Z","last_updated_date":"2025-10-22T12:33:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/mycophenolate-mofetil-teva-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"41059","name":"Osseor : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-12-04T00:09:00Z","last_updated_date":"2018-12-07T18:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/osseor-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"41065","name":"Luminity : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-09-18T02:00:00Z","last_updated_date":"2023-06-28T16:54:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/luminity-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"41133","name":"Bretaris Genuair : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2013-01-24T01:00:00Z","last_updated_date":"2025-02-25T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/bretaris-genuair-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"41136","name":"Duloxetine Zentiva : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2015-12-02T01:00:00Z","last_updated_date":"2022-08-16T15:58:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/duloxetine-zentiva-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"41137","name":"Ventavis : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-07-03T03:00:00Z","last_updated_date":"2025-12-16T14:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/ventavis-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"41143","name":"Tekturna : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-09-25T02:09:21Z","last_updated_date":"2009-09-25T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/tekturna-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"41197","name":"Lonsurf : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2017-05-31T02:00:00Z","last_updated_date":"2024-04-05T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/lonsurf-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"41221","name":"Chenodeoxycholic acid Leadiant : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2017-06-29T02:00:00Z","last_updated_date":"2025-08-13T10:30:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/chenodeoxycholic-acid-leadiant-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"41225","name":"Equilis StrepE : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-06-15T02:09:00Z","last_updated_date":"2025-09-05T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/equilis-strepe-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"41268","name":"Leflunomide medac : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2011-09-26T02:00:00Z","last_updated_date":"2025-07-04T13:44:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/leflunomide-medac-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"41289","name":"Stayveer : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2014-10-02T02:00:00Z","last_updated_date":"2024-10-24T09:58:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/stayveer-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"41293","name":"RotaTeq : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-12-04T00:09:00Z","last_updated_date":"2025-04-25T17:42:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/rotateq-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"41330","name":"Thyrogen : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-05-12T02:09:00Z","last_updated_date":"2025-02-19T15:42:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/thyrogen-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
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    {"id":"41361","name":"Zulvac 1+8 Bovis : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2013-06-04T16:22:00Z","last_updated_date":"2025-10-15T18:42:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/zulvac-18-bovis-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
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    {"id":"41700","name":"Ionsys : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2008-07-25T02:00:00Z","last_updated_date":"2011-01-28T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/ionsys-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
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    {"id":"41816","name":"Aerivio Spiromax : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2017-04-10T15:47:00Z","last_updated_date":"2020-01-15T15:47:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/aerivio-spiromax-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
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    {"id":"41911","name":"Suliqua : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2017-05-23T11:27:00Z","last_updated_date":"2024-10-25T12:18:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/suliqua-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"41953","name":"Krystexxa : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2014-12-01T01:00:00Z","last_updated_date":"2016-07-22T15:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/krystexxa-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"41980","name":"Pregabalin Zentiva k.s. : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2018-02-05T01:00:00Z","last_updated_date":"2023-03-20T11:33:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/pregabalin-zentiva-ks-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"41988","name":"Riximyo : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2017-11-23T11:23:00Z","last_updated_date":"2025-05-28T16:42:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/riximyo-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"42001","name":"Pemetrexed Pfizer (previously Pemetrexed Hospira) : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2016-07-07T02:00:00Z","last_updated_date":"2025-04-25T10:35:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/pemetrexed-pfizer-previously-pemetrexed-hospira-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"42056","name":"Stelara : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2010-02-17T01:00:00Z","last_updated_date":"2026-04-24T15:50:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/stelara-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"42058","name":"Trazimera : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2018-09-18T16:44:00Z","last_updated_date":"2026-01-05T15:30:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/trazimera-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"42345","name":"Prasugrel Viatris (previously Prasugrel Mylan) : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2018-10-15T18:27:00Z","last_updated_date":"2025-03-25T11:49:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/prasugrel-viatris-previously-prasugrel-mylan-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"42352","name":"Ivabradine Zentiva : EPAR - Procedural steps taken and scientific information after the authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2018-10-17T10:17:00Z","last_updated_date":"2025-07-17T11:53:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/ivabradine-zentiva-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"42407","name":"Nobivac LeuFel : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2018-10-19T18:08:00Z","last_updated_date":"2025-09-02T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/nobivac-leufel-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"42421","name":"Tremfya : EPAR - Procedural steps taken and scientific information after the authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2018-10-23T12:52:00Z","last_updated_date":"2025-09-08T16:32:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/tremfya-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"42431","name":"Kisplyx : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2018-10-25T15:07:00Z","last_updated_date":"2026-04-21T14:30:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/kisplyx-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"42537","name":"Intrarosa : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2018-11-05T13:11:00Z","last_updated_date":"2024-01-15T17:50:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/intrarosa-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"42540","name":"Cuprior : EPAR - Procedural steps taken and scientific information after the authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2018-11-06T10:52:00Z","last_updated_date":"2024-03-26T16:30:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/cuprior-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"42543","name":"Suvaxyn Circo : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2018-11-06T12:37:00Z","last_updated_date":"2025-10-14T11:51:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/suvaxyn-circo-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"42572","name":"Coagadex : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2018-11-07T16:17:00Z","last_updated_date":"2025-03-04T16:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/coagadex-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"42620","name":"Verzenios : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2019-01-21T16:19:00Z","last_updated_date":"2024-08-23T15:11:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/verzenios-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"42652","name":"Zessly : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2018-11-12T15:25:00Z","last_updated_date":"2025-06-24T13:38:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/zessly-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"42654","name":"Carmustine medac : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2018-11-12T17:55:00Z","last_updated_date":"2024-01-05T11:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/carmustine-medac-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"42660","name":"Hyrimoz : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2018-11-13T13:25:00Z","last_updated_date":"2025-04-29T10:08:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/hyrimoz-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"42662","name":"Entecavir Accord : EPAR - Procedural steps taken and scientific information after the authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2018-11-13T15:19:00Z","last_updated_date":"2024-07-24T16:30:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/entecavir-accord-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"42672","name":"Hefiya : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2018-11-13T17:30:00Z","last_updated_date":"2025-04-29T18:10:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/hefiya-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"42895","name":"Braftovi : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2018-11-30T15:01:00Z","last_updated_date":"2025-07-09T15:55:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/braftovi-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"42910","name":"Halimatoz : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2018-12-03T17:32:00Z","last_updated_date":"2021-01-29T12:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/halimatoz-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"42911","name":"Myalepta : EPAR - Procedural steps taken and scientific information after authorisation (archived)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2018-12-03T18:01:00Z","last_updated_date":"2025-02-12T16:53:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/myalepta-epar-procedural-steps-taken-scientific-information-after-authorisation-archived_en.pdf"},
    {"id":"42927","name":"Cablivi : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2018-12-04T17:26:00Z","last_updated_date":"2026-04-09T15:14:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/cablivi-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"42933","name":"Lamzede : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2018-12-05T16:45:00Z","last_updated_date":"2026-03-02T11:24:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/lamzede-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"42936","name":"Pelgraz : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2018-12-05T17:24:00Z","last_updated_date":"2025-05-19T16:08:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/pelgraz-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"42946","name":"Onpattro : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2018-12-06T12:08:00Z","last_updated_date":"2024-06-04T12:15:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/onpattro-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"42950","name":"Sifrol : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2018-12-06T17:13:00Z","last_updated_date":"2024-04-25T12:09:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/sifrol-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"42955","name":"Respiporc FLUpan H1N1 : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2018-12-07T12:10:00Z","last_updated_date":"2025-10-14T15:24:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/respiporc-flupan-h1n1-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"43035","name":"Biktarvy : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2018-12-13T11:06:00Z","last_updated_date":"2024-07-23T17:19:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/biktarvy-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"43161","name":"Rubraca : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2018-12-19T15:00:00Z","last_updated_date":"2025-11-27T16:38:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/rubraca-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
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    {"id":"43299","name":"Febuxostat Viatris : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2019-01-10T15:44:00Z","last_updated_date":"2025-07-14T12:41:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/febuxostat-viatris-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"43364","name":"Vihuma : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"Adopted","consultation_date":"","first_published_date":"2019-01-15T15:56:00Z","last_updated_date":"2022-11-07T16:55:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/vihuma-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"43419","name":"Tegsedi : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2020-01-06T14:37:00Z","last_updated_date":"2024-01-17T16:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/tegsedi-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"43454","name":"Yescarta : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2019-01-23T10:43:00Z","last_updated_date":"2025-10-20T14:30:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/yescarta-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"43554","name":"Kisqali : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2019-01-30T12:44:00Z","last_updated_date":"2025-09-25T11:20:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/kisqali-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"43670","name":"Clevor : EPAR - Procedural steps taken and scientific information after the authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2019-02-07T17:26:00Z","last_updated_date":"2025-09-03T11:11:11Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/clevor-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"43691","name":"Juluca : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2019-02-11T14:52:00Z","last_updated_date":"2025-11-14T16:41:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/juluca-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"43695","name":"Zycortal : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2019-02-12T16:06:00Z","last_updated_date":"2025-10-15T17:20:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/zycortal-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"43696","name":"Mektovi : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2019-02-12T17:52:00Z","last_updated_date":"2025-11-05T17:10:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/mektovi-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"43708","name":"Palonosetron Accord : EPAR - Procedural steps taken and scientific information after the authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2019-02-13T18:24:00Z","last_updated_date":"2024-05-21T14:40:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/palonosetron-accord-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"43728","name":"Kigabeq : EPAR - Procedural steps taken and scientific information after the authorisation (archived)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2019-02-14T15:07:00Z","last_updated_date":"2025-01-23T09:55:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/kigabeq-epar-procedural-steps-taken-scientific-information-after-authorisation-archived_en.pdf"},
    {"id":"43774","name":"Hulio : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2019-11-11T12:56:00Z","last_updated_date":"2025-04-09T12:06:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/hulio-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"43778","name":"Alunbrig : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2019-02-18T16:06:00Z","last_updated_date":"2025-04-25T15:35:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/alunbrig-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"43822","name":"Eptifibatide Accord : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2019-02-20T12:40:00Z","last_updated_date":"2023-04-21T11:42:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/eptifibatide-accord-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"43963","name":"Emgality : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2019-03-01T16:02:00Z","last_updated_date":"2025-05-28T14:26:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/emgality-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"44026","name":"Delstrigo : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2019-03-14T09:42:00Z","last_updated_date":"2025-07-31T11:53:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/delstrigo-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"44030","name":"Vaborem : EPAR - Procedural steps taken and scientific information after the authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2019-03-14T13:24:00Z","last_updated_date":"2025-10-16T12:22:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/vaborem-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"44049","name":"Zulvac BTV : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2019-03-19T10:57:00Z","last_updated_date":"2025-10-15T15:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/zulvac-btv-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"44063","name":"Slenyto : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2019-03-19T16:58:00Z","last_updated_date":"2025-11-11T15:35:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/slenyto-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"44099","name":"Mepsevii : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2019-03-25T09:42:00Z","last_updated_date":"2024-06-28T17:13:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/mepsevii-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"44109","name":"Symkevi : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2019-03-26T15:33:00Z","last_updated_date":"2025-12-08T13:35:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/symkevi-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"44205","name":"Tacforius : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2019-04-10T09:33:00Z","last_updated_date":"2024-12-11T17:14:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/tacforius-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"44263","name":"Lenalidomide Accord : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2019-04-15T13:06:00Z","last_updated_date":"2026-02-24T14:30:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/lenalidomide-accord-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"44264","name":"Luxturna : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2019-04-15T13:21:00Z","last_updated_date":"2025-10-21T10:52:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/luxturna-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"44268","name":"Fulvestrant Mylan : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2019-04-15T16:29:00Z","last_updated_date":"2024-05-22T11:07:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/fulvestrant-mylan-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"44278","name":"Ilumetri : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2019-04-16T15:37:00Z","last_updated_date":"2025-07-16T12:44:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/ilumetri-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"44346","name":"Anagrelide Viatris (previously Anagrelide Mylan) : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2019-04-25T14:50:00Z","last_updated_date":"2025-03-03T14:56:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/anagrelide-viatris-previously-anagrelide-mylan-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"44348","name":"Fulphila : EPAR - Procedural steps taken and scientific information after authorisation (archived)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2019-04-25T14:59:00Z","last_updated_date":"2023-12-04T11:28:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/fulphila-epar-procedural-steps-taken-scientific-information-after-authorisation-archived_en.pdf"},
    {"id":"44350","name":"Ogivri : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2019-04-25T15:50:00Z","last_updated_date":"2026-02-23T16:15:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/ogivri-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"44351","name":"Verkazia : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2019-04-25T15:50:00Z","last_updated_date":"2026-01-15T13:09:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/verkazia-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"44354","name":"Vepured : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2019-04-25T17:23:00Z","last_updated_date":"2025-10-15T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/vepured-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"44401","name":"Entecavir Viatris : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2019-04-30T12:41:00Z","last_updated_date":"2025-03-10T17:30:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/entecavir-viatris-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"44440","name":"Aimovig : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2019-05-06T18:44:00Z","last_updated_date":"2025-12-01T16:52:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/aimovig-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"44446","name":"Arti-Cell Forte : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2019-05-07T09:31:00Z","last_updated_date":"2024-10-14T10:22:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/arti-cell-forte-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"44478","name":"Apealea : EPAR - Procedural steps taken and scientific information after the authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2019-05-10T13:45:00Z","last_updated_date":"2024-03-06T11:06:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/apealea-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"44490","name":"Zirabev : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2019-05-14T11:37:00Z","last_updated_date":"2025-06-10T10:54:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/zirabev-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"44506","name":"MiPet Easecto : EPAR - Procedural steps taken and scientific information after the authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2019-05-15T17:35:00Z","last_updated_date":"2024-06-11T13:25:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/mipet-easecto-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"44578","name":"Nerlynx : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2019-05-23T12:23:00Z","last_updated_date":"2025-05-23T08:03:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/nerlynx-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"44595","name":"Pifeltro : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2019-05-27T15:43:00Z","last_updated_date":"2025-12-11T08:41:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/pifeltro-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"44690","name":"Alpivab : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2019-06-12T10:38:00Z","last_updated_date":"2020-12-09T14:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/alpivab-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"44720","name":"Flucelvax Tetra : EPAR - Procedural steps taken and scientific information after the authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2019-06-17T14:58:00Z","last_updated_date":"2026-02-27T15:20:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/flucelvax-tetra-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"44743","name":"Innovax-ND-IBD : EPAR - Procedural steps taken and scientific information after the authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2019-06-19T09:27:00Z","last_updated_date":"2021-11-04T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/innovax-nd-ibd-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"44759","name":"Veltassa : EPAR - Procedural steps taken and scientific information after the authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2019-06-19T17:04:00Z","last_updated_date":"2024-06-11T11:24:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/veltassa-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
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    {"id":"45140","name":"Kromeya : EPAR - Procedural steps taken and scientific information after the authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2019-07-29T10:40:00Z","last_updated_date":"2019-10-23T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/kromeya-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
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    {"id":"45261","name":"Vantobra (previously Tobramycin PARI) : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2019-08-16T15:08:00Z","last_updated_date":"2023-12-13T14:40:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/vantobra-previously-tobramycin-pari-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
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    {"id":"45298","name":"Shingrix : EPAR - Procedural steps taken and scientific information after the authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2019-08-22T10:57:00Z","last_updated_date":"2025-07-17T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/shingrix-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"45304","name":"Imfinzi : EPAR - Procedural steps taken and scientific information after authorisation (archived)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2019-08-22T15:08:00Z","last_updated_date":"2025-07-11T11:10:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/imfinzi-epar-procedural-steps-taken-scientific-information-after-authorisation-archived_en.pdf"},
    {"id":"45351","name":"Rizmoic : EPAR - Procedural steps taken and scientific information after the authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2019-08-29T15:40:00Z","last_updated_date":"2025-06-19T08:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/rizmoic-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
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    {"id":"45358","name":"Idacio : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2019-08-30T12:58:00Z","last_updated_date":"2025-10-27T09:15:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/idacio-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"45390","name":"Riarify : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2019-09-06T14:55:00Z","last_updated_date":"2025-03-18T17:50:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/riarify-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"45394","name":"Trydonis : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2019-09-09T09:23:00Z","last_updated_date":"2026-03-17T18:15:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/trydonis-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"45479","name":"Syvazul BTV : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2019-09-19T13:48:00Z","last_updated_date":"2025-09-02T11:11:11Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/syvazul-btv-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"45543","name":"Takhzyro : EPAR - Procedural steps taken and scientific information after the authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2019-10-01T11:02:00Z","last_updated_date":"2025-06-02T14:35:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/takhzyro-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"45550","name":"Pemetrexed Krka : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2019-10-02T17:09:00Z","last_updated_date":"2024-07-30T14:14:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/pemetrexed-krka-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"45596","name":"Duzallo : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2019-10-08T16:05:00Z","last_updated_date":"2020-08-06T11:03:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/duzallo-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"45597","name":"Vyxeos liposomal : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2019-10-08T16:18:00Z","last_updated_date":"2024-05-13T13:40:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/vyxeos-liposomal-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"45599","name":"Dzuveo : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2019-10-08T16:45:00Z","last_updated_date":"2024-09-12T14:26:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/dzuveo-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"45657","name":"Pelmeg : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2019-10-11T10:31:00Z","last_updated_date":"2025-04-02T11:39:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/pelmeg-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"45697","name":"Miglustat Dipharma : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2019-10-14T16:54:00Z","last_updated_date":"2025-06-25T11:32:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/miglustat-dipharma-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"45724","name":"Dectova : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2019-10-16T15:04:00Z","last_updated_date":"2025-09-11T16:13:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/dectova-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"45775","name":"Bevespi Aerosphere : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2019-10-23T12:41:00Z","last_updated_date":"2024-12-03T09:16:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/bevespi-aerosphere-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"45779","name":"Dengvaxia : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2019-10-23T16:56:00Z","last_updated_date":"2025-12-04T15:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/dengvaxia-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"45841","name":"Febuxostat Krka : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2019-10-29T15:55:00Z","last_updated_date":"2025-03-27T14:02:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/febuxostat-krka-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"45854","name":"Udenyca : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2019-10-30T09:17:00Z","last_updated_date":"2019-11-29T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/udenyca-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"45856","name":"Libtayo : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2019-10-30T13:52:00Z","last_updated_date":"2025-12-10T10:20:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/libtayo-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"45890","name":"Pazenir : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2023-09-22T17:45:00Z","last_updated_date":"2026-06-02T15:47:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/pazenir-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"45958","name":"Skyrizi : EPAR - Procedural steps taken and scientific information after the authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2019-11-11T16:08:00Z","last_updated_date":"2026-01-19T11:50:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/skyrizi-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"46018","name":"Zynteglo : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2019-11-14T01:00:00Z","last_updated_date":"2021-12-10T11:42:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/zynteglo-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"46174","name":"Deferiprone Lipomed : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2019-11-26T17:43:00Z","last_updated_date":"2023-07-14T15:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/deferiprone-lipomed-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"46185","name":"Suvaxyn CSF Marker : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2019-11-27T13:21:00Z","last_updated_date":"2025-09-02T11:35:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/suvaxyn-csf-marker-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"46233","name":"Ziextenzo : EPAR - Procedural steps taken and scientific information after the authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2019-12-04T12:10:00Z","last_updated_date":"2026-03-27T11:06:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/ziextenzo-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"46293","name":"Cufence : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2019-12-11T12:01:00Z","last_updated_date":"2025-07-02T02:00:00Z","reference_number":"EMA/115243/2020","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/cufence-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"46321","name":"Exzolt : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2019-12-16T14:14:00Z","last_updated_date":"2024-06-25T11:08:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/exzolt-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"46383","name":"Frontpro : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2020-01-06T14:23:00Z","last_updated_date":"2024-12-02T13:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/frontpro-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"46386","name":"VeraSeal : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2020-01-06T15:08:00Z","last_updated_date":"2025-03-27T10:37:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/veraseal-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"46401","name":"Nityr : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2020-01-09T11:54:00Z","last_updated_date":"2020-01-09T11:54:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/nityr-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"46410","name":"Poteligeo : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2020-01-10T14:30:00Z","last_updated_date":"2025-05-21T14:11:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/poteligeo-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"46413","name":"Lorviqua : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2020-01-13T09:31:00Z","last_updated_date":"2026-04-15T10:19:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/lorviqua-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"46458","name":"Ajovy : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2020-01-20T11:22:00Z","last_updated_date":"2025-04-04T14:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/ajovy-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"46573","name":"Doptelet : EPAR - Procedural steps taken and scientific information after the authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2020-01-27T10:42:00Z","last_updated_date":"2025-06-18T16:40:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/doptelet-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"46667","name":"Zynquista : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2020-02-04T11:39:00Z","last_updated_date":"2022-08-16T15:26:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/zynquista-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"46678","name":"Jivi : EPAR - Procedural steps taken and scientific information after authorisation (archived)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2020-02-05T02:00:00Z","last_updated_date":"2025-11-04T17:07:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/jivi-epar-procedural-steps-taken-scientific-information-after-authorisation-archived_en.pdf"},
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    {"id":"47521","name":"ReproCyc ParvoFLEX : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2020-04-30T10:57:00Z","last_updated_date":"2025-10-14T11:11:11Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/reprocyc-parvoflex-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"47565","name":"Tavlesse : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2020-05-05T01:00:00Z","last_updated_date":"2024-12-02T11:36:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/tavlesse-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"47582","name":"Isturisa : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2016-03-07T01:00:00Z","last_updated_date":"2024-12-12T15:33:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/isturisa-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"47648","name":"Quofenix : EPAR - Procedural steps taken and scientific information after the authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2020-12-21T13:57:00Z","last_updated_date":"2025-03-05T11:50:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/quofenix-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"47658","name":"Stelfonta : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2020-05-13T17:04:00Z","last_updated_date":"2025-10-14T12:22:02Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/stelfonta-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"47788","name":"Nubeqa : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2020-05-28T00:09:00Z","last_updated_date":"2025-07-24T11:18:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/nubeqa-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"47939","name":"Rybelsus : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2020-06-10T15:22:00Z","last_updated_date":"2025-07-08T14:57:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/rybelsus-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"48008","name":"Nustendi : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2020-06-15T14:10:00Z","last_updated_date":"2026-02-27T14:24:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/nustendi-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"48032","name":"Talzenna : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2020-06-17T11:18:00Z","last_updated_date":"2025-08-29T15:15:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/talzenna-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"48036","name":"Refixia : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2020-06-17T12:32:00Z","last_updated_date":"2025-11-25T12:56:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/refixia-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"48061","name":"Vaxchora : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2020-06-22T10:25:00Z","last_updated_date":"2025-09-24T15:55:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/vaxchora-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"48114","name":"Nilemdo : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2020-06-24T16:51:00Z","last_updated_date":"2026-02-27T10:52:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/nilemdo-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"48125","name":"Felisecto Plus : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2020-06-25T13:58:00Z","last_updated_date":"2025-08-27T11:45:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/felisecto-plus-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"48199","name":"Bortezomib Fresenius Kabi : EPAR - Procedural steps taken and scientific information after the authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2020-07-01T16:49:00Z","last_updated_date":"2025-02-13T13:30:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/bortezomib-fresenius-kabi-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"48260","name":"Arsenic trioxide Accord : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2020-07-08T11:03:00Z","last_updated_date":"2026-03-13T10:06:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/arsenic-trioxide-accord-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"48275","name":"Mirataz : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2020-07-10T11:10:00Z","last_updated_date":"2025-10-09T14:40:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/mirataz-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"48285","name":"Gumbohatch : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2020-07-10T16:30:00Z","last_updated_date":"2024-02-15T15:21:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/gumbohatch-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"48299","name":"UpCard : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2020-07-14T10:47:00Z","last_updated_date":"2025-10-15T11:46:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/upcard-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"48341","name":"Dexmedetomidine Accord : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2020-07-21T11:19:00Z","last_updated_date":"2023-01-25T13:38:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/dexmedetomidine-accord-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"48421","name":"Nepexto : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2020-07-24T16:33:00Z","last_updated_date":"2025-03-03T15:15:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/nepexto-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"48431","name":"Lyumjev : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2020-07-27T17:22:00Z","last_updated_date":"2026-01-21T11:50:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/lyumjev-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"48451","name":"Fetcroja : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2020-07-28T11:45:00Z","last_updated_date":"2025-01-22T15:36:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/fetcroja-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"48517","name":"Vitrakvi : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2020-07-31T12:15:00Z","last_updated_date":"2026-05-26T15:18:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/vitrakvi-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"48538","name":"Simparica Trio : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2020-08-03T16:40:00Z","last_updated_date":"2024-06-13T11:55:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/simparica-trio-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"48610","name":"Nuceiva : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2020-08-13T17:38:00Z","last_updated_date":"2024-05-28T09:14:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/nuceiva-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"48684","name":"Ruxience : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2020-08-24T11:24:00Z","last_updated_date":"2025-02-13T15:48:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/ruxience-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"48761","name":"Cinacalcet Accordpharma : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2020-09-04T17:21:00Z","last_updated_date":"2026-03-31T12:36:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/cinacalcet-accordpharma-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"48776","name":"Vectormune FP ILT + AE : EPAR - Procedural steps taken and scientific information after the authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2020-09-09T13:44:00Z","last_updated_date":"2025-10-15T12:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/vectormune-fp-ilt-ae-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"48823","name":"Azacitidine Mylan : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2020-09-16T01:00:00Z","last_updated_date":"2025-04-07T15:50:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/azacitidine-mylan-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"48873","name":"Clopidogrel / Acetylsalicylic acid Viatris : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2020-09-21T15:59:00Z","last_updated_date":"2025-03-03T14:19:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/clopidogrel-acetylsalicylic-acid-viatris-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"48924","name":"Ervebo : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2020-09-30T18:03:00Z","last_updated_date":"2025-09-19T14:05:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/ervebo-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"48945","name":"Ivozall : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2020-10-05T12:48:00Z","last_updated_date":"2023-12-07T16:37:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/ivozall-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"48962","name":"Hepcludex  : EPAR - Procedural steps taken and scientific information after authorisation (archived)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2020-10-07T18:02:00Z","last_updated_date":"2025-02-04T16:02:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/hepcludex-epar-procedural-steps-taken-scientific-information-after-authorisation-archived_en.pdf"},
    {"id":"48995","name":"Inbrija : EPAR - Procedural steps taken and scientific information after the authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2020-10-12T12:29:00Z","last_updated_date":"2025-12-09T16:08:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/inbrija-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"49105","name":"Sunosi : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2021-09-27T16:36:00Z","last_updated_date":"2026-05-27T17:26:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/sunosi-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"49108","name":"Beovu : EPAR - Procedural steps taken and scientific information after the authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2020-10-22T15:14:00Z","last_updated_date":"2025-05-19T09:20:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/beovu-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"49118","name":"Sixmo : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2020-10-23T12:33:00Z","last_updated_date":"2025-08-14T11:14:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/sixmo-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf-0"},
    {"id":"49126","name":"Zeposia: EPAR - Procedural steps taken and scientific information after the authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2020-10-26T09:44:00Z","last_updated_date":"2026-03-03T10:31:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/zeposia-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"49134","name":"Tulissin : EPAR - Procedural steps taken and scientific information after the authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2020-10-27T09:10:00Z","last_updated_date":"2025-10-14T08:30:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/tulissin-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"49135","name":"Rozlytrek: EPAR - Procedural steps taken and scientific information after the authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2020-10-27T11:17:00Z","last_updated_date":"2025-06-10T15:45:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/rozlytrek-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"49138","name":"Deferasirox Mylan : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2020-10-27T17:52:00Z","last_updated_date":"2025-05-02T11:44:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/deferasirox-mylan-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"49159","name":"Spravato : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2020-10-29T17:28:00Z","last_updated_date":"2025-09-10T12:43:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/spravato-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"49165","name":"Palynziq : EPAR - Procedural steps taken and scientific information after the authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2020-10-30T16:22:00Z","last_updated_date":"2024-07-12T17:17:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/palynziq-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"49194","name":"Ayvakyt : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2020-11-06T16:26:00Z","last_updated_date":"2025-08-06T17:45:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/ayvakyt-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"49200","name":"Zolgensma : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2020-11-09T10:31:00Z","last_updated_date":"2025-08-28T16:13:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/zolgensma-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"49201","name":"Gencebok : EPAR - Procedural steps taken and scientific information after the authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2020-11-09T16:56:00Z","last_updated_date":"2025-03-12T11:48:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/gencebok-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"49261","name":"Equidacent : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2020-11-16T01:00:00Z","last_updated_date":"2020-11-16T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/equidacent-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"49292","name":"Polivy : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2020-11-19T16:21:00Z","last_updated_date":"2025-10-17T16:45:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/polivy-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"49299","name":"Azacitidine betapharm : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2020-11-20T13:43:00Z","last_updated_date":"2024-01-10T14:10:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/azacitidine-betapharm-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"49325","name":"Posaconazole Accord : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2020-11-24T10:12:00Z","last_updated_date":"2024-12-05T12:37:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/posaconazole-accord-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"49373","name":"Zercepac : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2020-11-26T09:25:00Z","last_updated_date":"2026-01-07T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/zercepac-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"49379","name":"Chanhold : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2020-11-26T16:29:00Z","last_updated_date":"2025-09-03T11:27:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/chanhold-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"49401","name":"Veklury : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2020-11-30T10:58:00Z","last_updated_date":"2025-06-26T09:40:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/veklury-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"49411","name":"Amsparity : EPAR - Procedural steps taken and scientific information after the authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2020-12-01T11:07:00Z","last_updated_date":"2025-08-20T10:44:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/amsparity-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"49491","name":"Aybintio : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2020-12-09T15:43:00Z","last_updated_date":"2025-12-02T11:38:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/aybintio-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"49499","name":"Kaftrio : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2020-12-09T18:17:00Z","last_updated_date":"2025-07-02T13:14:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/kaftrio-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"49741","name":"Livogiva : EPAR - Procedural steps taken and scientific Information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2021-01-07T10:51:00Z","last_updated_date":"2025-11-28T09:15:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/livogiva-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"49761","name":"Daurismo : EPAR - Procedural steps taken and scientific information after the authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2021-01-08T14:47:00Z","last_updated_date":"2025-05-07T13:34:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/daurismo-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"49786","name":"Comirnaty : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2021-01-12T15:17:00Z","last_updated_date":"2024-11-28T16:34:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/comirnaty-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"49828","name":"Recarbrio : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2021-01-18T15:39:00Z","last_updated_date":"2026-01-26T11:38:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/recarbrio-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"49961","name":"Piqray : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2021-01-28T11:50:00Z","last_updated_date":"2025-02-12T12:10:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/piqray-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"49984","name":"Blenrep : EPAR - Procedural steps taken and scientific information after the authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2021-01-29T11:54:00Z","last_updated_date":"2024-03-13T12:29:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/blenrep-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"49985","name":"Lacosamide UCB : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2021-01-29T13:08:00Z","last_updated_date":"2025-05-23T12:05:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/lacosamide-ucb-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"50039","name":"Ulipristal Acetate Gedeon Richter : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2021-02-03T10:20:00Z","last_updated_date":"2021-07-02T11:52:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/ulipristal-acetate-gedeon-richter-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"50112","name":"Dovprela : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2021-02-09T17:10:00Z","last_updated_date":"2026-05-07T16:56:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/dovprela-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"50113","name":"Insulin aspart Sanofi : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2021-02-10T09:20:00Z","last_updated_date":"2026-02-06T12:10:00Z","reference_number":"EMA/76214/2021","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/insulin-aspart-sanofi-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"50250","name":"Vizimpro : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2021-02-22T11:01:00Z","last_updated_date":"2024-12-17T10:45:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/vizimpro-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"50251","name":"Besremi : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2021-02-22T13:10:00Z","last_updated_date":"2025-10-21T15:11:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/besremi-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"50499","name":"Libmeldy : EPAR - Procedural steps taken and scientific information after the authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2021-03-09T12:51:00Z","last_updated_date":"2025-07-28T16:35:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/libmeldy-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"50523","name":"Vocabria : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2021-03-11T10:10:00Z","last_updated_date":"2025-09-09T14:55:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/vocabria-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"50644","name":"Givlaari : EPAR - Procedural steps taken and scientific information after the authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2021-03-18T15:21:00Z","last_updated_date":"2025-05-08T14:14:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/givlaari-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"50655","name":"Nityr : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2021-03-19T13:44:00Z","last_updated_date":"2023-06-15T09:56:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/nityr-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf-0"},
    {"id":"50664","name":"Trepulmix : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2021-03-22T11:46:00Z","last_updated_date":"2025-04-10T17:12:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/trepulmix-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"50670","name":"Nyvepria : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2021-03-23T09:43:00Z","last_updated_date":"2025-11-24T16:08:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/nyvepria-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"50672","name":"Staquis : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2021-03-23T09:55:00Z","last_updated_date":"2022-02-08T11:47:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/staquis-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"50681","name":"Spikevax (previously COVID-19 Vaccine Moderna): EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2021-03-23T14:35:00Z","last_updated_date":"2025-05-05T09:46:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/spikevax-previously-covid-19-vaccine-moderna-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
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    {"id":"51148","name":"Enteroporc Coli : EPAR - Procedural steps taken and scientific information after the authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2021-05-12T15:46:00Z","last_updated_date":"2024-05-31T15:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/enteroporc-coli-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"51156","name":"Yuflyma : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2021-05-17T11:08:00Z","last_updated_date":"2025-03-27T13:04:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/yuflyma-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
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    {"id":"51255","name":"Arsenic trioxide Mylan : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2021-05-25T14:44:00Z","last_updated_date":"2025-05-06T11:28:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/arsenic-trioxide-mylan-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"51263","name":"Tulaven : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2021-05-25T16:36:00Z","last_updated_date":"2025-10-14T10:35:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/tulaven-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"51270","name":"Tukysa : EPAR - Procedural steps taken and scientific information after the authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2021-05-26T10:38:00Z","last_updated_date":"2025-04-03T09:32:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/tukysa-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"51340","name":"Ontozry : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2021-06-02T12:53:00Z","last_updated_date":"2025-04-08T16:18:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/ontozry-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"51347","name":"Kesimpta : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2021-06-02T16:08:00Z","last_updated_date":"2025-12-16T09:12:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/kesimpta-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"51348","name":"Hydrocortisone aceponate Ecuphar (previously Cortacare) : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2021-06-02T17:29:00Z","last_updated_date":"2025-10-07T15:45:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/hydrocortisone-aceponate-ecuphar-previously-cortacare-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"51353","name":"Xospata : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2021-06-03T12:57:00Z","last_updated_date":"2026-01-16T15:13:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/xospata-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"51449","name":"Lumeblue : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2021-06-16T10:35:00Z","last_updated_date":"2025-06-17T16:40:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/lumeblue-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"51557","name":"Fintepla : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2021-06-23T14:58:00Z","last_updated_date":"2025-05-02T13:22:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/fintepla-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"51568","name":"Azacitidine Celgene : EPAR - Procedural steps taken and scientific information after the authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2021-06-24T09:51:00Z","last_updated_date":"2021-08-04T17:32:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/azacitidine-celgene-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"51785","name":"Adakveo : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2021-07-05T14:35:00Z","last_updated_date":"2023-08-21T13:55:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/adakveo-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"51804","name":"Baqsimi : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2021-07-05T17:26:00Z","last_updated_date":"2025-09-15T15:27:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/baqsimi-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
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    {"id":"52112","name":"Rekambys : EPAR - Procedural steps taken and scientific information after the authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2021-07-28T10:36:00Z","last_updated_date":"2025-09-10T17:32:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/rekambys-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
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    {"id":"52293","name":"BroPair Spiromax : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2021-08-27T16:25:00Z","last_updated_date":"2025-06-30T09:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/bropair-spiromax-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"52301","name":"Idefirix : EPAR - Procedural steps taken and scientific information after the authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2021-08-31T12:16:00Z","last_updated_date":"2025-07-02T14:24:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/idefirix-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"52302","name":"Fingolimod Accord : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2021-08-31T14:52:00Z","last_updated_date":"2025-04-11T17:15:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/fingolimod-accord-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"52303","name":"Lenalidomide krka d.d. Novo mesto : EPAR - Procedural steps taken and scientific information after the authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2021-08-31T15:02:00Z","last_updated_date":"2021-12-17T13:51:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/lenalidomide-krka-dd-novo-mesto-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"52304","name":"Mvabea : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2021-08-31T14:52:00Z","last_updated_date":"2025-04-07T14:51:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/mvabea-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"52310","name":"Lenalidomide Krka : EPAR - Procedural steps taken and scientific information after the authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2021-09-01T10:48:00Z","last_updated_date":"2026-01-07T17:19:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/lenalidomide-krka-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"52315","name":"Pemazyre : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2021-09-01T12:51:00Z","last_updated_date":"2026-03-17T16:35:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/pemazyre-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"52339","name":"Inrebic : EPAR - Procedural steps taken and scientific information after the authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2021-09-06T13:54:00Z","last_updated_date":"2026-01-13T12:29:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/inrebic-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"52345","name":"Onureg : EPAR - Procedural steps taken and scientific information after the authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2021-09-06T15:19:00Z","last_updated_date":"2026-01-09T10:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/onureg-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"52365","name":"Posaconazole AHCL : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2021-09-08T14:36:00Z","last_updated_date":"2024-11-12T14:23:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/posaconazole-ahcl-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"52426","name":"Oxlumo : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2021-09-13T12:28:00Z","last_updated_date":"2025-10-02T15:46:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/oxlumo-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"52435","name":"Ryeqo : EPAR - Procedural steps taken and scientific information after the authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2021-09-13T17:33:00Z","last_updated_date":"2026-05-20T13:44:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/ryeqo-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"52441","name":"Kirsty (previously Kixelle) : EPAR - Procedural steps taken and scientific information after the authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2021-09-14T13:24:00Z","last_updated_date":"2026-03-11T17:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/kirsty-previously-kixelle-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"52446","name":"Enspryng : EPAR - Procedural steps taken and scientific information after the authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2021-09-15T10:58:00Z","last_updated_date":"2025-05-16T13:41:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/enspryng-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"52610","name":"Enteroporc Coli AC : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2021-09-24T15:59:00Z","last_updated_date":"2025-09-05T11:11:11Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/enteroporc-coli-ac-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"52724","name":"Minjuvi : EPAR - Procedural steps taken and scientific information after the authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2021-10-05T11:16:00Z","last_updated_date":"2025-10-06T10:53:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/minjuvi-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"52810","name":"Abecma : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2021-10-12T11:49:00Z","last_updated_date":"2025-12-09T14:52:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/abecma-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"52814","name":"Zabdeno : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2021-10-12T15:27:00Z","last_updated_date":"2025-04-07T15:04:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/zabdeno-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"52849","name":"Nexpovio : EPAR - Procedural steps taken and scientific information after the authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2021-10-14T14:35:00Z","last_updated_date":"2023-08-17T17:11:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/nexpovio-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"52875","name":"Tecartus : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2021-10-15T14:51:00Z","last_updated_date":"2025-11-20T14:17:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/tecartus-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"52876","name":"Evicto : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2021-10-18T11:33:00Z","last_updated_date":"2024-06-25T16:44:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/evicto-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"52911","name":"Lenalidomide Krka d.d. : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2021-10-26T16:52:00Z","last_updated_date":"2023-07-10T12:22:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/lenalidomide-krka-dd-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"52988","name":"Imcivree : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2021-11-04T10:28:00Z","last_updated_date":"2026-01-27T15:30:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/imcivree-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"53009","name":"Elzonris : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2021-11-08T11:39:00Z","last_updated_date":"2025-10-27T13:23:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/elzonris-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"53023","name":"Arikayce liposomal : Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2021-11-09T09:10:00Z","last_updated_date":"2025-07-10T12:38:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/arikayce-liposomal-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"53052","name":"LysaKare : EPAR -  Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2021-11-10T11:35:00Z","last_updated_date":"2025-05-21T14:05:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/lysakare-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"53053","name":"Koselugo : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2021-10-13T15:51:00Z","last_updated_date":"2026-05-26T11:41:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/koselugo-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"53054","name":"Copiktra : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2021-11-10T16:09:00Z","last_updated_date":"2026-04-09T15:33:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/copiktra-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"53138","name":"Byooviz : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2021-11-16T15:49:00Z","last_updated_date":"2026-01-23T13:27:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/byooviz-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"53139","name":"Nevanac : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2021-11-16T16:03:00Z","last_updated_date":"2021-11-16T16:03:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/nevanac-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf-0"},
    {"id":"53144","name":"Silodosin Recordati : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2021-11-18T09:19:00Z","last_updated_date":"2025-03-10T15:06:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/silodosin-recordati-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"53206","name":"Evenity : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2021-11-23T09:50:00Z","last_updated_date":"2025-02-17T15:32:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/evenity-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"53259","name":"Supemtek Tetra : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2021-11-24T14:18:00Z","last_updated_date":"2025-04-10T18:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/supemtek-tetra-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"53266","name":"Phelinun : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2021-11-24T16:55:00Z","last_updated_date":"2025-06-18T16:30:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/phelinun-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"53270","name":"Ghryvelin (previously Macimorelin Aeterna Zentaris) : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2021-11-25T14:03:00Z","last_updated_date":"2024-05-13T14:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/ghryvelin-previously-macimorelin-aeterna-zentaris-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"53316","name":"Drovelis : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2021-11-29T14:18:00Z","last_updated_date":"2026-03-10T12:55:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/drovelis-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"53323","name":"Lydisilka : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2021-11-29T15:07:00Z","last_updated_date":"2026-03-10T15:48:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/lydisilka-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"53324","name":"Tigecycline Accord : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2021-11-29T15:23:00Z","last_updated_date":"2025-06-05T11:13:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/tigecycline-accord-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"53390","name":"Ubac : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2021-12-07T13:00:00Z","last_updated_date":"2025-10-14T11:11:11Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/ubac-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"53425","name":"Rivaroxaban Accord : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2021-12-09T09:35:00Z","last_updated_date":"2025-08-28T12:18:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/rivaroxaban-accord-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"53435","name":"Atazanavir Krka : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2021-12-09T11:55:00Z","last_updated_date":"2026-03-27T12:18:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/atazanavir-krka-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"53448","name":"Gavreto : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2021-12-13T11:49:00Z","last_updated_date":"2025-01-17T10:07:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/gavreto-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"53459","name":"Qinlock : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2021-12-13T17:44:00Z","last_updated_date":"2025-10-15T11:51:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/qinlock-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"53460","name":"Regkirona : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2021-12-13T17:44:00Z","last_updated_date":"2024-10-30T11:10:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/regkirona-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"53505","name":"Sunitinib Accord : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2021-12-14T16:56:00Z","last_updated_date":"2025-05-06T14:30:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/sunitinib-accord-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"53506","name":"Abevmy : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2021-12-14T17:08:00Z","last_updated_date":"2025-09-09T13:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/abevmy-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"53646","name":"Brukinsa : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2022-01-06T12:19:00Z","last_updated_date":"2025-10-02T11:02:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/brukinsa-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"53680","name":"Heplisav B : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2022-01-11T14:49:00Z","last_updated_date":"2026-01-28T09:08:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/heplisav-b-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"53738","name":"Ozawade : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2022-01-14T17:02:00Z","last_updated_date":"2025-11-18T10:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/ozawade-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"53823","name":"Xofluza : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2022-01-18T17:18:00Z","last_updated_date":"2025-07-31T16:46:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/xofluza-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"53832","name":"Evrysdi : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2022-01-19T12:56:00Z","last_updated_date":"2025-07-14T09:24:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/evrysdi-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"53833","name":"Klisyri : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2022-01-19T14:17:00Z","last_updated_date":"2026-02-19T14:30:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/klisyri-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"53909","name":"Nyxthracis (previously Obiltoxaximab SFL) : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2022-01-26T08:41:00Z","last_updated_date":"2024-09-09T10:46:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/nyxthracis-previously-obiltoxaximab-sfl-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"53916","name":"Arsenic trioxide medac : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2022-01-26T11:36:00Z","last_updated_date":"2026-04-21T14:17:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/arsenic-trioxide-medac-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"53919","name":"Cabazitaxel Accord : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2022-01-26T12:44:00Z","last_updated_date":"2025-05-07T13:13:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/cabazitaxel-accord-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"53980","name":"Oyavas : EPAR - Procedural steps taken and scientific information after authorisation (archived)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2022-01-28T09:51:00Z","last_updated_date":"2025-11-10T14:02:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/oyavas-epar-procedural-steps-taken-scientific-information-after-authorisation-archived_en.pdf"},
    {"id":"54154","name":"Mhyosphere PCV ID : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2022-02-14T16:31:00Z","last_updated_date":"2025-03-14T11:11:11Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/mhyosphere-pcv-id-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"54188","name":"NexGard Combo : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2022-02-16T08:55:00Z","last_updated_date":"2024-10-03T12:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/nexgard-combo-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"54196","name":"Ogluo : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2022-02-16T16:10:00Z","last_updated_date":"2025-05-16T17:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/ogluo-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"54200","name":"Abiraterone Mylan : EPAR - Procedural steps taken and scientific information after the authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2022-02-16T17:04:00Z","last_updated_date":"2026-01-19T13:59:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/abiraterone-mylan-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"54227","name":"Librela : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2022-02-21T10:12:00Z","last_updated_date":"2024-05-31T14:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/librela-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"54231","name":"Aspaveli : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2022-02-21T13:13:00Z","last_updated_date":"2025-11-10T10:50:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/aspaveli-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"54326","name":"Roclanda : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2022-03-02T12:21:00Z","last_updated_date":"2025-09-17T11:27:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/roclanda-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"54330","name":"Jayempi : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2022-03-02T16:19:00Z","last_updated_date":"2025-03-19T17:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/jayempi-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"54355","name":"Evant : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2022-03-04T16:38:00Z","last_updated_date":"2025-09-09T16:39:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/evant-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"54460","name":"Ponvory : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2022-03-15T10:25:00Z","last_updated_date":"2026-03-10T18:03:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/ponvory-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"54480","name":"Forceris : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2022-03-16T12:20:00Z","last_updated_date":"2024-06-17T13:54:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/forceris-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"54515","name":"Ronapreve : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2022-03-18T10:47:00Z","last_updated_date":"2026-01-23T14:08:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/ronapreve-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"54525","name":"Ngenla : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2022-03-21T10:32:00Z","last_updated_date":"2025-04-23T14:39:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/ngenla-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"54528","name":"Nuvaxovid : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2022-03-21T14:11:00Z","last_updated_date":"2025-08-01T11:14:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/nuvaxovid-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"54643","name":"Vumerity : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2022-03-31T16:20:00Z","last_updated_date":"2025-02-05T01:18:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/vumerity-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"54661","name":"Oxervate : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2022-04-04T11:19:00Z","last_updated_date":"2024-10-25T12:07:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/oxervate-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"54752","name":"Oxbryta : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2022-04-13T14:46:00Z","last_updated_date":"2024-06-04T13:57:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/oxbryta-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"54820","name":"Vaxneuvance : EPAR - Procedural steps taken and scientific information after authorisation (archived)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2022-04-25T10:58:00Z","last_updated_date":"2025-01-16T14:20:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/vaxneuvance-epar-procedural-steps-taken-scientific-information-after-authorisation-archived_en.pdf"},
    {"id":"54835","name":"Sibnayal : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2022-04-26T16:39:00Z","last_updated_date":"2025-05-16T14:22:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/sibnayal-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"54859","name":"Byfavo : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2022-04-28T15:37:00Z","last_updated_date":"2025-11-28T14:52:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/byfavo-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"54863","name":"Paxlovid : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2022-04-29T11:00:00Z","last_updated_date":"2025-12-04T11:20:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/paxlovid-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"54914","name":"Xevudy : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2022-05-06T13:34:00Z","last_updated_date":"2026-03-04T15:39:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/xevudy-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"54928","name":"Fampridine Accord : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2022-05-10T14:10:00Z","last_updated_date":"2025-01-07T12:50:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/fampridine-accord-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"54941","name":"Rhokiinsa : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2022-05-11T14:07:00Z","last_updated_date":"2025-07-23T10:55:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/rhokiinsa-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"54974","name":"Bimzelx : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2022-05-17T13:56:00Z","last_updated_date":"2026-05-08T16:54:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/bimzelx-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"55045","name":"Riltrava Aerosphere : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2022-05-20T13:55:00Z","last_updated_date":"2025-09-30T16:30:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/riltrava-aerosphere-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"55113","name":"Bylvay : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2022-05-31T09:53:00Z","last_updated_date":"2025-05-19T18:39:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/bylvay-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"55140","name":"Vydura : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2022-06-07T14:29:00Z","last_updated_date":"2024-01-24T09:40:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/vydura-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"55144","name":"Quviviq : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2022-06-08T09:53:00Z","last_updated_date":"2025-04-30T16:42:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/quviviq-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"55167","name":"Fingolimod Mylan : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2022-06-09T12:12:00Z","last_updated_date":"2025-08-21T16:22:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/fingolimod-mylan-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"55186","name":"Orgovyx : EPAR - Procedural steps taken and scientific information after information (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2022-06-10T16:50:00Z","last_updated_date":"2025-06-24T16:35:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/orgovyx-epar-procedural-steps-taken-scientific-information-after-information-archive_en.pdf"},
    {"id":"55193","name":"Dasatinib Accord : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2022-06-10T17:35:00Z","last_updated_date":"2023-03-30T11:20:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/dasatinib-accord-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"55221","name":"Dimethyl fumarate Neuraxpharm : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2022-06-13T14:24:00Z","last_updated_date":"2023-12-22T14:16:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/dimethyl-fumarate-neuraxpharm-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"55267","name":"Zynrelef : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2022-06-16T16:43:00Z","last_updated_date":"2023-11-22T12:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/zynrelef-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"55284","name":"Dimethyl fumarate Polpharma : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2023-12-22T12:01:00Z","last_updated_date":"2023-12-22T12:01:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/dimethyl-fumarate-polpharma-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"55367","name":"Sapropterin Dipharma : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2022-06-24T14:16:00Z","last_updated_date":"2025-02-20T14:18:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/sapropterin-dipharma-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"55469","name":"Sogroya : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2022-07-06T11:01:00Z","last_updated_date":"2025-12-04T13:02:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/sogroya-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"55487","name":"Abiraterone Krka : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2022-07-06T15:24:00Z","last_updated_date":"2026-01-16T13:15:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/abiraterone-krka-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"55517","name":"Trodelvy : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2022-07-12T11:41:00Z","last_updated_date":"2025-08-21T11:11:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/trodelvy-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"55605","name":"Dimethyl fumarate Mylan : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2023-12-22T10:52:00Z","last_updated_date":"2023-12-22T10:52:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/dimethyl-fumarate-mylan-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf-0"},
    {"id":"55646","name":"Evrenzo : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2022-07-22T10:41:00Z","last_updated_date":"2025-09-30T11:46:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/evrenzo-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"55677","name":"Kapruvia : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2022-07-25T11:44:00Z","last_updated_date":"2026-02-12T15:06:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/kapruvia-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"55681","name":"Vypeti : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2022-07-25T14:44:00Z","last_updated_date":"2026-05-29T14:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/vypeti-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"55682","name":"Uplizna : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2022-07-25T15:45:00Z","last_updated_date":"2025-11-27T14:08:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/uplizna-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"55688","name":"Wegovy : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2022-07-26T17:55:00Z","last_updated_date":"2026-05-04T13:03:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/wegovy-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"55720","name":"Hukyndra :  EPAR - Procedural steps taken and scientific information after authorisation (archived)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2022-07-28T14:33:00Z","last_updated_date":"2025-02-05T13:10:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/hukyndra-epar-procedural-steps-taken-scientific-information-after-authorisation-archived_en.pdf"},
    {"id":"55744","name":"Okedi : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2022-08-01T11:42:00Z","last_updated_date":"2025-10-14T14:03:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/okedi-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"55760","name":"COVID-19 Vaccine (inactivated, adjuvanted) Valneva : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2022-08-02T12:15:00Z","last_updated_date":"2023-12-01T14:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/covid-19-vaccine-inactivated-adjuvanted-valneva-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"55844","name":"Yselty : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2022-08-19T11:36:00Z","last_updated_date":"2025-11-21T15:44:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/yselty-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"55865","name":"Cibinqo : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2022-08-23T10:56:00Z","last_updated_date":"2025-07-08T15:52:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/cibinqo-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"55871","name":"Skytrofa (previously Lonapegsomatropin Ascendis Pharma) : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2022-08-25T09:41:00Z","last_updated_date":"2025-06-19T10:08:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/skytrofa-previously-lonapegsomatropin-ascendis-pharma-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"55877","name":"Ontilyv : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2022-08-25T16:09:00Z","last_updated_date":"2025-03-28T11:46:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/ontilyv-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"55922","name":"Sitagliptin / Metformin hydrochloride Accord : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2022-09-01T11:18:00Z","last_updated_date":"2025-11-13T15:06:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/sitagliptin-metformin-hydrochloride-accord-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"56050","name":"Pirfenidone axunio : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2022-09-09T14:49:00Z","last_updated_date":"2024-04-25T14:35:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/pirfenidone-axunio-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"56137","name":"Upstaza : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2022-09-20T09:20:00Z","last_updated_date":"2025-12-02T14:31:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/upstaza-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"56165","name":"Kinpeygo : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2022-09-22T11:31:00Z","last_updated_date":"2025-02-11T14:28:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/kinpeygo-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"56178","name":"Evkeeza : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2022-09-23T16:16:00Z","last_updated_date":"2025-01-07T10:45:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/evkeeza-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"56181","name":"Evusheld : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2022-09-26T10:02:00Z","last_updated_date":"2025-10-14T16:47:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/evusheld-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"56183","name":"Prevenar 20 (previously Apexxnar) : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2022-09-26T11:27:00Z","last_updated_date":"2025-04-24T08:47:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/prevenar-20-previously-apexxnar-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"56185","name":"Vyvgart : Procedural steps taken and scientific information after the authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2022-09-26T15:11:00Z","last_updated_date":"2026-01-15T12:40:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/vyvgart-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"56188","name":"Vegzelma : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2022-09-26T15:48:00Z","last_updated_date":"2026-01-28T13:37:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/vegzelma-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"56190","name":"Rybrevant: EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2022-09-26T16:51:00Z","last_updated_date":"2025-06-19T13:50:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/rybrevant-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"56284","name":"Sugammadex Mylan: EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2022-10-03T13:40:00Z","last_updated_date":"2025-03-12T12:13:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/sugammadex-mylan-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"56324","name":"Ranivisio : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2022-10-05T13:17:00Z","last_updated_date":"2025-06-06T11:22:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/ranivisio-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"56325","name":"Vildagliptin / Metformin hydrochloride Accord : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2022-10-05T13:49:00Z","last_updated_date":"2025-04-04T16:14:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/vildagliptin-metformin-hydrochloride-accord-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"56429","name":"Saphnelo : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2022-10-18T13:38:00Z","last_updated_date":"2026-01-28T15:17:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/saphnelo-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"56455","name":"Dasatinib Accordpharma : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2022-10-24T11:52:00Z","last_updated_date":"2023-03-30T11:55:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/dasatinib-accordpharma-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"56486","name":"Sitagliptin SUN : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2022-10-27T10:46:00Z","last_updated_date":"2025-02-26T13:31:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/sitagliptin-sun-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"56556","name":"Tezspire : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2022-11-09T08:53:00Z","last_updated_date":"2025-07-21T14:14:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/tezspire-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"56557","name":"Roctavian : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2022-11-09T11:16:00Z","last_updated_date":"2025-10-28T17:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/roctavian-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"56609","name":"Exparel liposomal : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2022-11-14T11:58:00Z","last_updated_date":"2025-08-13T15:38:52Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/exparel-liposomal-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"56790","name":"Adtralza : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2022-11-25T11:37:00Z","last_updated_date":"2025-05-19T11:58:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/adtralza-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"56795","name":"Tavneos : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2022-11-25T14:25:00Z","last_updated_date":"2025-01-31T16:45:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/tavneos-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"56829","name":"Lumykras : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2022-11-29T15:19:00Z","last_updated_date":"2024-12-03T15:21:11Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/lumykras-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"56909","name":"Lutetium (177Lu) chloride Billev : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2022-12-08T10:52:00Z","last_updated_date":"2024-11-29T16:21:56Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/lutetium-177lu-chloride-billev-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"57031","name":"Scemblix : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2022-12-15T12:25:00Z","last_updated_date":"2025-12-08T17:32:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/scemblix-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"57097","name":"Pepaxti : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2022-12-19T15:56:00Z","last_updated_date":"2025-01-13T15:39:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/pepaxti-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"57204","name":"Amvuttra : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2023-01-10T15:27:00Z","last_updated_date":"2025-06-12T15:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/amvuttra-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"57226","name":"Libmyris : EPAR - Procedural steps taken and scientific information after authorisation (archived)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2023-01-11T16:47:00Z","last_updated_date":"2024-10-16T09:34:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/libmyris-epar-procedural-steps-taken-scientific-information-after-authorisation-archived_en.pdf"},
    {"id":"57295","name":"Teriflunomide Viatris : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2023-01-16T12:09:00Z","last_updated_date":"2025-12-11T10:42:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/teriflunomide-viatris-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"57299","name":"Livtencity : EPAR - Procedural steps taken and scientific information after authorisation (archived)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2023-01-16T16:42:00Z","last_updated_date":"2024-03-26T14:20:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/livtencity-epar-procedural-steps-taken-scientific-information-after-authorisation-archived_en.pdf"},
    {"id":"57302","name":"Carvykti : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2023-01-17T10:47:00Z","last_updated_date":"2025-07-11T14:49:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/carvykti-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"57351","name":"Filsuvez: EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2023-01-23T09:32:00Z","last_updated_date":"2025-05-15T10:42:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/filsuvez-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"57382","name":"Tabrecta : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2023-01-25T12:07:00Z","last_updated_date":"2025-06-19T15:35:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/tabrecta-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"57500","name":"Locametz: EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2023-02-02T10:37:00Z","last_updated_date":"2025-02-13T14:35:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/locametz-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"57502","name":"Pluvicto : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2023-02-02T11:00:00Z","last_updated_date":"2025-09-02T11:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/pluvicto-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"57543","name":"Lupkynis : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2023-02-07T15:44:00Z","last_updated_date":"2025-06-19T11:41:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/lupkynis-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"57692","name":"Ebvallo : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2023-02-16T11:01:00Z","last_updated_date":"2025-11-24T09:39:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/ebvallo-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"57722","name":"Nulibry : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2023-02-20T09:50:00Z","last_updated_date":"2024-07-25T08:50:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/nulibry-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"57723","name":"Kerendia : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2023-02-20T09:57:00Z","last_updated_date":"2026-01-16T15:35:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/kerendia-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"57804","name":"Mounjaro : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2023-02-23T15:39:00Z","last_updated_date":"2026-02-26T13:45:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/mounjaro-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"57882","name":"Rivaroxaban Viatris : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2023-03-06T10:25:00Z","last_updated_date":"2025-06-04T12:12:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/rivaroxaban-viatris-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"58094","name":"Beyfortus : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2023-03-21T15:04:00Z","last_updated_date":"2025-06-24T17:28:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/beyfortus-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"58119","name":"PreHevbri : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2023-03-22T12:16:00Z","last_updated_date":"2025-01-10T13:43:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/prehevbri-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"58122","name":"Zynlonta : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2023-03-22T13:58:00Z","last_updated_date":"2025-11-25T16:41:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/zynlonta-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"58134","name":"Truvelog Mix 30 : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2023-03-23T15:19:00Z","last_updated_date":"2026-05-07T17:11:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/truvelog-mix-30-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"58157","name":"Zokinvy : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2023-03-24T14:28:00Z","last_updated_date":"2026-04-07T10:44:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/zokinvy-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"58201","name":"Tecovirimat SIGA : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2023-03-29T13:14:00Z","last_updated_date":"2025-11-10T10:20:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/tecovirimat-siga-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"58253","name":"Enjaymo : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2023-03-31T14:20:00Z","last_updated_date":"2025-03-21T14:06:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/enjaymo-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"58303","name":"Nexviadyme : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2023-04-05T17:35:00Z","last_updated_date":"2026-01-23T17:12:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/nexviadyme-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"58335","name":"Hemgenix : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2023-04-13T11:23:00Z","last_updated_date":"2026-03-04T17:13:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/hemgenix-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"58336","name":"Celdoxome pegylated liposomal : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2023-09-05T12:15:00Z","last_updated_date":"2025-11-27T17:22:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/celdoxome-pegylated-liposomal-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"58482","name":"Lunsumio : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2023-04-20T15:06:00Z","last_updated_date":"2026-01-07T13:53:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/lunsumio-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"58504","name":"Artesunate Amivas : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2023-04-24T14:05:00Z","last_updated_date":"2025-05-20T14:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/artesunate-amivas-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"58572","name":"Xenpozyme : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2023-05-03T13:46:00Z","last_updated_date":"2026-01-19T14:45:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/xenpozyme-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"58578","name":"Padcev : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2023-05-03T17:12:00Z","last_updated_date":"2025-07-17T14:17:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/padcev-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"58585","name":"Zolsketil pegylated liposomal : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2023-05-04T13:36:00Z","last_updated_date":"2025-03-13T12:15:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/zolsketil-pegylated-liposomal-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"58657","name":"Camcevi : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2023-05-12T13:38:00Z","last_updated_date":"2025-04-03T15:51:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/camcevi-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"58737","name":"Eladynos : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2023-05-22T17:00:00Z","last_updated_date":"2024-04-12T12:24:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/eladynos-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"58783","name":"Livmarli: EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2023-05-25T16:48:00Z","last_updated_date":"2026-04-17T16:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/livmarli-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"58785","name":"Breyanzi : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2023-05-25T16:17:00Z","last_updated_date":"2025-05-07T17:30:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/breyanzi-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"58999","name":"Ximluci : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2023-06-20T08:42:00Z","last_updated_date":"2024-03-26T12:42:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/ximluci-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"59006","name":"Voxzogo : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2023-06-20T14:08:00Z","last_updated_date":"2024-07-17T16:32:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/voxzogo-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"59029","name":"Opzelura : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2023-06-22T09:41:00Z","last_updated_date":"2025-07-28T14:39:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/opzelura-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"59097","name":"Sunlenca : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2023-06-27T08:40:00Z","last_updated_date":"2025-12-16T15:20:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/sunlenca-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"59147","name":"Bimervax : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-05-26T15:01:00Z","last_updated_date":"2026-05-05T15:20:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/bimervax-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"59148","name":"Hyftor : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2023-06-29T15:11:00Z","last_updated_date":"2025-07-04T14:06:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/hyftor-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
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    {"id":"59563","name":"Plerixafor Accord : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2023-08-07T16:18:00Z","last_updated_date":"2024-05-13T14:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/plerixafor-accord-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"59918","name":"Imjudo : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2023-09-08T12:22:00Z","last_updated_date":"2025-08-14T15:40:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/imjudo-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"59925","name":"Teriparatide Sun : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2023-09-08T15:48:00Z","last_updated_date":"2024-09-13T14:10:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/teriparatide-sun-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"59928","name":"Tremelimumab AstraZeneca : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2023-09-11T11:02:00Z","last_updated_date":"2024-08-22T10:42:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/tremelimumab-astrazeneca-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"59968","name":"Lacosamide Adroiq : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2023-09-14T11:52:00Z","last_updated_date":"2025-09-25T16:24:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/lacosamide-adroiq-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"59996","name":"Melatonin Neurim : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2023-09-14T16:53:00Z","last_updated_date":"2023-09-14T16:53:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/melatonin-neurim-epar-procedural-steps-taken-and-scientific-information-after-authorisation_en.pdf"},
    {"id":"60115","name":"Opfolda: EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2023-09-22T14:38:00Z","last_updated_date":"2025-02-14T12:34:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/opfolda-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
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    {"id":"60268","name":"Kimmtrak : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2023-10-05T12:16:00Z","last_updated_date":"2025-03-07T16:11:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/kimmtrak-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"60409","name":"Sugammadex Adroiq : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2023-10-12T17:28:00Z","last_updated_date":"2025-04-08T14:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/sugammadex-adroiq-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"60452","name":"Briumvi : EPAR - Procedural steps taken and scientific information after the authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2023-10-18T19:22:00Z","last_updated_date":"2025-10-08T16:13:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/briumvi-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"60455","name":"Lytgobi : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2023-10-19T16:33:00Z","last_updated_date":"2025-10-29T13:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/lytgobi-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"60484","name":"Pedmarqsi : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2023-10-25T14:18:00Z","last_updated_date":"2025-05-23T15:23:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/pedmarqsi-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"60804","name":"VidPrevtyn Beta : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2023-11-08T14:45:00Z","last_updated_date":"2024-03-20T13:20:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/vidprevtyn-beta-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"60978","name":"Tyruko : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2023-11-24T12:29:38Z","last_updated_date":"2026-03-06T15:47:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/tyruko-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"61029","name":"Pirfenidone Viatris : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2023-11-28T18:10:09Z","last_updated_date":"2023-11-28T18:10:09Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/pirfenidone-viatris-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"61042","name":"Kauliv : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2023-11-20T14:45:24Z","last_updated_date":"2024-11-25T15:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/kauliv-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"61046","name":"Talvey : EPAR - Procedural steps taken and scientific information after the authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2023-11-29T15:20:28Z","last_updated_date":"2025-10-02T15:18:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/talvey-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"61058","name":"Pylclari : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2023-11-30T10:32:54Z","last_updated_date":"2025-05-26T10:54:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/pylclari-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"61222","name":"Yesafili : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2023-12-04T18:09:35Z","last_updated_date":"2024-12-09T10:36:15Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/yesafili-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"61275","name":"Epysqli : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2023-12-06T15:48:12Z","last_updated_date":"2024-03-18T10:15:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/epysqli-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"61566","name":"Dabigatran Etexilate Accord : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2023-12-21T13:19:02Z","last_updated_date":"2026-04-22T16:49:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/dabigatran-etexilate-accord-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"61579","name":"Sotyktu : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2023-12-21T16:47:04Z","last_updated_date":"2026-05-12T17:27:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/sotyktu-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"61633","name":"Finlee : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2024-01-04T16:32:13Z","last_updated_date":"2025-11-03T14:50:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/finlee-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"61638","name":"Columvi : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2024-01-05T13:04:05Z","last_updated_date":"2025-05-28T16:22:19Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/columvi-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"61676","name":"Tevimbra : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2024-01-09T16:17:20Z","last_updated_date":"2025-09-16T10:25:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/tevimbra-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"61764","name":"Tibsovo : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2024-01-15T14:17:14Z","last_updated_date":"2026-02-25T10:45:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/tibsovo-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"61807","name":"Dapagliflozin Viatris : EPAR - Procedural steps taken and scientific information after the authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2024-01-18T11:26:13Z","last_updated_date":"2026-01-26T09:09:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/dapagliflozin-viatris-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"61839","name":"Rayvow : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2024-01-23T11:06:43Z","last_updated_date":"2026-02-06T14:10:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/rayvow-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"61892","name":"Icatibant Accord : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2024-01-25T14:14:12Z","last_updated_date":"2026-04-16T17:56:29Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/icatibant-accord-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"62063","name":"Tyenne : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2024-02-09T15:26:55Z","last_updated_date":"2025-06-17T15:40:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/tyenne-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"62072","name":"Voraxaze : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2024-02-12T13:05:48Z","last_updated_date":"2026-01-07T14:05:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/voraxaze-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"62098","name":"Catiolanze : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2024-02-13T12:17:07Z","last_updated_date":"2024-02-13T12:17:07Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/catiolanze-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"62132","name":"Orserdu : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2024-02-14T12:23:56Z","last_updated_date":"2025-10-14T10:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/orserdu-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"62214","name":"Veoza :  EPAR - Procedural steps taken and scientific information after the authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2024-02-19T16:29:44Z","last_updated_date":"2025-03-21T12:50:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/veoza-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"62236","name":"Opdualag : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"Adopted","consultation_date":"","first_published_date":"2024-02-21T11:24:37Z","last_updated_date":"2025-07-11T11:34:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/opdualag-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"62287","name":"Arexvy : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2024-02-23T15:33:47Z","last_updated_date":"2025-06-26T14:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/arexvy-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"62306","name":"Sugammadex Piramal: EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2024-02-26T16:58:25Z","last_updated_date":"2024-02-26T16:58:25Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/sugammadex-piramal-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"62439","name":"Vafseo: EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2024-03-05T15:08:46Z","last_updated_date":"2025-03-27T11:29:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/vafseo-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"62497","name":"Skyclarys : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2024-03-08T14:06:19Z","last_updated_date":"2025-03-04T10:21:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/skyclarys-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"62647","name":"Ertapenem SUN : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2024-03-19T12:38:08Z","last_updated_date":"2024-04-03T16:16:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/ertapenem-sun-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"62649","name":"Abrysvo : EPAR - Procedural steps taken and scientific information after the authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2024-03-20T12:02:16Z","last_updated_date":"2025-08-20T08:12:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/abrysvo-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
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    {"id":"62986","name":"Tepkinly : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2024-04-17T13:37:00Z","last_updated_date":"2025-09-19T10:26:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/tepkinly-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"62988","name":"Teriflunomide Accord : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2024-04-17T15:12:58Z","last_updated_date":"2026-02-24T14:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/teriflunomide-accord-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"62994","name":"Dabigatran etexilate Teva : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2024-04-18T08:39:48Z","last_updated_date":"2025-01-21T11:20:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/dabigatran-etexilate-teva-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"63004","name":"Rosuvastatin/ perindopril /indapamide : List of nationally authorised medicinal products - PSUSA/00010752/202308","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2024-04-19T08:35:13Z","last_updated_date":"2024-04-19T08:35:13Z","reference_number":"EMA/170085/2024","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/rosuvastatin-perindopril-indapamide-list-nationally-authorised-medicinal-products-psusa-00010752-202308_en.pdf"},
    {"id":"63205","name":"Agamree : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2024-05-13T16:29:00Z","last_updated_date":"2025-12-16T12:09:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/agamree-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"63208","name":"Thalidomide Lipomed : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2024-05-14T13:32:00Z","last_updated_date":"2025-09-15T14:45:31Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/thalidomide-lipomed-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"63212","name":"Ryzneuta : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2024-05-15T12:26:00Z","last_updated_date":"2025-09-03T08:56:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/ryzneuta-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"63218","name":"Pregabalin Viatris : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2024-05-16T11:00:00Z","last_updated_date":"2026-05-08T08:56:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/pregabalin-viatris-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"63227","name":"Pregabalin Sandoz : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2024-05-16T11:00:00Z","last_updated_date":"2025-12-02T10:35:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/pregabalin-sandoz-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"63237","name":"Temozolomide Teva : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2024-05-16T14:00:00Z","last_updated_date":"2024-05-16T14:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/temozolomide-teva-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"63255","name":"Miglustat Gen.Orph : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2024-05-17T14:00:00Z","last_updated_date":"2025-06-24T16:59:27Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/miglustat-genorph-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"63284","name":"Mysildecard : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2024-05-21T14:21:19Z","last_updated_date":"2026-05-07T16:40:06Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/mysildecard-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
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    {"id":"63292","name":"Fulvestrant Mylan : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2024-05-22T10:00:00Z","last_updated_date":"2025-10-09T12:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/fulvestrant-mylan-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"63298","name":"Spexotras : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2024-05-22T11:50:00Z","last_updated_date":"2025-08-20T14:10:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/spexotras-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"63299","name":"Krazati : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2024-05-22T12:06:00Z","last_updated_date":"2025-12-02T10:10:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/krazati-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"63317","name":"Darunavir Viatris : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2024-05-24T11:57:00Z","last_updated_date":"2026-05-07T11:11:01Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/darunavir-viatris-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"63318","name":"Atazanavir Viatris : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2024-05-24T12:00:00Z","last_updated_date":"2026-05-07T11:11:11Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/atazanavir-viatris-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"63329","name":"Loargys : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2024-05-27T16:36:00Z","last_updated_date":"2025-11-05T10:44:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/loargys-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"63451","name":"Zilbrysq : EPAR - Procedural steps taken and scientific information after the authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2024-06-03T11:24:00Z","last_updated_date":"2025-04-29T14:06:24Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/zilbrysq-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"63476","name":"Pirfenidone Viatris : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2024-06-04T14:00:00Z","last_updated_date":"2025-12-19T12:12:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/pirfenidone-viatris-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"63504","name":"Qdenga : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2024-06-06T10:10:00Z","last_updated_date":"2026-01-30T08:50:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/qdenga-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"63512","name":"Sitagliptin/Metformin hydrochloride Sun : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2024-06-06T12:12:00Z","last_updated_date":"2024-06-06T12:12:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/sitagliptin-metformin-hydrochloride-sun-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"63513","name":"Litfulo : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2024-06-06T13:18:00Z","last_updated_date":"2025-03-03T14:22:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/litfulo-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"63688","name":"Sondelbay : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2024-06-19T15:57:00Z","last_updated_date":"2025-05-15T11:51:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/sondelbay-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"63693","name":"Atosiban SUN : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2024-06-20T09:56:48Z","last_updated_date":"2024-06-20T09:56:48Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/atosiban-sun-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"63707","name":"Nintedanib Accord : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2024-06-20T14:32:00Z","last_updated_date":"2025-08-14T11:35:50Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/nintedanib-accord-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"63744","name":"Imatinib Accord : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2024-06-25T11:59:25Z","last_updated_date":"2026-06-01T11:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/imatinib-accord-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"63762","name":"Vanflyta : EPAR - Procedural steps taken and scientific information after authorisation (archived)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2024-06-26T15:17:00Z","last_updated_date":"2024-12-18T15:08:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/vanflyta-epar-procedural-steps-taken-scientific-information-after-authorisation-archived_en.pdf"},
    {"id":"63766","name":"Uzprovo : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2024-06-27T12:08:00Z","last_updated_date":"2025-03-11T17:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/uzprovo-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"63799","name":"Aquipta : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2024-06-28T12:40:00Z","last_updated_date":"2026-05-28T13:49:26Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/aquipta-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"63842","name":"Filspari : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2024-07-02T11:54:00Z","last_updated_date":"2025-12-08T10:55:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/filspari-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"63852","name":"Duloxetine Zentiva : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2024-07-02T16:00:00Z","last_updated_date":"2024-11-29T11:11:01Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/duloxetine-zentiva-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"63853","name":"Memantine Mylan : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2024-07-02T16:57:01Z","last_updated_date":"2025-11-28T09:56:41Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/memantine-mylan-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"63869","name":"Emtricitabine/Tenofovir disoproxil Krka : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2024-07-04T09:46:00Z","last_updated_date":"2025-01-31T12:48:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/emtricitabine-tenofovir-disoproxil-krka-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"63982","name":"Qalsody : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2024-07-09T17:32:43Z","last_updated_date":"2026-05-11T09:32:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/qalsody-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"64013","name":"Ztalmy : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2024-07-11T09:40:15Z","last_updated_date":"2026-02-27T12:41:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/ztalmy-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"64080","name":"\tEmtricitabine/Tenofovir disoproxil Mylan : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2024-07-12T11:11:01Z","last_updated_date":"2025-06-30T09:59:37Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/emtricitabine-tenofovir-disoproxil-mylan-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"64083","name":"Emtricitabine/Tenofovir disoproxil Krka d.d. : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2024-07-12T11:11:01Z","last_updated_date":"2025-02-05T11:40:39Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/emtricitabine-tenofovir-disoproxil-krka-dd-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"64088","name":"Ebglyss : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2024-07-12T14:32:03Z","last_updated_date":"2025-04-07T16:11:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/ebglyss-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"64208","name":"Tenofovir disoproxil Mylan : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2024-07-19T09:10:00Z","last_updated_date":"2026-05-08T09:35:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/tenofovir-disoproxil-mylan-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"64230","name":"Fruzaqla : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2024-07-19T14:47:00Z","last_updated_date":"2024-11-27T16:05:24Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/fruzaqla-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"64254","name":"Lopinavir/Ritonavir Viatris : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2024-07-22T10:53:00Z","last_updated_date":"2026-06-01T11:11:01Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/lopinavir-ritonavir-viatris-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
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    {"id":"64368","name":"Efavirenz/Emtricitabine/Tenofovir disoproxil Krka : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2024-07-29T11:11:11Z","last_updated_date":"2025-01-22T16:01:16Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/efavirenz-emtricitabine-tenofovir-disoproxil-krka-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"64409","name":"Taxotere : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2024-07-31T13:44:21Z","last_updated_date":"2024-07-31T13:44:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/taxotere-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
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    {"id":"64427","name":"Mozobil : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2024-07-31T14:09:04Z","last_updated_date":"2024-07-31T14:09:04Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/mozobil-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"64479","name":"Jeraygo : EPAR Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2024-08-01T17:11:37Z","last_updated_date":"2025-08-29T09:29:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/jeraygo-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"64481","name":"Velsipity : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2024-08-01T17:18:50Z","last_updated_date":"2025-06-17T17:20:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/velsipity-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"64585","name":"Omlyclo : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2024-08-16T14:25:00Z","last_updated_date":"2025-04-24T15:06:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/omlyclo-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"64594","name":"Akeega : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2024-08-19T15:32:17Z","last_updated_date":"2026-03-17T12:50:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/akeega-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"64602","name":"Wezenla : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2024-08-20T15:15:00Z","last_updated_date":"2025-06-02T09:49:14Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/wezenla-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"64606","name":"Vueway : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2024-08-21T10:33:00Z","last_updated_date":"2025-10-20T12:30:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/vueway-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"64641","name":"Pioglitazone Accord : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2024-08-27T14:21:56Z","last_updated_date":"2024-08-27T14:21:56Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/pioglitazone-accord-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"64652","name":"Remicade : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2024-08-29T17:00:26Z","last_updated_date":"2025-12-15T12:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/remicade-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"64670","name":"Pazenir : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2019-11-05T12:20:34Z","last_updated_date":"2024-01-11T00:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/pazenir-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"64671","name":"Iasibon : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2024-08-30T13:59:03Z","last_updated_date":"2024-08-30T13:59:03Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/iasibon-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"64673","name":"Pregabalin Accord : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2024-08-30T14:28:30Z","last_updated_date":"2025-01-27T12:46:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/pregabalin-accord-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"64674","name":"Azacitidine Kabi : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2024-08-30T15:23:35Z","last_updated_date":"2024-08-30T15:23:35Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/azacitidine-kabi-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"64677","name":"Olanzapine Teva : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-11-24T11:11:39Z","last_updated_date":"2021-10-28T11:11:01Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/olanzapine-teva-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"64687","name":"Carmustine medac : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2024-09-03T13:15:40Z","last_updated_date":"2024-09-03T13:15:40Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/carmustine-medac-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"64709","name":"Apexelsin : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2024-09-05T10:24:00Z","last_updated_date":"2025-06-10T11:32:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/apexelsin-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"64723","name":"Lyxumia : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2024-09-05T16:15:00Z","last_updated_date":"2026-02-05T12:46:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/lyxumia-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"64725","name":"Viagra : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2024-09-05T16:22:00Z","last_updated_date":"2025-09-17T16:18:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/viagra-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"64764","name":"Lytenava : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2024-09-09T13:45:00Z","last_updated_date":"2026-02-09T14:48:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/lytenava-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"64777","name":"Ritonavir Viatris : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2024-09-10T14:15:00Z","last_updated_date":"2026-05-08T15:45:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/ritonavir-viatris-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"64810","name":"Tocilizumab STADA : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2024-09-12T11:20:00Z","last_updated_date":"2026-01-20T10:51:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/tocilizumab-stada-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"64842","name":"Rimmyrah : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2024-09-13T10:16:00Z","last_updated_date":"2025-08-20T12:02:20Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/rimmyrah-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"64992","name":"Caprelsa : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2024-09-23T23:00:00Z","last_updated_date":"2026-06-01T12:08:27Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/caprelsa-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"65001","name":"Repaglinide Accord : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2024-09-23T16:00:00Z","last_updated_date":"2024-09-23T16:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/repaglinide-accord-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"65026","name":"Steqeyma : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2024-09-25T11:00:00Z","last_updated_date":"2025-06-12T16:23:46Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/steqeyma-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"65216","name":"Elucirem : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2024-10-07T13:22:00Z","last_updated_date":"2025-11-14T21:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/elucirem-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"65217","name":"Fabhalta : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2024-10-07T13:29:00Z","last_updated_date":"2025-04-11T14:25:47Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/fabhalta-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"65228","name":"Axumin : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2024-10-08T10:58:00Z","last_updated_date":"2026-03-26T16:50:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/axumin-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"65240","name":"Comirnaty : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2024-10-08T16:32:00Z","last_updated_date":"2026-05-29T10:17:01Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/comirnaty-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"65258","name":"Enzalutamide Viatris : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2024-10-09T15:13:00Z","last_updated_date":"2025-12-05T19:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/enzalutamide-viatris-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"65265","name":"Spevigo : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2024-10-10T13:02:00Z","last_updated_date":"2025-08-21T16:42:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/spevigo-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"65301","name":"Irbesartan Zentiva : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2024-10-15T16:48:00Z","last_updated_date":"2026-04-22T16:44:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/irbesartan-zentiva-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"65305","name":"Mevlyq : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2024-10-16T11:15:00Z","last_updated_date":"2024-10-16T11:15:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/mevlyq-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"65356","name":"Cyramza : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2024-10-21T16:30:00Z","last_updated_date":"2026-01-16T14:20:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/cyramza-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"65373","name":"Beqvez : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2024-10-23T14:58:00Z","last_updated_date":"2025-06-04T11:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/beqvez-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"65413","name":"Eurneffy : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2024-10-24T09:40:00Z","last_updated_date":"2025-02-06T16:33:45Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/eurneffy-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"65456","name":"\tEfavirenz/Emtricitabine/Tenofovir disoproxil Mylan : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2024-10-28T13:34:00Z","last_updated_date":"2025-11-18T14:56:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/efavirenz-emtricitabine-tenofovir-disoproxil-mylan-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"65501","name":"Ibuprofen Gen.Orph : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2024-10-31T10:35:00Z","last_updated_date":"2025-05-28T10:44:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/ibuprofen-genorph-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"65558","name":"Wyost : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2024-11-06T16:47:01Z","last_updated_date":"2025-02-12T16:08:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/wyost-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"65564","name":"Zegalogue : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2024-11-07T14:57:33Z","last_updated_date":"2025-04-22T13:35:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/zegalogue-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"65620","name":"Zoledronic Acid Accord : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2024-11-13T16:31:28Z","last_updated_date":"2026-02-24T16:15:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/zoledronic-acid-accord-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"65678","name":"Celsunax : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2024-11-15T15:05:18Z","last_updated_date":"2024-11-15T15:05:18Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/celsunax-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"65719","name":"Elfabrio : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2024-11-20T10:49:01Z","last_updated_date":"2026-03-17T12:32:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/elfabrio-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
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    {"id":"65895","name":"Eribulin Baxter : EPAR - Procedural steps taken and scientific information after the authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2024-12-02T17:31:59Z","last_updated_date":"2026-02-24T15:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/eribulin-baxter-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"65934","name":"Tauvid : EPAR - Procedural steps taken and scientific information after the authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2024-12-03T16:33:21Z","last_updated_date":"2026-01-16T15:15:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/tauvid-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"66065","name":"Altuvoct : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2024-12-11T10:45:05Z","last_updated_date":"2025-12-19T08:22:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/altuvoct-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"66113","name":"Cejemly : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2024-12-13T11:44:01Z","last_updated_date":"2025-03-17T17:08:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/cejemly-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"66170","name":"Neuraceq : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2024-12-17T16:15:02Z","last_updated_date":"2026-04-28T13:36:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/neuraceq-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"66172","name":"Uptravi : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2024-12-17T16:39:46Z","last_updated_date":"2026-02-19T14:20:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/uptravi-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"66192","name":"Vevizye : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2024-12-18T10:47:12Z","last_updated_date":"2025-02-19T09:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/vevizye-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"66216","name":"Piasky : EPAR - Procedural steps taken and scientific information after the authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2024-12-18T15:24:15Z","last_updated_date":"2025-04-25T17:33:16Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/piasky-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"66225","name":"Axitinib Accord : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2024-12-19T12:22:12Z","last_updated_date":"2025-07-22T17:33:34Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/axitinib-accord-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"66245","name":"Levetiracetam Sun : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-01-06T15:37:06Z","last_updated_date":"2026-01-05T17:50:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/levetiracetam-sun-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"66246","name":"Pomalidomide Viatris : EPAR - Procedural steps taken and scientific information after the authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-01-06T16:23:46Z","last_updated_date":"2026-05-08T09:38:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/pomalidomide-viatris-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"66255","name":"Fampridine Accord : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-01-07T14:22:06Z","last_updated_date":"2025-07-18T14:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/fampridine-accord-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"66258","name":"Emselex : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-01-07T14:44:23Z","last_updated_date":"2025-09-15T16:24:07Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/emselex-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"66265","name":"Jubbonti : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-01-08T09:16:00Z","last_updated_date":"2025-11-27T16:31:11Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/jubbonti-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"66269","name":"Vyloy : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-01-08T17:47:00Z","last_updated_date":"2026-03-03T14:17:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/vyloy-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"66278","name":"Leflunomide Zentiva : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-01-09T14:04:43Z","last_updated_date":"2026-01-28T15:52:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/leflunomide-zentiva-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"66283","name":"Levetiracetam Accord : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-01-09T16:22:56Z","last_updated_date":"2025-12-09T14:15:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/levetiracetam-accord-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"66285","name":"Eksunbi : EPAR - Procedural steps taken and scientific information after the authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-01-10T11:00:12Z","last_updated_date":"2025-09-08T16:03:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/eksunbi-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"66333","name":"Palforzia : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-01-16T15:37:27Z","last_updated_date":"2025-12-08T17:24:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/palforzia-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"66337","name":"Rivastigmine Sandoz : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-01-16T17:02:11Z","last_updated_date":"2026-01-16T13:36:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/rivastigmine-sandoz-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"66360","name":"Balversa : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-01-17T15:30:21Z","last_updated_date":"2026-04-20T16:41:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/balversa-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"66368","name":"Rivastigmine Hexal : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-01-20T10:17:31Z","last_updated_date":"2026-01-16T13:15:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/rivastigmine-hexal-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"66381","name":"Rivastigmine 1 A Pharma : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-01-20T15:44:48Z","last_updated_date":"2026-01-16T11:55:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/rivastigmine-1-pharma-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"66385","name":"Posaconazole Accord : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-01-21T09:39:10Z","last_updated_date":"2025-05-06T09:10:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/posaconazole-accord-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"66386","name":"Posaconazole AHCL : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-01-21T09:54:16Z","last_updated_date":"2025-01-21T09:54:16Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/posaconazole-ahcl-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"66398","name":"Afqlir : EPAR -Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-01-21T15:02:33Z","last_updated_date":"2025-04-24T14:58:29Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/afqlir-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"66467","name":"Lojuxta : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-01-27T13:34:43Z","last_updated_date":"2025-01-27T13:34:43Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/lojuxta-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"66468","name":"Inaqovi : EPAR - Procedural steps taken and scientific information after the authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-01-27T13:53:18Z","last_updated_date":"2025-01-27T13:53:18Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/inaqovi-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"66469","name":"Inaqovi : EPAR - Procedural steps taken and scientific information after the authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-01-27T13:56:41Z","last_updated_date":"2025-03-10T17:16:05Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/inaqovi-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"66475","name":"Sitagliptin Accord : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-01-27T15:35:45Z","last_updated_date":"2025-01-27T15:35:45Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/sitagliptin-accord-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"66477","name":"Darunavir Krka : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-01-28T10:13:21Z","last_updated_date":"2025-01-28T10:13:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/darunavir-krka-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"66478","name":"Telmisartan Actavis : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-01-28T11:36:20Z","last_updated_date":"2025-01-28T11:36:20Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/telmisartan-actavis-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"66495","name":"Irbesartan / Hydrochlorothiazide Teva : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-01-29T08:50:15Z","last_updated_date":"2026-01-16T12:30:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/irbesartan-hydrochlorothiazide-teva-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"66504","name":"Edarbi : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-01-29T13:54:17Z","last_updated_date":"2025-01-29T13:54:17Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/edarbi-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"66506","name":"Zykadia : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-01-29T14:01:38Z","last_updated_date":"2026-01-29T17:16:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/zykadia-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"66512","name":"Irbesartan Hydrochlorothiazide Zentiva: EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-01-29T16:21:06Z","last_updated_date":"2026-01-16T12:38:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/irbesartan-hydrochlorothiazide-zentiva-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"66513","name":"Celldemic : Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-01-29T16:35:18Z","last_updated_date":"2025-01-29T16:35:18Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/celldemic-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"66515","name":"Supemtek Tetra : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-01-29T17:01:59Z","last_updated_date":"2025-07-23T16:00:54Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/supemtek-tetra-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"66565","name":"Eucreas : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-02-03T10:55:10Z","last_updated_date":"2025-12-08T16:42:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/eucreas-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"66566","name":"Jalra : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-02-03T11:13:26Z","last_updated_date":"2026-01-05T17:35:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/jalra-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"66567","name":"Zomarist : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-02-03T11:23:22Z","last_updated_date":"2025-12-05T16:43:34Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/zomarist-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"66577","name":"Trazimera : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-02-03T15:31:24Z","last_updated_date":"2026-02-03T10:10:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/trazimera-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"66596","name":"Omvoh : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-02-04T14:22:55Z","last_updated_date":"2026-01-28T15:20:31Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/omvoh-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"66597","name":"Repaglinide Krka : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-02-04T14:31:43Z","last_updated_date":"2025-02-04T14:31:43Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/repaglinide-krka-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"66598","name":"Rapamune : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-02-04T15:30:21Z","last_updated_date":"2026-05-04T10:37:38Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/rapamune-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"66599","name":"Blitzima : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-02-04T15:48:05Z","last_updated_date":"2025-09-29T15:05:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/blitzima-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
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    {"id":"66618","name":"Icandra : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-09-21T09:54:02Z","last_updated_date":"2025-02-06T09:58:56Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/icandra-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"66625","name":"Epruvy : EPAR - Procedural steps taken and scientific information after the authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-02-06T15:26:36Z","last_updated_date":"2025-11-14T09:40:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/epruvy-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"66678","name":"Kinpeygo : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-02-11T14:25:11Z","last_updated_date":"2026-04-23T13:58:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/kinpeygo-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
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    {"id":"66681","name":"\tRepaglinide Teva : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-02-11T15:51:20Z","last_updated_date":"2025-02-11T15:51:20Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/repaglinide-teva-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"66685","name":"\tKarvezide : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-02-11T16:37:17Z","last_updated_date":"2025-09-25T13:50:22Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/karvezide-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
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    {"id":"66687","name":"Emblaveo : EPAR - Procedural steps taken and scientific information after the authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-02-12T08:26:05Z","last_updated_date":"2025-09-17T09:47:42Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/emblaveo-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
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    {"id":"66704","name":"Dafiro : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-02-12T15:33:39Z","last_updated_date":"2025-11-19T12:55:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/dafiro-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"66705","name":"Exforge HCT : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-02-12T15:40:08Z","last_updated_date":"2026-02-06T10:35:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/exforge-hct-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"66706","name":"Copalia HCT : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-02-12T15:49:08Z","last_updated_date":"2026-02-06T10:26:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/copalia-hct-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"66707","name":"Dafiro HCT : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-02-12T15:55:24Z","last_updated_date":"2026-02-06T10:33:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/dafiro-hct-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"66708","name":"Actelsar HCT : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-02-12T16:04:08Z","last_updated_date":"2025-05-13T14:25:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/actelsar-hct-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"66712","name":"Locametz: EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-02-13T08:57:05Z","last_updated_date":"2025-03-31T15:42:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/locametz-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"66739","name":"Ozempic : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-02-13T14:07:20Z","last_updated_date":"2026-04-22T10:36:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/ozempic-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"66742","name":"\tRuxience : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-02-13T14:17:25Z","last_updated_date":"2025-07-14T16:55:34Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/ruxience-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"66753","name":"Docetaxel Accord : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-02-13T16:27:02Z","last_updated_date":"2025-02-13T16:27:02Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/docetaxel-accord-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"66755","name":"Nimenrix : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-02-13T16:38:35Z","last_updated_date":"2025-02-13T16:38:35Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/nimenrix-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"66758","name":"Dimethyl fumarate Neuraxpharm : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-02-13T16:48:29Z","last_updated_date":"2025-02-13T16:48:29Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/dimethyl-fumarate-neuraxpharm-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"66761","name":"Dimethyl fumarate Mylan : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-02-13T16:52:03Z","last_updated_date":"2025-05-12T17:32:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/dimethyl-fumarate-mylan-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"66763","name":"Bortezomib Fresenius Kabi : EPAR - Procedural steps taken and scientific information after the authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-02-13T16:58:51Z","last_updated_date":"2025-02-13T16:58:51Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/bortezomib-fresenius-kabi-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"66795","name":"Beyfortus : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-02-14T16:12:03Z","last_updated_date":"2026-04-01T12:45:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/beyfortus-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"66799","name":"Paxlovid : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-02-14T16:22:10Z","last_updated_date":"2026-05-18T16:35:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/paxlovid-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"66801","name":"\tKarvea : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-02-14T16:40:44Z","last_updated_date":"2026-01-16T12:51:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/karvea-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"66802","name":"Zinforo : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-02-14T16:47:17Z","last_updated_date":"2025-09-09T12:05:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/zinforo-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"66816","name":"Evenity : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-02-17T10:31:07Z","last_updated_date":"2025-05-07T13:57:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/evenity-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"66820","name":"\tUlunar Breezhaler : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-02-17T11:50:39Z","last_updated_date":"2025-07-25T10:25:54Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/ulunar-breezhaler-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"66822","name":"\tCibinqo : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-02-17T12:10:55Z","last_updated_date":"2025-02-17T12:10:55Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/cibinqo-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"66823","name":"Nuvaxovid : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-02-17T12:21:04Z","last_updated_date":"2026-01-22T16:48:33Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/nuvaxovid-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"66824","name":"Daptomycin Hospira : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-02-17T12:33:46Z","last_updated_date":"2026-01-20T10:05:05Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/daptomycin-hospira-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"66837","name":"Azacitidine Accord : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-02-18T09:28:24Z","last_updated_date":"2025-10-07T12:16:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/azacitidine-accord-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"66840","name":"Onureg : EPAR - Procedural steps taken and scientific information after the authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-02-18T10:00:46Z","last_updated_date":"2026-01-09T12:35:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/onureg-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"66841","name":"Vyndaqel : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-02-18T11:16:44Z","last_updated_date":"2026-04-22T10:46:38Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/vyndaqel-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"66856","name":"Balversa : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-02-19T16:42:02Z","last_updated_date":"2026-04-28T09:10:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/balversa-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"66858","name":"\tVevizye : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-02-19T08:56:10Z","last_updated_date":"2025-04-24T11:31:55Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/vevizye-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"66869","name":"Neupro : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-02-19T09:47:00Z","last_updated_date":"2026-04-07T16:23:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/neupro-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"66872","name":"Apretude : EPAR - Procedural steps taken and scientific information after the authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-02-19T13:44:17Z","last_updated_date":"2025-02-19T13:44:17Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/apretude-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"66876","name":"\tPluvicto : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-02-19T14:59:58Z","last_updated_date":"2026-02-18T11:20:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/pluvicto-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"66878","name":"Obgemsa : EPAR - Procedural steps taken and scientific information after the authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-02-19T15:56:00Z","last_updated_date":"2025-07-08T09:57:44Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/obgemsa-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"66889","name":"Qaialdo : EPAR -  Procedural steps taken and scientific information after the authorisation (archived)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-02-20T08:47:53Z","last_updated_date":"2025-02-20T08:47:53Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/qaialdo-epar-procedural-steps-taken-scientific-information-after-authorisation-archived_en.pdf"},
    {"id":"66892","name":"Jakavi : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-02-20T09:47:29Z","last_updated_date":"2025-11-10T17:10:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/jakavi-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"66902","name":"Sapropterin Dipharma : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-02-20T12:36:01Z","last_updated_date":"2026-05-18T10:49:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/sapropterin-dipharma-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"66903","name":"Tuznue : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-02-20T12:43:04Z","last_updated_date":"2025-10-23T09:45:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/tuznue-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"66907","name":"Fabhalta : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-02-20T16:24:17Z","last_updated_date":"2025-12-19T16:20:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/fabhalta-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"66920","name":"Avastin : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-02-24T10:35:59Z","last_updated_date":"2026-01-27T12:03:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/avastin-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"66921","name":"Entresto : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-02-24T11:35:13Z","last_updated_date":"2026-01-13T10:16:29Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/entresto-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"66922","name":"Neparvis : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-02-24T11:41:15Z","last_updated_date":"2026-01-13T10:26:16Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/neparvis-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"66934","name":"Lyrica : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-02-24T17:11:26Z","last_updated_date":"2026-03-25T13:29:29Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/lyrica-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"66943","name":"Pregabalin Viatris Pharma : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-02-25T13:18:35Z","last_updated_date":"2025-11-05T12:55:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/pregabalin-viatris-pharma-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"66948","name":"Tacforius : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-02-25T13:57:22Z","last_updated_date":"2025-05-08T12:06:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/tacforius-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"66954","name":"Eptifibatide Accord : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-02-25T14:56:05Z","last_updated_date":"2025-05-02T16:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/eptifibatide-accord-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"66986","name":"Aripiprazole Accord : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-02-26T13:31:56Z","last_updated_date":"2025-02-26T13:31:56Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/aripiprazole-accord-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"66987","name":"Sitagliptin SUN : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-02-26T13:34:38Z","last_updated_date":"2025-11-10T12:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/sitagliptin-sun-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"66990","name":"Herzuma : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-02-26T13:55:28Z","last_updated_date":"2026-01-28T17:05:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/herzuma-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"66991","name":"MicardisPlus : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-10-15T13:56:35Z","last_updated_date":"2025-01-17T10:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/micardisplus-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"66994","name":"Micardis : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-02-26T14:24:31Z","last_updated_date":"2025-02-26T14:24:31Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/micardis-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"67000","name":"Somavert : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-02-27T09:35:51Z","last_updated_date":"2025-02-27T09:35:51Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/somavert-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67001","name":"Biktarvy : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-02-27T09:46:53Z","last_updated_date":"2026-01-28T16:02:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/biktarvy-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67003","name":"Evkeeza : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-02-27T09:54:08Z","last_updated_date":"2026-02-26T12:49:26Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/evkeeza-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67004","name":"Voydeya : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-02-27T10:08:05Z","last_updated_date":"2025-07-08T10:55:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/voydeya-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"67005","name":"Xalkori : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-02-27T10:26:24Z","last_updated_date":"2026-01-08T11:04:09Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/xalkori-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67012","name":"Litfulo : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-02-27T13:39:37Z","last_updated_date":"2025-02-27T13:39:37Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/litfulo-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67014","name":"Omlyclo : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-02-27T13:57:26Z","last_updated_date":"2026-05-11T10:06:08Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/omlyclo-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67023","name":"mResvia : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-02-27T15:51:08Z","last_updated_date":"2025-05-05T14:58:07Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/mresvia-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"67037","name":"Fluenz : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-02-28T09:57:34Z","last_updated_date":"2025-07-14T11:54:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/fluenz-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67070","name":"Efient : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-03-03T13:52:56Z","last_updated_date":"2025-07-22T17:33:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/efient-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67073","name":"Spherox : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-03-03T14:15:44Z","last_updated_date":"2025-03-03T14:15:44Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/spherox-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67075","name":"MenQuadfi : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-03-03T14:18:53Z","last_updated_date":"2026-03-24T18:17:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/menquadfi-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67079","name":"Anagrelide Viatris : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-03-03T14:45:42Z","last_updated_date":"2025-11-14T15:34:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/anagrelide-viatris-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67086","name":"Vegzelma : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-03-03T16:19:19Z","last_updated_date":"2026-01-28T14:35:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/vegzelma-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67088","name":"Fymskina : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-03-03T16:49:42Z","last_updated_date":"2026-02-24T14:10:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/fymskina-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67089","name":"Clopidogrel / Acetylsalicylic acid Viatris : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-03-03T17:29:31Z","last_updated_date":"2025-05-05T11:25:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/clopidogrel-acetylsalicylic-acid-viatris-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67097","name":"\tLutathera : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-03-04T13:51:09Z","last_updated_date":"2025-04-03T16:22:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/lutathera-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67098","name":"Skyclarys : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-03-04T13:58:52Z","last_updated_date":"2026-03-13T13:44:14Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/skyclarys-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67099","name":"\tSomaKit TOC : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-03-04T14:10:26Z","last_updated_date":"2026-03-25T12:54:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/somakit-toc-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67100","name":"Toviaz : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-03-04T14:17:02Z","last_updated_date":"2025-03-04T14:17:02Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/toviaz-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67102","name":"Coagadex : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-03-04T14:44:05Z","last_updated_date":"2025-12-15T14:20:32Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/coagadex-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67104","name":"Ibandronic acid Accord : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-03-04T14:51:31Z","last_updated_date":"2025-09-26T16:57:46Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/ibandronic-acid-accord-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67107","name":"Awiqli : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-03-05T09:31:46Z","last_updated_date":"2025-11-17T16:18:08Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/awiqli-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67108","name":"\tTarceva : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-03-05T09:44:10Z","last_updated_date":"2025-03-05T09:44:10Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/tarceva-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67112","name":"Remsima : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-03-05T14:00:38Z","last_updated_date":"2026-05-08T18:58:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/remsima-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67114","name":"Lenalidomide Mylan : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-03-05T14:10:08Z","last_updated_date":"2026-05-11T17:14:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/lenalidomide-mylan-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67115","name":"Benepali : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-07-24T12:19:36Z","last_updated_date":"2025-12-01T15:30:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/benepali-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67117","name":"Dynastat : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-03-05T17:27:29Z","last_updated_date":"2025-03-05T17:27:29Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/dynastat-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67118","name":"Hexacima : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-03-05T17:31:21Z","last_updated_date":"2025-09-29T13:32:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/hexacima-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67124","name":"Tygacil : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-03-06T13:41:49Z","last_updated_date":"2025-10-22T12:30:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/tygacil-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67125","name":"Eltrombopag Viatris : EPAR - Procedural steps and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-03-06T14:22:12Z","last_updated_date":"2026-05-07T09:48:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/eltrombopag-viatris-epar-procedural-steps-scientific-information-after-authorisation_en.pdf"},
    {"id":"67126","name":"Hexyon : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-03-06T16:20:26Z","last_updated_date":"2025-09-29T15:28:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/hexyon-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67138","name":"Truqap : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-03-07T12:22:30Z","last_updated_date":"2025-03-07T12:22:30Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/truqap-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"67139","name":"Kimmtrak : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-03-07T12:32:53Z","last_updated_date":"2025-12-09T11:44:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/kimmtrak-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67145","name":"BeneFIX : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-03-07T13:52:33Z","last_updated_date":"2025-03-07T13:52:33Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/benefix-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67147","name":"\tIbrance : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-03-07T13:58:18Z","last_updated_date":"2025-03-07T13:58:18Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/ibrance-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67154","name":"Verzenios : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-03-07T15:41:30Z","last_updated_date":"2026-05-27T14:25:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/verzenios-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67163","name":"Entecavir Viatris : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-03-10T11:53:18Z","last_updated_date":"2026-05-07T14:30:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/entecavir-viatris-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67166","name":"Dimethyl fumarate Accord : EPAR - Procedural steps taken and scientific information after the authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-03-10T13:21:46Z","last_updated_date":"2025-08-26T14:43:49Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/dimethyl-fumarate-accord-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67169","name":"Sutent : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-03-10T15:06:28Z","last_updated_date":"2025-03-10T15:06:28Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/sutent-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67187","name":"Uzprovo : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-03-11T14:34:53Z","last_updated_date":"2026-05-07T10:30:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/uzprovo-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67233","name":"Sugammadex Mylan: EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-03-12T14:37:15Z","last_updated_date":"2025-06-11T11:16:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/sugammadex-mylan-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67246","name":"Naveruclif : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-03-13T11:08:43Z","last_updated_date":"2025-07-01T11:56:50Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/naveruclif-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"67247","name":"\tImraldi : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-03-13T11:17:59Z","last_updated_date":"2026-02-04T11:40:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/imraldi-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67249","name":"Entyvio : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-03-13T12:16:27Z","last_updated_date":"2026-03-03T15:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/entyvio-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67253","name":"\tZolsketil pegylated liposomal : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-03-13T15:11:56Z","last_updated_date":"2026-04-16T15:41:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/zolsketil-pegylated-liposomal-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67286","name":"Yesafili : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-03-14T14:35:23Z","last_updated_date":"2026-02-26T14:42:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/yesafili-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67292","name":"Revinty Ellipta : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-03-14T16:06:40Z","last_updated_date":"2025-03-14T16:06:40Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/revinty-ellipta-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67304","name":"Cejemly : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-03-17T14:10:03Z","last_updated_date":"2026-02-18T09:20:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/cejemly-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67305","name":"Skilarence : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-03-17T14:33:21Z","last_updated_date":"2025-03-17T14:33:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/skilarence-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67334","name":"\tEfavirenz/Emtricitabine/Tenofovir disoproxil Zentiva : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-03-18T14:43:06Z","last_updated_date":"2025-03-18T14:43:06Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/efavirenz-emtricitabine-tenofovir-disoproxil-zentiva-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67341","name":"Fymskina : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-03-19T10:55:16Z","last_updated_date":"2025-03-19T10:55:16Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/fymskina-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"67342","name":"\tRasagiline ratiopharm : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-03-19T11:37:20Z","last_updated_date":"2025-04-09T10:43:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/rasagiline-ratiopharm-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67343","name":"Emtricitabine/Tenofovir disoproxil Zentiva : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-03-19T11:56:57Z","last_updated_date":"2025-03-19T11:56:57Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/emtricitabine-tenofovir-disoproxil-zentiva-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67346","name":"Rivastigmine Actavis : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-03-19T12:47:56Z","last_updated_date":"2025-06-13T15:10:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/rivastigmine-actavis-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67352","name":"\tTolura : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-03-19T15:33:50Z","last_updated_date":"2025-07-18T14:24:11Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/tolura-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67353","name":"Jayempi : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-03-19T16:10:25Z","last_updated_date":"2026-04-23T11:15:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/jayempi-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67356","name":"Pomalidomide Krka - EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-03-19T16:21:44Z","last_updated_date":"2025-03-19T16:21:44Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/pomalidomide-krka-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67357","name":"Tenofovir disoproxil Zentiva : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-03-19T16:44:36Z","last_updated_date":"2025-03-19T16:44:36Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/tenofovir-disoproxil-zentiva-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67358","name":"Pomalidomide Krka - EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-03-19T16:57:49Z","last_updated_date":"2025-07-14T17:41:58Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/pomalidomide-krka-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf-0"},
    {"id":"67372","name":"\tScintimun : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-03-20T16:06:54Z","last_updated_date":"2025-03-20T16:06:54Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/scintimun-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67373","name":"\tHumira : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-03-20T16:18:13Z","last_updated_date":"2026-05-07T16:15:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/humira-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67378","name":"Veoza : EPAR - Procedural steps taken and scientific information after the authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-03-21T11:21:23Z","last_updated_date":"2026-04-21T11:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/veoza-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67379","name":"\tBuvidal : EPAR - Procedural steps taken and scientific information after the authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-03-21T11:28:51Z","last_updated_date":"2025-03-21T11:28:51Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/buvidal-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67394","name":"Enjaymo : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-03-21T14:32:58Z","last_updated_date":"2025-08-01T17:40:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/enjaymo-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67414","name":"Siiltibcy : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-03-24T12:19:08Z","last_updated_date":"2025-10-24T11:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/siiltibcy-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67416","name":"Lyvdelzi : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-03-24T14:28:16Z","last_updated_date":"2026-02-20T10:30:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/lyvdelzi-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67429","name":"Sugammadex Fresenius Kabi : EPAR - Procedural steps taken and scientific information after the authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-03-25T10:40:44Z","last_updated_date":"2025-07-11T14:30:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/sugammadex-fresenius-kabi-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67438","name":"EndolucinBeta : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-03-25T13:20:36Z","last_updated_date":"2026-05-13T12:08:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/endolucinbeta-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67439","name":"Onpattro : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-03-25T13:50:27Z","last_updated_date":"2025-03-25T13:50:27Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/onpattro-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67440","name":"Sugammadex Amomed : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-03-25T14:01:21Z","last_updated_date":"2026-02-04T13:36:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/sugammadex-amomed-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67447","name":"Prasugrel Viatris (previously Prasugrel Mylan) : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-03-25T17:08:23Z","last_updated_date":"2025-09-26T11:40:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/prasugrel-viatris-previously-prasugrel-mylan-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67449","name":"Emadine : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-03-25T17:26:53Z","last_updated_date":"2026-06-01T15:44:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/emadine-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67451","name":"\tNyxoid : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-03-26T10:27:26Z","last_updated_date":"2025-06-12T15:38:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/nyxoid-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67453","name":"Cosentyx : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-03-26T11:26:16Z","last_updated_date":"2025-10-21T14:05:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/cosentyx-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67470","name":"Columvi : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-03-26T16:14:00Z","last_updated_date":"2025-10-24T23:10:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/columvi-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67473","name":"Nimvastid : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-03-26T16:43:38Z","last_updated_date":"2025-07-17T15:42:26Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/nimvastid-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67474","name":"Korjuny : EPAR - Procedural steps taken and scientific information after the authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-03-26T17:05:56Z","last_updated_date":"2026-05-06T16:10:10Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/korjuny-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67478","name":"Vafseo: EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-03-27T10:40:07Z","last_updated_date":"2026-03-24T11:55:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/vafseo-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67481","name":"Eurneffy : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-03-27T11:41:11Z","last_updated_date":"2026-06-01T10:33:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/eurneffy-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67482","name":"INOmax : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-03-27T11:45:26Z","last_updated_date":"2026-01-29T16:34:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/inomax-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67483","name":"Strimvelis : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-03-27T11:49:20Z","last_updated_date":"2026-05-08T18:10:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/strimvelis-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67484","name":"\tFebuxostat Krka : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-03-27T11:57:08Z","last_updated_date":"2025-03-27T11:57:08Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/febuxostat-krka-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67485","name":"Brukinsa : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-03-27T11:57:54Z","last_updated_date":"2025-11-24T09:12:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/brukinsa-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67486","name":"Yuflyma : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-03-27T12:03:43Z","last_updated_date":"2026-02-05T09:37:35Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/yuflyma-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67501","name":"Uplizna : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-03-27T14:33:24Z","last_updated_date":"2026-05-22T12:35:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/uplizna-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67502","name":"\tVeraSeal : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-03-27T14:43:04Z","last_updated_date":"2025-03-27T14:43:04Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/veraseal-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67510","name":"Respreeza : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-03-27T16:56:03Z","last_updated_date":"2025-03-27T16:56:03Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/respreeza-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67527","name":"Ofev : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-03-28T11:33:38Z","last_updated_date":"2026-01-06T09:27:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/ofev-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67529","name":"Kevzara : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-03-28T11:44:39Z","last_updated_date":"2026-02-20T11:11:01Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/kevzara-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67542","name":"Vimpat : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-03-28T13:56:13Z","last_updated_date":"2025-05-08T11:50:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/vimpat-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67544","name":"Winrevair : EPAR - Procedural steps taken and scientific information after the authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-03-28T14:49:41Z","last_updated_date":"2026-04-01T09:50:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/winrevair-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67548","name":"Rukobia : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-03-31T09:58:44Z","last_updated_date":"2025-09-11T10:40:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/rukobia-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67549","name":"\tNplate : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-03-31T10:22:08Z","last_updated_date":"2025-10-15T11:35:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/nplate-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67550","name":"Amgevita : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-03-31T11:07:56Z","last_updated_date":"2026-04-23T11:50:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/amgevita-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67553","name":"Zebinix : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-03-31T15:36:17Z","last_updated_date":"2025-08-06T13:35:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/zebinix-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67556","name":"Giotrif : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-03-31T16:32:58Z","last_updated_date":"2026-05-11T09:18:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/giotrif-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67572","name":"Evista : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-04-01T12:29:09Z","last_updated_date":"2025-04-01T12:29:09Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/evista-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67575","name":"Zubsolv : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-04-01T13:13:37Z","last_updated_date":"2025-12-08T11:52:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/zubsolv-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67579","name":"Glyxambi : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-04-01T15:21:32Z","last_updated_date":"2026-03-30T15:40:11Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/glyxambi-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67584","name":"\tBortezomib Accord : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-04-01T16:27:14Z","last_updated_date":"2026-03-25T14:18:51Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/bortezomib-accord-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67592","name":"\tBroPair Spiromax : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-04-02T09:03:09Z","last_updated_date":"2025-06-30T16:12:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/bropair-spiromax-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67596","name":"\tPelmeg : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-04-02T12:00:23Z","last_updated_date":"2026-03-18T10:48:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/pelmeg-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67597","name":"Synjardy : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-04-02T12:13:23Z","last_updated_date":"2025-11-19T11:59:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/synjardy-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67598","name":"Jardiance : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-04-02T12:19:28Z","last_updated_date":"2026-03-24T16:20:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/jardiance-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67607","name":"Hetronifly : EPAR - Procedural steps taken and scientific information after the authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-04-03T09:45:58Z","last_updated_date":"2026-05-13T15:25:37Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/hetronifly-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67618","name":"Tukysa : EPAR - Procedural steps taken and scientific information after the authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-04-03T13:10:26Z","last_updated_date":"2025-11-25T14:42:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/tukysa-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67619","name":"Camcevi : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-04-03T13:15:44Z","last_updated_date":"2026-05-11T15:20:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/camcevi-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67620","name":"ellaOne : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-04-03T13:23:10Z","last_updated_date":"2025-09-29T15:04:24Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/ellaone-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67621","name":"Seffalair Spiromax : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-04-03T13:31:19Z","last_updated_date":"2025-12-16T13:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/seffalair-spiromax-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67623","name":"\tMabThera : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-04-03T14:19:09Z","last_updated_date":"2025-05-06T16:59:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/mabthera-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67624","name":"RoActemra : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-05-06T14:52:49Z","last_updated_date":"2026-04-01T11:53:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/roactemra-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67625","name":"Perjeta : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-04-03T15:55:37Z","last_updated_date":"2026-04-28T15:44:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/perjeta-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67626","name":"Ronapreve : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-04-03T16:07:41Z","last_updated_date":"2026-01-23T09:09:59Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/ronapreve-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67632","name":"Vildagliptin / Metformin hydrochloride Accord : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-04-04T11:57:39Z","last_updated_date":"2025-07-25T17:48:51Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/vildagliptin-metformin-hydrochloride-accord-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67633","name":"\tOpsumit : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-04-04T13:01:04Z","last_updated_date":"2026-04-23T09:25:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/opsumit-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67638","name":"Sitagliptin / Metformin hydrochloride Mylan : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-04-04T13:25:13Z","last_updated_date":"2025-09-30T15:24:49Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/sitagliptin-metformin-hydrochloride-mylan-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67660","name":"Elrexfio : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-04-07T11:00:17Z","last_updated_date":"2026-01-16T18:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/elrexfio-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67670","name":"Avtozma: EPAR - Procedural steps taken and scientific information after the authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-04-07T16:04:19Z","last_updated_date":"2026-01-26T14:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/avtozma-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67671","name":"Ebglyss : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-04-07T16:12:21Z","last_updated_date":"2026-03-20T15:05:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/ebglyss-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67682","name":"Lysodren : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-04-08T11:53:45Z","last_updated_date":"2026-03-11T11:11:01Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/lysodren-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67688","name":"Ontozry : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-04-08T12:15:57Z","last_updated_date":"2025-12-03T08:40:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/ontozry-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67694","name":"Azilect : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-04-08T13:25:18Z","last_updated_date":"2025-04-08T13:25:18Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/azilect-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67696","name":"\tKentera : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-04-08T13:37:31Z","last_updated_date":"2025-04-08T13:37:31Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/kentera-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67698","name":"Azacitidine Mylan : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-04-08T14:13:01Z","last_updated_date":"2025-12-12T16:40:51Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/azacitidine-mylan-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67700","name":"Loqtorzi : EPAR - Procedural steps taken and scientific information after the authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-04-08T15:02:55Z","last_updated_date":"2026-05-07T10:55:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/loqtorzi-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67701","name":"Qarziba : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-04-08T15:19:58Z","last_updated_date":"2025-11-26T15:50:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/qarziba-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67703","name":"Sugammadex Adroiq : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-04-08T16:07:09Z","last_updated_date":"2026-01-16T23:09:25Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/sugammadex-adroiq-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67710","name":"Hulio : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-04-09T12:28:48Z","last_updated_date":"2026-02-19T11:11:01Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/hulio-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67713","name":"Talmanco: EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-04-09T14:02:10Z","last_updated_date":"2026-05-08T12:48:08Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/talmanco-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67714","name":"Esbriet : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-04-09T14:21:53Z","last_updated_date":"2026-05-08T09:50:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/esbriet-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67721","name":"Competact : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-04-09T16:05:30Z","last_updated_date":"2025-04-09T16:05:30Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/competact-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67725","name":"Kaletra : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-04-10T11:49:05Z","last_updated_date":"2025-12-02T15:50:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/kaletra-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67726","name":"Bylvay : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-04-10T11:59:22Z","last_updated_date":"2026-05-08T12:35:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/bylvay-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67728","name":"Kayfanda : EPAR - Procedural steps taken and scientific information after the authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-04-10T12:06:40Z","last_updated_date":"2025-07-11T09:30:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/kayfanda-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67729","name":"\tRelvar Ellipta : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-04-10T12:17:44Z","last_updated_date":"2025-04-10T12:17:44Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/relvar-ellipta-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67734","name":"Kaftrio : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-04-10T14:54:48Z","last_updated_date":"2026-03-19T17:16:44Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/kaftrio-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67735","name":"\tTrepulmix : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-04-10T15:13:48Z","last_updated_date":"2025-07-31T11:08:30Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/trepulmix-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67743","name":"Breyanzi : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-04-11T08:28:20Z","last_updated_date":"2025-12-18T12:19:30Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/breyanzi-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67750","name":"Xermelo : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-04-11T13:10:52Z","last_updated_date":"2025-12-08T09:30:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/xermelo-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67760","name":"Effentora : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-04-11T15:07:55Z","last_updated_date":"2026-01-19T12:44:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/effentora-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67761","name":"\tEdurant : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-04-11T15:15:11Z","last_updated_date":"2025-04-11T15:15:11Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/edurant-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67763","name":"\tCinqaero : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-04-11T15:22:49Z","last_updated_date":"2025-04-11T15:22:49Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/cinqaero-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67765","name":"\tExelon : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-04-11T15:50:38Z","last_updated_date":"2026-02-24T15:26:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/exelon-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67768","name":"Vydura : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-04-14T10:17:34Z","last_updated_date":"2026-02-26T09:42:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/vydura-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67769","name":"Sugammadex Piramal: EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-04-14T10:35:53Z","last_updated_date":"2025-06-12T13:10:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/sugammadex-piramal-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67770","name":"Trumenba : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-04-14T10:47:33Z","last_updated_date":"2026-05-27T16:29:38Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/trumenba-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67790","name":"Rezolsta : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-04-14T14:35:47Z","last_updated_date":"2025-04-14T14:35:47Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/rezolsta-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67833","name":"Inlyta : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-04-14T17:08:47Z","last_updated_date":"2025-04-14T17:08:47Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/inlyta-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"67848","name":"Flucelvax : EPAR - Procedural steps taken and scientific information after the authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-04-15T12:43:24Z","last_updated_date":"2025-07-14T15:25:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/flucelvax-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"67852","name":"Zefylti : EPAR - Procedural steps taken and scientific information after the authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-04-15T14:00:39Z","last_updated_date":"2025-09-29T12:24:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/zefylti-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67857","name":"Prometax : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-04-15T14:50:15Z","last_updated_date":"2025-04-15T14:50:15Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/prometax-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67859","name":"Mounjaro : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-04-15T15:52:06Z","last_updated_date":"2026-02-06T17:05:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/mounjaro-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67861","name":"Valdoxan : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-04-15T16:21:49Z","last_updated_date":"2025-04-15T16:21:49Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/valdoxan-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67863","name":"Tamiflu : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-04-15T17:25:32Z","last_updated_date":"2025-04-15T17:25:32Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/tamiflu-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67866","name":"Spikevax (previously COVID-19 Vaccine Moderna): EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-04-16T10:44:17Z","last_updated_date":"2026-02-24T12:05:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/spikevax-previously-covid-19-vaccine-moderna-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67878","name":"Prevymis : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-04-16T13:40:14Z","last_updated_date":"2025-12-12T10:16:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/prevymis-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67879","name":"Cometriq : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-04-16T14:09:52Z","last_updated_date":"2026-02-27T10:30:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/cometriq-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67880","name":"\tElaprase : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-04-16T14:11:20Z","last_updated_date":"2025-04-16T14:11:20Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/elaprase-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67881","name":"\tZerbaxa : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-04-16T16:30:20Z","last_updated_date":"2025-04-16T16:30:20Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/zerbaxa-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67882","name":"Epysqli : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-04-16T16:30:51Z","last_updated_date":"2026-02-18T10:30:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/epysqli-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67893","name":"Evra : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-04-22T12:15:02Z","last_updated_date":"2025-04-22T12:15:02Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/evra-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67894","name":"Lenvima : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-04-22T12:32:22Z","last_updated_date":"2026-03-26T17:20:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/lenvima-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67895","name":"Kisplyx : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-04-22T13:00:29Z","last_updated_date":"2026-03-26T17:24:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/kisplyx-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67896","name":"Zegalogue : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-04-22T13:35:58Z","last_updated_date":"2026-01-26T11:55:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/zegalogue-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67917","name":"Ivemend : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-04-22T16:22:41Z","last_updated_date":"2025-11-05T09:45:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/ivemend-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67919","name":"\tTemodal : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-04-22T16:31:30Z","last_updated_date":"2025-11-06T14:50:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/temodal-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67920","name":"Scemblix : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-04-22T09:18:23Z","last_updated_date":"2026-04-30T15:44:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/scemblix-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67928","name":"Emend : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-04-23T10:56:09Z","last_updated_date":"2025-10-24T15:40:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/emend-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67929","name":"Zinplava : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-04-23T11:05:59Z","last_updated_date":"2025-12-01T11:30:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/zinplava-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67930","name":"Noxafil : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-04-23T11:15:40Z","last_updated_date":"2026-03-24T16:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/noxafil-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67934","name":"Pritor : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-04-23T13:59:02Z","last_updated_date":"2025-04-23T13:59:02Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/pritor-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67936","name":"Micardis : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-04-23T14:19:23Z","last_updated_date":"2026-04-17T15:40:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/micardis-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67939","name":"Ngenla : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-04-23T14:53:36Z","last_updated_date":"2025-12-16T15:08:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/ngenla-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67941","name":"Pyzchiva : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-04-23T15:45:09Z","last_updated_date":"2025-11-03T14:14:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/pyzchiva-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67943","name":"Nilotinib Accord : EPAR - Procedural steps taken and scientific information after the authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-04-23T15:58:36Z","last_updated_date":"2025-08-27T17:51:32Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/nilotinib-accord-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67944","name":"Kinzalmono : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-04-23T16:00:30Z","last_updated_date":"2025-04-23T16:00:30Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/kinzalmono-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67954","name":"Movymia : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-04-24T14:52:19Z","last_updated_date":"2026-04-22T13:20:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/movymia-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67956","name":"Prevenar 20 (previously Apexxnar) : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-04-24T15:20:53Z","last_updated_date":"2025-11-18T14:40:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/prevenar-20-previously-apexxnar-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67957","name":"Kayfanda : EPAR - Procedural steps taken and scientific information (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-04-24T15:44:47Z","last_updated_date":"2025-04-24T15:44:47Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/kayfanda-epar-procedural-steps-taken-scientific-information-archive_en.pdf"},
    {"id":"67960","name":"Prevenar 13 : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-04-24T16:17:55Z","last_updated_date":"2026-02-05T10:20:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/prevenar-13-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67962","name":"\tCancidas : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-04-24T16:42:49Z","last_updated_date":"2026-01-08T15:40:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/cancidas-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67963","name":"Afqlir : EPAR -Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-04-24T16:52:28Z","last_updated_date":"2026-03-03T16:01:47Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/afqlir-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67964","name":"Dyrupeg : EPAR -  Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-04-25T08:15:41Z","last_updated_date":"2025-05-13T14:00:06Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/dyrupeg-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"67982","name":"Ahzantive : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-04-25T12:21:34Z","last_updated_date":"2025-11-07T12:43:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/ahzantive-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67995","name":"RotaTeq : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-04-25T16:26:37Z","last_updated_date":"2025-12-18T12:55:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/rotateq-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"67996","name":"Elocta : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-04-25T16:37:15Z","last_updated_date":"2025-04-25T16:37:15Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/elocta-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
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    {"id":"67999","name":"Pemetrexed Pfizer (previously Pemetrexed Hospira) : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-04-25T17:11:07Z","last_updated_date":"2026-01-15T10:29:05Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/pemetrexed-pfizer-previously-pemetrexed-hospira-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68001","name":"Piasky : EPAR - Procedural steps taken and scientific information after the authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-04-25T17:33:34Z","last_updated_date":"2025-10-21T11:15:27Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/piasky-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68009","name":"Twynsta : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-04-28T14:24:16Z","last_updated_date":"2026-04-23T17:15:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/twynsta-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68015","name":"Bimzelx : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-04-28T15:47:16Z","last_updated_date":"2026-05-08T14:20:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/bimzelx-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68021","name":"\tSpedra : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-04-28T16:48:14Z","last_updated_date":"2026-01-06T09:18:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/spedra-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68022","name":"Hympavzi : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-04-28T17:08:50Z","last_updated_date":"2026-03-19T15:05:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/hympavzi-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68026","name":"Zilbrysq : EPAR - Procedural steps taken and scientific information after the authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-04-29T14:06:39Z","last_updated_date":"2026-04-23T10:50:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/zilbrysq-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68027","name":"Hefiya : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-04-29T14:46:22Z","last_updated_date":"2025-12-11T15:33:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/hefiya-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68033","name":"Hyrimoz : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-04-29T17:35:13Z","last_updated_date":"2025-12-11T15:30:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/hyrimoz-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68034","name":"Cimzia : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-04-29T17:47:14Z","last_updated_date":"2026-05-19T16:30:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/cimzia-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68038","name":"Quviviq : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-04-30T11:46:15Z","last_updated_date":"2026-03-12T12:20:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/quviviq-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
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    {"id":"68059","name":"\tBekemv : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-05-02T12:41:57Z","last_updated_date":"2026-01-15T16:10:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/bekemv-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68065","name":"Fintepla : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-05-02T13:57:01Z","last_updated_date":"2026-05-07T15:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/fintepla-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68069","name":"Alprolix : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-05-02T15:42:58Z","last_updated_date":"2025-05-02T15:42:58Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/alprolix-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68077","name":"NeoRecormon : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-05-02T19:51:11Z","last_updated_date":"2025-05-02T19:51:11Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/neorecormon-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68079","name":"Stoboclo : EPAR - Procedural steps taken and scientific information after the authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-05-05T10:27:06Z","last_updated_date":"2025-09-17T12:19:04Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/stoboclo-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"68085","name":"Ketoconazole Esteve : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-05-05T14:16:48Z","last_updated_date":"2025-05-05T14:16:48Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/ketoconazole-esteve-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68087","name":"Circadin : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-05-05T14:30:06Z","last_updated_date":"2025-07-07T16:12:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/circadin-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68089","name":"Trelegy Ellipta : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-05-05T15:26:03Z","last_updated_date":"2026-05-08T15:40:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/trelegy-ellipta-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68091","name":"Kavigale : EPAR - Procedural steps taken and scientific information after the authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-05-05T15:57:42Z","last_updated_date":"2026-04-07T11:15:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/kavigale-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68092","name":"mResvia : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-05-05T16:02:26Z","last_updated_date":"2026-04-30T11:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/mresvia-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68100","name":"Abiraterone Accord : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-05-06T08:40:19Z","last_updated_date":"2026-01-14T15:33:06Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/abiraterone-accord-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68105","name":"Elebrato Ellipta : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-05-06T09:28:52Z","last_updated_date":"2026-05-08T15:44:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/elebrato-ellipta-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68116","name":"Sunitinib Accord : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-05-06T15:07:23Z","last_updated_date":"2025-12-04T09:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/sunitinib-accord-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68117","name":"Obodence : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-05-06T15:15:05Z","last_updated_date":"2025-09-18T16:52:01Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/obodence-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"68118","name":"Sitagliptin/Metformin hydrochloride Sun : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-05-06T15:23:33Z","last_updated_date":"2025-05-06T15:23:33Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/sitagliptin-metformin-hydrochloride-sun-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68124","name":"Iqirvo : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-05-06T15:45:57Z","last_updated_date":"2025-08-13T16:37:16Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/iqirvo-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68128","name":"Bortezomib Sun : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-05-06T15:26:12Z","last_updated_date":"2025-10-14T17:16:06Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/bortezomib-sun-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68135","name":"Ocrevus : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-05-06T18:32:15Z","last_updated_date":"2026-04-16T15:18:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/ocrevus-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68136","name":"Urorec : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-05-07T09:40:34Z","last_updated_date":"2025-05-07T09:40:34Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/urorec-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68139","name":"Cabazitaxel Accord : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-05-07T12:03:18Z","last_updated_date":"2026-01-07T17:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/cabazitaxel-accord-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68155","name":"Zepatier : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-05-07T16:28:10Z","last_updated_date":"2025-11-07T10:44:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/zepatier-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68165","name":"Jentadueto : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-05-08T11:50:56Z","last_updated_date":"2025-12-18T12:22:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/jentadueto-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68168","name":"\tGivlaari : EPAR - Procedural steps taken and scientific information after the authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-05-08T12:48:39Z","last_updated_date":"2025-05-08T12:48:39Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/givlaari-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68212","name":"Rystiggo : EPAR - Procedural steps taken and scientific information after the authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-05-12T09:26:41Z","last_updated_date":"2026-01-16T16:15:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/rystiggo-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68213","name":"Aqumeldi : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-05-12T09:38:54Z","last_updated_date":"2025-10-21T12:34:16Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/aqumeldi-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"68216","name":"Targretin : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-05-12T10:57:05Z","last_updated_date":"2025-08-12T14:32:27Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/targretin-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68223","name":"Omjjara : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-05-12T14:10:20Z","last_updated_date":"2025-05-12T14:10:20Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/omjjara-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68224","name":"Pomalidomide Zentiva : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-05-12T14:22:10Z","last_updated_date":"2026-05-26T15:48:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/pomalidomide-zentiva-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68230","name":"Levetiracetam Hospira : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-05-12T15:00:08Z","last_updated_date":"2025-12-15T10:17:56Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/levetiracetam-hospira-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68233","name":"Voriconazole Accord : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-05-12T15:16:35Z","last_updated_date":"2025-10-21T13:19:05Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/voriconazole-accord-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68235","name":"Amlodipine / Valsartan Mylan : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-05-12T15:32:07Z","last_updated_date":"2025-07-24T13:34:43Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/amlodipine-valsartan-mylan-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf-0"},
    {"id":"68242","name":"Dimethyl fumarate Mylan : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-05-12T17:25:25Z","last_updated_date":"2026-05-07T13:02:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/dimethyl-fumarate-mylan-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68244","name":"Xyrem : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-05-12T18:02:25Z","last_updated_date":"2025-05-12T18:02:25Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/xyrem-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68256","name":"Enbrel : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-05-13T14:16:44Z","last_updated_date":"2025-08-13T09:14:31Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/enbrel-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68262","name":"Kanjinti : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-05-13T16:28:56Z","last_updated_date":"2025-05-13T16:28:56Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/kanjinti-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68264","name":"Clopidogrel TAD : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-05-13T16:37:05Z","last_updated_date":"2025-05-13T16:37:05Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/clopidogrel-tad-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68267","name":"\tClopidogrel Krka d.d.: EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-05-13T16:52:33Z","last_updated_date":"2025-05-13T16:52:33Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/clopidogrel-krka-dd-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68272","name":"\tZyllt : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-05-14T08:58:43Z","last_updated_date":"2025-05-14T08:58:43Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/zyllt-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68279","name":"Clopidogrel Krka : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-05-14T12:09:23Z","last_updated_date":"2025-05-14T12:09:23Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/clopidogrel-krka-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68281","name":"Lyfnua : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-05-14T14:02:22Z","last_updated_date":"2025-12-08T09:40:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/lyfnua-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68283","name":"Isentress : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-05-14T14:36:14Z","last_updated_date":"2025-11-17T15:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/isentress-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68291","name":"Kymriah : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-05-15T09:44:48Z","last_updated_date":"2025-11-06T12:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/kymriah-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68292","name":"Rytelo : EPAR - Procedural steps taken and scientific information after information","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-05-15T09:59:25Z","last_updated_date":"2025-05-15T09:59:25Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/rytelo-epar-procedural-steps-taken-scientific-information-after-information_en.pdf"},
    {"id":"68295","name":"Tevimbra : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-05-15T11:02:38Z","last_updated_date":"2026-05-27T20:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/tevimbra-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68296","name":"Faslodex : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-05-15T11:26:14Z","last_updated_date":"2025-05-15T11:26:14Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/faslodex-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68297","name":"Sondelbay : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-05-15T11:52:22Z","last_updated_date":"2026-03-23T17:45:06Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/sondelbay-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68301","name":"\tFilsuvez: EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-05-15T12:43:34Z","last_updated_date":"2025-05-15T12:43:34Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/filsuvez-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68302","name":"Eltrombopag Accord : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-05-15T12:52:13Z","last_updated_date":"2025-05-20T14:03:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/eltrombopag-accord-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"68304","name":"Opuviz : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-05-15T13:49:47Z","last_updated_date":"2026-01-19T12:58:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/opuviz-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68305","name":"Sprycel : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-05-15T14:20:22Z","last_updated_date":"2026-02-25T08:42:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/sprycel-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68306","name":"Riluzole Zentiva : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-05-15T14:34:38Z","last_updated_date":"2025-05-15T14:34:38Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/riluzole-zentiva-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68320","name":"\tOgluo : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-05-16T13:08:56Z","last_updated_date":"2025-09-17T16:18:40Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/ogluo-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68322","name":"Sibnayal : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-05-16T13:27:40Z","last_updated_date":"2026-04-09T11:11:01Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/sibnayal-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68323","name":"Buprenorphine Neuraxpharm : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-05-16T13:36:12Z","last_updated_date":"2025-05-16T13:36:12Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/buprenorphine-neuraxpharm-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68325","name":"Enspryng : EPAR - Procedural steps taken and scientific information after the authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-05-16T13:45:10Z","last_updated_date":"2026-02-16T11:11:11Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/enspryng-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68326","name":"Matever : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-05-16T14:40:34Z","last_updated_date":"2025-12-16T15:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/matever-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68329","name":"Bortezomib Hospira : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-05-16T14:53:45Z","last_updated_date":"2026-04-15T11:44:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/bortezomib-hospira-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68333","name":"Eydenzelt : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-05-16T15:03:08Z","last_updated_date":"2025-12-10T09:10:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/eydenzelt-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68336","name":"Cerdelga : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-05-16T15:23:36Z","last_updated_date":"2026-05-20T11:11:01Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/cerdelga-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68343","name":"Vipdomet : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-05-19T14:33:29Z","last_updated_date":"2025-05-19T14:33:29Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/vipdomet-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68351","name":"Adtralza : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-05-19T15:41:15Z","last_updated_date":"2026-05-28T14:49:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/adtralza-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68355","name":"Beovu : EPAR - Procedural steps taken and scientific information after the authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-05-19T16:18:49Z","last_updated_date":"2026-05-07T14:40:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/beovu-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68356","name":"Briviact : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-05-19T16:26:00Z","last_updated_date":"2025-05-19T16:26:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/briviact-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68357","name":"Sitagliptin / Metformin hydrochloride Accord : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-05-19T16:48:05Z","last_updated_date":"2025-11-13T09:46:59Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/sitagliptin-metformin-hydrochloride-accord-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68358","name":"Pelgraz : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-05-19T16:52:43Z","last_updated_date":"2025-05-19T16:52:43Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/pelgraz-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68360","name":"Beqvez : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-05-20T10:58:34Z","last_updated_date":"2025-06-04T11:51:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/beqvez-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68363","name":"Herceptin : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-05-06T11:40:54Z","last_updated_date":"2026-03-02T15:44:18Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/herceptin-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68364","name":"Duavive : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-05-20T11:57:42Z","last_updated_date":"2025-11-06T14:25:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/duavive-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68365","name":"Conbriza : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-05-20T12:06:20Z","last_updated_date":"2025-05-20T12:06:20Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/conbriza-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68369","name":"Eltrombopag Accord : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-05-20T14:03:38Z","last_updated_date":"2026-02-25T10:18:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/eltrombopag-accord-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68371","name":"Artesunate Amivas : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-05-20T14:22:47Z","last_updated_date":"2026-03-24T11:32:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/artesunate-amivas-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68373","name":"LysaKare : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-05-21T14:30:27Z","last_updated_date":"2026-04-01T15:53:39Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/lysakare-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68374","name":"Instanyl : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-05-21T14:39:32Z","last_updated_date":"2025-08-13T15:23:43Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/instanyl-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68375","name":"Teysuno : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-05-21T14:45:14Z","last_updated_date":"2025-10-30T16:40:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/teysuno-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68376","name":"Poteligeo : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-05-21T14:51:47Z","last_updated_date":"2026-04-08T11:00:02Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/poteligeo-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68377","name":"Pedea : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-05-21T15:33:02Z","last_updated_date":"2025-05-21T15:33:02Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/pedea-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68391","name":"Xydalba : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-05-23T08:22:44Z","last_updated_date":"2025-11-20T12:40:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/xydalba-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68392","name":"Nerlynx : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-05-23T08:42:38Z","last_updated_date":"2025-05-23T08:42:38Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/nerlynx-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68393","name":"Revestive : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-05-23T08:52:44Z","last_updated_date":"2025-05-23T08:52:44Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/revestive-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68426","name":"Inhixa : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-05-23T15:50:07Z","last_updated_date":"2026-03-05T14:08:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/inhixa-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68427","name":"Kostaive : EPAR - Procedural steps taken and scientific information after the authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-05-23T15:56:52Z","last_updated_date":"2026-06-03T09:50:11Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/kostaive-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68428","name":"Epidyolex : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-05-23T16:01:58Z","last_updated_date":"2026-04-24T12:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/epidyolex-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68429","name":"Xigduo : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-05-23T16:13:14Z","last_updated_date":"2026-03-13T09:12:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/xigduo-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68431","name":"Komboglyze : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-05-23T16:20:38Z","last_updated_date":"2025-05-23T16:20:38Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/komboglyze-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68432","name":"Ebymect : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-05-23T18:02:30Z","last_updated_date":"2026-03-13T09:26:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/ebymect-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68433","name":"Janumet : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-05-23T18:16:11Z","last_updated_date":"2025-11-10T15:36:06Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/janumet-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68434","name":"Velmetia : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-05-23T18:26:24Z","last_updated_date":"2025-12-01T13:50:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/velmetia-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68435","name":"Ristfor : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-05-23T18:31:46Z","last_updated_date":"2025-11-17T16:50:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/ristfor-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68436","name":"Menveo : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-05-23T18:37:54Z","last_updated_date":"2025-10-14T14:52:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/menveo-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68437","name":"Ifirmasta : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-05-23T18:49:45Z","last_updated_date":"2026-05-06T11:11:01Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/ifirmasta-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68438","name":"Ifirmacombi : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-05-23T18:54:43Z","last_updated_date":"2026-01-16T12:32:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/ifirmacombi-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68439","name":"Enzalutamide Viatris : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-05-23T19:03:57Z","last_updated_date":"2026-02-24T15:23:08Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/enzalutamide-viatris-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68440","name":"Pedmarqsi : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-05-23T19:14:21Z","last_updated_date":"2025-05-23T19:14:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/pedmarqsi-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68441","name":"Advate : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-05-23T19:27:33Z","last_updated_date":"2025-05-23T19:27:33Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/advate-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68442","name":"Retsevmo : EPAR - Procedural steps taken and scientific information after the authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-05-23T19:34:56Z","last_updated_date":"2026-02-12T15:54:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/retsevmo-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68443","name":"Sixmo : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-05-23T19:46:53Z","last_updated_date":"2025-05-23T19:46:53Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/sixmo-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68444","name":"Ovitrelle : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-05-23T19:58:11Z","last_updated_date":"2025-05-23T19:58:11Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/ovitrelle-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68445","name":"Lacosamide UCB : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-05-23T20:02:54Z","last_updated_date":"2025-05-23T20:02:54Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/lacosamide-ucb-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68453","name":"Rixathon : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-05-26T14:10:33Z","last_updated_date":"2025-08-05T16:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/rixathon-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68454","name":"Pylclari : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-05-26T14:18:40Z","last_updated_date":"2026-03-02T16:13:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/pylclari-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68455","name":"Bimervax : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2023-06-29T14:21:32Z","last_updated_date":"2025-04-30T14:22:17Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/bimervax-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"68458","name":"Eksunbi : EPAR - Procedural steps taken and scientific information after the authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-05-26T16:37:55Z","last_updated_date":"2025-09-08T16:04:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/eksunbi-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68462","name":"Epruvy : EPAR - Procedural steps taken and scientific information after the authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-05-27T09:53:47Z","last_updated_date":"2025-05-27T09:53:47Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/epruvy-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"68464","name":"Voxzogo : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-05-27T12:05:13Z","last_updated_date":"2025-11-18T13:30:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/voxzogo-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68477","name":"Inflectra : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-05-27T16:07:30Z","last_updated_date":"2026-02-17T12:26:06Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/inflectra-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68478","name":"Sorafenib Accord : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-05-27T16:24:18Z","last_updated_date":"2026-04-09T10:12:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/sorafenib-accord-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68479","name":"Ovaleap : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-05-27T16:32:51Z","last_updated_date":"2025-05-27T16:32:51Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/ovaleap-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68484","name":"Lyfnua : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-05-28T10:32:44Z","last_updated_date":"2025-05-28T10:32:44Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/lyfnua-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"68485","name":"Ibuprofen Gen.Orph : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-05-28T10:44:06Z","last_updated_date":"2026-02-16T11:11:01Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/ibuprofen-genorph-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68492","name":"Emgality : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-05-28T15:28:52Z","last_updated_date":"2026-01-27T12:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/emgality-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68493","name":"Pemetrexed medac : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-05-28T16:00:09Z","last_updated_date":"2025-05-28T16:00:09Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/pemetrexed-medac-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68495","name":"Lacosamide Accord : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-05-28T16:24:46Z","last_updated_date":"2025-05-28T16:24:46Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/lacosamide-accord-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68496","name":"Cubicin : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-05-28T16:25:15Z","last_updated_date":"2025-11-07T10:48:08Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/cubicin-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68499","name":"Xolair : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-05-28T17:10:37Z","last_updated_date":"2025-05-28T17:10:37Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/xolair-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68501","name":"Efficib : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-05-28T17:55:53Z","last_updated_date":"2025-12-01T11:25:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/efficib-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68502","name":"Riximyo : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-05-28T18:11:55Z","last_updated_date":"2025-08-05T16:10:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/riximyo-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68503","name":"NovoRapid : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-05-28T18:29:52Z","last_updated_date":"2025-05-28T18:29:52Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/novorapid-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68505","name":"Absimky : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-05-28T19:26:20Z","last_updated_date":"2025-12-18T11:00:02Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/absimky-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68519","name":"Temozolomide Accord : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-06-02T11:28:37Z","last_updated_date":"2025-06-02T11:28:37Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/temozolomide-accord-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68523","name":"Camzyos: EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-06-02T13:02:26Z","last_updated_date":"2025-06-02T13:02:26Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/camzyos-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68524","name":"Wezenla : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-06-02T13:47:33Z","last_updated_date":"2025-06-02T13:47:33Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/wezenla-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf-0"},
    {"id":"68529","name":"Ztalmy : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-06-02T15:03:40Z","last_updated_date":"2026-02-27T09:26:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/ztalmy-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68539","name":"Corbilta (previously Levodopa/Carbidopa/Entacapone Sandoz) : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-06-02T19:08:04Z","last_updated_date":"2025-06-02T19:08:04Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/corbilta-previously-levodopa-carbidopa-entacapone-sandoz-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68540","name":"Tecartus : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-06-02T19:53:51Z","last_updated_date":"2026-05-19T16:39:45Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/tecartus-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68541","name":"Atazanavir Krka : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-06-03T11:41:10Z","last_updated_date":"2026-03-27T11:32:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/atazanavir-krka-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68542","name":"Leqembi : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-06-03T11:47:20Z","last_updated_date":"2026-05-04T11:42:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/leqembi-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68549","name":"Cholestagel : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-06-03T14:42:11Z","last_updated_date":"2025-06-03T14:42:11Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/cholestagel-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68561","name":"Zeffix : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-06-03T15:34:52Z","last_updated_date":"2025-06-03T15:34:52Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/zeffix-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68563","name":"Veklury : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-06-04T09:41:09Z","last_updated_date":"2026-01-06T15:52:18Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/veklury-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68566","name":"Tecvayli : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-06-04T10:48:42Z","last_updated_date":"2025-10-08T10:42:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/tecvayli-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68575","name":"Rivaroxaban Viatris : EPAR - Procedural steps taken and scientific information after authorisation ","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-06-04T14:25:20Z","last_updated_date":"2026-05-08T10:34:17Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/rivaroxaban-viatris-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68577","name":"Ixchiq : EPAR - Procedural steps taken and scientific information after authorisation (archived)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-04-09T12:00:00Z","last_updated_date":"2025-04-09T12:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/ixchiq-epar-procedural-steps-taken-scientific-information-after-authorisation-archived_en.pdf"},
    {"id":"68578","name":"IVF Media G5 - Procedural steps and scientific information after initial consultation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-06-04T16:00:00Z","last_updated_date":"2026-04-16T13:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/ivf-media-g5-procedural-steps-scientific-information-after-initial-consultation_en.pdf"},
    {"id":"68583","name":"Tigecycline Accord : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-06-05T12:19:05Z","last_updated_date":"2025-09-26T16:52:42Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/tigecycline-accord-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68588","name":"Ixchiq : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-04-09T13:00:00Z","last_updated_date":"2026-05-18T12:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/ixchiq-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68593","name":"HBVaxPro : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-06-06T08:52:56Z","last_updated_date":"2025-11-07T13:05:09Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/hbvaxpro-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68595","name":"Zyprexa : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-06-06T09:02:36Z","last_updated_date":"2026-02-27T11:25:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/zyprexa-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68597","name":"Ranivisio : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-06-06T09:28:41Z","last_updated_date":"2025-11-14T11:21:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/ranivisio-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68626","name":"Imuldosa : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-06-06T16:56:16Z","last_updated_date":"2026-05-11T14:06:25Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/imuldosa-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68631","name":"Apexelsin : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-06-10T11:32:44Z","last_updated_date":"2025-06-10T11:32:44Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/apexelsin-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68632","name":"Capvaxive : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-06-10T11:58:34Z","last_updated_date":"2026-06-01T09:50:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/capvaxive-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68633","name":"Zirabev : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-06-10T12:02:36Z","last_updated_date":"2026-03-25T16:49:48Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/zirabev-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68639","name":"\tVokanamet : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-06-10T13:37:41Z","last_updated_date":"2025-06-10T13:37:41Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/vokanamet-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68687","name":"Skyrizi : EPAR - Procedural steps taken and scientific information after the authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-06-11T11:09:52Z","last_updated_date":"2025-11-25T10:05:40Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/skyrizi-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68688","name":"Dexdor : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-06-11T11:21:46Z","last_updated_date":"2026-01-28T12:46:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/dexdor-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68719","name":"Steqeyma : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-06-12T15:05:42Z","last_updated_date":"2026-04-16T16:53:44Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/steqeyma-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68737","name":"Baiama : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-06-13T12:30:18Z","last_updated_date":"2025-11-07T10:38:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/baiama-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68747","name":"Invokana : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-06-13T14:34:25Z","last_updated_date":"2025-06-13T14:34:25Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/invokana-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68766","name":"Yargesa : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-06-16T12:12:21Z","last_updated_date":"2025-12-19T12:08:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/yargesa-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68768","name":"Imvanex : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-06-16T15:09:08Z","last_updated_date":"2026-05-18T16:22:35Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/imvanex-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68777","name":"Foclivia : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-06-16T15:50:17Z","last_updated_date":"2025-06-16T15:50:17Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/foclivia-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68779","name":"Spevigo : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-06-16T16:42:30Z","last_updated_date":"2026-04-14T14:04:44Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/spevigo-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68780","name":"Xbryk : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-06-16T17:00:09Z","last_updated_date":"2025-07-10T17:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/xbryk-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68783","name":"Xromi : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-06-17T11:28:44Z","last_updated_date":"2026-04-28T10:45:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/xromi-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68786","name":"Lumeblue : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-06-17T11:53:37Z","last_updated_date":"2025-06-17T11:53:37Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/lumeblue-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68788","name":"Xevudy : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-06-17T12:06:43Z","last_updated_date":"2026-03-04T11:06:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/xevudy-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68791","name":"Tecentriq : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-06-17T13:58:05Z","last_updated_date":"2026-04-28T10:44:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/tecentriq-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68795","name":"Tyenne : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-06-17T15:42:52Z","last_updated_date":"2025-10-02T11:17:55Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/tyenne-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68797","name":"Velsipity : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-06-17T16:31:31Z","last_updated_date":"2025-09-12T11:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/velsipity-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68799","name":"Aripiprazole Zentiva : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-06-17T17:04:44Z","last_updated_date":"2026-04-08T14:26:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/aripiprazole-zentiva-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68800","name":"Prolia : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-06-18T10:32:29Z","last_updated_date":"2025-06-18T10:32:29Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/prolia-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68802","name":"Doptelet : EPAR - Procedural steps taken and scientific information after the authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-06-18T11:04:52Z","last_updated_date":"2026-04-08T13:30:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/doptelet-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68804","name":"Rezzayo : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-06-18T11:20:31Z","last_updated_date":"2025-06-18T11:20:31Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/rezzayo-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"68806","name":"Anzupgo : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-06-18T11:22:27Z","last_updated_date":"2025-12-08T15:54:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/anzupgo-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68821","name":"Pergoveris : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-06-18T17:06:54Z","last_updated_date":"2025-06-18T17:06:54Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/pergoveris-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68830","name":"Rybrevant: EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-06-19T12:23:00Z","last_updated_date":"2025-10-29T11:31:31Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/rybrevant-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68832","name":"Zelboraf : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-06-19T12:34:19Z","last_updated_date":"2025-06-19T12:34:19Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/zelboraf-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68837","name":"Lupkynis : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-06-19T13:54:38Z","last_updated_date":"2025-11-24T14:24:04Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/lupkynis-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68845","name":"Rizmoic : EPAR - Procedural steps taken and scientific information after the authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-06-19T17:31:51Z","last_updated_date":"2025-12-10T14:05:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/rizmoic-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68869","name":"Axura : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-06-20T14:29:18Z","last_updated_date":"2025-06-20T14:29:18Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/axura-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68870","name":"Yorvipath : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-06-20T14:34:44Z","last_updated_date":"2025-06-20T14:34:44Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/yorvipath-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68871","name":"Memantine Merz : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-06-20T14:49:13Z","last_updated_date":"2025-06-20T14:49:13Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/memantine-merz-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68872","name":"Lemtrada : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-06-20T14:58:26Z","last_updated_date":"2025-10-27T13:20:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/lemtrada-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68885","name":"Grepid : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-06-23T13:24:52Z","last_updated_date":"2025-06-23T13:24:52Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/grepid-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68922","name":"\tAripiprazole Sandoz : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-06-24T13:08:57Z","last_updated_date":"2026-04-13T12:52:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/aripiprazole-sandoz-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68924","name":"Tolucombi : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-06-24T14:17:57Z","last_updated_date":"2026-05-06T11:11:01Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/tolucombi-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68925","name":"Zessly : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-06-24T14:25:30Z","last_updated_date":"2025-06-24T14:25:30Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/zessly-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68926","name":"Cotellic : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-06-24T15:06:04Z","last_updated_date":"2025-06-24T15:06:04Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/cotellic-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68928","name":"Datroway : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-06-24T15:20:38Z","last_updated_date":"2026-02-09T12:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/datroway-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68931","name":"Jemperli : EPAR - Procedural steps taken and scientific information after the authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-06-24T15:49:15Z","last_updated_date":"2026-04-23T12:55:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/jemperli-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68933","name":"Orgovyx : EPAR - Procedural steps taken and scientific information after information","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-06-24T15:56:17Z","last_updated_date":"2025-09-30T13:26:27Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/orgovyx-epar-procedural-steps-taken-scientific-information-after-information_en.pdf"},
    {"id":"68944","name":"Beyonttra : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-06-24T17:26:01Z","last_updated_date":"2025-11-05T11:32:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/beyonttra-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68973","name":"Miglustat Dipharma : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-06-25T17:09:17Z","last_updated_date":"2025-06-25T17:09:17Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/miglustat-dipharma-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"68986","name":"Pavblu : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-06-26T11:55:47Z","last_updated_date":"2026-04-14T09:44:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/pavblu-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69005","name":"Zoonotic Influenza Vaccine Seqirus: EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-06-27T12:24:13Z","last_updated_date":"2025-06-27T12:24:13Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/zoonotic-influenza-vaccine-seqirus-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69007","name":"\tSaxenda : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-06-27T12:42:43Z","last_updated_date":"2025-07-31T15:58:10Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/saxenda-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69009","name":"\tTresiba : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-06-27T12:54:18Z","last_updated_date":"2025-06-27T12:54:18Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/tresiba-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69012","name":"Eylea : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-06-27T13:03:35Z","last_updated_date":"2026-03-04T10:40:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/eylea-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69018","name":"Avamys : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-06-27T15:16:34Z","last_updated_date":"2025-06-27T15:16:34Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/avamys-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69026","name":"Vyjuvek : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-06-30T07:24:12Z","last_updated_date":"2025-06-30T07:24:12Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/vyjuvek-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69027","name":"Busulfan Fresenius Kabi : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-06-30T07:29:37Z","last_updated_date":"2025-07-01T15:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/busulfan-fresenius-kabi-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69046","name":"Levetiracetam Teva  : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-06-30T13:30:15Z","last_updated_date":"2026-01-26T17:08:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/levetiracetam-teva-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69049","name":"Levetiracetam ratiopharm : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-06-30T14:32:46Z","last_updated_date":"2026-01-26T17:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/levetiracetam-ratiopharm-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69050","name":"Levetiracetam Actavis Group : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-06-30T14:47:12Z","last_updated_date":"2026-01-26T17:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/levetiracetam-actavis-group-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69057","name":"Keppra : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-06-30T15:31:38Z","last_updated_date":"2026-04-01T13:33:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/keppra-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69058","name":"Levetiracetam Actavis : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-06-30T15:37:19Z","last_updated_date":"2026-01-26T17:10:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/levetiracetam-actavis-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69063","name":"Naveruclif : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-07-01T11:57:51Z","last_updated_date":"2025-08-12T12:03:52Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/naveruclif-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69076","name":"Idefirix : EPAR - Procedural steps taken and scientific information after the authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-07-02T09:57:59Z","last_updated_date":"2025-07-02T09:57:59Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/idefirix-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69080","name":"Stivarga : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-07-02T12:27:36Z","last_updated_date":"2026-03-24T15:14:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/stivarga-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69082","name":"Tivdak : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-07-03T09:59:16Z","last_updated_date":"2026-02-24T14:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/tivdak-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69102","name":"Leflunomide medac : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-07-04T11:58:20Z","last_updated_date":"2025-12-19T12:11:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/leflunomide-medac-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69105","name":"Orfadin : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-07-04T12:23:47Z","last_updated_date":"2025-07-04T12:23:47Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/orfadin-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69111","name":"Neoatricon : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-07-04T13:36:32Z","last_updated_date":"2025-07-04T13:36:32Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/neoatricon-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69117","name":"Hyftor : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-07-04T18:29:53Z","last_updated_date":"2025-07-04T18:29:53Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/hyftor-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69153","name":"Latuda : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-07-07T16:20:43Z","last_updated_date":"2026-05-08T16:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/latuda-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69158","name":"Holoclar : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-07-08T09:50:01Z","last_updated_date":"2025-07-08T09:50:01Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/holoclar-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69159","name":"Rybelsus : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-07-08T10:42:48Z","last_updated_date":"2026-04-22T14:01:54Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/rybelsus-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69160","name":"Voydeya : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-07-08T10:55:28Z","last_updated_date":"2026-01-13T10:08:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/voydeya-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69171","name":"Gohibic : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-07-08T15:49:14Z","last_updated_date":"2025-07-08T15:49:14Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/gohibic-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69175","name":"Ituxredi : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-07-09T10:03:14Z","last_updated_date":"2025-07-09T10:03:14Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/ituxredi-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69192","name":"Braftovi : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-07-09T15:19:51Z","last_updated_date":"2025-11-05T10:36:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/braftovi-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69199","name":"Toujeo : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-07-09T15:54:59Z","last_updated_date":"2026-03-05T15:30:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/toujeo-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69223","name":"Temozolomide Sun : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2024-05-21T12:32:38Z","last_updated_date":"2025-07-10T12:35:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/temozolomide-sun-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69227","name":"Apremilast Accord : EPAR - Procedural steps taken and scientific information after authorisation (archived)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-07-10T13:48:10Z","last_updated_date":"2025-07-18T16:41:36Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/apremilast-accord-epar-procedural-steps-taken-scientific-information-after-authorisation-archived_en.pdf"},
    {"id":"69235","name":"Capecitabine Teva : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-07-11T09:22:16Z","last_updated_date":"2025-07-11T09:22:16Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/capecitabine-teva-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69244","name":"Opdualag : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-07-11T13:49:16Z","last_updated_date":"2026-05-27T15:09:32Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/opdualag-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69245","name":"Abseamed : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-07-11T13:56:54Z","last_updated_date":"2025-07-11T13:56:54Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/abseamed-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69247","name":"Binocrit : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-07-11T14:07:43Z","last_updated_date":"2025-07-11T14:07:43Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/binocrit-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69249","name":"Epoetin Alfa Hexal : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-07-11T14:17:03Z","last_updated_date":"2025-07-11T14:17:03Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/epoetin-alfa-hexal-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69252","name":"Carvykti : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-07-11T15:13:50Z","last_updated_date":"2026-06-01T16:50:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/carvykti-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69253","name":"Idacio : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-07-11T15:20:31Z","last_updated_date":"2026-06-02T12:26:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/idacio-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69255","name":"Febuxostat Viatris : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-07-14T10:00:50Z","last_updated_date":"2026-05-07T16:50:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/febuxostat-viatris-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69262","name":"Fluad : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-07-14T14:16:38Z","last_updated_date":"2025-07-14T14:16:38Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/fluad-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69263","name":"Waylivra : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-07-14T14:19:42Z","last_updated_date":"2026-03-23T13:10:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/waylivra-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69264","name":"Flucelvax : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-07-14T15:25:39Z","last_updated_date":"2026-03-30T10:55:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/flucelvax-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69270","name":"Plavix : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-07-14T17:03:09Z","last_updated_date":"2025-07-14T17:03:09Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/plavix-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69273","name":"Evrysdi : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-07-14T18:11:26Z","last_updated_date":"2026-04-21T15:20:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/evrysdi-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69274","name":"Scenesse : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-07-15T09:07:08Z","last_updated_date":"2025-07-15T09:07:08Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/scenesse-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69280","name":"Natpar : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-07-15T10:04:11Z","last_updated_date":"2025-07-15T10:04:11Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/natpar-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69304","name":"Ilumetri : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-07-16T09:51:45Z","last_updated_date":"2026-05-07T14:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/ilumetri-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69309","name":"Javlor : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-07-16T13:13:07Z","last_updated_date":"2025-07-16T13:13:07Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/javlor-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69310","name":"Crysvita : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-07-16T13:58:18Z","last_updated_date":"2026-04-08T12:22:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/crysvita-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69333","name":"Padcev : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-07-17T09:48:37Z","last_updated_date":"2025-09-25T12:25:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/padcev-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69334","name":"Nemluvio : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-07-17T09:56:59Z","last_updated_date":"2026-06-01T12:40:24Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/nemluvio-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69342","name":"Byooviz : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-07-17T10:57:20Z","last_updated_date":"2026-02-25T09:06:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/byooviz-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69345","name":"Mepact : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-07-17T11:49:56Z","last_updated_date":"2025-12-18T09:55:05Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/mepact-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69347","name":"Shingrix : EPAR - Procedural steps taken and scientific information after the authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-07-17T12:36:03Z","last_updated_date":"2026-03-23T13:50:30Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/shingrix-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69348","name":"Ketamine : List of nationally authorised medicinal products - PSUSA/00001804/202412","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-07-17T12:56:20Z","last_updated_date":"2025-07-17T12:56:20Z","reference_number":"EMADOC-1700519818-2297263","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/ketamine-list-nationally-authorised-medicinal-products-psusa-00001804-202412_en.pdf"},
    {"id":"69351","name":"Ivabradine Zentiva : EPAR - Procedural steps taken and scientific information after the authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-07-17T14:37:36Z","last_updated_date":"2025-07-17T14:37:36Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/ivabradine-zentiva-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69353","name":"Gardasil 9 : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-07-17T14:48:14Z","last_updated_date":"2025-10-09T14:25:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/gardasil-9-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69354","name":"Zavicefta : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2017-04-04T09:58:49Z","last_updated_date":"2020-05-20T15:23:52Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/zavicefta-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"69355","name":"Zavicefta : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-05-20T15:21:20Z","last_updated_date":"2025-11-14T10:10:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/zavicefta-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69358","name":"Nordimet : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-07-17T18:47:38Z","last_updated_date":"2025-07-17T18:47:38Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/nordimet-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69381","name":"Soliris : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-07-18T14:16:50Z","last_updated_date":"2025-07-18T14:16:50Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/soliris-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69383","name":"Aldara : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-07-18T14:56:29Z","last_updated_date":"2025-07-18T14:56:29Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/aldara-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69384","name":"Lynparza : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-07-18T15:17:05Z","last_updated_date":"2026-06-03T16:20:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/lynparza-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69386","name":"Duvyzat : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-07-18T15:24:16Z","last_updated_date":"2025-07-18T15:24:16Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/duvyzat-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69390","name":"Lazcluze : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-07-18T16:09:06Z","last_updated_date":"2026-03-26T12:42:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/lazcluze-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69392","name":"Talzenna : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-07-18T16:37:46Z","last_updated_date":"2025-07-18T16:37:46Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/talzenna-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69398","name":"Aybintio : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-07-21T16:15:51Z","last_updated_date":"2026-01-28T11:15:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/aybintio-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69401","name":"Tezspire : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-07-21T18:23:26Z","last_updated_date":"2025-10-22T15:58:25Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/tezspire-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69408","name":"Zyclara : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-07-22T16:18:36Z","last_updated_date":"2025-07-22T16:18:36Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/zyclara-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69410","name":"Lynozyfic : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-07-22T16:28:07Z","last_updated_date":"2025-07-22T16:28:07Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/lynozyfic-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69411","name":"Incruse Ellipta : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-07-22T16:50:39Z","last_updated_date":"2025-07-22T16:50:39Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/incruse-ellipta-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69412","name":"Axitinib Accord : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-07-22T17:34:18Z","last_updated_date":"2025-09-11T16:30:50Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/axitinib-accord-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69415","name":"Taltz : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-07-22T17:53:13Z","last_updated_date":"2026-04-23T14:15:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/taltz-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69416","name":"Rhokiinsa : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-07-23T10:54:49Z","last_updated_date":"2026-01-15T14:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/rhokiinsa-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69417","name":"Celsentri : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-07-23T11:04:37Z","last_updated_date":"2026-01-12T14:46:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/celsentri-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69422","name":"Blincyto : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-07-23T17:24:05Z","last_updated_date":"2026-01-13T11:04:07Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/blincyto-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69423","name":"Tafinlar : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-07-23T17:31:35Z","last_updated_date":"2026-05-19T09:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/tafinlar-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69433","name":"Nubeqa : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-07-24T13:52:27Z","last_updated_date":"2025-08-21T15:00:25Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/nubeqa-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69442","name":"Amlodipine / Valsartan Mylan : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-07-24T15:37:30Z","last_updated_date":"2025-07-24T15:37:30Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/amlodipine-valsartan-mylan-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69452","name":"Vitrakvi : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-07-24T16:15:09Z","last_updated_date":"2026-03-11T16:39:41Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/vitrakvi-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69463","name":"Cresemba : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-07-24T18:59:52Z","last_updated_date":"2025-07-24T18:59:52Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/cresemba-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69480","name":"Armisarte : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-07-25T10:35:40Z","last_updated_date":"2025-07-25T10:35:40Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/armisarte-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69481","name":"Ultibro Breezhaler : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-07-25T10:42:02Z","last_updated_date":"2025-07-25T10:42:02Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/ultibro-breezhaler-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69486","name":"Volibris : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-07-25T11:07:04Z","last_updated_date":"2026-04-22T15:35:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/volibris-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69492","name":"Xoterna Breezhaler : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-07-25T11:30:40Z","last_updated_date":"2025-07-25T11:30:40Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/xoterna-breezhaler-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69535","name":"Libmeldy : EPAR - Procedural steps taken and scientific information after the authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-07-28T14:19:29Z","last_updated_date":"2025-12-16T15:08:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/libmeldy-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69542","name":"Xofigo : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-07-28T14:33:25Z","last_updated_date":"2025-07-28T14:33:25Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/xofigo-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69543","name":"Opzelura : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-07-28T14:42:03Z","last_updated_date":"2026-03-23T13:49:10Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/opzelura-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69550","name":"Nubeqa : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2020-05-27T16:03:39Z","last_updated_date":"2025-07-28T16:05:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/nubeqa-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf-0"},
    {"id":"69554","name":"Hukyndra : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-07-28T16:24:35Z","last_updated_date":"2026-01-28T15:22:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/hukyndra-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69561","name":"Xgeva : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-07-29T15:06:35Z","last_updated_date":"2026-03-19T16:33:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/xgeva-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69562","name":"Duaklir Genuair : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-07-29T15:25:35Z","last_updated_date":"2025-07-29T15:25:35Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/duaklir-genuair-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69564","name":"Eklira Genuair : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-07-29T15:36:43Z","last_updated_date":"2025-07-29T15:36:43Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/eklira-genuair-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69591","name":"Anoro Ellipta : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-07-31T09:31:28Z","last_updated_date":"2025-07-31T09:31:28Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/anoro-ellipta-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69595","name":"Libmyris : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-07-31T11:18:45Z","last_updated_date":"2026-03-19T11:02:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/libmyris-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69599","name":"Xtandi : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-07-31T15:59:48Z","last_updated_date":"2026-03-26T10:07:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/xtandi-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69602","name":"Xofluza : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-07-31T16:23:48Z","last_updated_date":"2026-05-20T17:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/xofluza-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69604","name":"Delstrigo : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-07-31T16:42:15Z","last_updated_date":"2025-12-03T15:50:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/delstrigo-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69638","name":"Kalydeco : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-08-04T12:53:53Z","last_updated_date":"2025-08-04T12:53:53Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/kalydeco-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69640","name":"Mycamine : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-08-04T13:04:50Z","last_updated_date":"2025-10-13T10:50:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/mycamine-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69641","name":"Gems Medium Suite - Procedural steps and scientific information after initial consultation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-08-04T14:45:04Z","last_updated_date":"2025-08-04T14:45:04Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/gems-medium-suite-procedural-steps-scientific-information-after-initial-consultation_en.pdf"},
    {"id":"69643","name":"Darzalex : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-08-04T15:36:03Z","last_updated_date":"2026-04-28T13:05:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/darzalex-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69644","name":"Docetaxel Kabi : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-08-04T16:43:32Z","last_updated_date":"2025-08-04T16:43:32Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/docetaxel-kabi-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69655","name":"Glivec : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-08-05T09:46:26Z","last_updated_date":"2025-11-12T12:10:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/glivec-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69664","name":"Livtencity : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-08-05T14:24:20Z","last_updated_date":"2025-10-22T12:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/livtencity-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69666","name":"Omnitrope : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-08-05T15:28:10Z","last_updated_date":"2025-08-05T15:28:10Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/omnitrope-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69669","name":"Seebri Breezhaler : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-08-06T08:39:09Z","last_updated_date":"2026-01-26T15:05:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/seebri-breezhaler-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69671","name":"Tovanor Breezhaler : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-08-06T10:51:44Z","last_updated_date":"2026-01-26T15:12:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/tovanor-breezhaler-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69673","name":"Adempas : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-08-06T11:16:14Z","last_updated_date":"2026-05-22T14:12:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/adempas-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69675","name":"Kengrexal : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-08-06T11:55:17Z","last_updated_date":"2026-03-10T15:42:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/kengrexal-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69676","name":"Enurev Breezhaler : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-08-06T11:58:54Z","last_updated_date":"2026-01-26T15:16:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/enurev-breezhaler-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69679","name":"Abecma : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-08-06T15:33:13Z","last_updated_date":"2025-12-09T16:07:49Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/abecma-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69684","name":"Brintellix : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-08-07T15:42:10Z","last_updated_date":"2026-01-19T16:55:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/brintellix-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69689","name":"Jinarc : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-08-08T14:01:51Z","last_updated_date":"2026-06-01T15:30:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/jinarc-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69703","name":"\tDyrupeg : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-08-12T15:38:00Z","last_updated_date":"2025-08-12T15:38:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/dyrupeg-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69723","name":"Jivi : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-08-13T14:22:22Z","last_updated_date":"2025-08-13T14:22:22Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/jivi-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69725","name":"Ferriprox : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-08-13T15:11:15Z","last_updated_date":"2026-04-21T13:24:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/ferriprox-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69727","name":"Lokelma : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-08-13T15:30:01Z","last_updated_date":"2025-09-03T15:35:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/lokelma-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69728","name":"Stribild : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-08-13T15:31:29Z","last_updated_date":"2025-08-13T15:31:29Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/stribild-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69730","name":"Exparel liposomal : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-08-13T15:39:01Z","last_updated_date":"2025-08-13T15:39:01Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/exparel-liposomal-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69731","name":"Kovaltry : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-08-13T15:41:04Z","last_updated_date":"2025-08-13T15:41:04Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/kovaltry-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69749","name":"Nintedanib Accord : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-08-14T17:05:24Z","last_updated_date":"2025-08-29T10:42:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/nintedanib-accord-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69751","name":"Keytruda : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-08-14T17:43:58Z","last_updated_date":"2026-04-22T16:20:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/keytruda-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69760","name":"Trixeo Aerosphere : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-08-19T11:23:43Z","last_updated_date":"2025-09-19T15:50:38Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/trixeo-aerosphere-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69765","name":"M-M-RVaxPro : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-08-19T13:55:14Z","last_updated_date":"2025-10-30T12:45:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/m-m-rvaxpro-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69766","name":"ProQuad : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-08-19T14:03:16Z","last_updated_date":"2025-09-25T12:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/proquad-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69767","name":"\tUltomiris : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-08-19T14:09:30Z","last_updated_date":"2025-10-22T10:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/ultomiris-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69768","name":"Invanz : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-08-19T14:16:57Z","last_updated_date":"2025-11-21T15:10:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/invanz-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69788","name":"Abrysvo : EPAR - Procedural steps taken and scientific information after the authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-08-20T13:36:01Z","last_updated_date":"2026-06-01T15:08:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/abrysvo-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69789","name":"Rimmyrah : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-08-20T13:56:18Z","last_updated_date":"2026-01-09T11:20:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/rimmyrah-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69790","name":"Xaluprine : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-08-20T14:02:46Z","last_updated_date":"2025-09-25T16:45:30Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/xaluprine-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69791","name":"Elahere : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-08-20T14:25:21Z","last_updated_date":"2025-10-02T15:40:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/elahere-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"69793","name":"Amsparity : EPAR - Procedural steps taken and scientific information after the authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-08-20T14:29:32Z","last_updated_date":"2025-10-22T15:28:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/amsparity-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69797","name":" Spexotras : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-08-20T14:51:14Z","last_updated_date":"2026-05-19T11:45:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/spexotras-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69802","name":"Qaialdo : EPAR - Procedural steps taken and scientific information after the authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-08-20T16:03:55Z","last_updated_date":"2026-03-24T16:05:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/qaialdo-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69803","name":"Yescarta : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-08-20T16:12:11Z","last_updated_date":"2026-05-19T16:25:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/yescarta-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69804","name":"Raxone : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-08-20T17:01:47Z","last_updated_date":"2025-08-20T17:01:47Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/raxone-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69806","name":"Votubia : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-08-20T17:40:54Z","last_updated_date":"2025-11-20T15:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/votubia-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69826","name":"Fampyra : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-08-21T15:07:34Z","last_updated_date":"2025-08-21T15:07:34Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/fampyra-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69830","name":"Dasatinib Accord Healthcare : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-08-21T15:22:17Z","last_updated_date":"2026-02-05T09:25:05Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/dasatinib-accord-healthcare-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69831","name":"Exjade : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-08-21T15:32:58Z","last_updated_date":"2026-02-05T15:30:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/exjade-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69836","name":"Fingolimod Mylan : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-08-21T15:58:21Z","last_updated_date":"2025-11-28T09:08:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/fingolimod-mylan-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69848","name":"Galafold : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-08-25T14:17:28Z","last_updated_date":"2025-08-25T14:17:28Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/galafold-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69850","name":"Tyverb : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-08-25T15:15:47Z","last_updated_date":"2026-01-06T11:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/tyverb-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69851","name":"Truqap : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-08-25T15:46:45Z","last_updated_date":"2026-05-06T09:40:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/truqap-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69858","name":"Klisyri : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-08-26T12:56:16Z","last_updated_date":"2026-02-19T15:45:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/klisyri-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69863","name":"Kyntheum : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-08-27T13:52:42Z","last_updated_date":"2025-08-27T13:52:42Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/kyntheum-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69864","name":"Lixiana : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-08-27T14:03:52Z","last_updated_date":"2026-04-20T15:02:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/lixiana-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69865","name":"Roteas : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-08-27T14:13:47Z","last_updated_date":"2026-04-20T15:06:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/roteas-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69869","name":"Betmiga : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-08-27T15:03:23Z","last_updated_date":"2025-08-27T15:03:23Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/betmiga-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69871","name":"Laventair Ellipta : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-08-27T15:12:24Z","last_updated_date":"2025-08-27T15:12:24Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/laventair-ellipta-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69877","name":"Tabrecta : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-08-27T17:44:22Z","last_updated_date":"2025-08-27T17:44:22Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/tabrecta-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69879","name":"Icatibant Accord : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-08-27T17:56:38Z","last_updated_date":"2026-04-16T10:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/icatibant-accord-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69885","name":"Zolgensma : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-08-28T12:36:10Z","last_updated_date":"2025-08-28T12:36:10Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/zolgensma-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69887","name":"Rivaroxaban Accord : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-08-28T13:18:21Z","last_updated_date":"2025-08-28T13:18:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/rivaroxaban-accord-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69889","name":"Afinitor : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-08-28T15:12:07Z","last_updated_date":"2025-11-20T16:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/afinitor-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69903","name":"Vevzuo : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-08-29T09:09:54Z","last_updated_date":"2026-03-27T11:11:01Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/vevzuo-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69904","name":"Sephience : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-09-05T17:52:00Z","last_updated_date":"2026-05-22T13:52:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/sephience-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69905","name":"Jeraygo : EPAR Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-08-29T12:11:00Z","last_updated_date":"2026-02-27T11:55:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/jeraygo-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69918","name":"Caelyx pegylated liposomal : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-09-02T08:48:49Z","last_updated_date":"2026-04-24T09:50:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/caelyx-pegylated-liposomal-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69920","name":"Ebilfumin : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-09-02T09:05:44Z","last_updated_date":"2025-09-02T09:05:44Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/ebilfumin-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69921","name":"Simbrinza : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-09-02T09:13:51Z","last_updated_date":"2026-01-23T12:55:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/simbrinza-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69923","name":"Blenrep : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-09-02T11:19:12Z","last_updated_date":"2026-04-08T15:32:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/blenrep-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf-0"},
    {"id":"69924","name":"Azarga : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-09-02T14:01:30Z","last_updated_date":"2026-02-06T09:55:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/azarga-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69933","name":"Hepcludex : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-09-03T10:11:34Z","last_updated_date":"2026-03-31T11:40:11Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/hepcludex-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69939","name":"Ryzneuta : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-09-03T11:07:41Z","last_updated_date":"2026-04-01T17:50:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/ryzneuta-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69940","name":"Casgevy : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-09-03T11:25:04Z","last_updated_date":"2026-02-19T12:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/casgevy-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69946","name":"Rapiscan : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-09-03T15:39:46Z","last_updated_date":"2025-12-17T09:26:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/rapiscan-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69951","name":"Topotecan Hospira : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-09-04T13:49:57Z","last_updated_date":"2026-03-31T14:15:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/topotecan-hospira-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69952","name":"Eurartesim : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-09-04T14:00:37Z","last_updated_date":"2025-09-04T14:00:37Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/eurartesim-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69978","name":"Ozawade : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-09-05T15:43:55Z","last_updated_date":"2025-09-05T15:43:55Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/ozawade-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69979","name":"Wakix : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-09-05T15:51:48Z","last_updated_date":"2026-03-27T15:32:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/wakix-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69993","name":"Tremfya : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-09-08T13:53:43Z","last_updated_date":"2026-03-23T16:15:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/tremfya-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69995","name":"Nevanac : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-09-08T15:01:02Z","last_updated_date":"2026-01-23T12:44:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/nevanac-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"69998","name":"Procysbi : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-09-08T15:31:42Z","last_updated_date":"2025-09-08T15:31:42Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/procysbi-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"70016","name":"Qoyvolma : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-09-09T11:24:57Z","last_updated_date":"2026-04-16T16:06:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/qoyvolma-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"70018","name":"Vocabria : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-09-09T14:24:38Z","last_updated_date":"2025-10-30T12:18:08Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/vocabria-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"70028","name":"Ecalta : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-09-09T15:56:17Z","last_updated_date":"2025-09-09T15:56:17Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/ecalta-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"70031","name":"Abevmy : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-09-09T17:30:10Z","last_updated_date":"2026-02-25T11:15:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/abevmy-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"70033","name":"Arexvy : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-09-10T09:48:22Z","last_updated_date":"2026-05-19T15:12:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/arexvy-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"70046","name":"Rekambys : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-09-10T13:45:49Z","last_updated_date":"2025-11-04T11:15:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/rekambys-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"70049","name":"Tasmar : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-09-10T14:11:55Z","last_updated_date":"2025-09-10T14:11:55Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/tasmar-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"70052","name":"Hemlibra : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-09-10T14:19:37Z","last_updated_date":"2025-09-10T14:19:37Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/hemlibra-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"70061","name":"Dectova : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-09-11T10:23:05Z","last_updated_date":"2025-11-10T10:45:05Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/dectova-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"70064","name":"Champix : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-09-11T10:48:18Z","last_updated_date":"2025-09-11T10:48:18Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/champix-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"70067","name":"Otulfi : EPAR - Procedural steps taken and scientific information after the authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-01-06T17:21:35Z","last_updated_date":"2025-05-06T17:22:32Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/otulfi-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"70068","name":"Otulfi : EPAR - Procedural steps taken and scientific information after the authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-09-11T17:22:57Z","last_updated_date":"2026-05-27T15:15:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/otulfi-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"70081","name":"Thalidomide Lipomed : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-09-15T14:45:42Z","last_updated_date":"2025-09-15T14:45:42Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/thalidomide-lipomed-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"70088","name":"Baqsimi : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-09-15T17:25:16Z","last_updated_date":"2025-09-15T17:25:16Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/baqsimi-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"70101","name":" Emblaveo : EPAR - Procedural steps taken and scientific information after the authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-09-17T09:48:08Z","last_updated_date":"2026-02-23T13:05:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/emblaveo-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"70103","name":"Besponsa : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-09-17T09:58:25Z","last_updated_date":"2026-05-18T12:39:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/besponsa-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"70108","name":"Mylotarg : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-09-17T10:23:49Z","last_updated_date":"2025-09-17T10:23:49Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/mylotarg-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"70121","name":"Stoboclo : EPAR - Procedural steps taken and scientific information after the authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-09-17T12:19:12Z","last_updated_date":"2026-01-14T10:21:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/stoboclo-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"70134","name":"Roclanda : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-09-17T16:12:25Z","last_updated_date":"2026-03-24T12:46:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/roclanda-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"70140","name":"Replagal : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-09-18T11:54:07Z","last_updated_date":"2025-12-19T12:33:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/replagal-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"70141","name":"Leqvio : EPAR - Procedural steps taken and scientific information after the authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-09-18T12:01:43Z","last_updated_date":"2026-03-04T10:45:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/leqvio-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"70145","name":"Increlex : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-09-18T13:39:25Z","last_updated_date":"2026-03-30T11:48:08Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/increlex-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"70160","name":"Obodence : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-09-18T16:52:12Z","last_updated_date":"2026-01-06T09:18:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/obodence-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"70163","name":"Zonegran : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-09-18T16:59:05Z","last_updated_date":"2025-09-18T16:59:05Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/zonegran-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"70189","name":"Ervebo : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-09-19T15:36:26Z","last_updated_date":"2026-01-16T13:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/ervebo-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"70190","name":"Tepkinly : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-09-19T15:44:33Z","last_updated_date":"2026-02-06T15:54:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/tepkinly-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"70191","name":"Ordspono : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-09-19T15:56:42Z","last_updated_date":"2025-09-19T15:56:42Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/ordspono-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"70192","name":"Calquence : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-09-19T16:05:49Z","last_updated_date":"2025-09-19T16:05:49Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/calquence-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"70217","name":"Cegfila : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-09-23T10:32:37Z","last_updated_date":"2026-03-18T08:55:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/cegfila-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"70220","name":"Vizamyl : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-09-23T11:03:16Z","last_updated_date":"2026-03-13T11:05:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/vizamyl-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"70221","name":"Gilenya : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-09-23T11:11:58Z","last_updated_date":"2026-02-03T14:54:19Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/gilenya-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"70244","name":"Vaxchora : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-09-24T10:34:10Z","last_updated_date":"2025-09-24T10:34:10Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/vaxchora-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"70246","name":"Rinvoq : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-09-24T10:45:36Z","last_updated_date":"2025-11-17T10:30:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/rinvoq-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"70265","name":"\tLacosamide Adroiq : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-09-25T11:32:11Z","last_updated_date":"2026-01-21T16:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/lacosamide-adroiq-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"70267","name":"Riulvy : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-09-25T11:42:40Z","last_updated_date":"2025-09-25T11:42:40Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/riulvy-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
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    {"id":"70286","name":"Zoledronic acid Teva : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-09-25T17:24:39Z","last_updated_date":"2026-05-21T15:30:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/zoledronic-acid-teva-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"70288","name":"Alhemo : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-09-25T17:46:58Z","last_updated_date":"2025-09-25T17:46:58Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/alhemo-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"70306","name":"Dovato : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-09-26T16:44:09Z","last_updated_date":"2025-11-14T10:38:08Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/dovato-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"70312","name":"Eliquis : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-09-29T09:59:29Z","last_updated_date":"2026-04-01T09:59:49Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/eliquis-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"70316","name":"Talvey : EPAR - Procedural steps taken and scientific information after the authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-09-29T11:43:28Z","last_updated_date":"2025-11-28T11:06:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/talvey-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"70318","name":"Retacrit : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-04-22T13:47:03Z","last_updated_date":"2026-03-02T13:45:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/retacrit-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"70320","name":"Empliciti : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-09-29T14:24:01Z","last_updated_date":"2025-09-29T14:24:01Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/empliciti-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"70354","name":"Onbrez Breezhaler : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-09-30T11:13:49Z","last_updated_date":"2025-11-18T16:21:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/onbrez-breezhaler-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"70355","name":"Oslif Breezhaler : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-09-30T11:21:46Z","last_updated_date":"2025-11-18T16:26:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/oslif-breezhaler-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"70357","name":"Orkambi : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-09-30T11:29:32Z","last_updated_date":"2026-06-02T13:20:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/orkambi-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"70359","name":"Wegovy : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-09-30T13:47:53Z","last_updated_date":"2026-03-30T16:45:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/wegovy-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"70360","name":"Hirobriz Breezhaler : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-09-30T13:56:43Z","last_updated_date":"2025-11-18T16:31:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/hirobriz-breezhaler-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"70361","name":"Riltrava Aerosphere : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-09-30T14:02:00Z","last_updated_date":"2025-09-30T14:02:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/riltrava-aerosphere-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"70363","name":"Jevtana : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-09-30T13:57:49Z","last_updated_date":"2025-09-30T13:57:49Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/jevtana-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"70366","name":"Siklos : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-09-30T14:19:31Z","last_updated_date":"2026-04-28T12:30:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/siklos-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"70374","name":"Deferasirox Accord : EPAR - Procedural steps taken and scientific information after the authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-09-30T16:22:45Z","last_updated_date":"2025-09-30T16:22:45Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/deferasirox-accord-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"70378","name":"Evrenzo : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-09-30T16:44:44Z","last_updated_date":"2026-05-12T14:54:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/evrenzo-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"70381","name":"Bosulif : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-09-30T17:19:49Z","last_updated_date":"2026-01-12T12:32:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/bosulif-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"70401","name":"Oxlumo : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-10-02T11:40:40Z","last_updated_date":"2025-10-02T11:40:40Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/oxlumo-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"70409","name":"Elahere : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-08-20T15:42:10Z","last_updated_date":"2026-01-23T11:35:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/elahere-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"70454","name":"\tImlygic : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-10-06T13:33:34Z","last_updated_date":"2026-01-06T14:37:13Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/imlygic-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"70458","name":"Imnovid : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-10-06T16:40:00Z","last_updated_date":"2025-10-06T16:40:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/imnovid-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"70461","name":"Minjuvi : EPAR - Procedural steps taken and scientific information after the authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-10-06T17:18:59Z","last_updated_date":"2026-01-27T12:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/minjuvi-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"70464","name":"Tepadina : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-10-07T10:37:42Z","last_updated_date":"2026-02-24T13:50:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/tepadina-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"70466","name":"Daxas : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-10-07T11:34:31Z","last_updated_date":"2026-02-25T14:36:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/daxas-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"70468","name":"Cinacalcet Mylan : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-10-07T12:22:10Z","last_updated_date":"2026-05-07T16:05:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/cinacalcet-mylan-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"70470","name":"Benlysta : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-10-07T15:09:59Z","last_updated_date":"2025-10-07T15:09:59Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/benlysta-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"70471","name":"\tSelincro : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-10-07T15:19:35Z","last_updated_date":"2025-10-07T15:19:35Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/selincro-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"70477","name":"Bemrist Breezhaler : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-10-07T16:09:16Z","last_updated_date":"2025-10-07T16:09:16Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/bemrist-breezhaler-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"70488","name":"Gazyvaro : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-10-08T10:28:28Z","last_updated_date":"2026-03-17T11:46:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/gazyvaro-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"70491","name":"Briumvi : EPAR - Procedural steps taken and scientific information after the authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-10-08T11:06:09Z","last_updated_date":"2025-10-08T11:06:09Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/briumvi-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"70498","name":"Memantine Accord : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-10-09T09:36:02Z","last_updated_date":"2025-10-09T09:36:02Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/memantine-accord-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"70508","name":"Zadenvi - EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-10-09T14:03:15Z","last_updated_date":"2025-10-09T14:03:15Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/zadenvi-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"70529","name":"Teriparatide Sun : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-10-10T17:03:05Z","last_updated_date":"2025-10-10T17:03:05Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/teriparatide-sun-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"70544","name":"Okedi : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-10-14T14:29:16Z","last_updated_date":"2025-10-14T14:29:16Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/okedi-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"70545","name":"Arikayce liposomal : Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-10-14T14:33:56Z","last_updated_date":"2025-10-14T14:33:56Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/arikayce-liposomal-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"70547","name":"Vaxelis : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-10-14T14:43:50Z","last_updated_date":"2026-03-31T11:11:01Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/vaxelis-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"70556","name":"Orserdu : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-10-14T17:22:43Z","last_updated_date":"2026-03-25T12:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/orserdu-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"70568","name":"Zutectra : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-10-15T11:42:28Z","last_updated_date":"2025-10-15T11:42:28Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/zutectra-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"70569","name":"Simponi : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-10-15T11:53:05Z","last_updated_date":"2025-10-15T11:53:05Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/simponi-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"70571","name":"Qinlock : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-10-15T14:02:37Z","last_updated_date":"2026-02-11T11:22:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/qinlock-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"70573","name":"Kineret : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-10-15T14:15:29Z","last_updated_date":"2026-01-30T10:35:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/kineret-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"70575","name":"Ondexxya : EPAR - Procedural steps taken and scientific information after the authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-10-15T14:34:17Z","last_updated_date":"2025-11-14T11:32:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/ondexxya-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"70578","name":"Mayzent : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-10-15T16:21:54Z","last_updated_date":"2026-05-08T09:28:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/mayzent-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"70581","name":"Duloxetine Viatris : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-10-15T18:35:41Z","last_updated_date":"2026-05-07T16:28:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/duloxetine-viatris-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"70583","name":"Mvasi : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-10-16T09:13:53Z","last_updated_date":"2026-01-27T09:55:05Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/mvasi-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"70595","name":"Vaborem : EPAR - Procedural steps taken and scientific information after the authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-10-16T13:04:24Z","last_updated_date":"2026-03-23T15:44:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/vaborem-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"70603","name":"Avonex : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-10-16T14:45:12Z","last_updated_date":"2026-05-26T16:17:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/avonex-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"70605","name":"Plegridy : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-10-16T14:49:58Z","last_updated_date":"2026-02-11T11:25:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/plegridy-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"70626","name":"Arava : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-10-17T11:26:58Z","last_updated_date":"2026-05-19T12:50:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/arava-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"70632","name":"Polivy : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-10-17T12:20:38Z","last_updated_date":"2026-05-27T11:38:59Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/polivy-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"70648","name":"Izamby : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-10-17T15:26:57Z","last_updated_date":"2025-11-20T15:15:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/izamby-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"70658","name":"Insuman : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-10-20T09:51:31Z","last_updated_date":"2026-03-05T14:58:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/insuman-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"70665","name":"Xeljanz : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-10-20T12:26:40Z","last_updated_date":"2026-01-12T12:05:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/xeljanz-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"70669","name":"Diacomit : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-10-20T13:34:54Z","last_updated_date":"2025-10-20T13:34:54Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/diacomit-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"70689","name":"Vueway : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-10-20T16:27:54Z","last_updated_date":"2026-02-10T13:44:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/vueway-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"70691","name":"Herwenda : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-10-20T17:31:50Z","last_updated_date":"2025-10-20T17:31:50Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/herwenda-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"70692","name":"Gardasil : EPAR - Procedural steps taken and scientific information after authorisation ","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-10-20T17:38:25Z","last_updated_date":"2025-10-20T17:38:25Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/gardasil-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"70731","name":"Aqumeldi : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-10-21T12:34:25Z","last_updated_date":"2025-10-21T12:34:25Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/aqumeldi-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"70732","name":"Luxturna : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-10-21T12:39:17Z","last_updated_date":"2026-02-16T14:15:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/luxturna-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"70734","name":"Besremi : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-10-21T13:55:38Z","last_updated_date":"2026-04-24T10:15:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/besremi-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"70753","name":"Zonisamide Viatris : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-10-22T10:39:00Z","last_updated_date":"2025-10-22T10:39:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/zonisamide-viatris-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"70755","name":"Venclyxto : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-10-22T11:38:13Z","last_updated_date":"2025-10-22T11:38:13Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/venclyxto-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"70758","name":"Myfenax : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-10-22T12:05:52Z","last_updated_date":"2026-04-10T12:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/myfenax-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"70759","name":"Mycophenolate mofetil Teva : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-10-22T12:18:22Z","last_updated_date":"2026-04-10T12:30:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/mycophenolate-mofetil-teva-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"70781","name":"Rolcya : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-10-23T10:47:15Z","last_updated_date":"2025-11-27T16:20:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/rolcya-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"70808","name":"Alkindi : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-10-24T12:07:09Z","last_updated_date":"2026-03-10T10:42:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/alkindi-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"70818","name":"Ozurdex : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-10-24T14:01:32Z","last_updated_date":"2026-05-29T13:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/ozurdex-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"70821","name":"Sylvant : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-10-24T14:57:28Z","last_updated_date":"2026-03-24T15:28:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/sylvant-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"70842","name":"Elzonris : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-10-27T12:34:25Z","last_updated_date":"2025-10-27T12:34:25Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/elzonris-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"70843","name":"Imbruvica : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-10-27T12:49:16Z","last_updated_date":"2026-02-17T10:30:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/imbruvica-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"70865","name":"Multaq : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-10-28T11:07:20Z","last_updated_date":"2025-10-28T11:07:20Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/multaq-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"70877","name":"Usymro : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-10-28T13:11:01Z","last_updated_date":"2026-01-09T15:44:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/usymro-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"70882","name":"Abilify Maintena : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-10-28T14:05:42Z","last_updated_date":"2025-10-28T14:05:42Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/abilify-maintena-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"70884","name":"Roctavian : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-10-28T14:53:42Z","last_updated_date":"2026-01-14T11:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/roctavian-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"70885","name":"Votrient : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-10-28T15:06:18Z","last_updated_date":"2025-10-28T15:06:18Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/votrient-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"70886","name":"Phesgo : EPAR - Procedural steps taken and scientific information after the authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-10-28T15:17:00Z","last_updated_date":"2025-10-28T15:17:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/phesgo-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"70896","name":"Quadramet : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-10-31T12:10:36Z","last_updated_date":"2025-10-31T12:10:36Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/quadramet-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"70899","name":"Lytgobi : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-10-29T13:08:15Z","last_updated_date":"2025-10-29T13:08:15Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/lytgobi-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"70928","name":"Zimbus Breezhaler : EPAR - Procedural steps taken and scientific information after the authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-10-30T09:48:34Z","last_updated_date":"2025-10-30T09:48:34Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/zimbus-breezhaler-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"70929","name":"Enerzair Breezhaler : EPAR - Procedural steps taken and scientific information after the authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-10-30T09:55:54Z","last_updated_date":"2025-11-20T12:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/enerzair-breezhaler-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"70937","name":"Myalepta : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-08-21T13:53:58Z","last_updated_date":"2025-11-03T10:50:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/myalepta-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"70946","name":"Ristaben : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-10-30T15:58:50Z","last_updated_date":"2025-10-30T15:58:50Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/ristaben-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"70948","name":"Elonva : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-10-30T16:34:15Z","last_updated_date":"2025-10-30T16:34:15Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/elonva-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"70953","name":"Puregon : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-10-30T17:19:06Z","last_updated_date":"2025-12-18T15:24:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/puregon-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"70958","name":"Januvia : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-10-31T11:10:12Z","last_updated_date":"2025-10-31T11:10:12Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/januvia-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"70960","name":"Zurzuvae  : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-10-31T11:17:40Z","last_updated_date":"2025-10-31T11:17:40Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/zurzuvae-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"70980","name":"Finlee : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-11-04T16:51:40Z","last_updated_date":"2026-03-30T12:22:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/finlee-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"70981","name":"Mekinist : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-11-03T16:58:26Z","last_updated_date":"2026-05-22T17:05:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/mekinist-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"70993","name":"Tuzulby : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-11-04T11:11:00Z","last_updated_date":"2025-12-19T12:17:07Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/tuzulby-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"71003","name":"Mektovi : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-11-05T10:44:20Z","last_updated_date":"2025-11-05T10:44:20Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/mektovi-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"71005","name":"Grasustek : EPAR - Procedural steps taken and scientific information after the authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-11-05T11:45:13Z","last_updated_date":"2026-03-24T12:05:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/grasustek-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"71006","name":"Erivedge : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-11-05T12:05:23Z","last_updated_date":"2025-11-05T12:05:23Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/erivedge-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"71008","name":"Loargys : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-11-05T12:32:00Z","last_updated_date":"2025-12-09T13:12:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/loargys-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"71011","name":"Pegasys : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-11-05T15:32:46Z","last_updated_date":"2025-11-05T15:32:46Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/pegasys-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"71012","name":"Cabometyx : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-05-11T16:05:08Z","last_updated_date":"2025-11-07T16:16:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/cabometyx-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"71013","name":"Cabometyx : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-04-16T16:11:27Z","last_updated_date":"2026-02-27T16:12:30Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/cabometyx-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"71035","name":"Revolade : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-11-06T14:11:12Z","last_updated_date":"2026-02-26T09:52:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/revolade-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"71038","name":"Mysimba : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-11-06T15:13:05Z","last_updated_date":"2026-04-10T11:11:01Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/mysimba-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"71044","name":"Bridion : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-11-06T16:40:50Z","last_updated_date":"2025-11-06T16:40:50Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/bridion-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"71046","name":"Yesintek : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-11-07T09:52:57Z","last_updated_date":"2026-05-27T10:15:34Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/yesintek-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"71047","name":"Zoledronic acid Mylan : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-11-07T10:11:36Z","last_updated_date":"2026-03-31T13:23:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/zoledronic-acid-mylan-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"71069","name":"Aspaveli : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-11-10T12:27:18Z","last_updated_date":"2026-05-13T15:40:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/aspaveli-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"71075","name":"Verquvo : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-11-10T16:11:19Z","last_updated_date":"2026-04-21T14:55:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/verquvo-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"71092","name":"Norvir : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-11-11T11:32:24Z","last_updated_date":"2026-01-07T16:15:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/norvir-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"71095","name":"Slenyto : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-11-11T11:54:22Z","last_updated_date":"2025-11-11T11:54:22Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/slenyto-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"71106","name":"Iclusig : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-11-12T15:43:23Z","last_updated_date":"2026-05-13T08:47:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/iclusig-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"71164","name":"Triumeq : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-11-14T10:19:11Z","last_updated_date":"2026-01-26T14:22:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/triumeq-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"71165","name":"Tivicay : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-11-14T10:25:35Z","last_updated_date":"2025-11-14T10:25:35Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/tivicay-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"71167","name":"Zypadhera : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-11-14T10:32:39Z","last_updated_date":"2026-02-09T15:38:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/zypadhera-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"71168","name":"Juluca : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-11-14T10:42:35Z","last_updated_date":"2025-11-14T10:42:35Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/juluca-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"71171","name":"Tysabri : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-11-14T11:02:26Z","last_updated_date":"2026-05-26T11:50:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/tysabri-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"71174","name":"Alyftrek : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-11-14T11:10:29Z","last_updated_date":"2026-03-30T10:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/alyftrek-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"71180","name":"Elucirem : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-11-14T13:30:30Z","last_updated_date":"2026-02-10T14:02:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/elucirem-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"71186","name":"Procoralan : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-11-17T10:36:04Z","last_updated_date":"2025-11-17T10:36:04Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/procoralan-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"71187","name":"Corlentor : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-11-17T10:46:22Z","last_updated_date":"2025-11-17T10:46:22Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/corlentor-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"71188","name":"Ivabradine Anpharm : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-11-17T10:52:45Z","last_updated_date":"2025-11-17T10:52:45Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/ivabradine-anpharm-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"71200","name":"Odomzo : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-11-17T15:41:20Z","last_updated_date":"2025-11-17T15:41:20Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/odomzo-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"71228","name":"Truvada : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-11-18T14:49:11Z","last_updated_date":"2025-11-18T14:49:11Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/truvada-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"71233","name":"Viread : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-11-18T16:54:55Z","last_updated_date":"2025-11-18T16:54:55Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/viread-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"71248","name":"Erleada : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-11-19T12:59:08Z","last_updated_date":"2026-04-22T13:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/erleada-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"71256","name":"Atectura Breezhaler : EPAR - Procedural steps taken and scientific information after the authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-11-20T12:07:39Z","last_updated_date":"2025-11-20T12:07:39Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/atectura-breezhaler-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"71272","name":"Yselty : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-11-21T10:27:47Z","last_updated_date":"2025-11-21T10:27:47Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/yselty-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"71284","name":"Opdivo : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-11-21T12:30:50Z","last_updated_date":"2026-06-02T15:18:08Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/opdivo-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"71288","name":"Yervoy : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-11-21T14:58:09Z","last_updated_date":"2025-11-21T14:58:09Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/yervoy-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"71290","name":"Obizur : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-11-21T15:06:00Z","last_updated_date":"2025-11-21T15:06:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/obizur-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"71296","name":"Steglatro : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-11-21T15:32:24Z","last_updated_date":"2026-02-11T14:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/steglatro-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"71297","name":"Steglujan : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-11-21T15:41:19Z","last_updated_date":"2025-11-21T15:41:19Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/steglujan-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"71298","name":"Ebvallo : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-11-24T09:13:52Z","last_updated_date":"2025-11-24T09:13:52Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/ebvallo-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"71304","name":"Pradaxa : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-11-24T10:04:39Z","last_updated_date":"2025-11-24T10:04:39Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/pradaxa-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"71306","name":"Denbrayce : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-11-24T10:55:56Z","last_updated_date":"2026-05-11T08:48:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/denbrayce-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"71310","name":"Nyvepria : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-11-24T12:35:30Z","last_updated_date":"2026-01-20T14:18:08Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/nyvepria-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"71312","name":"SonoVue : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-11-24T13:45:58Z","last_updated_date":"2026-03-20T09:20:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/sonovue-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"71314","name":"Reblozyl : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-11-24T15:16:20Z","last_updated_date":"2025-11-24T15:16:20Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/reblozyl-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"71316","name":"Sirturo : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-11-24T16:20:57Z","last_updated_date":"2026-06-03T10:30:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/sirturo-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"71318","name":"Cetrotide : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-11-24T16:45:36Z","last_updated_date":"2026-01-27T16:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/cetrotide-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"71323","name":"Zynlonta : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-11-25T09:17:39Z","last_updated_date":"2025-11-25T09:17:39Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/zynlonta-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"71324","name":"Erelzi : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-11-25T09:29:03Z","last_updated_date":"2025-12-16T12:12:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/erelzi-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"71330","name":"Jaypirca : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-11-25T11:34:15Z","last_updated_date":"2026-01-28T12:15:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/jaypirca-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"71332","name":"Refixia : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-11-25T11:54:04Z","last_updated_date":"2025-11-25T11:54:04Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/refixia-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"71345","name":"Zejula : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-11-26T15:04:29Z","last_updated_date":"2025-11-26T15:04:29Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/zejula-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"71361","name":"Bildyos : EPAR - Procedural steps taken and scientific information after the authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-11-27T11:05:05Z","last_updated_date":"2026-02-06T15:50:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/bildyos-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"71363","name":"Rubraca : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-11-27T11:38:02Z","last_updated_date":"2025-11-27T11:38:02Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/rubraca-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"71376","name":"Jubbonti : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-11-27T16:15:50Z","last_updated_date":"2025-11-27T16:15:50Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/jubbonti-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"71381","name":"Byfavo : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-11-28T09:28:43Z","last_updated_date":"2025-11-28T09:28:43Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/byfavo-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"71385","name":"Bilprevda : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-11-28T11:03:29Z","last_updated_date":"2026-01-09T15:05:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/bilprevda-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"71412","name":"Tesavel : EPAR - Procedural steps taken and scientific information after authorisation ","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-12-01T10:41:00Z","last_updated_date":"2025-12-01T10:41:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/tesavel-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"71414","name":"Akynzeo : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-12-01T10:53:50Z","last_updated_date":"2026-06-02T14:53:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/akynzeo-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"71415","name":"Aimovig : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-12-01T10:59:05Z","last_updated_date":"2025-12-10T15:42:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/aimovig-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"71439","name":"Xelevia : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-12-01T14:29:56Z","last_updated_date":"2025-12-01T14:29:56Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/xelevia-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"71446","name":"Upstaza : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-12-02T10:00:40Z","last_updated_date":"2025-12-02T10:00:40Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/upstaza-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"71457","name":"Protopic : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-12-03T16:24:23Z","last_updated_date":"2025-12-03T16:24:23Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/protopic-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"71467","name":"Oczyesa : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-12-03T10:31:05Z","last_updated_date":"2025-12-03T10:31:05Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/oczyesa-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"71475","name":"NexoBrid : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-12-03T14:19:34Z","last_updated_date":"2025-12-03T14:19:34Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/nexobrid-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"71478","name":"Incellipan : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-12-03T15:15:40Z","last_updated_date":"2025-12-03T15:15:40Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/incellipan-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"71483","name":"Baraclude : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-12-03T16:24:06Z","last_updated_date":"2025-12-03T16:24:06Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/baraclude-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"71485","name":"Tryngolza : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-12-03T16:30:55Z","last_updated_date":"2025-12-03T16:30:55Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/tryngolza-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"71490","name":"Tagrisso : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-12-04T08:39:45Z","last_updated_date":"2025-12-04T08:39:45Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/tagrisso-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"71509","name":"Sogroya : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-12-04T15:25:11Z","last_updated_date":"2025-12-04T15:25:11Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/sogroya-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"71534","name":"Voraxaze : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-12-05T14:05:37Z","last_updated_date":"2025-12-05T14:05:37Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/voraxaze-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"71557","name":"Ravicti : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-12-05T16:12:45Z","last_updated_date":"2025-12-05T16:12:45Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/ravicti-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"71564","name":"Filspari : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-12-08T09:57:17Z","last_updated_date":"2025-12-08T09:57:17Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/filspari-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"71581","name":"Symkevi : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-12-08T11:44:07Z","last_updated_date":"2025-12-08T11:44:07Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/symkevi-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"71592","name":"Neulasta : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-12-08T15:56:25Z","last_updated_date":"2025-12-08T15:56:25Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/neulasta-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"71599","name":"Eviplera : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-12-09T10:06:06Z","last_updated_date":"2025-12-09T10:06:06Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/eviplera-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"71600","name":"Aubagio : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-12-09T10:15:07Z","last_updated_date":"2025-12-09T10:15:07Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/aubagio-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"71615","name":"Gohibic : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-12-09T12:21:01Z","last_updated_date":"2026-03-17T16:15:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/gohibic-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf-0"},
    {"id":"71619","name":"Inbrija : EPAR - Procedural steps taken and scientific information after the authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-12-09T13:16:41Z","last_updated_date":"2025-12-09T13:16:41Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/inbrija-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"71620","name":"Anzupgo : EPAR - Procedural steps taken and scientific information (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-12-09T14:07:59Z","last_updated_date":"2025-12-09T14:07:59Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/anzupgo-epar-procedural-steps-taken-scientific-information-archive_en.pdf"},
    {"id":"71629","name":"Carbaglu : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-12-09T16:14:35Z","last_updated_date":"2025-12-09T16:14:35Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/carbaglu-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"71642","name":"Libtayo : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-12-10T11:54:41Z","last_updated_date":"2025-12-10T11:54:41Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/libtayo-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"71644","name":"Pandemic influenza vaccine H5N1 AstraZeneca : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-12-10T14:13:37Z","last_updated_date":"2026-05-08T12:45:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/pandemic-influenza-vaccine-h5n1-astrazeneca-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"71695","name":"Pifeltro : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-12-11T15:25:17Z","last_updated_date":"2025-12-11T15:25:17Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/pifeltro-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"71697","name":"Tobi Podhaler : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-12-11T15:53:06Z","last_updated_date":"2026-05-11T11:11:01Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/tobi-podhaler-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"71702","name":"Teriflunomide Viatris : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-12-11T16:39:59Z","last_updated_date":"2026-05-29T12:06:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/teriflunomide-viatris-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"71727","name":"Prialt : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-12-12T13:32:22Z","last_updated_date":"2026-04-15T15:25:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/prialt-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"71742","name":"Clopidogrel Viatris : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-12-12T15:22:27Z","last_updated_date":"2025-12-12T15:22:27Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/clopidogrel-viatris-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"71752","name":"Repatha : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-12-15T09:29:14Z","last_updated_date":"2025-12-15T09:29:14Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/repatha-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"71762","name":"Agamree : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-12-16T08:19:07Z","last_updated_date":"2026-04-08T17:10:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/agamree-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"71763","name":"Cholib : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-12-16T08:30:30Z","last_updated_date":"2025-12-16T08:30:30Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/cholib-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"71764","name":"Ambrisentan Viatris : EPAR - Procedural steps taken and scientific information after the authorisation ","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-12-16T08:35:23Z","last_updated_date":"2026-05-07T15:30:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/ambrisentan-viatris-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"71765","name":"Trisenox : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-12-16T08:41:07Z","last_updated_date":"2026-01-30T14:55:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/trisenox-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"71767","name":"Cyanokit : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-12-16T09:29:35Z","last_updated_date":"2025-12-16T09:29:35Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/cyanokit-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"71770","name":"Ventavis : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-12-16T09:57:21Z","last_updated_date":"2025-12-16T09:57:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/ventavis-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"71771","name":"Sunlenca : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-12-16T10:33:24Z","last_updated_date":"2026-02-26T11:45:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/sunlenca-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"71774","name":"Kesimpta : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-12-16T11:46:39Z","last_updated_date":"2026-02-05T14:52:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/kesimpta-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"71795","name":"Tasigna : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-12-17T09:58:40Z","last_updated_date":"2025-12-17T09:58:40Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/tasigna-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"71800","name":"Adjupanrix (previously Pandemic influenza vaccine (H5N1) (split virion, inactivated, adjuvanted) GlaxoSmithKline Biologicals): EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-12-17T12:04:29Z","last_updated_date":"2025-12-17T12:04:29Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/adjupanrix-previously-pandemic-influenza-vaccine-h5n1-split-virion-inactivated-adjuvanted-glaxosmithkline-biologicals-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"71822","name":"Ziihera : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-12-17T16:10:11Z","last_updated_date":"2025-12-17T16:10:11Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/ziihera-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"71827","name":"Lucentis : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-12-17T16:35:49Z","last_updated_date":"2026-05-13T17:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/lucentis-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"71833","name":"Azacitidine Kabi : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-12-18T09:44:14Z","last_updated_date":"2025-12-18T09:44:14Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/azacitidine-kabi-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"71842","name":"Orgalutran : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-12-18T12:28:12Z","last_updated_date":"2025-12-18T12:28:12Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/orgalutran-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"71854","name":"Altuvoct : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-12-19T08:22:53Z","last_updated_date":"2025-12-19T08:22:53Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/altuvoct-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"71864","name":"Ruconest : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-12-19T09:24:35Z","last_updated_date":"2026-05-20T11:20:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/ruconest-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"71867","name":"Methylthioninium chloride Proveblue : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-12-19T11:36:13Z","last_updated_date":"2025-12-19T11:36:13Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/methylthioninium-chloride-proveblue-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"71868","name":"Simulect : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-12-19T12:03:14Z","last_updated_date":"2025-12-19T12:03:14Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/simulect-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"71870","name":"Olumiant : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-12-19T12:53:04Z","last_updated_date":"2026-05-07T12:11:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/olumiant-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"71889","name":"Attrogy : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-12-19T15:28:27Z","last_updated_date":"2025-12-19T15:28:27Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/attrogy-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"71909","name":"Zemcelpro : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-12-22T14:59:13Z","last_updated_date":"2026-02-18T11:30:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/zemcelpro-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"71910","name":"Osvyrti : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-12-22T15:18:48Z","last_updated_date":"2026-05-22T09:22:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/osvyrti-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"71917","name":"Junod : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-01-05T13:12:00Z","last_updated_date":"2026-01-05T13:12:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/junod-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"71918","name":"Alymsys : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-01-05T13:28:57Z","last_updated_date":"2026-02-06T15:30:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/alymsys-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"71936","name":"Voriconazole Hikma (previously Voriconazole Hospira): EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-01-06T10:05:23Z","last_updated_date":"2026-01-06T10:05:23Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/voriconazole-hikma-previously-voriconazole-hospira-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"71944","name":"Vaxneuvance : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-01-06T10:44:20Z","last_updated_date":"2026-01-06T10:44:20Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/vaxneuvance-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"71946","name":"Itovebi : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-01-06T11:50:48Z","last_updated_date":"2026-05-08T09:45:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/itovebi-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"71947","name":"Kapruvia : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-01-06T11:56:09Z","last_updated_date":"2026-06-01T09:32:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/kapruvia-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"71950","name":"Lenalidomide Krka : EPAR - Procedural steps taken and scientific information after the authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-01-07T13:32:25Z","last_updated_date":"2026-03-12T16:02:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/lenalidomide-krka-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"71954","name":"Kuvan : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-01-07T14:20:27Z","last_updated_date":"2026-01-07T14:21:03Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/kuvan-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"71956","name":"Apremilast Accord : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-01-07T14:36:48Z","last_updated_date":"2026-03-20T16:50:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/apremilast-accord-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"71981","name":"Olanzapine Viatris : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-01-07T16:39:08Z","last_updated_date":"2026-01-07T16:39:08Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/olanzapine-viatris-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"71993","name":"Reagila : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-01-08T13:55:50Z","last_updated_date":"2026-01-08T13:55:50Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/reagila-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"72000","name":"Sovaldi : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-01-09T09:59:59Z","last_updated_date":"2026-01-09T09:59:59Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/sovaldi-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"72001","name":"Harvoni : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-01-09T10:11:53Z","last_updated_date":"2026-01-09T10:11:53Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/harvoni-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"72003","name":"Ayvakyt : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-01-09T11:23:16Z","last_updated_date":"2026-01-09T11:23:16Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/ayvakyt-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"72004","name":"Praluent : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-10-21T13:57:31Z","last_updated_date":"2025-10-21T13:57:31Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/praluent-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"72005","name":"Tolvaptan Accord : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-01-09T14:07:43Z","last_updated_date":"2026-01-09T14:07:43Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/tolvaptan-accord-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"72007","name":"Abilify : EPAR – Product information – tracked changes","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-01-12T12:17:23Z","last_updated_date":"2026-01-12T12:17:23Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/abilify-epar-product-information-tracked-changes_en.docx","translations":{"bg":"https://www.ema.europa.eu/bg/documents/procedural-steps-after/abilify-epar-product-information-tracked-changes_bg.docx","es":"https://www.ema.europa.eu/es/documents/procedural-steps-after/abilify-epar-product-information-tracked-changes_es.docx","cs":"https://www.ema.europa.eu/cs/documents/procedural-steps-after/abilify-epar-product-information-tracked-changes_cs.docx","da":"https://www.ema.europa.eu/da/documents/procedural-steps-after/abilify-epar-product-information-tracked-changes_da.docx","de":"https://www.ema.europa.eu/de/documents/procedural-steps-after/abilify-epar-product-information-tracked-changes_de.docx","et":"https://www.ema.europa.eu/et/documents/procedural-steps-after/abilify-epar-product-information-tracked-changes_et.docx","el":"https://www.ema.europa.eu/el/documents/procedural-steps-after/abilify-epar-product-information-tracked-changes_el.docx","fr":"https://www.ema.europa.eu/fr/documents/procedural-steps-after/abilify-epar-product-information-tracked-changes_fr.docx","hr":"https://www.ema.europa.eu/hr/documents/procedural-steps-after/abilify-epar-product-information-tracked-changes_hr.docx","it":"https://www.ema.europa.eu/it/documents/procedural-steps-after/abilify-epar-product-information-tracked-changes_it.docx","lv":"https://www.ema.europa.eu/lv/documents/procedural-steps-after/abilify-epar-product-information-tracked-changes_lv.docx","lt":"https://www.ema.europa.eu/lt/documents/procedural-steps-after/abilify-epar-product-information-tracked-changes_lt.docx","hu":"https://www.ema.europa.eu/hu/documents/procedural-steps-after/abilify-epar-product-information-tracked-changes_hu.docx","mt":"https://www.ema.europa.eu/mt/documents/procedural-steps-after/abilify-epar-product-information-tracked-changes_mt.docx","nl":"https://www.ema.europa.eu/nl/documents/procedural-steps-after/abilify-epar-product-information-tracked-changes_nl.docx","pl":"https://www.ema.europa.eu/pl/documents/procedural-steps-after/abilify-epar-product-information-tracked-changes_pl.docx","pt":"https://www.ema.europa.eu/pt/documents/procedural-steps-after/abilify-epar-product-information-tracked-changes_pt.docx","ro":"https://www.ema.europa.eu/ro/documents/procedural-steps-after/abilify-epar-product-information-tracked-changes_ro.docx","sk":"https://www.ema.europa.eu/sk/documents/procedural-steps-after/abilify-epar-product-information-tracked-changes_sk.docx","sl":"https://www.ema.europa.eu/sl/documents/procedural-steps-after/abilify-epar-product-information-tracked-changes_sl.docx","fi":"https://www.ema.europa.eu/fi/documents/procedural-steps-after/abilify-epar-product-information-tracked-changes_fi.docx","sv":"https://www.ema.europa.eu/sv/documents/procedural-steps-after/abilify-epar-product-information-tracked-changes_sv.docx","is":"https://www.ema.europa.eu/is/documents/procedural-steps-after/abilify-epar-product-information-tracked-changes_is.docx","no":"https://www.ema.europa.eu/no/documents/procedural-steps-after/abilify-epar-product-information-tracked-changes_no.docx"}},
    {"id":"72022","name":"Kisunla : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-01-13T10:19:59Z","last_updated_date":"2026-02-26T10:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/kisunla-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"72024","name":"Mavenclad : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-01-13T10:55:09Z","last_updated_date":"2026-01-13T10:55:09Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/mavenclad-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"72036","name":"Welireg : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-01-13T15:32:05Z","last_updated_date":"2026-01-13T15:32:05Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/welireg-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"72037","name":"Inrebic : EPAR - Procedural steps taken and scientific information after the authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-01-13T15:40:45Z","last_updated_date":"2026-01-13T15:40:45Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/inrebic-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"72038","name":"Aranesp : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-01-13T16:12:13Z","last_updated_date":"2026-01-23T16:35:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/aranesp-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"72040","name":"Rydapt : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-01-14T11:01:48Z","last_updated_date":"2026-01-14T11:01:48Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/rydapt-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"72044","name":"Zvogra : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-01-14T11:42:53Z","last_updated_date":"2026-01-14T11:42:53Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/zvogra-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"72045","name":"Otezla : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-01-14T11:47:59Z","last_updated_date":"2026-01-14T11:47:59Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/otezla-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"72055","name":"Vyvgart : Procedural steps taken and scientific information after the authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-01-15T10:14:38Z","last_updated_date":"2026-01-15T10:14:38Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/vyvgart-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"72061","name":"Ikervis : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-01-15T14:16:13Z","last_updated_date":"2026-01-15T14:16:13Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/ikervis-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"72062","name":"Verkazia : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-01-15T14:21:59Z","last_updated_date":"2026-01-15T14:21:59Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/verkazia-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"72105","name":"Terrosa : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-01-16T12:56:38Z","last_updated_date":"2026-04-23T14:26:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/terrosa-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"72110","name":"Alimta : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-01-16T13:48:33Z","last_updated_date":"2026-01-16T13:48:33Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/alimta-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"72112","name":"Intuniv : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-01-16T13:53:15Z","last_updated_date":"2026-01-16T13:53:15Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/intuniv-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"72113","name":"Amyvid : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-01-16T14:00:04Z","last_updated_date":"2026-01-16T14:00:04Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/amyvid-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"72117","name":"Kerendia : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-01-16T16:30:55Z","last_updated_date":"2026-01-16T16:30:55Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/kerendia-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"72118","name":"Namuscla : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-01-16T17:40:31Z","last_updated_date":"2026-06-03T14:22:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/namuscla-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"72121","name":"Kivexa : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-01-19T10:46:47Z","last_updated_date":"2026-01-19T10:46:47Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/kivexa-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"72123","name":"Trizivir : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-01-19T10:55:24Z","last_updated_date":"2026-01-19T10:55:24Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/trizivir-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"72125","name":"Ziagen : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-01-19T11:16:07Z","last_updated_date":"2026-01-19T11:16:07Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/ziagen-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"72127","name":"Zercepac : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-01-19T11:48:05Z","last_updated_date":"2026-05-18T12:10:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/zercepac-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"72129","name":"Relistor : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-01-19T12:28:55Z","last_updated_date":"2026-01-19T12:28:55Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/relistor-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"72140","name":"Xenpozyme : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-01-19T17:14:16Z","last_updated_date":"2026-01-19T17:14:16Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/xenpozyme-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"72142","name":"Abiraterone Mylan : EPAR - Procedural steps taken and scientific information after the authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-01-19T17:23:04Z","last_updated_date":"2026-01-19T17:23:04Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/abiraterone-mylan-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"72165","name":"Elfabrio : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-01-20T12:33:33Z","last_updated_date":"2026-01-20T12:33:33Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/elfabrio-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"72166","name":"Hycamtin : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-01-20T13:44:22Z","last_updated_date":"2026-01-20T13:44:22Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/hycamtin-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"72170","name":"Veyvondi : EPAR - Procedural steps taken and scientific information after the authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-01-20T15:32:54Z","last_updated_date":"2026-01-20T15:32:54Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/veyvondi-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"72175","name":"Ponlimsi : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-01-20T17:00:19Z","last_updated_date":"2026-01-20T17:00:19Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/ponlimsi-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"72181","name":"Abasaglar : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-01-21T14:08:52Z","last_updated_date":"2026-01-21T14:08:52Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/abasaglar-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"72185","name":"Humalog : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-01-21T14:36:34Z","last_updated_date":"2026-01-21T14:36:34Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/humalog-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"72196","name":"Lyumjev : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-01-21T15:32:33Z","last_updated_date":"2026-01-21T15:32:33Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/lyumjev-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"72199","name":"Liprolog : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-01-21T16:28:36Z","last_updated_date":"2026-01-21T16:28:36Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/liprolog-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"72202","name":"Abraxane : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-01-21T08:10:05Z","last_updated_date":"2026-01-21T08:10:05Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/abraxane-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"72204","name":"Bavencio : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-01-22T12:46:09Z","last_updated_date":"2026-05-21T12:50:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/bavencio-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"72221","name":"Ontruzant : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-01-23T10:35:53Z","last_updated_date":"2026-01-23T10:35:53Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/ontruzant-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"72224","name":"Aripiprazole Mylan Pharma : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-01-23T10:56:27Z","last_updated_date":"2026-01-23T10:56:27Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/aripiprazole-mylan-pharma-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"72227","name":"Travatan : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-01-23T13:45:32Z","last_updated_date":"2026-01-23T13:45:32Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/travatan-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"72228","name":"Nexviadyme : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-01-23T13:57:46Z","last_updated_date":"2026-01-23T13:57:46Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/nexviadyme-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"72244","name":"Dapagliflozin Viatris : EPAR - Procedural steps taken and scientific information after the authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-01-26T10:41:22Z","last_updated_date":"2026-05-07T16:10:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/dapagliflozin-viatris-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"72246","name":"Erbitux : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-01-26T10:56:20Z","last_updated_date":"2026-01-28T15:55:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/erbitux-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"72252","name":"Triumeq : EPAR – Product information – tracked changes","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-01-26T13:29:05Z","last_updated_date":"2026-01-26T13:29:05Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/triumeq-epar-product-information-tracked-changes_en.docx","translations":{"bg":"https://www.ema.europa.eu/bg/documents/procedural-steps-after/xeljanz-epar-product-information-tracked-changes_bg.docx","es":"https://www.ema.europa.eu/es/documents/procedural-steps-after/xeljanz-epar-product-information-tracked-changes_es.docx","cs":"https://www.ema.europa.eu/cs/documents/procedural-steps-after/xeljanz-epar-product-information-tracked-changes_cs.docx","da":"https://www.ema.europa.eu/da/documents/procedural-steps-after/xeljanz-epar-product-information-tracked-changes_da.docx","de":"https://www.ema.europa.eu/de/documents/procedural-steps-after/xeljanz-epar-product-information-tracked-changes_de.docx","et":"https://www.ema.europa.eu/et/documents/procedural-steps-after/xeljanz-epar-product-information-tracked-changes_et.docx","el":"https://www.ema.europa.eu/el/documents/procedural-steps-after/xeljanz-epar-product-information-tracked-changes_el.docx","fr":"https://www.ema.europa.eu/fr/documents/procedural-steps-after/xeljanz-epar-product-information-tracked-changes_fr.docx","hr":"https://www.ema.europa.eu/hr/documents/procedural-steps-after/xeljanz-epar-product-information-tracked-changes_hr.docx","it":"https://www.ema.europa.eu/it/documents/procedural-steps-after/xeljanz-epar-product-information-tracked-changes_it.docx","lv":"https://www.ema.europa.eu/lv/documents/procedural-steps-after/xeljanz-epar-product-information-tracked-changes_lv.docx","lt":"https://www.ema.europa.eu/lt/documents/procedural-steps-after/xeljanz-epar-product-information-tracked-changes_lt.docx","hu":"https://www.ema.europa.eu/hu/documents/procedural-steps-after/xeljanz-epar-product-information-tracked-changes_hu.docx","mt":"https://www.ema.europa.eu/mt/documents/procedural-steps-after/xeljanz-epar-product-information-tracked-changes_mt.docx","nl":"https://www.ema.europa.eu/nl/documents/procedural-steps-after/xeljanz-epar-product-information-tracked-changes_nl.docx","pl":"https://www.ema.europa.eu/pl/documents/procedural-steps-after/xeljanz-epar-product-information-tracked-changes_pl.docx","pt":"https://www.ema.europa.eu/pt/documents/procedural-steps-after/xeljanz-epar-product-information-tracked-changes_pt.docx","ro":"https://www.ema.europa.eu/ro/documents/procedural-steps-after/xeljanz-epar-product-information-tracked-changes_ro.docx","sk":"https://www.ema.europa.eu/sk/documents/procedural-steps-after/xeljanz-epar-product-information-tracked-changes_sk.docx","sl":"https://www.ema.europa.eu/sl/documents/procedural-steps-after/xeljanz-epar-product-information-tracked-changes_sl.docx","fi":"https://www.ema.europa.eu/fi/documents/procedural-steps-after/xeljanz-epar-product-information-tracked-changes_fi.docx","sv":"https://www.ema.europa.eu/sv/documents/procedural-steps-after/xeljanz-epar-product-information-tracked-changes_sv.docx","is":"https://www.ema.europa.eu/is/documents/procedural-steps-after/xeljanz-epar-product-information-tracked-changes_is.docx","no":"https://www.ema.europa.eu/no/documents/procedural-steps-after/xeljanz-epar-product-information-tracked-changes_no.docx"}},
    {"id":"72254","name":"Zynyz : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-01-26T14:24:23Z","last_updated_date":"2026-03-18T12:28:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/zynyz-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"72259","name":"Recarbrio : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-01-26T16:22:21Z","last_updated_date":"2026-01-26T16:22:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/recarbrio-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"72268","name":"Wainzua : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-01-27T09:57:22Z","last_updated_date":"2026-01-27T09:57:22Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/wainzua-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"72274","name":"Avzivi : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-01-27T10:29:49Z","last_updated_date":"2026-02-05T14:21:03Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/avzivi-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"72289","name":"Constella : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-01-27T12:08:10Z","last_updated_date":"2026-01-27T12:08:10Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/constella-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"72292","name":"Imcivree : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-01-27T13:59:59Z","last_updated_date":"2026-06-02T11:11:01Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/imcivree-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"72298","name":"Adcirca : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-01-27T16:04:33Z","last_updated_date":"2026-01-27T16:04:33Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/adcirca-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"72299","name":"Optruma : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-01-27T16:11:35Z","last_updated_date":"2026-01-27T16:11:35Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/optruma-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"72303","name":"Forsteo : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-01-28T09:22:52Z","last_updated_date":"2026-01-28T09:22:52Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/forsteo-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"72304","name":"Cialis : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-01-28T09:57:07Z","last_updated_date":"2026-01-28T09:57:07Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/cialis-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"72305","name":"Abilify : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2004-11-15T10:34:31Z","last_updated_date":"2026-01-12T10:38:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/abilify-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"72306","name":"Tadalafil Lilly : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-01-28T10:54:35Z","last_updated_date":"2026-01-28T10:54:35Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/tadalafil-lilly-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"72312","name":"Genvoya : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-01-28T12:41:24Z","last_updated_date":"2026-01-28T12:41:24Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/genvoya-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"72319","name":"Oyavas : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-01-28T13:33:41Z","last_updated_date":"2026-01-28T13:33:41Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/oyavas-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"72326","name":"Koselugo : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-01-28T14:24:28Z","last_updated_date":"2026-01-28T14:24:28Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/koselugo-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"72330","name":"Pomalidomide Teva : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-01-28T15:28:31Z","last_updated_date":"2026-05-28T17:02:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/pomalidomide-teva-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"72331","name":"Saphnelo : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-01-28T15:41:06Z","last_updated_date":"2026-01-28T15:41:06Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/saphnelo-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"72335","name":"Heplisav B : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-01-28T16:06:47Z","last_updated_date":"2026-01-28T16:06:47Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/heplisav-b-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"72342","name":"Arixtra : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-01-29T12:13:46Z","last_updated_date":"2026-05-07T11:11:01Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/arixtra-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"72346","name":"Insulin lispro Sanofi : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-01-29T12:58:46Z","last_updated_date":"2026-01-29T12:58:46Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/insulin-lispro-sanofi-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"72348","name":"Firazyr : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-01-29T13:20:19Z","last_updated_date":"2026-04-01T11:46:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/firazyr-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"72359","name":"Qdenga : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-01-30T08:30:39Z","last_updated_date":"2026-05-27T14:38:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/qdenga-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"72360","name":"Trulicity : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-01-30T08:46:07Z","last_updated_date":"2026-01-30T08:46:07Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/trulicity-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"72378","name":"Pemetrexed Accord : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-01-30T11:30:58Z","last_updated_date":"2026-01-30T11:30:58Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/pemetrexed-accord-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"72404","name":"GalliaPharm : EPAR - Procedural steps taken and scientific information after the authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-02-03T09:47:15Z","last_updated_date":"2026-02-03T09:47:15Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/galliapharm-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"72423","name":"Vazkepa : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-02-05T12:59:32Z","last_updated_date":"2026-03-13T11:33:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/vazkepa-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"72424","name":"Yuvanci : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-02-05T14:04:58Z","last_updated_date":"2026-05-22T13:08:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/yuvanci-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"72427","name":"DuoTrav : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-02-05T14:26:56Z","last_updated_date":"2026-02-05T14:26:56Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/duotrav-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"72430","name":"Vanflyta : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-02-05T16:01:39Z","last_updated_date":"2026-02-05T16:01:39Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/vanflyta-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"72435","name":"Xerava : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-02-06T09:28:41Z","last_updated_date":"2026-03-13T11:12:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/xerava-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"72440","name":"Insulin aspart Sanofi : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-02-06T10:06:56Z","last_updated_date":"2026-02-06T10:06:56Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/insulin-aspart-sanofi-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"72441","name":"Tuznue : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-02-06T10:42:09Z","last_updated_date":"2026-02-06T10:42:09Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/tuznue-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"72444","name":"Helicobacter Test INFAI : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-02-06T12:03:57Z","last_updated_date":"2026-02-06T12:03:57Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/helicobacter-test-infai-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"72453","name":"Xadago : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-02-09T13:57:17Z","last_updated_date":"2026-02-09T13:57:17Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/xadago-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"72457","name":"Kirsty (previously Kixelle) : EPAR - Procedural steps taken and scientific information after the authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2021-09-14T12:00:00Z","last_updated_date":"2021-09-14T12:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/kirsty-previously-kixelle-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"72458","name":"Azopt : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-02-09T15:33:49Z","last_updated_date":"2026-02-09T15:33:49Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/azopt-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"72461","name":"Lytenava : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-02-09T17:39:14Z","last_updated_date":"2026-02-09T17:39:14Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/lytenava-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"72496","name":"Adenuric : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-02-10T16:56:23Z","last_updated_date":"2026-02-10T16:56:23Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/adenuric-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf-0"},
    {"id":"72506","name":"Romvimza  : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-02-11T11:37:00Z","last_updated_date":"2026-02-11T11:37:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/romvimza-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"72526","name":"Fosavance : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-02-12T11:07:17Z","last_updated_date":"2026-02-12T11:07:17Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/fosavance-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"72535","name":"Adrovance : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-02-12T15:07:45Z","last_updated_date":"2026-02-12T15:07:45Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/adrovance-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"72538","name":"Infanrix Hexa : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-02-12T15:28:46Z","last_updated_date":"2026-02-12T15:28:46Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/infanrix-hexa-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"72544","name":"Vantavo : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-02-12T16:57:17Z","last_updated_date":"2026-02-12T16:57:17Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/vantavo-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"72556","name":"Emtricitabine / Rilpivirine / Tenofovir Alafenamide Viatris : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-02-13T15:14:52Z","last_updated_date":"2026-05-08T09:32:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/emtricitabine-rilpivirine-tenofovir-alafenamide-viatris-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"72570","name":"Orphacol : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-02-16T14:49:14Z","last_updated_date":"2026-04-21T12:30:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/orphacol-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"72576","name":"Usrenty : EPAR - Procedural steps taken and scientific information after the authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-02-17T09:23:28Z","last_updated_date":"2026-05-18T10:30:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/usrenty-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"72579","name":" Trecondi : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-02-17T10:46:22Z","last_updated_date":"2026-02-17T10:46:22Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/trecondi-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"72586","name":"Enrylaze : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-02-18T09:28:38Z","last_updated_date":"2026-02-18T09:28:38Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/enrylaze-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"72597","name":"Evfraxy : EPAR - Procedural steps taken and scientific information after the authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-02-19T10:18:09Z","last_updated_date":"2026-03-20T15:18:08Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/evfraxy-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"72598","name":"Fulphila : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-02-19T10:25:58Z","last_updated_date":"2026-02-19T10:25:58Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/fulphila-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"72602","name":"Adzynma : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-02-19T13:54:51Z","last_updated_date":"2026-02-19T13:54:51Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/adzynma-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"72603","name":"Kigabeq : EPAR - Procedural steps taken and scientific information after the authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-02-19T14:08:42Z","last_updated_date":"2026-02-19T14:08:42Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/kigabeq-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"72610","name":"\tImfinzi : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-02-19T16:03:54Z","last_updated_date":"2026-05-18T10:41:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/imfinzi-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"72615","name":"Orladeyo : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2021-07-12T09:00:00Z","last_updated_date":"2021-07-12T09:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/orladeyo-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"72619","name":"Ameluz : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-02-20T10:05:45Z","last_updated_date":"2026-06-03T14:40:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/ameluz-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"72631","name":"Semglee : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-02-20T15:51:38Z","last_updated_date":"2026-02-20T15:51:38Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/semglee-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"72646","name":"Ogivri : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-02-23T15:18:40Z","last_updated_date":"2026-02-23T15:18:40Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/ogivri-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"72647","name":"Efmody : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-01-06T15:48:47Z","last_updated_date":"2026-02-23T15:50:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/efmody-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"72649","name":"Inluriyo : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-02-23T15:57:29Z","last_updated_date":"2026-02-23T15:57:29Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/inluriyo-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"72658","name":"Teriflunomide Accord : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-02-24T09:38:34Z","last_updated_date":"2026-02-24T09:38:34Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/teriflunomide-accord-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"72679","name":"Vivlipeg : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-02-24T15:43:17Z","last_updated_date":"2026-02-24T15:43:17Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/vivlipeg-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"72693","name":"Tibsovo : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-02-25T12:52:54Z","last_updated_date":"2026-02-25T12:52:54Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/tibsovo-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"72695","name":"Tadalafil Mylan : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-02-25T13:12:15Z","last_updated_date":"2026-02-25T13:12:15Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/tadalafil-mylan-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"72698","name":"DaTSCAN : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-02-25T14:28:45Z","last_updated_date":"2026-02-25T14:28:45Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/datscan-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"72700","name":"Sycrest : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-02-25T14:43:58Z","last_updated_date":"2026-02-25T14:43:58Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/sycrest-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
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    {"id":"72718","name":"Yeytuo : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-02-26T12:02:40Z","last_updated_date":"2026-05-04T11:11:01Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/yeytuo-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"72737","name":"Alecensa : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-02-27T11:01:15Z","last_updated_date":"2026-02-27T11:01:15Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/alecensa-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"72740","name":"Nilemdo : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-02-27T11:11:00Z","last_updated_date":"2026-02-27T11:11:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/nilemdo-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"72742","name":"Nustendi : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-02-27T11:19:16Z","last_updated_date":"2026-02-27T11:19:16Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/nustendi-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"72767","name":"Xbonzy : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-03-02T10:08:17Z","last_updated_date":"2026-05-12T10:53:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/xbonzy-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"72768","name":"Nexium Control : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-03-02T10:16:16Z","last_updated_date":"2026-03-02T10:16:16Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/nexium-control-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"72769","name":"Azomyr : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-03-02T10:32:15Z","last_updated_date":"2026-03-02T10:32:15Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/azomyr-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"72771","name":"Neoclarityn : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-03-02T10:45:04Z","last_updated_date":"2026-03-02T10:45:04Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/neoclarityn-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"72773","name":"Rasilez : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-03-02T12:22:06Z","last_updated_date":"2026-03-02T12:22:06Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/rasilez-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"72774","name":"Aerius : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-03-02T13:17:00Z","last_updated_date":"2026-03-02T13:17:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/aerius-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"72779","name":"Lamzede : EPAR - Procedural steps taken and scientific information after authorisation ","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-03-02T16:24:22Z","last_updated_date":"2026-03-02T16:24:22Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/lamzede-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"72790","name":"Nivestim : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-03-02T16:39:51Z","last_updated_date":"2026-03-02T16:39:51Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/nivestim-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"72798","name":"Aqneursa : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-03-03T11:36:45Z","last_updated_date":"2026-03-03T11:36:45Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/aqneursa-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"72799","name":"Vyloy : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-03-03T13:48:09Z","last_updated_date":"2026-03-03T13:48:09Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/vyloy-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"72805","name":"Zeposia: EPAR - Procedural steps taken and scientific information after the authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-03-03T14:26:58Z","last_updated_date":"2026-03-03T14:26:58Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/zeposia-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"72815","name":"Hemgenix : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-03-04T10:49:32Z","last_updated_date":"2026-03-04T10:49:32Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/hemgenix-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"72829","name":"Kefdensis : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-03-04T14:05:27Z","last_updated_date":"2026-03-04T14:05:27Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/kefdensis-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"72858","name":"Imatinib Teva : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-03-05T14:53:35Z","last_updated_date":"2026-03-05T14:53:35Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/imatinib-teva-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"72859","name":"Lantus : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-03-05T15:04:52Z","last_updated_date":"2026-03-05T15:04:52Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/lantus-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"72861","name":"VacPertagen : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-03-05T15:13:19Z","last_updated_date":"2026-03-05T15:13:19Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/vacpertagen-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"72862","name":"Apidra : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-03-05T15:21:10Z","last_updated_date":"2026-03-05T15:21:10Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/apidra-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"72873","name":"Tyruko : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-03-06T13:37:15Z","last_updated_date":"2026-03-06T13:37:15Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/tyruko-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"72885","name":"Cayston : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-03-09T10:04:29Z","last_updated_date":"2026-03-09T10:04:29Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/cayston-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"72892","name":"Nucala : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-03-09T10:40:58Z","last_updated_date":"2026-03-09T10:40:58Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/nucala-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"72895","name":"Enhertu : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2025-12-03T14:35:48Z","last_updated_date":"2025-12-03T14:35:48Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/enhertu-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"72922","name":"Teduglutide Viatris : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-03-10T11:21:03Z","last_updated_date":"2026-05-08T15:47:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/teduglutide-viatris-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"72928","name":"Amversio : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-03-10T13:49:47Z","last_updated_date":"2026-03-10T13:49:47Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/amversio-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"72929","name":"Drovelis : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-03-10T15:00:24Z","last_updated_date":"2026-03-10T15:00:24Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/drovelis-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"72930","name":"Lydisilka : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-03-10T15:08:20Z","last_updated_date":"2026-03-10T15:08:20Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/lydisilka-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"72965","name":"Rxulti : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-03-12T09:06:39Z","last_updated_date":"2026-03-23T13:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/rxulti-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"72988","name":"Forxiga : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-03-12T16:36:12Z","last_updated_date":"2026-03-12T16:36:12Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/forxiga-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"72995","name":"Edistride : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-03-13T09:22:06Z","last_updated_date":"2026-03-13T09:22:06Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/edistride-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"72999","name":"Vabysmo : EPAR - Procedural steps taken and scientific information after authorisation (archived)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-03-13T10:12:17Z","last_updated_date":"2026-03-13T10:12:17Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/vabysmo-epar-procedural-steps-taken-scientific-information-after-authorisation-archived_en.pdf"},
    {"id":"73002","name":"Arsenic trioxide Accord : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-03-13T11:17:39Z","last_updated_date":"2026-03-13T11:17:39Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/arsenic-trioxide-accord-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"73058","name":"Trimbow : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-03-17T12:31:33Z","last_updated_date":"2026-03-17T12:31:33Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/trimbow-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"73059","name":"Trydonis : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-03-17T12:41:49Z","last_updated_date":"2026-03-17T12:41:49Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/trydonis-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"73060","name":"Akeega : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-03-17T12:51:45Z","last_updated_date":"2026-03-17T12:51:45Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/akeega-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"73103","name":"Strensiq : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-03-18T15:03:15Z","last_updated_date":"2026-03-18T15:03:15Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/strensiq-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"73107","name":"Deltyba : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-03-18T16:21:04Z","last_updated_date":"2026-03-18T16:21:04Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/deltyba-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"73109","name":"Voranigo : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-03-18T16:34:17Z","last_updated_date":"2026-05-19T10:55:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/voranigo-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"73136","name":"Adcetris : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-03-20T15:26:18Z","last_updated_date":"2026-03-20T15:26:18Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/adcetris-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"73155","name":"Velphoro : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-03-24T10:55:14Z","last_updated_date":"2026-03-24T10:55:14Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/velphoro-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"73167","name":"Kadcyla : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-03-24T14:15:04Z","last_updated_date":"2026-03-24T14:15:04Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/kadcyla-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"73169","name":"Kanuma : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-03-24T15:06:18Z","last_updated_date":"2026-03-24T15:06:18Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/kanuma-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"73185","name":"Trabectedin Accord : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-03-25T09:01:28Z","last_updated_date":"2026-03-25T09:01:28Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/trabectedin-accord-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"73187","name":"Tepezza : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-03-25T09:46:43Z","last_updated_date":"2026-03-25T09:46:43Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/tepezza-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"73194","name":"Bemfola : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-03-25T10:34:55Z","last_updated_date":"2026-03-25T10:34:55Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/bemfola-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"73237","name":"Ziextenzo : EPAR - Procedural steps taken and scientific information after the authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-03-27T10:29:25Z","last_updated_date":"2026-03-27T10:29:25Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/ziextenzo-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"73271","name":"Ogsiveo : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-03-31T10:10:05Z","last_updated_date":"2026-05-06T11:11:01Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/ogsiveo-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"73276","name":"Brilique : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-03-31T12:39:00Z","last_updated_date":"2026-03-31T12:39:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/brilique-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"73278","name":"Cinacalcet Accordpharma : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-03-31T13:02:32Z","last_updated_date":"2026-03-31T13:02:32Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/cinacalcet-accordpharma-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"73318","name":"Zokinvy : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-04-07T12:53:12Z","last_updated_date":"2026-04-07T12:53:12Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/zokinvy-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"73319","name":"Aerinaze : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-04-07T12:59:47Z","last_updated_date":"2026-04-07T12:59:47Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/aerinaze-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"73342","name":"Viramune : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-04-07T16:40:14Z","last_updated_date":"2026-04-07T16:40:14Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/viramune-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"73348","name":"Rezzayo : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-04-08T11:33:15Z","last_updated_date":"2026-04-08T11:33:15Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/rezzayo-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"73350","name":"Rebif : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-04-08T13:44:27Z","last_updated_date":"2026-04-08T13:44:27Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/rebif-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"73356","name":"Yellox : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-04-08T15:26:35Z","last_updated_date":"2026-04-08T15:26:35Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/yellox-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"73372","name":"Neofordex : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-04-09T10:35:19Z","last_updated_date":"2026-04-09T10:35:19Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/neofordex-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"73374","name":"Theralugand : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-04-09T10:54:48Z","last_updated_date":"2026-06-02T16:45:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/theralugand-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"73402","name":"Cablivi : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-04-09T16:55:19Z","last_updated_date":"2026-05-27T12:05:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/cablivi-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"73404","name":"CellCept : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-10-27T09:41:16Z","last_updated_date":"2026-02-24T09:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/cellcept-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"73408","name":"Myclausen : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-04-10T10:10:54Z","last_updated_date":"2026-04-10T10:10:54Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/myclausen-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"73411","name":"Mynzepli : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-04-10T10:51:12Z","last_updated_date":"2026-04-10T10:51:12Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/mynzepli-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"73425","name":"Teizeild : EPAR - Procedural steps taken and scientific information after the authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-04-13T12:58:53Z","last_updated_date":"2026-04-13T12:58:53Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/teizeild-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"73436","name":"Vfend : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-04-14T12:00:00Z","last_updated_date":"2026-04-14T12:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/vfend-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"73444","name":"Jorveza : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-04-15T11:59:43Z","last_updated_date":"2026-04-15T11:59:43Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/jorveza-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"73446","name":"Lorviqua : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-04-15T12:18:28Z","last_updated_date":"2026-04-15T12:18:28Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/lorviqua-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"73470","name":"Enwylma : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-04-16T08:43:34Z","last_updated_date":"2026-04-16T08:43:34Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/enwylma-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"73471","name":"Myqorzo : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-04-16T08:49:13Z","last_updated_date":"2026-04-16T08:49:13Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/myqorzo-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"73472","name":"Emtricitabine / Tenofovir alafenamide Viatris Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-04-16T13:26:56Z","last_updated_date":"2026-04-16T13:26:56Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/emtricitabine-tenofovir-alafenamide-viatris-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"73480","name":"Atriance : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-04-16T19:47:49Z","last_updated_date":"2026-04-16T19:47:49Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/atriance-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"73492","name":"Aclasta : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-04-20T10:56:00Z","last_updated_date":"2026-04-20T10:56:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/aclasta-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"73495","name":"Nulojix : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-04-20T13:41:13Z","last_updated_date":"2026-04-20T13:41:13Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/nulojix-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"73503","name":"Arsenic trioxide medac : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-04-21T13:11:00Z","last_updated_date":"2026-04-21T13:11:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/arsenic-trioxide-medac-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"73504","name":"Ezmekly : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-04-21T14:45:34Z","last_updated_date":"2026-05-12T11:05:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/ezmekly-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"73519","name":"Rotarix : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-04-22T11:55:39Z","last_updated_date":"2026-04-22T11:55:39Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/rotarix-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"73537","name":"Praxbind : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-04-23T13:01:51Z","last_updated_date":"2026-04-23T13:01:51Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/praxbind-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"73538","name":"Aptivus : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-04-23T13:07:58Z","last_updated_date":"2026-04-23T13:07:58Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/aptivus-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"73544","name":"Nulojix : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-04-23T14:57:54Z","last_updated_date":"2026-04-23T14:57:54Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/nulojix-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf-0"},
    {"id":"73548","name":"Vysribli : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-04-23T16:57:27Z","last_updated_date":"2026-04-23T16:57:27Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/vysribli-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"73550","name":"Ondibta : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-04-24T08:43:40Z","last_updated_date":"2026-04-24T08:43:40Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/ondibta-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"73551","name":"Striascan : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-04-24T08:49:00Z","last_updated_date":"2026-04-24T08:49:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/striascan-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"73553","name":"Stelara : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-04-24T09:16:55Z","last_updated_date":"2026-04-24T09:16:55Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/stelara-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"73571","name":"Ranluspec : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-04-24T14:13:53Z","last_updated_date":"2026-05-29T14:43:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/ranluspec-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"73575","name":"Dazublys : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-04-28T09:36:17Z","last_updated_date":"2026-04-28T09:36:17Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/dazublys-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"73613","name":"Qutenza : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2009-11-16T10:44:30Z","last_updated_date":"2023-12-04T11:11:01Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/qutenza-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"73638","name":"Usgena : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-05-07T09:57:15Z","last_updated_date":"2026-05-07T09:57:15Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/usgena-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"73641","name":"\tOncaspar : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-05-07T10:47:12Z","last_updated_date":"2026-05-07T10:47:12Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/oncaspar-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"73643","name":"Comtan : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-05-07T13:54:52Z","last_updated_date":"2026-05-07T13:54:52Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/comtan-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"73647","name":"Afiveg : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-05-07T15:37:40Z","last_updated_date":"2026-05-07T15:37:40Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/afiveg-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"73650","name":"Nintedanib Viatris : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-05-08T09:23:37Z","last_updated_date":"2026-05-08T09:23:37Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/nintedanib-viatris-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"73651","name":"Pomalidomide Viatris : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-05-08T09:38:33Z","last_updated_date":"2026-05-08T09:38:33Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/pomalidomide-viatris-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"73666","name":"Ixiaro : EPAR - Procedural steps taken and scientific information after authorisation ","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-05-08T12:26:43Z","last_updated_date":"2026-05-08T12:26:43Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/ixiaro-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"73676","name":"Olanzapine Glenmark : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-05-08T15:49:33Z","last_updated_date":"2026-05-08T15:49:33Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/olanzapine-glenmark-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"73678","name":"Olanzapine Glenmark Europe : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-05-08T15:59:31Z","last_updated_date":"2026-05-08T15:59:31Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/olanzapine-glenmark-europe-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"73688","name":"Orencia : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-05-11T09:01:17Z","last_updated_date":"2026-05-11T09:01:17Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/orencia-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"73691","name":"Amglidia : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-05-11T09:24:12Z","last_updated_date":"2026-05-11T09:24:12Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/amglidia-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"73692","name":"Qalsody : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-05-11T09:33:41Z","last_updated_date":"2026-05-11T09:33:41Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/qalsody-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"73693","name":"Exdensur : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-05-11T09:55:29Z","last_updated_date":"2026-05-11T09:55:29Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/exdensur-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"73707","name":"Olazax : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-05-11T15:46:11Z","last_updated_date":"2026-05-11T15:46:11Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/olazax-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"73717","name":"Olazax Disperzi : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-05-12T10:47:44Z","last_updated_date":"2026-05-12T10:47:44Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/olazax-disperzi-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
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    {"id":"73778","name":"Ryeqo : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-05-20T10:31:20Z","last_updated_date":"2026-05-20T10:31:20Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/ryeqo-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"73791","name":"Pyrukynd : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-05-21T13:33:21Z","last_updated_date":"2026-05-21T13:33:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/pyrukynd-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"73794","name":"Nuwiq : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-05-21T14:17:09Z","last_updated_date":"2026-05-21T14:17:09Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/nuwiq-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"73823","name":"Jubereq : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-05-22T09:54:37Z","last_updated_date":"2026-05-22T09:54:37Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/jubereq-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"73835","name":"Yttriga : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-05-22T13:14:11Z","last_updated_date":"2026-05-22T13:14:11Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/yttriga-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"73844","name":"Ucedane : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-05-26T09:18:57Z","last_updated_date":"2026-05-26T09:18:57Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/ucedane-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"73850","name":"Fycompa : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-05-26T11:18:58Z","last_updated_date":"2026-05-26T11:18:58Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/fycompa-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"73858","name":"Rezdiffra : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-05-27T11:02:00Z","last_updated_date":"2026-05-27T11:02:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/rezdiffra-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"73860","name":"Poherdy : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-05-27T12:21:51Z","last_updated_date":"2026-05-27T12:21:51Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/poherdy-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"73862","name":"Xenleta : EPAR - Procedural steps taken and scientific information after the authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-05-27T12:39:33Z","last_updated_date":"2026-05-27T12:39:33Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/xenleta-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"73863","name":"Sunosi : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-05-27T14:21:50Z","last_updated_date":"2026-05-27T14:21:50Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/sunosi-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"73865","name":"Calquence : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-05-27T15:20:04Z","last_updated_date":"2026-05-27T15:20:04Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/calquence-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf-0"},
    {"id":"73879","name":"Beromun : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-05-28T13:29:09Z","last_updated_date":"2026-05-28T13:29:09Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/beromun-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"73883","name":"Aquipta : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-05-28T14:12:54Z","last_updated_date":"2026-05-28T14:12:54Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/aquipta-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"73895","name":"Vypeti : EPAR - Procedural steps taken and scientific information after authorisation","type":"procedural-steps-after","status":"unknown","consultation_date":"","first_published_date":"2026-05-29T12:32:17Z","last_updated_date":"2026-05-29T12:32:17Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps-after/vypeti-epar-procedural-steps-taken-scientific-information-after-authorisation_en.pdf"},
    {"id":"2519","name":"ProMeris : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2007-01-10T00:09:21Z","last_updated_date":"2015-07-14T01:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/promeris-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"2626","name":"Actos : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-04-03T02:00:00Z","last_updated_date":"2006-04-03T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/actos-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"2660","name":"Nobilis Influenza H5N2 : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-09-19T02:00:00Z","last_updated_date":"2006-09-19T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/nobilis-influenza-h5n2-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"2682","name":"GONAL-f : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-08-31T02:09:21Z","last_updated_date":"2006-08-31T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/gonal-f-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"2823","name":"Champix : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-10-11T02:09:00Z","last_updated_date":"2006-10-11T02:09:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/champix-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"2898","name":"Fendrix : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2005-12-22T00:09:21Z","last_updated_date":"2005-12-22T00:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/fendrix-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"2920","name":"Olanzapine Cipla : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2007-12-17T01:00:00Z","last_updated_date":"2014-07-24T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/olanzapine-cipla-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"2926","name":"Avastin : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-01-24T01:00:00Z","last_updated_date":"2006-01-24T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/avastin-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"3065","name":"NutropinAq : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-07-12T02:09:21Z","last_updated_date":"2006-07-12T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/nutropinaq-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"3122","name":"Levemir : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-08-15T02:00:00Z","last_updated_date":"2006-08-15T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/levemir-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"3134","name":"Econor : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2005-10-21T02:09:21Z","last_updated_date":"2005-10-21T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/econor-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"3300","name":"Tandemact : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2007-01-26T01:00:00Z","last_updated_date":"2007-01-26T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/tandemact-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"3447","name":"Humalog : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-01-09T00:09:21Z","last_updated_date":"2006-01-09T00:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/humalog-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"3467","name":"Mixtard : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-08-31T02:09:21Z","last_updated_date":"2006-08-31T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/mixtard-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"3567","name":"Epivir : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2005-11-25T01:00:00Z","last_updated_date":"2005-11-25T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/epivir-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"3809","name":"Zulvac 8 Bovis : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2010-01-21T01:00:00Z","last_updated_date":"2010-01-21T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/zulvac-8-bovis-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"3815","name":"Equilis Prequenza : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2005-10-21T02:09:21Z","last_updated_date":"2005-10-21T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/equilis-prequenza-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"3821","name":"PhotoBarr : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2008-11-25T01:00:00Z","last_updated_date":"2012-05-07T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/photobarr-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"3827","name":"Axura : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2005-10-21T02:00:00Z","last_updated_date":"2005-10-21T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/axura-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"3857","name":"Rotarix : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-09-11T02:09:21Z","last_updated_date":"2006-09-11T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/rotarix-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"4558","name":"Emadine : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2005-10-21T02:00:00Z","last_updated_date":"2005-10-21T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/emadine-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"4600","name":"DuoTrav : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2007-05-31T02:00:00Z","last_updated_date":"2007-05-31T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/duotrav-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"4671","name":"Trisenox : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2005-10-28T02:09:21Z","last_updated_date":"2005-10-28T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/trisenox-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"4838","name":"Cerezyme : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2005-10-21T02:09:21Z","last_updated_date":"2005-10-21T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/cerezyme-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"4975","name":"Suprelorin : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2007-07-11T02:00:00Z","last_updated_date":"2007-07-11T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/suprelorin-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"5087","name":"Litak : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2005-10-21T02:00:00Z","last_updated_date":"2005-10-21T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/litak-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"5156","name":"Liprolog: EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-06-19T02:00:00Z","last_updated_date":"2006-06-19T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/liprolog-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"5306","name":"Actraphane : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-04-03T02:00:00Z","last_updated_date":"2006-04-03T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/actraphane-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"5338","name":"Velcade : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-08-15T02:00:00Z","last_updated_date":"2006-08-15T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/velcade-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"5414","name":"Sprycel : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-11-30T01:00:00Z","last_updated_date":"2006-11-30T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/sprycel-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"5445","name":"Tasigna : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2007-11-29T00:09:21Z","last_updated_date":"2007-11-29T00:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/tasigna-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"5450","name":"Imprida : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2007-02-21T01:00:00Z","last_updated_date":"2017-05-11T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/imprida-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"5501","name":"Circadin : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2007-07-11T02:09:21Z","last_updated_date":"2007-07-11T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/circadin-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"5506","name":"Isentress : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2008-01-14T01:00:00Z","last_updated_date":"2008-01-14T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/isentress-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"5620","name":"Cymbalta : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-02-07T01:00:00Z","last_updated_date":"2006-02-07T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/cymbalta-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"5663","name":"Velosulin : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2009-04-17T02:09:21Z","last_updated_date":"2009-04-17T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/velosulin-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"5699","name":"ReFacto AF : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-09-08T02:00:00Z","last_updated_date":"2006-09-08T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/refacto-af-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"5811","name":"Infanrix Hexa : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2005-10-21T02:00:00Z","last_updated_date":"2005-10-21T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/infanrix-hexa-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"5883","name":"Suboxone : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-10-19T02:00:00Z","last_updated_date":"2006-10-19T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/suboxone-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"5917","name":"Kivexa : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-08-07T02:00:00Z","last_updated_date":"2023-11-27T12:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/kivexa-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"6027","name":"Ionsys : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-02-02T01:00:00Z","last_updated_date":"2011-01-28T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/ionsys-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"6253","name":"Nonafact : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2005-11-15T00:09:00Z","last_updated_date":"2020-04-29T00:09:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/nonafact-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"6296","name":"Zometa : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2005-10-21T02:00:00Z","last_updated_date":"2005-10-21T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/zometa-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"6347","name":"Noxafil : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2005-11-04T00:09:21Z","last_updated_date":"2005-11-04T00:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/noxafil-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"6371","name":"Zyprexa : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2005-10-21T02:00:00Z","last_updated_date":"2005-10-21T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/zyprexa-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"6398","name":"Lumigan : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2005-12-08T01:00:00Z","last_updated_date":"2005-12-08T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/lumigan-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"6604","name":"Daronrix : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2007-04-11T02:00:00Z","last_updated_date":"2013-07-02T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/daronrix-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"6658","name":"Zerene : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2005-10-21T02:09:21Z","last_updated_date":"2012-10-15T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/zerene-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"6670","name":"Purevax RCP : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2005-11-22T00:09:00Z","last_updated_date":"2005-11-22T00:09:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/purevax-rcp-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"6699","name":"NovoMix : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2005-10-21T02:00:00Z","last_updated_date":"2005-10-21T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/novomix-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"6776","name":"Teslascan : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-10-30T00:09:21Z","last_updated_date":"2012-08-02T16:15:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/teslascan-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"6834","name":"Agenerase : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2005-10-21T02:00:00Z","last_updated_date":"2011-06-21T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/agenerase-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"6847","name":"Keppra : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2005-10-21T02:00:00Z","last_updated_date":"2005-10-21T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/keppra-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"6861","name":"Zolvix : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2009-11-26T00:09:21Z","last_updated_date":"2009-11-26T00:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/zolvix-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"6902","name":"Yttriga : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-10-30T00:09:21Z","last_updated_date":"2006-10-30T00:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/yttriga-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"6920","name":"Karvea : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-07-11T02:00:00Z","last_updated_date":"2006-07-11T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/karvea-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"7109","name":"Altargo : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2007-06-05T02:00:00Z","last_updated_date":"2019-03-15T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/altargo-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"7113","name":"Kogenate Bayer : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-09-08T02:00:00Z","last_updated_date":"2006-09-08T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/kogenate-bayer-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"7120","name":"Paxene : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2005-12-15T01:00:00Z","last_updated_date":"2010-03-22T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/paxene-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"7210","name":"Vistide : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2005-11-17T01:00:00Z","last_updated_date":"2015-01-19T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/vistide-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"7312","name":"Zevalin : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-11-13T01:00:00Z","last_updated_date":"2006-11-13T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/zevalin-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"7352","name":"Xolair : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2005-11-25T01:00:00Z","last_updated_date":"2005-11-25T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/xolair-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"7471","name":"Focetria : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2007-05-07T02:00:00Z","last_updated_date":"2007-05-07T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/focetria-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"7505","name":"Virbagen Omega : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-08-29T02:09:21Z","last_updated_date":"2006-08-29T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/virbagen-omega-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"7522","name":"Azomyr : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2005-10-21T02:00:00Z","last_updated_date":"2005-10-21T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/azomyr-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"7611","name":"Procoralan : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2005-11-04T01:00:00Z","last_updated_date":"2023-12-21T16:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/procoralan-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"7822","name":"Rapamune : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2009-06-16T02:00:00Z","last_updated_date":"2009-06-16T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/rapamune-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"7870","name":"Posatex : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2008-07-01T02:09:21Z","last_updated_date":"2008-07-01T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/posatex-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"7991","name":"ProMeris Duo : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2007-01-10T00:09:21Z","last_updated_date":"2015-07-14T01:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/promeris-duo-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"8025","name":"Palladia : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2009-10-01T02:09:21Z","last_updated_date":"2009-10-01T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/palladia-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"8108","name":"Avaglim : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-10-20T02:00:00Z","last_updated_date":"2011-01-17T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/avaglim-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"8135","name":"Myozyme : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2009-05-19T02:00:00Z","last_updated_date":"2024-02-15T10:23:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/myozyme-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"8176","name":"NeuroBloc : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2008-06-01T02:09:00Z","last_updated_date":"2023-05-04T10:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/neurobloc-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"8179","name":"Xeloda : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2005-12-07T01:00:00Z","last_updated_date":"2005-12-07T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/xeloda-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"8185","name":"Beromun : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2005-10-21T02:09:21Z","last_updated_date":"2005-10-21T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/beromun-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"8214","name":"Metalyse : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-07-10T02:00:00Z","last_updated_date":"2006-07-10T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/metalyse-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"8296","name":"Ambirix : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2005-11-23T01:00:00Z","last_updated_date":"2005-11-23T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/ambirix-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"8327","name":"Circovac : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2007-08-01T01:09:21Z","last_updated_date":"2007-08-01T01:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/circovac-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"8350","name":"Irbesartan Hydrochlorothiazide BMS : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2009-11-24T01:00:00Z","last_updated_date":"2009-11-24T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/irbesartan-hydrochlorothiazide-bms-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"8428","name":"Competact : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2007-05-31T02:09:21Z","last_updated_date":"2007-05-31T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/competact-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"8502","name":"Leucogen : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2009-06-30T02:00:00Z","last_updated_date":"2009-06-30T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/leucogen-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"8513","name":"Hexavac : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2005-10-25T02:00:00Z","last_updated_date":"2012-08-16T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/hexavac-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"8578","name":"Xeristar : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-02-07T01:00:00Z","last_updated_date":"2021-06-22T14:15:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/xeristar-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"8661","name":"Increlex : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2007-08-13T02:00:00Z","last_updated_date":"2007-08-13T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/increlex-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"8676","name":"Medicinal Oxygen Air Liquide Sante : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2007-01-12T01:00:00Z","last_updated_date":"2007-01-12T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/medicinal-oxygen-air-liquide-sante-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"8799","name":"PritorPlus : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2005-10-21T02:00:00Z","last_updated_date":"2005-10-21T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/pritorplus-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"8806","name":"Valtropin : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2007-05-31T02:00:00Z","last_updated_date":"2012-08-14T18:50:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/valtropin-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"8829","name":"Zenapax : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2008-04-08T03:09:21Z","last_updated_date":"2008-04-08T03:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/zenapax-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"8841","name":"ProQuad : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-06-02T02:00:00Z","last_updated_date":"2006-06-02T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/proquad-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"8847","name":"Raptiva : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2009-08-04T02:00:00Z","last_updated_date":"2009-08-04T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/raptiva-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"8895","name":"Gonazon : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2007-01-15T01:00:00Z","last_updated_date":"2012-08-15T12:20:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/gonazon-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"8953","name":"Revlimid : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2007-06-26T02:00:00Z","last_updated_date":"2007-06-26T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/revlimid-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"9089","name":"Reyataz : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-08-08T02:00:00Z","last_updated_date":"2006-08-08T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/reyataz-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"9114","name":"Irbesartan Hydrochlorothiazide Winthrop : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2007-02-05T01:00:00Z","last_updated_date":"2007-02-05T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/irbesartan-hydrochlorothiazide-winthrop-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"9349","name":"Kinzalmono : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-07-10T02:00:00Z","last_updated_date":"2006-07-10T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/kinzalmono-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"9433","name":"Zimulti : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2009-01-30T02:09:21Z","last_updated_date":"2009-01-30T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/zimulti-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"9474","name":"Visudyne : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-01-23T01:00:00Z","last_updated_date":"2006-01-23T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/visudyne-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"9583","name":"Fevaxyn Pentofel : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2007-03-08T01:00:00Z","last_updated_date":"2024-11-21T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/fevaxyn-pentofel-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"9666","name":"Aptivus : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2005-11-04T01:00:00Z","last_updated_date":"2005-11-04T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/aptivus-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"9757","name":"Pirsue : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-11-23T00:09:21Z","last_updated_date":"2025-05-02T01:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/pirsue-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"9946","name":"Quintanrix : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2008-09-10T02:00:00Z","last_updated_date":"2008-09-10T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/quintanrix-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"10024","name":"Vasovist : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2005-11-04T01:00:00Z","last_updated_date":"2005-11-04T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/vasovist-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"10048","name":"Toviaz : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2007-12-05T01:00:00Z","last_updated_date":"2007-12-05T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/toviaz-epar-procedural-steps-taken-authorisation_en.pdf"},
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    {"id":"10751","name":"Iscover : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-10-24T02:00:00Z","last_updated_date":"2006-10-24T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/iscover-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"10870","name":"Cerenia : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-10-05T01:09:21Z","last_updated_date":"2006-10-05T01:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/cerenia-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"10974","name":"Ypozane : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2007-01-18T01:00:00Z","last_updated_date":"2007-01-18T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/ypozane-epar-procedural-steps-taken-authorisation_en.pdf"},
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    {"id":"11484","name":"Respiporc Flu3 : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2010-01-19T01:00:00Z","last_updated_date":"2010-01-19T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/respiporc-flu3-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"11530","name":"Ytracis : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2005-10-21T02:09:00Z","last_updated_date":"2022-01-17T02:09:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/ytracis-epar-procedural-steps-taken-authorisation_en.pdf"},
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    {"id":"12433","name":"Galvus : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2007-04-04T02:09:21Z","last_updated_date":"2007-04-04T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/galvus-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"12652","name":"Fosavance : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2005-10-21T02:09:21Z","last_updated_date":"2005-10-21T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/fosavance-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"12758","name":"Ketek : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2007-07-06T02:00:00Z","last_updated_date":"2019-06-19T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/ketek-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"12805","name":"NovoNorm : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2005-10-21T02:00:00Z","last_updated_date":"2005-10-21T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/novonorm-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"13055","name":"Rebetol : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-08-11T02:00:00Z","last_updated_date":"2023-11-07T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/rebetol-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"13085","name":"Prac-tic : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-12-22T00:09:21Z","last_updated_date":"2006-12-22T00:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/prac-tic-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"13156","name":"Exforge : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2007-02-21T01:00:00Z","last_updated_date":"2007-02-21T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/exforge-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"13174","name":"Tasmar : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-01-25T00:09:21Z","last_updated_date":"2006-01-25T00:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/tasmar-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"13497","name":"Xenical : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2005-12-19T01:00:00Z","last_updated_date":"2005-12-19T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/xenical-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"13535","name":"Trizivir : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-08-07T02:09:00Z","last_updated_date":"2006-08-07T02:09:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/trizivir-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"13611","name":"Pegasys : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-08-08T02:00:00Z","last_updated_date":"2006-08-08T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/pegasys-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"13848","name":"Aloxi : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-08-16T02:00:00Z","last_updated_date":"2006-08-16T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/aloxi-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"14061","name":"Tekturna : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2009-09-09T02:09:21Z","last_updated_date":"2009-09-09T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/tekturna-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"14085","name":"Silapo : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2008-01-15T01:00:00Z","last_updated_date":"2008-01-15T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/silapo-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"14103","name":"Betaferon : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-08-09T02:09:21Z","last_updated_date":"2006-08-09T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/betaferon-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"14203","name":"Ovitrelle : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-11-10T00:09:21Z","last_updated_date":"2006-11-10T00:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/ovitrelle-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"14226","name":"Bovalto Ibraxion : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-08-07T02:00:00Z","last_updated_date":"2019-08-13T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/bovalto-ibraxion-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"14360","name":"SonoVue : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2005-10-21T02:00:00Z","last_updated_date":"2005-10-21T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/sonovue-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"14415","name":"Coxevac : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2010-10-14T02:00:00Z","last_updated_date":"2010-10-14T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/coxevac-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"14428","name":"Actrapid : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-04-03T02:00:00Z","last_updated_date":"2006-04-03T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/actrapid-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"14598","name":"Sonata : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2005-10-21T02:00:00Z","last_updated_date":"2015-10-21T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/sonata-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"14604","name":"Prevenar : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2005-10-21T02:00:00Z","last_updated_date":"2017-11-24T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/prevenar-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"14616","name":"Vaxxitek HVT+IBD : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-01-30T01:00:00Z","last_updated_date":"2006-01-30T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/vaxxitek-hvtibd-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"14627","name":"Byetta : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-12-15T00:09:21Z","last_updated_date":"2006-12-15T00:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/byetta-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"14721","name":"Copalia : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2007-02-21T00:09:21Z","last_updated_date":"2007-02-21T00:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/copalia-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"14767","name":"Olanzapine Teva : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2008-01-14T01:00:00Z","last_updated_date":"2008-01-14T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/olanzapine-teva-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"14845","name":"Zactran : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2008-07-24T02:09:21Z","last_updated_date":"2008-07-24T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/zactran-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"14864","name":"Helicobacter Test INFAI : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2005-10-21T02:09:21Z","last_updated_date":"2005-10-21T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/helicobacter-test-infai-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"14870","name":"Refludan : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-07-10T02:00:00Z","last_updated_date":"2012-07-27T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/refludan-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"14941","name":"Avandamet : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-08-15T02:00:00Z","last_updated_date":"2016-06-08T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/avandamet-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"14956","name":"SevoFlo : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-08-03T02:00:00Z","last_updated_date":"2006-08-03T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/sevoflo-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"15110","name":"Yarvitan : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2007-09-04T02:00:00Z","last_updated_date":"2007-09-04T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/yarvitan-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"15236","name":"Nespo : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2009-01-29T00:09:21Z","last_updated_date":"2009-01-29T00:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/nespo-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"15310","name":"Prialt : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-08-31T02:00:00Z","last_updated_date":"2006-08-31T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/prialt-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"15501","name":"Quadramet : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2005-10-21T02:09:21Z","last_updated_date":"2005-10-21T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/quadramet-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"15685","name":"Advocate : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2009-07-28T01:09:00Z","last_updated_date":"2009-07-28T01:09:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/advocate-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"15752","name":"Ibaflin : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-07-24T02:00:00Z","last_updated_date":"2006-07-24T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/ibaflin-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"15764","name":"Dafiro : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2007-02-21T01:00:00Z","last_updated_date":"2007-02-21T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/dafiro-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"15790","name":"Ammonaps : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-11-10T01:00:00Z","last_updated_date":"2006-11-10T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/ammonaps-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"15804","name":"Twinrix Adult : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2005-12-01T00:09:21Z","last_updated_date":"2005-12-01T00:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/twinrix-adult-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"15891","name":"Dynepo : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2008-03-13T00:09:21Z","last_updated_date":"2008-03-13T00:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/dynepo-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"15946","name":"Slentrol : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2007-05-03T02:00:00Z","last_updated_date":"2015-02-24T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/slentrol-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"15992","name":"Bondronat : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2005-10-21T02:09:21Z","last_updated_date":"2005-10-21T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/bondronat-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"16021","name":"Crixivan : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2005-10-21T02:00:00Z","last_updated_date":"2022-07-07T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/crixivan-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"16067","name":"Baraclude : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2007-05-21T02:09:21Z","last_updated_date":"2007-05-21T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/baraclude-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"16182","name":"Epoetin Alfa Hexal : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2007-09-17T02:00:00Z","last_updated_date":"2007-09-17T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/epoetin-alfa-hexal-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"16186","name":"Humira : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-03-30T02:09:21Z","last_updated_date":"2006-03-30T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/humira-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"16232","name":"Abilify : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-10-30T01:00:00Z","last_updated_date":"2006-10-30T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/abilify-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"16285","name":"Loxicom : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2009-02-12T01:00:00Z","last_updated_date":"2009-02-12T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/loxicom-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"16321","name":"Rilutek : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2005-10-21T02:09:21Z","last_updated_date":"2005-10-21T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/rilutek-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"16373","name":"Pruban : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-08-14T02:00:00Z","last_updated_date":"2010-07-26T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/pruban-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"16395","name":"Easotic : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2008-11-28T00:09:21Z","last_updated_date":"2008-11-28T00:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/easotic-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"16494","name":"Starlix : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-08-09T02:00:00Z","last_updated_date":"2022-06-28T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/starlix-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"16588","name":"Xyrem : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-08-09T02:00:00Z","last_updated_date":"2006-08-09T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/xyrem-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"16696","name":"Quixidar : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2008-05-16T02:00:00Z","last_updated_date":"2008-05-16T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/quixidar-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"16752","name":"Flebogammadif : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2007-09-13T02:00:00Z","last_updated_date":"2007-09-13T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/flebogammadif-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"17017","name":"Rabigen SAG2 : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-07-31T02:00:00Z","last_updated_date":"2006-07-31T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/rabigen-sag2-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"17203","name":"Kaletra : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-08-09T02:00:00Z","last_updated_date":"2006-08-09T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/kaletra-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"17238","name":"DepoCyte : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2005-10-21T02:00:00Z","last_updated_date":"2005-10-21T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/depocyte-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"17303","name":"Temodal : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2005-12-13T00:09:21Z","last_updated_date":"2005-12-13T00:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/temodal-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"17310","name":"Optaflu : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2007-08-01T02:09:21Z","last_updated_date":"2007-08-01T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/optaflu-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"17358","name":"ProteqFlu-Te : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2007-08-10T02:00:00Z","last_updated_date":"2007-08-10T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/proteqflu-te-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"17398","name":"Zyprexa Velotab : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2005-10-21T02:00:00Z","last_updated_date":"2005-10-21T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/zyprexa-velotab-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"17405","name":"Alli : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2007-07-27T02:00:00Z","last_updated_date":"2007-07-27T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/alli-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"17585","name":"Tritanrix HepB : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2005-10-21T02:09:21Z","last_updated_date":"2014-01-07T01:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/tritanrix-hepb-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"17601","name":"Onsenal : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2005-11-15T01:00:00Z","last_updated_date":"2011-04-06T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/onsenal-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"17716","name":"Invega : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2007-07-10T02:00:00Z","last_updated_date":"2007-07-10T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/invega-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"17726","name":"Prandin : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-08-31T02:00:00Z","last_updated_date":"2006-08-31T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/prandin-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"17993","name":"Viramune : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2005-10-21T02:00:00Z","last_updated_date":"2005-10-21T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/viramune-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"18011","name":"Omnitrope : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-04-25T02:00:00Z","last_updated_date":"2006-04-25T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/omnitrope-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"18051","name":"Glivec : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2005-10-28T02:09:21Z","last_updated_date":"2005-10-28T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/glivec-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"18137","name":"Exubera : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2008-11-17T00:09:21Z","last_updated_date":"2008-11-17T00:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/exubera-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"18143","name":"Zalasta : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2007-10-29T00:09:21Z","last_updated_date":"2007-10-29T00:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/zalasta-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"18168","name":"Neulasta : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2009-06-19T02:00:00Z","last_updated_date":"2009-06-19T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/neulasta-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"18334","name":"IntronA : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-08-11T02:00:00Z","last_updated_date":"2022-12-15T10:04:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/introna-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"18427","name":"Halocur : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2005-11-22T01:00:00Z","last_updated_date":"2005-11-22T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/halocur-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"18461","name":"Kinzalkomb : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2005-10-21T02:00:00Z","last_updated_date":"2005-10-21T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/kinzalkomb-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"18513","name":"Rasilez : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2007-09-03T02:00:00Z","last_updated_date":"2007-09-03T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/rasilez-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"18531","name":"Incurin : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-08-07T02:00:00Z","last_updated_date":"2006-08-07T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/incurin-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"18574","name":"Sutent : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-08-01T02:00:00Z","last_updated_date":"2006-08-01T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/sutent-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"18709","name":"Nobivac Bb : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2005-11-16T01:00:00Z","last_updated_date":"2005-11-16T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/nobivac-bb-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"18729","name":"Evoltra : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2007-05-31T02:00:00Z","last_updated_date":"2007-05-31T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/evoltra-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"18757","name":"Ultratard : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2008-02-15T00:09:21Z","last_updated_date":"2008-02-15T00:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/ultratard-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"18768","name":"Ingelvac CircoFLEX : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2008-02-25T01:00:00Z","last_updated_date":"2008-02-25T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/ingelvac-circoflex-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"18781","name":"Suvaxyn Aujeszky 783 + O/W : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-03-29T02:00:00Z","last_updated_date":"2006-03-29T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/suvaxyn-aujeszky-783-ow-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"18924","name":"Nexavar : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2007-03-05T00:09:21Z","last_updated_date":"2007-03-05T00:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/nexavar-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"18936","name":"Stocrin : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2005-11-03T01:00:00Z","last_updated_date":"2005-11-03T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/stocrin-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"19051","name":"Onsior : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2008-11-20T01:00:00Z","last_updated_date":"2008-11-20T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/onsior-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"19096","name":"Aprovel : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-10-16T02:00:00Z","last_updated_date":"2006-10-16T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/aprovel-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"19219","name":"Fareston : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2005-11-29T00:09:00Z","last_updated_date":"2005-11-29T00:09:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/fareston-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"19294","name":"Rebif : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-08-09T02:00:00Z","last_updated_date":"2006-08-09T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/rebif-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"19446","name":"Poulvac Flufend H5N3 RG : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-09-19T02:09:21Z","last_updated_date":"2012-05-07T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/poulvac-flufend-h5n3-rg-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"19508","name":"Aclasta : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-04-03T02:00:00Z","last_updated_date":"2006-04-03T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/aclasta-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"19527","name":"Meloxidyl : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2007-04-02T02:00:00Z","last_updated_date":"2007-04-02T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/meloxidyl-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"19642","name":"Aerius : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-04-03T02:00:00Z","last_updated_date":"2006-04-03T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/aerius-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"19720","name":"Celsentri : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2007-10-15T02:09:21Z","last_updated_date":"2007-10-15T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/celsentri-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"19778","name":"Metacam : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2005-11-22T01:00:00Z","last_updated_date":"2005-11-22T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/metacam-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"19820","name":"Orencia : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2007-06-05T02:09:21Z","last_updated_date":"2007-06-05T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/orencia-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"19880","name":"Revatio : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-10-11T02:00:00Z","last_updated_date":"2006-10-11T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/revatio-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"19957","name":"NovoRapid : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2009-06-19T02:00:00Z","last_updated_date":"2009-06-19T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/novorapid-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"20054","name":"Thelin : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2007-04-17T02:09:21Z","last_updated_date":"2011-03-02T01:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/thelin-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"20097","name":"Ebixa : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2005-10-21T02:00:00Z","last_updated_date":"2005-10-21T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/ebixa-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"20175","name":"Orfadin : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2007-04-04T02:00:00Z","last_updated_date":"2007-04-04T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/orfadin-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"20263","name":"Exjade : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2007-04-17T02:00:00Z","last_updated_date":"2007-04-17T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/exjade-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"20294","name":"Invanz : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-10-13T02:00:00Z","last_updated_date":"2006-10-13T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/invanz-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"20412","name":"Trudexa : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2008-02-15T00:09:21Z","last_updated_date":"2008-02-15T00:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/trudexa-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"20483","name":"Evista : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2005-10-21T02:00:00Z","last_updated_date":"2005-10-21T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/evista-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"20527","name":"Prilactone : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2007-07-18T02:09:00Z","last_updated_date":"2007-07-18T02:09:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/prilactone-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"20544","name":"Targretin : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-08-08T02:09:21Z","last_updated_date":"2006-08-08T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/targretin-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"20555","name":"Telzir : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2005-12-06T00:09:21Z","last_updated_date":"2026-01-05T00:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/telzir-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"20573","name":"Clomicalm : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2008-07-31T01:09:21Z","last_updated_date":"2008-07-31T01:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/clomicalm-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"20613","name":"Protopy : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2008-10-29T01:00:00Z","last_updated_date":"2008-10-29T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/protopy-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"20657","name":"HBVaxPro : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-09-05T02:09:21Z","last_updated_date":"2006-09-05T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/hbvaxpro-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"20748","name":"Stronghold : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-08-03T02:00:00Z","last_updated_date":"2006-08-03T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/stronghold-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"20798","name":"Protelos : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2005-11-21T01:00:00Z","last_updated_date":"2005-11-21T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/protelos-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"20916","name":"Cholestagel : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2005-10-21T02:09:21Z","last_updated_date":"2005-10-21T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/cholestagel-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"21040","name":"Preotact : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2007-05-31T02:00:00Z","last_updated_date":"2014-07-02T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/preotact-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"21187","name":"Acomplia : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2009-01-30T01:00:00Z","last_updated_date":"2009-01-30T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/acomplia-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"21215","name":"Ferriprox : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-07-10T02:09:21Z","last_updated_date":"2006-07-10T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/ferriprox-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"21238","name":"Truvada : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2005-11-23T00:09:21Z","last_updated_date":"2005-11-23T00:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/truvada-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"21359","name":"Gripovac 3 : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2010-01-25T01:00:00Z","last_updated_date":"2018-09-04T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/gripovac-3-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"21382","name":"Ganfort : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-06-12T02:09:21Z","last_updated_date":"2006-06-12T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/ganfort-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"21394","name":"ViraferonPeg : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-08-11T02:00:00Z","last_updated_date":"2021-01-22T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/viraferonpeg-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"21519","name":"Optisulin : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2005-10-21T02:09:21Z","last_updated_date":"2005-10-21T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/optisulin-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"21690","name":"Erbitux : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-10-30T01:00:00Z","last_updated_date":"2006-10-30T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/erbitux-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"21766","name":"Arixtra : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2005-11-04T01:00:00Z","last_updated_date":"2005-11-04T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/arixtra-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"21976","name":"Panretin : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-01-26T01:00:00Z","last_updated_date":"2006-01-26T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/panretin-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"22098","name":"INOmax : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-08-15T02:00:00Z","last_updated_date":"2023-04-20T11:03:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/inomax-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"22163","name":"Optison : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2008-08-01T02:00:00Z","last_updated_date":"2008-08-01T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/optison-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"22191","name":"Exelon : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-01-12T01:00:00Z","last_updated_date":"2006-01-12T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/exelon-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"22372","name":"Sustiva : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-11-20T01:00:00Z","last_updated_date":"2024-03-14T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/sustiva-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"22418","name":"Purevax RCP FeLV : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2005-11-22T01:00:00Z","last_updated_date":"2005-11-22T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/purevax-rcp-felv-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"22552","name":"Cetrotide : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2005-10-21T02:09:21Z","last_updated_date":"2005-10-21T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/cetrotide-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"22566","name":"Januvia : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2007-03-26T02:09:21Z","last_updated_date":"2007-03-26T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/januvia-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"22744","name":"NeoSpect : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-05-12T02:09:21Z","last_updated_date":"2010-11-18T01:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/neospect-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"22766","name":"Gliolan : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2007-09-24T02:09:21Z","last_updated_date":"2007-09-24T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/gliolan-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"22918","name":"Integrilin : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-07-10T02:00:00Z","last_updated_date":"2006-07-10T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/integrilin-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"22964","name":"Synagis : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2005-10-21T02:00:00Z","last_updated_date":"2005-10-21T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/synagis-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"23124","name":"Viagra : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-09-22T02:00:00Z","last_updated_date":"2006-09-22T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/viagra-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"23125","name":"Aerinaze : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2007-08-03T02:00:00Z","last_updated_date":"2007-08-03T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/aerinaze-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"23151","name":"Mircera : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2007-08-02T02:00:00Z","last_updated_date":"2007-08-02T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/mircera-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"23339","name":"Dukoral : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2005-12-07T01:00:00Z","last_updated_date":"2005-12-07T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/dukoral-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"23390","name":"Zavesca : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2005-10-21T02:09:21Z","last_updated_date":"2005-10-21T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/zavesca-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"23544","name":"Nobivac Piro : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-07-31T02:00:00Z","last_updated_date":"2006-07-31T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/nobivac-piro-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"23568","name":"Melovem : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2007-07-09T02:00:00Z","last_updated_date":"2007-07-09T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/melovem-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"23571","name":"Norvir : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2005-10-21T02:09:21Z","last_updated_date":"2005-10-21T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/norvir-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"23630","name":"Improvac : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2009-05-13T02:00:00Z","last_updated_date":"2009-05-13T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/improvac-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"23670","name":"Startvac : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2009-02-17T01:00:00Z","last_updated_date":"2009-02-17T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/startvac-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"23695","name":"Ventavis : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2005-10-21T02:00:00Z","last_updated_date":"2005-10-21T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/ventavis-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"23753","name":"Busilvex : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2005-10-21T02:09:00Z","last_updated_date":"2023-08-04T12:55:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/busilvex-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"23892","name":"MabCampath : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2005-10-21T02:09:21Z","last_updated_date":"2012-08-15T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/mabcampath-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"23923","name":"Porcilis AR-T DF : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-08-16T02:09:21Z","last_updated_date":"2006-08-16T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/porcilis-ar-t-df-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"24085","name":"Helixate NexGen : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-11-06T00:09:00Z","last_updated_date":"2020-06-02T00:09:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/helixate-nexgen-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"24098","name":"MicardisPlus : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-07-20T02:09:21Z","last_updated_date":"2006-07-20T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/micardisplus-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"24114","name":"Dicural : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2008-10-31T00:09:21Z","last_updated_date":"2015-10-30T00:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/dicural-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"24167","name":"Replagal : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-07-21T02:00:00Z","last_updated_date":"2006-07-21T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/replagal-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"24218","name":"Lyrica : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2005-10-21T02:00:00Z","last_updated_date":"2005-10-21T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/lyrica-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"24547","name":"Mimpara : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2005-10-21T02:09:21Z","last_updated_date":"2026-05-20T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/mimpara-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"24736","name":"Diacomit : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2009-01-29T01:00:00Z","last_updated_date":"2009-01-29T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/diacomit-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"24761","name":"Tractocile : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-08-15T02:00:00Z","last_updated_date":"2006-08-15T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/tractocile-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"24792","name":"Sebivo : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2007-05-08T02:00:00Z","last_updated_date":"2021-01-14T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/sebivo-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"24844","name":"BeneFIX : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2005-12-06T01:00:00Z","last_updated_date":"2005-12-06T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/benefix-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"24877","name":"CellCept : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-04-06T02:09:21Z","last_updated_date":"2006-04-06T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/cellcept-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"24906","name":"Karvezide : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-10-16T02:00:00Z","last_updated_date":"2006-10-16T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/karvezide-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"24932","name":"Procomvax : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2009-07-29T02:00:00Z","last_updated_date":"2009-07-29T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/procomvax-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"25361","name":"NeoRecormon : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2005-10-21T02:09:21Z","last_updated_date":"2005-10-21T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/neorecormon-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"25521","name":"Optimark : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2007-08-02T02:09:21Z","last_updated_date":"2007-08-02T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/optimark-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"25533","name":"Bondenza : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-10-16T02:09:21Z","last_updated_date":"2013-05-13T19:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/bondenza-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"25594","name":"Pylobactell : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2005-12-07T01:00:00Z","last_updated_date":"2005-12-07T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/pylobactell-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"26038","name":"Herceptin : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2005-10-21T02:09:21Z","last_updated_date":"2005-10-21T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/herceptin-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"26134","name":"NovoSeven : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2005-10-21T02:00:00Z","last_updated_date":"2005-10-21T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/novoseven-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"26160","name":"Foscan : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-01-10T00:09:21Z","last_updated_date":"2006-01-10T00:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/foscan-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"26249","name":"Purevax RCCh : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2005-11-22T00:09:21Z","last_updated_date":"2015-01-23T00:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/purevax-rcch-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"26322","name":"Revasc : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-07-11T02:00:00Z","last_updated_date":"2014-07-29T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/revasc-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"26398","name":"Neupro : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-03-09T01:00:00Z","last_updated_date":"2006-03-09T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/neupro-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"26417","name":"Neocolipor : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-08-09T02:00:00Z","last_updated_date":"2025-01-31T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/neocolipor-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"26436","name":"Comtan : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2005-10-21T02:00:00Z","last_updated_date":"2005-10-21T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/comtan-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"26497","name":"Vivanza : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2005-10-21T02:00:00Z","last_updated_date":"2022-02-28T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/vivanza-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"26581","name":"Equilis StrepE : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2007-10-08T02:09:00Z","last_updated_date":"2007-10-08T02:09:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/equilis-strepe-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"26659","name":"Savene : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-09-07T02:00:00Z","last_updated_date":"2006-09-07T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/savene-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"26683","name":"Protaphane : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2005-10-21T02:00:00Z","last_updated_date":"2005-10-21T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/protaphane-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"26695","name":"Dexdomitor : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2005-10-21T02:09:21Z","last_updated_date":"2024-09-17T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/dexdomitor-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"26732","name":"Levitra : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2005-10-21T02:00:00Z","last_updated_date":"2005-10-21T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/levitra-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"26946","name":"Levviax : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2008-02-15T00:09:21Z","last_updated_date":"2008-02-15T00:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/levviax-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"26985","name":"Naglazyme : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-10-30T00:09:21Z","last_updated_date":"2006-10-30T00:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/naglazyme-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"27000","name":"Travatan : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-10-26T02:09:21Z","last_updated_date":"2006-10-26T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/travatan-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"27054","name":"Purevax RCPCh : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2005-11-22T01:00:00Z","last_updated_date":"2005-11-22T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/purevax-rcpch-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"27140","name":"Avandia : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-08-15T02:00:00Z","last_updated_date":"2016-06-08T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/avandia-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"27193","name":"Retacrit : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2008-01-15T01:00:00Z","last_updated_date":"2008-01-15T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/retacrit-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"27231","name":"Equilis Te : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2005-10-21T02:09:21Z","last_updated_date":"2005-10-21T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/equilis-te-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"27313","name":"Optruma : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2005-10-21T02:09:21Z","last_updated_date":"2005-10-21T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/optruma-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"27349","name":"Porcilis Porcoli : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-09-14T02:09:21Z","last_updated_date":"2006-09-14T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/porcilis-porcoli-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"27352","name":"Elaprase : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2007-01-18T01:00:00Z","last_updated_date":"2007-01-18T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/elaprase-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"27355","name":"Puregon : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2008-08-31T02:00:00Z","last_updated_date":"2008-08-31T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/puregon-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"27417","name":"Insuman : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-08-09T02:00:00Z","last_updated_date":"2006-08-09T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/insuman-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"27446","name":"Glubrava : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2008-04-16T02:00:00Z","last_updated_date":"2022-10-18T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/glubrava-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"27504","name":"RotaTeq : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-09-21T02:09:21Z","last_updated_date":"2006-09-21T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/rotateq-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"27549","name":"Viread : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-04-06T02:00:00Z","last_updated_date":"2006-04-06T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/viread-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"27607","name":"Trazec : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2009-08-24T02:00:00Z","last_updated_date":"2009-08-24T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/trazec-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"27629","name":"Angiox : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2005-12-07T01:00:00Z","last_updated_date":"2018-09-14T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/angiox-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"27803","name":"Binocrit : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2007-09-17T02:09:21Z","last_updated_date":"2007-09-17T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/binocrit-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"27842","name":"Intrinsa : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-09-05T02:00:00Z","last_updated_date":"2012-06-18T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/intrinsa-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"27860","name":"Cortavance : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2007-01-31T00:09:21Z","last_updated_date":"2007-01-31T00:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/cortavance-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"27884","name":"Ceprotin : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2005-10-21T02:09:21Z","last_updated_date":"2005-10-21T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/ceprotin-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"28015","name":"Luminity : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-10-19T02:00:00Z","last_updated_date":"2014-06-17T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/luminity-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"28056","name":"Nobilis Influenza H5N6 : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2008-02-13T01:00:00Z","last_updated_date":"2010-07-26T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/nobilis-influenza-h5n6-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"28180","name":"Arava : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2005-11-23T01:00:00Z","last_updated_date":"2005-11-23T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/arava-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"28297","name":"Inductos : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2005-10-21T02:00:00Z","last_updated_date":"2017-06-15T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/inductos-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"28487","name":"Zerit : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-08-11T02:00:00Z","last_updated_date":"2006-08-11T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/zerit-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"28493","name":"Osigraft : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2005-10-21T02:09:21Z","last_updated_date":"2016-07-27T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/osigraft-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"28539","name":"Tamiflu : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2005-10-21T02:00:00Z","last_updated_date":"2005-10-21T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/tamiflu-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"28764","name":"Prezista : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2008-11-25T01:00:00Z","last_updated_date":"2008-11-25T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/prezista-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"28807","name":"Hepsera : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-10-24T02:09:00Z","last_updated_date":"2023-03-01T02:49:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/hepsera-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"28819","name":"BTVPUR Alsap 8 : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2009-03-24T00:09:21Z","last_updated_date":"2018-05-17T01:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/btvpur-alsap-8-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"28831","name":"Riprazo : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2007-09-03T02:00:00Z","last_updated_date":"2007-09-03T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/riprazo-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"29086","name":"Adrovance : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2007-01-18T01:00:00Z","last_updated_date":"2007-01-18T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/adrovance-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"29301","name":"Cubicin : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-08-11T02:00:00Z","last_updated_date":"2006-08-11T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/cubicin-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"29481","name":"Vaniqa : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2005-10-21T02:00:00Z","last_updated_date":"2005-10-21T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/vaniqa-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"29565","name":"Viraferon : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2008-05-27T03:09:21Z","last_updated_date":"2008-05-27T03:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/viraferon-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"29637","name":"Ecalta : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2007-10-09T02:00:00Z","last_updated_date":"2007-10-09T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/ecalta-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"29767","name":"Azilect : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-08-11T02:00:00Z","last_updated_date":"2006-08-11T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/azilect-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"29778","name":"Zeffix : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-08-07T02:09:21Z","last_updated_date":"2006-08-07T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/zeffix-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"30037","name":"Mirapexin : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2005-10-26T02:09:21Z","last_updated_date":"2005-10-26T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/mirapexin-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"30203","name":"TachoSil : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-01-24T01:00:00Z","last_updated_date":"2006-01-24T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/tachosil-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"30220","name":"Zulvac 8 Ovis : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2010-01-21T01:00:00Z","last_updated_date":"2010-01-21T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/zulvac-8-ovis-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"30244","name":"Draxxin : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2008-09-02T02:09:21Z","last_updated_date":"2008-09-02T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/draxxin-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"30278","name":"Torisel : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2007-12-05T01:00:00Z","last_updated_date":"2010-12-03T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/torisel-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"30282","name":"Flexicam : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-05-11T02:00:00Z","last_updated_date":"2014-05-20T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/flexicam-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"30339","name":"Aldara : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-07-21T02:00:00Z","last_updated_date":"2006-07-21T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/aldara-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"30492","name":"Acticam : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2009-01-05T01:00:00Z","last_updated_date":"2021-03-24T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/acticam-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"30516","name":"Eucreas : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2007-12-03T01:00:00Z","last_updated_date":"2007-12-03T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/eucreas-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"30543","name":"Irbesartan Winthrop : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2007-02-05T01:00:00Z","last_updated_date":"2007-02-05T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/irbesartan-winthrop-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"30570","name":"Somavert : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2005-10-21T02:00:00Z","last_updated_date":"2005-10-21T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/somavert-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"30685","name":"Fuzeon : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-08-11T02:09:21Z","last_updated_date":"2006-08-11T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/fuzeon-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"30690","name":"Trocoxil : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2008-09-22T02:00:00Z","last_updated_date":"2008-09-22T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/trocoxil-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"30726","name":"Suvaxyn PCV : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2009-07-24T02:00:00Z","last_updated_date":"2020-04-15T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/suvaxyn-pcv-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"31005","name":"Emend : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-09-05T02:00:00Z","last_updated_date":"2006-09-05T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/emend-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"31098","name":"Thyrogen : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-01-24T00:09:00Z","last_updated_date":"2006-01-24T00:09:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/thyrogen-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"31236","name":"Atriance : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2007-09-20T02:00:00Z","last_updated_date":"2007-09-20T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/atriance-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"31357","name":"Insulin Human Winthrop : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2007-02-20T01:00:00Z","last_updated_date":"2018-04-30T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/insulin-human-winthrop-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"31410","name":"Neoclarityn : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-07-21T02:09:21Z","last_updated_date":"2006-07-21T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/neoclarityn-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"31573","name":"Corlentor : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2005-11-04T01:00:00Z","last_updated_date":"2005-11-04T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/corlentor-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"31653","name":"Micardis : EPAR - Procedural steps taken before authorisation (archive)","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-07-10T02:09:21Z","last_updated_date":"2025-02-26T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/micardis-epar-procedural-steps-taken-authorisation-archive_en.pdf"},
    {"id":"31709","name":"CoAprovel : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-10-17T02:09:21Z","last_updated_date":"2006-10-17T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/coaprovel-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"32066","name":"Siklos : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2007-08-10T02:00:00Z","last_updated_date":"2007-08-10T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/siklos-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"32165","name":"Twinrix Paediatric : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2005-10-21T02:09:21Z","last_updated_date":"2005-10-21T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/twinrix-paediatric-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"32167","name":"Faslodex : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-01-09T00:09:21Z","last_updated_date":"2006-01-09T00:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/faslodex-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"32239","name":"Azopt : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2005-10-21T02:00:00Z","last_updated_date":"2005-10-21T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/azopt-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"32334","name":"Posaconazole SP : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2009-07-31T02:00:00Z","last_updated_date":"2009-07-31T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/posaconazole-sp-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"32340","name":"Caelyx : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2005-10-21T02:09:21Z","last_updated_date":"2005-10-21T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/caelyx-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"32412","name":"Naxcel : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2005-11-22T01:00:00Z","last_updated_date":"2005-11-22T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/naxcel-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"32572","name":"Leucofeligen FeLV/RCP : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2009-07-02T02:00:00Z","last_updated_date":"2009-07-02T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/leucofeligen-felvrcp-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"32582","name":"Meloxivet : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2007-11-28T01:00:00Z","last_updated_date":"2018-05-28T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/meloxivet-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"32892","name":"Cystadane : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2007-03-05T00:09:21Z","last_updated_date":"2007-03-05T00:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/cystadane-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"33022","name":"Opatanol : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2005-10-21T02:00:00Z","last_updated_date":"2005-10-21T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/opatanol-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"33320","name":"Lysodren : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-01-24T01:00:00Z","last_updated_date":"2006-01-24T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/lysodren-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"33418","name":"Macugen : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2007-05-31T02:00:00Z","last_updated_date":"2019-06-27T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/macugen-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"33429","name":"Vectibix : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2007-12-19T01:00:00Z","last_updated_date":"2007-12-19T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/vectibix-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"33483","name":"Previcox : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-08-14T02:09:21Z","last_updated_date":"2006-08-14T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/previcox-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"33520","name":"Lantus : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2005-10-21T02:00:00Z","last_updated_date":"2005-10-21T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/lantus-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"33573","name":"MabThera : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-09-29T02:00:00Z","last_updated_date":"2006-09-29T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/mabthera-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"33702","name":"BTVPUR AlSap 2-4 : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2010-11-09T01:00:00Z","last_updated_date":"2018-11-13T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/btvpur-alsap-2-4-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"33809","name":"Livensa : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-09-08T02:00:00Z","last_updated_date":"2012-04-16T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/livensa-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"33850","name":"Sifrol : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2005-10-26T02:00:00Z","last_updated_date":"2005-10-26T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/sifrol-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"33984","name":"Comtess : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2005-10-21T02:00:00Z","last_updated_date":"2005-10-21T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/comtess-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"34003","name":"Tysabri : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2007-05-31T02:09:00Z","last_updated_date":"2020-05-04T02:09:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/tysabri-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"34093","name":"Locatim : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-07-24T02:00:00Z","last_updated_date":"2006-07-24T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/locatim-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"34227","name":"Duvaxyn WNV : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2008-12-01T00:09:21Z","last_updated_date":"2008-12-01T00:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/duvaxyn-wnv-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"34285","name":"Ariclaim : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-02-07T01:00:00Z","last_updated_date":"2018-08-07T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/ariclaim-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"34431","name":"Pergoveris : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2007-08-06T02:00:00Z","last_updated_date":"2023-05-31T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/pergoveris-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"34474","name":"Stalevo : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-10-30T01:00:00Z","last_updated_date":"2006-10-30T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/stalevo-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"34479","name":"Forcaltonin : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2008-11-21T00:09:21Z","last_updated_date":"2008-11-21T00:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/forcaltonin-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"34522","name":"Irbesartan BMS : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2009-11-26T01:00:00Z","last_updated_date":"2009-11-26T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/irbesartan-bms-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"34590","name":"Fabrazyme : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2005-12-21T00:09:00Z","last_updated_date":"2005-12-21T00:09:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/fabrazyme-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"34698","name":"Osseor : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2005-11-21T00:09:00Z","last_updated_date":"2005-11-21T00:09:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/osseor-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"34711","name":"Pritor : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-07-11T02:00:00Z","last_updated_date":"2006-07-11T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/pritor-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"34729","name":"Evra : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2005-10-21T02:00:00Z","last_updated_date":"2005-10-21T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/evra-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"34745","name":"Masivet : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2008-11-17T01:00:00Z","last_updated_date":"2008-11-17T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/masivet-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"34782","name":"Remicade : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2005-12-07T01:00:00Z","last_updated_date":"2005-12-07T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/remicade-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"34882","name":"Taxotere : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2005-12-22T00:09:21Z","last_updated_date":"2005-12-22T00:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/taxotere-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"34946","name":"Viracept : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-11-20T01:00:00Z","last_updated_date":"2014-06-10T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/viracept-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"34952","name":"Cyanokit : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2007-12-18T01:00:00Z","last_updated_date":"2007-12-18T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/cyanokit-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"35006","name":"Porcilis Pesti : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2009-02-26T00:09:00Z","last_updated_date":"2009-02-26T00:09:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/porcilis-pesti-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"35159","name":"Carbaglu : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-11-10T00:09:21Z","last_updated_date":"2006-11-10T00:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/carbaglu-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"35203","name":"Fasturtec : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2005-11-25T00:09:00Z","last_updated_date":"2005-11-25T00:09:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/fasturtec-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"35483","name":"Cervarix : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2007-10-03T02:00:00Z","last_updated_date":"2007-10-03T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/cervarix-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"35684","name":"Pedea : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2005-10-21T02:00:00Z","last_updated_date":"2005-10-21T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/pedea-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"35705","name":"Tygacil : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2007-04-04T02:09:21Z","last_updated_date":"2007-04-04T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/tygacil-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"35723","name":"Soliris : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2007-06-29T02:00:00Z","last_updated_date":"2007-06-29T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/soliris-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"35769","name":"Tesavel : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2008-02-11T00:09:00Z","last_updated_date":"2008-02-11T00:09:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/tesavel-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"35916","name":"Rapilysin : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-07-11T02:00:00Z","last_updated_date":"2006-07-11T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/rapilysin-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"36126","name":"Monotard : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2008-02-15T00:09:21Z","last_updated_date":"2008-02-15T00:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/monotard-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"36218","name":"Advasure : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2008-03-18T00:09:21Z","last_updated_date":"2008-03-18T00:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/advasure-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"36235","name":"Netvax : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2009-04-27T02:00:00Z","last_updated_date":"2014-06-11T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/netvax-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"36255","name":"Regranex : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2009-08-17T02:00:00Z","last_updated_date":"2012-08-15T16:50:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/regranex-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"36451","name":"Purevax FeLV : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2005-11-22T01:00:00Z","last_updated_date":"2005-11-22T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/purevax-felv-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"36457","name":"LeukoScan : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2005-10-21T02:00:00Z","last_updated_date":"2018-02-09T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/leukoscan-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"36560","name":"Enbrel : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-10-18T02:00:00Z","last_updated_date":"2006-10-18T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/enbrel-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"36639","name":"M-M-RVaxPro : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-08-09T02:09:00Z","last_updated_date":"2006-08-09T02:09:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/m-m-rvaxpro-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"36765","name":"Simulect : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2005-11-28T01:00:00Z","last_updated_date":"2005-11-28T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/simulect-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"36800","name":"Kineret : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-07-21T02:00:00Z","last_updated_date":"2006-07-21T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/kineret-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"36819","name":"Xelevia : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2007-03-26T02:00:00Z","last_updated_date":"2007-03-26T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/xelevia-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"36830","name":"Tarceva : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2005-11-03T00:09:21Z","last_updated_date":"2005-11-03T00:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/tarceva-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"36970","name":"Alimta : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-02-09T01:00:00Z","last_updated_date":"2006-02-09T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/alimta-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"36983","name":"Zostavax : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2007-01-17T01:00:00Z","last_updated_date":"2025-06-11T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/zostavax-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"36992","name":"Cancidas : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2005-10-21T02:09:21Z","last_updated_date":"2005-10-21T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/cancidas-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"37056","name":"Ziagen : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2005-11-21T00:09:00Z","last_updated_date":"2005-11-21T00:09:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/ziagen-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"37068","name":"Bovilis BTV8 : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2010-09-09T02:00:00Z","last_updated_date":"2022-07-27T11:26:00Z","reference_number":"EMA/CVMP/234339/2009","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/bovilis-btv8-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"37305","name":"Docetaxel Winthrop : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2007-05-15T02:00:00Z","last_updated_date":"2022-05-20T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/docetaxel-winthrop-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"37435","name":"Equilis Prequenza Te : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2005-10-21T02:09:21Z","last_updated_date":"2005-10-21T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/equilis-prequenza-te-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"37448","name":"Nobilis IB 4-91 : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-08-29T02:00:00Z","last_updated_date":"2006-08-29T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/nobilis-ib-4-91-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"37472","name":"Silgard : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-10-13T02:00:00Z","last_updated_date":"2006-10-13T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/silgard-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"37499","name":"Zubrin : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-03-27T02:00:00Z","last_updated_date":"2012-05-08T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/zubrin-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"37589","name":"Forsteo : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2005-10-21T02:09:21Z","last_updated_date":"2005-10-21T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/forsteo-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"37609","name":"Orgalutran : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2005-10-21T02:00:00Z","last_updated_date":"2005-10-21T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/orgalutran-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"38032","name":"Kepivance : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-08-08T02:00:00Z","last_updated_date":"2016-04-08T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/kepivance-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"38067","name":"Infanrix Penta : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2005-10-21T02:00:00Z","last_updated_date":"2013-07-10T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/infanrix-penta-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"38208","name":"Avonex : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-08-16T02:00:00Z","last_updated_date":"2006-08-16T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/avonex-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"38394","name":"Emtriva : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-08-11T02:00:00Z","last_updated_date":"2006-08-11T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/emtriva-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"38395","name":"Nevanac : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2008-01-14T00:09:21Z","last_updated_date":"2008-01-14T00:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/nevanac-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"38672","name":"Porcilis PCV : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2009-01-27T00:09:21Z","last_updated_date":"2009-01-27T00:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/porcilis-pcv-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"38678","name":"Protopic : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-08-29T02:00:00Z","last_updated_date":"2006-08-29T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/protopic-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"38771","name":"Hycamtin : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-02-20T00:09:21Z","last_updated_date":"2006-02-20T00:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/hycamtin-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"38812","name":"Insulatard : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-09-06T02:00:00Z","last_updated_date":"2006-09-06T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/insulatard-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"38831","name":"Aivlosin : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2008-11-26T00:09:21Z","last_updated_date":"2008-11-26T00:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/aivlosin-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"38940","name":"PegIntron : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-08-11T02:00:00Z","last_updated_date":"2021-06-03T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/pegintron-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"39106","name":"Aranesp : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-06-14T02:00:00Z","last_updated_date":"2006-06-14T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/aranesp-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"39129","name":"Myocet : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2008-08-16T02:00:00Z","last_updated_date":"2008-08-16T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/myocet-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"39147","name":"Purevax RC : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2005-11-22T01:00:00Z","last_updated_date":"2005-11-22T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/purevax-rc-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"39164","name":"Xagrid : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2007-04-24T02:09:21Z","last_updated_date":"2007-04-24T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/xagrid-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"39212","name":"Invirase : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-10-31T01:00:00Z","last_updated_date":"2023-09-25T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/invirase-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"39264","name":"Apidra : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2005-10-21T02:00:00Z","last_updated_date":"2005-10-21T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/apidra-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"39277","name":"Convenia : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2007-09-05T02:09:21Z","last_updated_date":"2007-09-05T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/convenia-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"39294","name":"Luveris : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-11-10T01:00:00Z","last_updated_date":"2006-11-10T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/luveris-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"39439","name":"Plavix : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-10-24T02:00:00Z","last_updated_date":"2006-10-24T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/plavix-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"39595","name":"Rhiniseng : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2010-09-28T02:00:00Z","last_updated_date":"2010-09-28T02:00:00Z","reference_number":"EMA/544561/2010","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/rhiniseng-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"39615","name":"Neupopeg : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2009-01-26T00:09:21Z","last_updated_date":"2009-01-26T00:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/neupopeg-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"39750","name":"Cialis : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2005-10-21T02:09:21Z","last_updated_date":"2005-10-21T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/cialis-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"39811","name":"Quadrisol : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2005-11-28T01:00:00Z","last_updated_date":"2005-11-28T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/quadrisol-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"39886","name":"Emselex : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-01-19T01:00:00Z","last_updated_date":"2006-01-19T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/emselex-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"39949","name":"Yentreve : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-02-07T00:09:21Z","last_updated_date":"2006-02-07T00:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/yentreve-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"40019","name":"Lucentis : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2007-03-14T01:00:00Z","last_updated_date":"2007-03-14T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/lucentis-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"40082","name":"Parareg : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2009-05-14T02:00:00Z","last_updated_date":"2009-05-14T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/parareg-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"40254","name":"Glustin : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-09-06T02:09:00Z","last_updated_date":"2022-10-17T02:09:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/glustin-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"40334","name":"Atripla : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2007-12-18T01:00:00Z","last_updated_date":"2022-01-21T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/atripla-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"40401","name":"Gardasil : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-10-05T02:09:21Z","last_updated_date":"2006-10-05T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/gardasil-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"40422","name":"Abseamed : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2007-09-17T02:00:00Z","last_updated_date":"2007-09-17T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/abseamed-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"40580","name":"Eurican Herpes 205 : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-05-31T02:09:21Z","last_updated_date":"2006-05-31T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/eurican-herpes-205-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"40702","name":"Renagel : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2005-10-21T02:00:00Z","last_updated_date":"2005-10-21T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/renagel-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"40745","name":"ATryn : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2007-01-11T01:00:00Z","last_updated_date":"2019-07-02T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/atryn-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"40835","name":"Vfend : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2006-11-07T01:00:00Z","last_updated_date":"2006-11-07T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/vfend-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"40860","name":"Dynastat : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2005-11-15T01:00:00Z","last_updated_date":"2005-11-15T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/dynastat-epar-procedural-steps-taken-authorisation_en.pdf"},
    {"id":"40901","name":"Sprimeo : EPAR - Procedural steps taken before authorisation","type":"procedural-steps-before","status":"unknown","consultation_date":"","first_published_date":"2007-09-03T02:00:00Z","last_updated_date":"2012-08-20T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/procedural-steps/sprimeo-epar-procedural-steps-taken-authorisation_en.pdf"},
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    {"id":"49332","name":"Rivaroxaban Accord : EPAR - Product information","type":"product-information","status":"unknown","consultation_date":"","first_published_date":"2020-11-24T12:02:00Z","last_updated_date":"2025-08-28T12:05:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/product-information/rivaroxaban-accord-epar-product-information_en.pdf","translations":{"bg":"https://www.ema.europa.eu/bg/documents/product-information/rivaroxaban-accord-epar-product-information_bg.pdf","es":"https://www.ema.europa.eu/es/documents/product-information/rivaroxaban-accord-epar-product-information_es.pdf","cs":"https://www.ema.europa.eu/cs/documents/product-information/rivaroxaban-accord-epar-product-information_cs.pdf","da":"https://www.ema.europa.eu/da/documents/product-information/rivaroxaban-accord-epar-product-information_da.pdf","de":"https://www.ema.europa.eu/de/documents/product-information/rivaroxaban-accord-epar-product-information_de.pdf","et":"https://www.ema.europa.eu/et/documents/product-information/rivaroxaban-accord-epar-product-information_et.pdf","el":"https://www.ema.europa.eu/el/documents/product-information/rivaroxaban-accord-epar-product-information_el.pdf","fr":"https://www.ema.europa.eu/fr/documents/product-information/rivaroxaban-accord-epar-product-information_fr.pdf","hr":"https://www.ema.europa.eu/hr/documents/product-information/rivaroxaban-accord-epar-product-information_hr.pdf","it":"https://www.ema.europa.eu/it/documents/product-information/rivaroxaban-accord-epar-product-information_it.pdf","lv":"https://www.ema.europa.eu/lv/documents/product-information/rivaroxaban-accord-epar-product-information_lv.pdf","lt":"https://www.ema.europa.eu/lt/documents/product-information/rivaroxaban-accord-epar-product-information_lt.pdf","hu":"https://www.ema.europa.eu/hu/documents/product-information/rivaroxaban-accord-epar-product-information_hu.pdf","mt":"https://www.ema.europa.eu/mt/documents/product-information/rivaroxaban-accord-epar-product-information_mt.pdf","nl":"https://www.ema.europa.eu/nl/documents/product-information/rivaroxaban-accord-epar-product-information_nl.pdf","pl":"https://www.ema.europa.eu/pl/documents/product-information/rivaroxaban-accord-epar-product-information_pl.pdf","pt":"https://www.ema.europa.eu/pt/documents/product-information/rivaroxaban-accord-epar-product-information_pt.pdf","ro":"https://www.ema.europa.eu/ro/documents/product-information/rivaroxaban-accord-epar-product-information_ro.pdf","sk":"https://www.ema.europa.eu/sk/documents/product-information/rivaroxaban-accord-epar-product-information_sk.pdf","sl":"https://www.ema.europa.eu/sl/documents/product-information/rivaroxaban-accord-epar-product-information_sl.pdf","fi":"https://www.ema.europa.eu/fi/documents/product-information/rivaroxaban-accord-epar-product-information_fi.pdf","sv":"https://www.ema.europa.eu/sv/documents/product-information/rivaroxaban-accord-epar-product-information_sv.pdf","is":"https://www.ema.europa.eu/is/documents/product-information/rivaroxaban-accord-epar-product-information_is.pdf","no":"https://www.ema.europa.eu/no/documents/product-information/rivaroxaban-accord-epar-product-information_no.pdf"}},
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    {"id":"51337","name":"Drovelis : EPAR - Product information","type":"product-information","status":"unknown","consultation_date":"","first_published_date":"2021-06-02T11:11:00Z","last_updated_date":"2026-03-10T12:55:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/product-information/drovelis-epar-product-information_en.pdf","translations":{"bg":"https://www.ema.europa.eu/bg/documents/product-information/drovelis-epar-product-information_bg.pdf","es":"https://www.ema.europa.eu/es/documents/product-information/drovelis-epar-product-information_es.pdf","cs":"https://www.ema.europa.eu/cs/documents/product-information/drovelis-epar-product-information_cs.pdf","da":"https://www.ema.europa.eu/da/documents/product-information/drovelis-epar-product-information_da.pdf","de":"https://www.ema.europa.eu/de/documents/product-information/drovelis-epar-product-information_de.pdf","et":"https://www.ema.europa.eu/et/documents/product-information/drovelis-epar-product-information_et.pdf","el":"https://www.ema.europa.eu/el/documents/product-information/drovelis-epar-product-information_el.pdf","fr":"https://www.ema.europa.eu/fr/documents/product-information/drovelis-epar-product-information_fr.pdf","hr":"https://www.ema.europa.eu/hr/documents/product-information/drovelis-epar-product-information_hr.pdf","it":"https://www.ema.europa.eu/it/documents/product-information/drovelis-epar-product-information_it.pdf","lv":"https://www.ema.europa.eu/lv/documents/product-information/drovelis-epar-product-information_lv.pdf","lt":"https://www.ema.europa.eu/lt/documents/product-information/drovelis-epar-product-information_lt.pdf","hu":"https://www.ema.europa.eu/hu/documents/product-information/drovelis-epar-product-information_hu.pdf","mt":"https://www.ema.europa.eu/mt/documents/product-information/drovelis-epar-product-information_mt.pdf","nl":"https://www.ema.europa.eu/nl/documents/product-information/drovelis-epar-product-information_nl.pdf","pl":"https://www.ema.europa.eu/pl/documents/product-information/drovelis-epar-product-information_pl.pdf","pt":"https://www.ema.europa.eu/pt/documents/product-information/drovelis-epar-product-information_pt.pdf","ro":"https://www.ema.europa.eu/ro/documents/product-information/drovelis-epar-product-information_ro.pdf","sk":"https://www.ema.europa.eu/sk/documents/product-information/drovelis-epar-product-information_sk.pdf","sl":"https://www.ema.europa.eu/sl/documents/product-information/drovelis-epar-product-information_sl.pdf","fi":"https://www.ema.europa.eu/fi/documents/product-information/drovelis-epar-product-information_fi.pdf","sv":"https://www.ema.europa.eu/sv/documents/product-information/drovelis-epar-product-information_sv.pdf","is":"https://www.ema.europa.eu/is/documents/product-information/drovelis-epar-product-information_is.pdf","no":"https://www.ema.europa.eu/no/documents/product-information/drovelis-epar-product-information_no.pdf"}},
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    {"id":"51521","name":"Evkeeza : EPAR - Product Information","type":"product-information","status":"unknown","consultation_date":"","first_published_date":"2021-06-21T15:12:00Z","last_updated_date":"2026-02-26T11:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/product-information/evkeeza-epar-product-information_en.pdf","translations":{"bg":"https://www.ema.europa.eu/bg/documents/product-information/evkeeza-epar-product-information_bg.pdf","es":"https://www.ema.europa.eu/es/documents/product-information/evkeeza-epar-product-information_es.pdf","cs":"https://www.ema.europa.eu/cs/documents/product-information/evkeeza-epar-product-information_cs.pdf","da":"https://www.ema.europa.eu/da/documents/product-information/evkeeza-epar-product-information_da.pdf","de":"https://www.ema.europa.eu/de/documents/product-information/evkeeza-epar-product-information_de.pdf","et":"https://www.ema.europa.eu/et/documents/product-information/evkeeza-epar-product-information_et.pdf","el":"https://www.ema.europa.eu/el/documents/product-information/evkeeza-epar-product-information_el.pdf","fr":"https://www.ema.europa.eu/fr/documents/product-information/evkeeza-epar-product-information_fr.pdf","hr":"https://www.ema.europa.eu/hr/documents/product-information/evkeeza-epar-product-information_hr.pdf","it":"https://www.ema.europa.eu/it/documents/product-information/evkeeza-epar-product-information_it.pdf","lv":"https://www.ema.europa.eu/lv/documents/product-information/evkeeza-epar-product-information_lv.pdf","lt":"https://www.ema.europa.eu/lt/documents/product-information/evkeeza-epar-product-information_lt.pdf","hu":"https://www.ema.europa.eu/hu/documents/product-information/evkeeza-epar-product-information_hu.pdf","mt":"https://www.ema.europa.eu/mt/documents/product-information/evkeeza-epar-product-information_mt.pdf","nl":"https://www.ema.europa.eu/nl/documents/product-information/evkeeza-epar-product-information_nl.pdf","pl":"https://www.ema.europa.eu/pl/documents/product-information/evkeeza-epar-product-information_pl.pdf","pt":"https://www.ema.europa.eu/pt/documents/product-information/evkeeza-epar-product-information_pt.pdf","ro":"https://www.ema.europa.eu/ro/documents/product-information/evkeeza-epar-product-information_ro.pdf","sk":"https://www.ema.europa.eu/sk/documents/product-information/evkeeza-epar-product-information_sk.pdf","sl":"https://www.ema.europa.eu/sl/documents/product-information/evkeeza-epar-product-information_sl.pdf","fi":"https://www.ema.europa.eu/fi/documents/product-information/evkeeza-epar-product-information_fi.pdf","sv":"https://www.ema.europa.eu/sv/documents/product-information/evkeeza-epar-product-information_sv.pdf","is":"https://www.ema.europa.eu/is/documents/product-information/evkeeza-epar-product-information_is.pdf","no":"https://www.ema.europa.eu/no/documents/product-information/evkeeza-epar-product-information_no.pdf"}},
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    {"id":"61909","name":"Pseudoephedrine-containing medicinal products  Article-31 referral - Annex I (Aerinaze)","type":"amended-product-information","status":"Adopted","consultation_date":"","first_published_date":"2024-01-30T11:57:06Z","last_updated_date":"2024-01-30T11:57:06Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/amended-product-information/pseudoephedrine-containing-medicinal-products-article-31-referral-annex-i-aerinaze_en.pdf"},
    {"id":"2460","name":"Pandemic influenza vaccine (H5N1) (split virion, inactivated, adjuvanted) GlaxoSmithKline Biologicals : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2009-12-17T01:00:00Z","last_updated_date":"2009-12-17T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/pandemic-influenza-vaccine-h5n1-split-virion-inactivated-adjuvanted-glaxosmithkline-biologicals-epar-public-assessment-report_en.pdf"},
    {"id":"2485","name":"Clopidogrel BMS : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2008-11-07T01:00:00Z","last_updated_date":"2008-11-07T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/clopidogrel-bms-epar-public-assessment-report_en.pdf"},
    {"id":"2605","name":"Veraflox : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2011-07-18T02:00:00Z","last_updated_date":"2011-07-18T02:00:00Z","reference_number":"EMA/142130/2011","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/veraflox-epar-public-assessment-report_en.pdf"},
    {"id":"2613","name":"Paliperidone Janssen : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2015-01-21T01:00:00Z","last_updated_date":"2015-01-21T01:00:00Z","reference_number":"EMA/664603/2014","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/paliperidone-janssen-epar-public-assessment-report_en.pdf"},
    {"id":"2653","name":"Versican Plus Pi/L4 : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2014-10-20T02:00:00Z","last_updated_date":"2014-10-20T02:00:00Z","reference_number":"EMA/317641/2014","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/versican-plus-pil4-epar-public-assessment-report_en.pdf"},
    {"id":"2678","name":"Rivastigmine 1 A Pharma  : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2009-12-21T01:00:00Z","last_updated_date":"2009-12-21T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/rivastigmine-1-pharma-epar-public-assessment-report_en.pdf"},
    {"id":"2729","name":"Spinraza : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2017-06-21T16:39:00Z","last_updated_date":"2017-06-21T16:39:00Z","reference_number":"EMA/289068/2017","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/spinraza-epar-public-assessment-report_en.pdf"},
    {"id":"2731","name":"Coagadex : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2016-04-04T02:00:00Z","last_updated_date":"2016-04-04T02:00:00Z","reference_number":"EMA/CHMP/139881/2016","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/coagadex-epar-public-assessment-report_en.pdf"},
    {"id":"2769","name":"Ontruzant : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2018-01-26T01:00:00Z","last_updated_date":"2018-01-26T01:00:00Z","reference_number":"EMA/CHMP/9855/2018","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/ontruzant-epar-public-assessment-report_en.pdf"},
    {"id":"2896","name":"Enzepi : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2016-07-19T02:00:00Z","last_updated_date":"2016-07-19T02:00:00Z","reference_number":"EMA/340098/2016","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/enzepi-epar-public-assessment-report_en.pdf"},
    {"id":"2994","name":"Dany's BienenWohl : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2018-07-17T11:31:00Z","last_updated_date":"2025-01-10T11:31:00Z","reference_number":"EMA/247684/2018","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/danys-bienenwohl-epar-public-assessment-report_en.pdf"},
    {"id":"3314","name":"NexoBrid : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2013-01-07T01:00:00Z","last_updated_date":"2013-01-07T01:00:00Z","reference_number":"EMA/648483/2012","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/nexobrid-epar-public-assessment-report_en.pdf"},
    {"id":"3390","name":"Lumark : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2015-07-16T02:00:00Z","last_updated_date":"2026-02-11T02:00:00Z","reference_number":"EMA/427491/2015","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/lumark-epar-public-assessment-report_en.pdf"},
    {"id":"3405","name":"Biopoin : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2009-12-16T01:00:00Z","last_updated_date":"2009-12-16T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/biopoin-epar-public-assessment-report_en.pdf"},
    {"id":"3416","name":"Shingrix : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2018-03-28T02:00:00Z","last_updated_date":"2018-03-28T02:00:00Z","reference_number":"EMA/88588/2018","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/shingrix-epar-public-assessment-report_en.pdf"},
    {"id":"3443","name":"Duloxetine Zentiva : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2015-08-27T02:00:00Z","last_updated_date":"2015-08-27T02:00:00Z","reference_number":"EMA/CHMP/373461/2015","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/duloxetine-zentiva-epar-public-assessment-report_en.pdf"},
    {"id":"3454","name":"Temomedac : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2010-02-11T01:00:00Z","last_updated_date":"2010-02-11T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/temomedac-epar-public-assessment-report_en.pdf"},
    {"id":"3532","name":"Meloxidolor : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2013-05-13T02:00:00Z","last_updated_date":"2025-10-09T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/meloxidolor-epar-public-assessment-report_en.pdf"},
    {"id":"3673","name":"Aripiprazole Zentiva : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2015-07-30T02:00:00Z","last_updated_date":"2015-07-30T02:00:00Z","reference_number":"EMA/CHMP/232319/2015","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/aripiprazole-zentiva-epar-public-assessment-report_en.pdf"},
    {"id":"3689","name":"Jinarc : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2015-06-12T02:00:00Z","last_updated_date":"2015-06-12T02:00:00Z","reference_number":"EMA/154879/2015","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/jinarc-epar-public-assessment-report_en.pdf"},
    {"id":"3702","name":"Inflacam : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2011-12-16T01:00:00Z","last_updated_date":"2025-10-08T01:00:00Z","reference_number":"EMA/847392/2011","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/inflacam-epar-public-assessment-report_en.pdf"},
    {"id":"3722","name":"Bronchitol : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2012-08-02T17:44:00Z","last_updated_date":"2012-08-02T17:44:00Z","reference_number":"EMA/CHMP/121817/2012","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/bronchitol-epar-public-assessment-report_en.pdf"},
    {"id":"3744","name":"Prepandemic Influenza Vaccine (H5N1) (Split Virion, Inactivated, Adjuvanted) GlaxoSmithKline Biologicals : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2008-10-23T02:00:00Z","last_updated_date":"2012-03-21T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/prepandemic-influenza-vaccine-h5n1-split-virion-inactivated-adjuvanted-glaxosmithkline-biologicals-epar-public-assessment-report_en.pdf"},
    {"id":"3756","name":"Parvoduk : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2014-05-20T02:00:00Z","last_updated_date":"2019-04-15T02:00:00Z","reference_number":"EMA/103539/2014","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/parvoduk-epar-public-assessment-report_en.pdf"},
    {"id":"3787","name":"Tecentriq : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2017-09-29T02:00:00Z","last_updated_date":"2018-03-16T01:00:00Z","reference_number":"EMA/505694/2017","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/tecentriq-epar-public-assessment-report_en.pdf"},
    {"id":"3790","name":"Purevax Rabies : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2011-03-23T01:00:00Z","last_updated_date":"2024-10-17T10:29:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/purevax-rabies-epar-public-assessment-report_en.pdf"},
    {"id":"3842","name":"Dupixent : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2017-10-11T02:00:00Z","last_updated_date":"2017-10-11T02:00:00Z","reference_number":"EMA/358525/2023","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/dupixent-epar-public-assessment-report_en.pdf"},
    {"id":"3851","name":"Onglyza : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2009-10-27T01:00:00Z","last_updated_date":"2009-10-27T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/onglyza-epar-public-assessment-report_en.pdf"},
    {"id":"3860","name":"Adasuve : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2013-02-28T01:00:00Z","last_updated_date":"2013-02-28T01:00:00Z","reference_number":"EMA/91055/2013","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/adasuve-epar-public-assessment-report_en.pdf"},
    {"id":"3953","name":"Zoledronic Acid Accord : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2014-02-06T01:00:00Z","last_updated_date":"2014-02-06T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/zoledronic-acid-accord-epar-public-assessment-report_en.pdf"},
    {"id":"3955","name":"Galafold : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2016-06-09T02:00:00Z","last_updated_date":"2016-06-09T02:00:00Z","reference_number":"EMA/272226/2016","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/galafold-epar-public-assessment-report_en.pdf"},
    {"id":"4068","name":"Rivastigmine Hexal  : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2009-12-21T01:00:00Z","last_updated_date":"2009-12-21T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/rivastigmine-hexal-epar-public-assessment-report_en.pdf"},
    {"id":"4089","name":"Mysildecard : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2016-12-08T01:00:00Z","last_updated_date":"2016-12-08T01:00:00Z","reference_number":"EMA/533666/2016","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/mysildecard-epar-public-assessment-report_en.pdf"},
    {"id":"4091","name":"Onzeald : EPAR - Refusal public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2018-02-02T01:00:00Z","last_updated_date":"2018-02-02T01:00:00Z","reference_number":"EMA/795015/2017","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/onzeald-epar-refusal-public-assessment-report_en.pdf"},
    {"id":"4128","name":"Spherox : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2017-07-24T02:00:00Z","last_updated_date":"2017-07-24T02:00:00Z","reference_number":"EMA/349863/2017","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/spherox-epar-public-assessment-report_en.pdf"},
    {"id":"4136","name":"Brintellix : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2014-01-14T01:00:00Z","last_updated_date":"2014-01-14T01:00:00Z","reference_number":"EMA/699150/2013","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/brintellix-epar-public-assessment-report_en.pdf"},
    {"id":"4165","name":"Nulojix : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2011-07-07T02:00:00Z","last_updated_date":"2011-07-07T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/nulojix-epar-public-assessment-report_en.pdf"},
    {"id":"4190","name":"Odefsey : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2016-07-08T02:00:00Z","last_updated_date":"2016-07-08T02:00:00Z","reference_number":"EMA/335723/2016","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/odefsey-epar-public-assessment-report_en.pdf"},
    {"id":"4246","name":"Sildenafil ratiopharm : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2010-01-26T01:00:00Z","last_updated_date":"2010-01-26T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/sildenafil-ratiopharm-epar-public-assessment-report_en.pdf"},
    {"id":"4251","name":"Temozolomide Teva : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2010-02-11T01:00:00Z","last_updated_date":"2010-02-11T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/temozolomide-teva-epar-public-assessment-report_en.pdf"},
    {"id":"4259","name":"Colobreathe : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2012-03-07T01:00:00Z","last_updated_date":"2012-03-07T01:00:00Z","reference_number":"EMA/913717/2011","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/colobreathe-epar-public-assessment-report_en.pdf"},
    {"id":"4270","name":"Nityr : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2018-08-09T02:00:00Z","last_updated_date":"2018-08-09T02:00:00Z","reference_number":"EMA/413721/2018","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/nityr-epar-public-assessment-report_en.pdf"},
    {"id":"4362","name":"Folotyn : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2012-07-11T02:00:00Z","last_updated_date":"2012-07-11T02:00:00Z","reference_number":"EMA/453346/2012","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/folotyn-epar-public-assessment-report_en.pdf"},
    {"id":"4402","name":"Lokelma : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2018-04-05T16:34:00Z","last_updated_date":"2018-04-05T16:34:00Z","reference_number":"EMA/93250/2018","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/lokelma-epar-public-assessment-report_en.pdf"},
    {"id":"4405","name":"Ribavirin Three Rivers : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2010-07-02T02:00:00Z","last_updated_date":"2010-07-02T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/ribavirin-three-rivers-epar-public-assessment-report_en.pdf"},
    {"id":"4418","name":"Tepadina : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2010-05-06T02:00:00Z","last_updated_date":"2010-05-06T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/tepadina-epar-public-assessment-report_en.pdf"},
    {"id":"4534","name":"Memantine Merz : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2012-12-14T16:00:00Z","last_updated_date":"2012-12-14T16:00:00Z","reference_number":"EMA/741024/2012","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/memantine-merz-epar-public-assessment-report_en.pdf"},
    {"id":"4763","name":"Levetiracetam Hospira : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2014-01-20T01:00:00Z","last_updated_date":"2014-01-20T01:00:00Z","reference_number":"EMA/777160/2013","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/levetiracetam-hospira-epar-public-assessment-report_en.pdf"},
    {"id":"4764","name":"Temozolomide Hexal : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2010-03-26T01:00:00Z","last_updated_date":"2023-02-27T15:46:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/temozolomide-hexal-epar-public-assessment-report_en.pdf"},
    {"id":"4813","name":"Sevocalm : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2016-07-06T02:00:00Z","last_updated_date":"2025-10-14T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/sevocalm-epar-public-assessment-report_en.pdf"},
    {"id":"4827","name":"Esmya : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2012-03-15T01:00:00Z","last_updated_date":"2018-08-03T02:00:00Z","reference_number":"EMA/141637/2012","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/esmya-epar-public-assessment-report_en.pdf"},
    {"id":"4879","name":"Pioglitazone Krka : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2012-04-26T02:00:00Z","last_updated_date":"2014-09-26T02:00:00Z","reference_number":"EMA/CHMP/423161/2011","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/pioglitazone-krka-epar-public-assessment-report_en.pdf"},
    {"id":"4915","name":"Vepacel : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2012-03-16T01:00:00Z","last_updated_date":"2012-03-16T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/vepacel-epar-public-assessment-report_en.pdf"},
    {"id":"4961","name":"NovoThirteen : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2012-09-25T02:00:00Z","last_updated_date":"2012-09-25T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/novothirteen-epar-public-assessment-report_en.pdf"},
    {"id":"4979","name":"Inlyta : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2012-09-13T02:00:00Z","last_updated_date":"2012-09-13T02:00:00Z","reference_number":"EMA/CHMP/453325/2012","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/inlyta-epar-public-assessment-report_en.pdf"},
    {"id":"4984","name":"Simparica : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2015-12-18T01:00:00Z","last_updated_date":"2024-06-11T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/simparica-epar-public-assessment-report_en.pdf"},
    {"id":"5004","name":"Pregabalin Pfizer : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2014-05-07T02:00:00Z","last_updated_date":"2014-05-07T02:00:00Z","reference_number":"EMA/174304/2014","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/pregabalin-pfizer-epar-public-assessment-report_en.pdf"},
    {"id":"5075","name":"Mozobil : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2009-08-20T02:09:21Z","last_updated_date":"2009-08-20T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/mozobil-epar-public-assessment-report_en.pdf"},
    {"id":"5121","name":"Voriconazole Hospira : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2015-06-25T02:00:00Z","last_updated_date":"2015-06-25T02:00:00Z","reference_number":"EMA/CHMP/151531/2015","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/voriconazole-hospira-epar-public-assessment-report_en.pdf"},
    {"id":"5142","name":"Duloxetine Lilly : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2015-01-26T01:00:00Z","last_updated_date":"2015-01-26T01:00:00Z","reference_number":"EMA/753230/2014","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/duloxetine-lilly-epar-public-assessment-report_en.pdf"},
    {"id":"5215","name":"Edurant : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2011-12-12T01:00:00Z","last_updated_date":"2011-12-12T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/edurant-epar-public-assessment-report_en.pdf"},
    {"id":"5225","name":"Labazenit : EPAR - Refusal public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2013-10-10T11:42:00Z","last_updated_date":"2013-10-10T11:42:00Z","reference_number":"EMA/465765/2013","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/labazenit-epar-refusal-public-assessment-report_en.pdf"},
    {"id":"5228","name":"Ongentys : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2016-07-01T02:00:00Z","last_updated_date":"2016-07-01T02:00:00Z","reference_number":"EMA/343011/2016","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/ongentys-epar-public-assessment-report_en.pdf"},
    {"id":"5232","name":"Truxima : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2017-03-08T01:00:00Z","last_updated_date":"2017-03-08T01:00:00Z","reference_number":"EMA/CHMP/75695/2017","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/truxima-epar-public-assessment-report_en.pdf"},
    {"id":"5245","name":"Qtern : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2016-07-27T02:00:00Z","last_updated_date":"2016-07-27T02:00:00Z","reference_number":"EMA/428168/2016","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/qtern-epar-public-assessment-report_en.pdf"},
    {"id":"5250","name":"Methylthioninium chloride Proveblue : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2011-06-06T02:00:00Z","last_updated_date":"2011-06-06T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/methylthioninium-chloride-proveblue-epar-public-assessment-report_en.pdf"},
    {"id":"5308","name":"Darunavir Krka : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2018-02-06T01:00:00Z","last_updated_date":"2018-02-06T01:00:00Z","reference_number":"EMA/786959/2018","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/darunavir-krka-epar-public-assessment-report_en.pdf"},
    {"id":"5334","name":"Zulvac BTV Ovis : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2017-05-12T02:00:00Z","last_updated_date":"2025-10-15T15:00:00Z","reference_number":"EMA/118000/2017","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/zulvac-btv-ovis-epar-public-assessment-report_en.pdf"},
    {"id":"5349","name":"Acrescent : EPAR - Refusal public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2013-03-11T01:00:00Z","last_updated_date":"2013-03-11T01:00:00Z","reference_number":"EMA/111381/2013","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/acrescent-epar-refusal-public-assessment-report_en.pdf"},
    {"id":"5367","name":"Roteas : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2017-05-04T02:00:00Z","last_updated_date":"2017-05-04T02:00:00Z","reference_number":"EMA/158410/2017","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/roteas-epar-public-assessment-report_en.pdf"},
    {"id":"5381","name":"Emtricitabine/Tenofovir disoproxil Zentiva : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2016-11-23T01:00:00Z","last_updated_date":"2016-11-23T01:00:00Z","reference_number":"EMA/650230/2016","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/emtricitabinetenofovir-disoproxil-zentiva-epar-public-assessment-report_en.pdf"},
    {"id":"5461","name":"Ivabradine Accord : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2017-06-07T02:00:00Z","last_updated_date":"2017-06-07T02:00:00Z","reference_number":"EMA/263015/2017","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/ivabradine-accord-epar-public-assessment-report_en.pdf"},
    {"id":"5529","name":"Oncaspar : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2016-01-29T16:15:00Z","last_updated_date":"2016-01-29T16:15:00Z","reference_number":"EMA/826135/2016","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/oncaspar-epar-public-assessment-report_en.pdf"},
    {"id":"5533","name":"Orphacol : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2013-10-02T02:00:00Z","last_updated_date":"2013-10-02T02:00:00Z","reference_number":"EMA/596651/2013","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/orphacol-epar-public-assessment-report_en.pdf"},
    {"id":"5550","name":"Lamivudine/Zidovudine Teva : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2011-03-15T01:00:00Z","last_updated_date":"2023-03-21T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/lamivudinezidovudine-teva-epar-public-assessment-report_en.pdf"},
    {"id":"5593","name":"Clopidogrel / Acetylsalicylic acid Teva : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2014-09-26T19:00:00Z","last_updated_date":"2017-04-28T19:00:00Z","reference_number":"EMA/CHMP/333195/2014","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/clopidogrel-acetylsalicylic-acid-teva-epar-public-assessment-report_en.pdf"},
    {"id":"5608","name":"Modigraf : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2009-06-12T02:09:21Z","last_updated_date":"2009-06-12T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/modigraf-epar-public-assessment-report_en.pdf"},
    {"id":"5631","name":"Xultophy : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2014-11-21T01:00:00Z","last_updated_date":"2014-11-21T01:00:00Z","reference_number":"EMA/CHMP/369341/2014","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/xultophy-epar-public-assessment-report_en.pdf"},
    {"id":"5731","name":"Alecensa : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2017-04-11T16:55:00Z","last_updated_date":"2017-04-11T16:55:00Z","reference_number":"EMA/197343/2017","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/alecensa-epar-public-assessment-report_en.pdf"},
    {"id":"5739","name":"Caspofungin Accord : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2016-03-21T01:00:00Z","last_updated_date":"2016-03-21T01:00:00Z","reference_number":"EMA/32587/2016","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/caspofungin-accord-epar-public-assessment-report_en.pdf"},
    {"id":"5761","name":"Certifect : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2018-07-27T02:00:00Z","last_updated_date":"2018-07-27T02:00:00Z","reference_number":"EMA/CVMP/152336/2011","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/certifect-epar-public-assessment-report_en.pdf"},
    {"id":"5799","name":"Poulvac E. coli : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2013-01-29T01:00:00Z","last_updated_date":"2013-01-29T01:00:00Z","reference_number":"EMA/CVMP/298291/2012","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/poulvac-e-coli-epar-public-assessment-report_en.pdf","translations":{"bg":"https://www.ema.europa.eu/bg/documents/assessment-report/poulvac-e-coli-epar-public-assessment-report_bg.pdf","es":"https://www.ema.europa.eu/es/documents/assessment-report/poulvac-e-coli-epar-public-assessment-report_es.pdf","cs":"https://www.ema.europa.eu/cs/documents/assessment-report/poulvac-e-coli-epar-public-assessment-report_cs.pdf","da":"https://www.ema.europa.eu/da/documents/assessment-report/poulvac-e-coli-epar-public-assessment-report_da.pdf","de":"https://www.ema.europa.eu/de/documents/assessment-report/poulvac-e-coli-epar-public-assessment-report_de.pdf","et":"https://www.ema.europa.eu/et/documents/assessment-report/poulvac-e-coli-epar-public-assessment-report_et.pdf","el":"https://www.ema.europa.eu/el/documents/assessment-report/poulvac-e-coli-epar-public-assessment-report_el.pdf","fr":"https://www.ema.europa.eu/fr/documents/assessment-report/poulvac-e-coli-epar-public-assessment-report_fr.pdf","ga":"https://www.ema.europa.eu/ga/documents/assessment-report/poulvac-e-coli-epar-public-assessment-report_ga.pdf","hr":"https://www.ema.europa.eu/hr/documents/assessment-report/poulvac-e-coli-epar-public-assessment-report_hr.pdf","it":"https://www.ema.europa.eu/it/documents/assessment-report/poulvac-e-coli-epar-public-assessment-report_it.pdf","lv":"https://www.ema.europa.eu/lv/documents/assessment-report/poulvac-e-coli-epar-public-assessment-report_lv.pdf","lt":"https://www.ema.europa.eu/lt/documents/assessment-report/poulvac-e-coli-epar-public-assessment-report_lt.pdf","hu":"https://www.ema.europa.eu/hu/documents/assessment-report/poulvac-e-coli-epar-public-assessment-report_hu.pdf","mt":"https://www.ema.europa.eu/mt/documents/assessment-report/poulvac-e-coli-epar-public-assessment-report_mt.pdf","nl":"https://www.ema.europa.eu/nl/documents/assessment-report/poulvac-e-coli-epar-public-assessment-report_nl.pdf","pl":"https://www.ema.europa.eu/pl/documents/assessment-report/poulvac-e-coli-epar-public-assessment-report_pl.pdf","pt":"https://www.ema.europa.eu/pt/documents/assessment-report/poulvac-e-coli-epar-public-assessment-report_pt.pdf","ro":"https://www.ema.europa.eu/ro/documents/assessment-report/poulvac-e-coli-epar-public-assessment-report_ro.pdf","sk":"https://www.ema.europa.eu/sk/documents/assessment-report/poulvac-e-coli-epar-public-assessment-report_sk.pdf","sl":"https://www.ema.europa.eu/sl/documents/assessment-report/poulvac-e-coli-epar-public-assessment-report_sl.pdf","fi":"https://www.ema.europa.eu/fi/documents/assessment-report/poulvac-e-coli-epar-public-assessment-report_fi.pdf","sv":"https://www.ema.europa.eu/sv/documents/assessment-report/poulvac-e-coli-epar-public-assessment-report_sv.pdf","is":"https://www.ema.europa.eu/is/documents/assessment-report/poulvac-e-coli-epar-public-assessment-report_is.pdf","no":"https://www.ema.europa.eu/no/documents/assessment-report/poulvac-e-coli-epar-public-assessment-report_no.pdf"}},
    {"id":"5812","name":"Vipidia : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2013-10-15T02:00:00Z","last_updated_date":"2013-10-15T02:00:00Z","reference_number":"EMA/CHMP/207780/2013","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/vipidia-epar-public-assessment-report_en.pdf"},
    {"id":"5891","name":"Pregabalin Zentiva : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2015-07-27T02:00:00Z","last_updated_date":"2015-07-27T02:00:00Z","reference_number":"EMA/CHMP/408316/2015","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/pregabalin-zentiva-epar-public-assessment-report_en.pdf"},
    {"id":"5895","name":"Raloxifene Teva : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2010-05-28T02:00:00Z","last_updated_date":"2010-05-28T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/raloxifene-teva-epar-public-assessment-report_en.pdf"},
    {"id":"5915","name":"Zalviso : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2015-10-02T02:00:00Z","last_updated_date":"2022-09-27T11:27:00Z","reference_number":"EMA/612007/2015","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/zalviso-epar-public-assessment-report_en.pdf"},
    {"id":"5965","name":"Vpriv : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2010-09-10T02:00:00Z","last_updated_date":"2010-09-10T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/vpriv-epar-public-assessment-report_en.pdf"},
    {"id":"5970","name":"Rasilamlo : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2011-06-06T13:09:00Z","last_updated_date":"2017-03-28T13:09:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/rasilamlo-epar-public-assessment-report_en.pdf"},
    {"id":"5983","name":"Repaglinide Accord : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2012-01-23T17:45:00Z","last_updated_date":"2012-01-23T17:45:00Z","reference_number":"EMA/9712/2012","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/repaglinide-accord-epar-public-assessment-report_en.pdf"},
    {"id":"6007","name":"Tobi Podhaler : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2011-08-25T02:00:00Z","last_updated_date":"2011-08-25T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/tobi-podhaler-epar-public-assessment-report_en.pdf"},
    {"id":"6070","name":"Anoro : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2014-06-16T02:00:00Z","last_updated_date":"2014-06-16T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/anoro-epar-public-assessment-report_en.pdf"},
    {"id":"6083","name":"Xarelto : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2008-11-10T00:09:21Z","last_updated_date":"2008-11-10T00:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/xarelto-epar-public-assessment-report_en.pdf"},
    {"id":"6163","name":"Iclusig : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2013-07-11T02:00:00Z","last_updated_date":"2013-07-11T02:00:00Z","reference_number":"EMA/CHMP/220290/2013","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/iclusig-epar-public-assessment-report_en.pdf"},
    {"id":"6195","name":"Genasense : EPAR - Refusal public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2007-10-31T01:00:00Z","last_updated_date":"2007-10-31T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/genasense-epar-refusal-public-assessment-report_en.pdf"},
    {"id":"6270","name":"Velactis : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2016-02-11T01:00:00Z","last_updated_date":"2021-01-25T02:00:00Z","reference_number":"EMA/673468/2015","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/velactis-epar-public-assessment-report_en.pdf"},
    {"id":"6313","name":"Ritemvia : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2017-08-15T02:00:00Z","last_updated_date":"2021-08-16T02:00:00Z","reference_number":"EMA/CHMP/421799/2017","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/ritemvia-epar-public-assessment-report_en.pdf"},
    {"id":"6327","name":"Equilis West Nile : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2013-07-09T02:00:00Z","last_updated_date":"2025-09-09T02:00:00Z","reference_number":"EMA/250545/2013","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/equilis-west-nile-epar-public-assessment-report_en.pdf"},
    {"id":"6363","name":"Zoledronic acid Medac : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2012-08-17T02:00:00Z","last_updated_date":"2026-05-19T02:00:00Z","reference_number":"EMA/CHMP/271077/2012","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/zoledronic-acid-medac-epar-public-assessment-report_en.pdf"},
    {"id":"6374","name":"Zulvac 1+8 Bovis : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2012-03-15T01:00:00Z","last_updated_date":"2025-10-15T01:00:00Z","reference_number":"EMA/CVMP/973396/2011","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/zulvac-18-bovis-epar-public-assessment-report_en.pdf"},
    {"id":"6487","name":"Onivyde : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2016-10-25T17:29:00Z","last_updated_date":"2016-10-25T17:29:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/onivyde-epar-public-assessment-report_en.pdf"},
    {"id":"6513","name":"Vectra 3D : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2014-03-26T01:00:00Z","last_updated_date":"2024-06-13T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/vectra-3d-epar-public-assessment-report_en.pdf"},
    {"id":"6584","name":"Blincyto : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2015-12-07T01:00:00Z","last_updated_date":"2015-12-07T01:00:00Z","reference_number":"EMA/CHMP/469312/2015","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/blincyto-epar-public-assessment-report_en.pdf"},
    {"id":"6806","name":"Bravecto Plus : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2018-06-07T02:00:00Z","last_updated_date":"2024-06-28T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/bravecto-plus-epar-public-assessment-report_en.pdf"},
    {"id":"6841","name":"IDflu : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2009-04-07T02:00:00Z","last_updated_date":"2018-03-28T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/idflu-epar-public-assessment-report_en.pdf"},
    {"id":"6843","name":"Cystadrops : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2017-02-22T01:00:00Z","last_updated_date":"2017-02-22T01:00:00Z","reference_number":"EMA/738656/2016","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/cystadrops-epar-public-assessment-report_en.pdf"},
    {"id":"6872","name":"Eklira Genuair : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2012-09-19T02:00:00Z","last_updated_date":"2012-09-19T02:00:00Z","reference_number":"EMA/CHMP/169578/2012","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/eklira-genuair-epar-public-assessment-report_en.pdf"},
    {"id":"6874","name":"PecFent : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2010-09-14T02:00:00Z","last_updated_date":"2010-09-14T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/pecfent-epar-public-assessment-report_en.pdf"},
    {"id":"6883","name":"Ryzodeg : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2013-02-20T01:00:00Z","last_updated_date":"2013-02-20T01:00:00Z","reference_number":"EMA/700472/2012","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/ryzodeg-epar-public-assessment-report_en.pdf"},
    {"id":"6932","name":"Innovax-ILT : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2015-10-08T02:00:00Z","last_updated_date":"2024-10-25T02:00:00Z","reference_number":"EMA/309739/2015","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/innovax-ilt-epar-public-assessment-report_en.pdf"},
    {"id":"7085","name":"Gemesis : EPAR - Refusal public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2010-05-27T02:00:00Z","last_updated_date":"2010-05-27T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/gemesis-epar-refusal-public-assessment-report_en.pdf"},
    {"id":"7091","name":"Olanzapine Apotex : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2010-06-23T02:00:00Z","last_updated_date":"2010-06-23T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/olanzapine-apotex-epar-public-assessment-report_en.pdf"},
    {"id":"7134","name":"Solymbic : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2017-04-07T12:27:00Z","last_updated_date":"2017-04-07T12:27:00Z","reference_number":"EMA/106921/2017","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/solymbic-epar-public-assessment-report_en.pdf"},
    {"id":"7179","name":"Lutathera : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2018-01-17T10:20:00Z","last_updated_date":"2018-01-17T10:20:00Z","reference_number":"EMA/506460/2017","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/lutathera-epar-public-assessment-report_en.pdf"},
    {"id":"7181","name":"Aripiprazole Pharmathen : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2015-07-20T02:00:00Z","last_updated_date":"2015-07-20T02:00:00Z","reference_number":"EMA/CHMP/747323/2015","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/aripiprazole-pharmathen-epar-public-assessment-report_en.pdf"},
    {"id":"7197","name":"Cytopoint : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2017-05-05T02:00:00Z","last_updated_date":"2025-03-17T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/cytopoint-epar-public-assessment-report_en.pdf"},
    {"id":"7230","name":"Abasria : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2014-10-14T02:00:00Z","last_updated_date":"2014-10-14T02:00:00Z","reference_number":"EMA/CHMP/340840/2014","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/abasria-epar-public-assessment-report_en.pdf"},
    {"id":"7364","name":"Zinbryta : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2016-07-19T02:00:00Z","last_updated_date":"2018-05-02T02:00:00Z","reference_number":"EMA/458317/2016","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/zinbryta-epar-public-assessment-report_en.pdf"},
    {"id":"7418","name":"Nexgard Spectra : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2015-02-10T01:00:00Z","last_updated_date":"2024-06-13T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/nexgard-spectra-epar-public-assessment-report_en.pdf"},
    {"id":"7422","name":"Neuraceq : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2014-03-11T01:00:00Z","last_updated_date":"2014-03-11T01:00:00Z","reference_number":"EMA/5028/2014","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/neuraceq-epar-public-assessment-report_en.pdf"},
    {"id":"7462","name":"Aftovaxpur DOE : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2013-08-16T18:00:00Z","last_updated_date":"2023-07-04T18:00:00Z","reference_number":"EMA/389517/2013","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/aftovaxpur-doe-epar-public-assessment-report_en.pdf"},
    {"id":"7472","name":"Enurev Breezhaler : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2012-10-17T02:00:00Z","last_updated_date":"2012-10-17T02:00:00Z","reference_number":"EMA/CHMP/508338/2012","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/enurev-breezhaler-epar-public-assessment-report_en.pdf"},
    {"id":"7474","name":"Riarify : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2018-04-26T02:00:00Z","last_updated_date":"2025-03-18T02:00:00Z","reference_number":"EMA/155339/2018","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/riarify-epar-public-assessment-report_en.pdf"},
    {"id":"7486","name":"Ketoconazole HRA : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2015-01-30T01:00:00Z","last_updated_date":"2015-01-30T01:00:00Z","reference_number":"EMA/CHMP/534845/2014","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/ketoconazole-hra-epar-public-assessment-report_en.pdf"},
    {"id":"7529","name":"Zypadhera : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2009-01-05T01:09:21Z","last_updated_date":"2009-01-05T01:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/zypadhera-epar-public-assessment-report_en.pdf"},
    {"id":"7547","name":"Febuxostat Mylan : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2017-10-19T02:00:00Z","last_updated_date":"2017-10-19T02:00:00Z","reference_number":"EMA/368110/2017","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/febuxostat-mylan-epar-public-assessment-report_en.pdf"},
    {"id":"7552","name":"Privigen : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2008-05-20T02:00:00Z","last_updated_date":"2008-05-20T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/privigen-epar-public-assessment-report_en.pdf"},
    {"id":"7595","name":"Ibandronic acid Sandoz : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2011-08-04T02:00:00Z","last_updated_date":"2011-08-04T02:00:00Z","reference_number":"EMA/CHMP/94879/2011","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/ibandronic-acid-sandoz-epar-public-assessment-report_en.pdf"},
    {"id":"7824","name":"Canigen L4 : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2015-07-30T02:00:00Z","last_updated_date":"2024-11-07T15:40:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/canigen-l4-epar-public-assessment-report_en.pdf"},
    {"id":"7853","name":"Leflunomide Winthrop : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2010-01-22T01:00:00Z","last_updated_date":"2010-01-22T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/leflunomide-winthrop-epar-public-assessment-report_en.pdf"},
    {"id":"7944","name":"Nordimet : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2016-09-29T02:00:00Z","last_updated_date":"2016-09-29T02:00:00Z","reference_number":"EMA/527385/2016","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/nordimet-epar-public-assessment-report_en.pdf"},
    {"id":"8105","name":"Xadago : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2015-03-30T02:00:00Z","last_updated_date":"2015-03-30T02:00:00Z","reference_number":"EMA/CHMP/393951/2014","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/xadago-epar-public-assessment-report_en.pdf"},
    {"id":"8128","name":"Clopidogrel Sandoz : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2009-10-16T02:00:00Z","last_updated_date":"2011-10-26T14:05:05Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/clopidogrel-sandoz-epar-public-assessment-report_en.pdf"},
    {"id":"8223","name":"Pixuvri : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2012-05-31T02:00:00Z","last_updated_date":"2012-05-31T02:00:00Z","reference_number":"EMA/309145/2012","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/pixuvri-epar-public-assessment-report_en.pdf"},
    {"id":"8283","name":"Steglujan : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2018-04-05T02:00:00Z","last_updated_date":"2018-04-05T02:00:00Z","reference_number":"EMA/86941/2018","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/steglujan-epar-public-assessment-report_en.pdf"},
    {"id":"8338","name":"Libertek : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2011-03-11T01:00:00Z","last_updated_date":"2018-02-08T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/libertek-epar-public-assessment-report_en.pdf"},
    {"id":"8377","name":"Deltyba : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2014-05-08T02:00:00Z","last_updated_date":"2014-05-08T02:00:00Z","reference_number":"EMA/55567/2014","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/deltyba-epar-public-assessment-report_en.pdf"},
    {"id":"8383","name":"Perjeta : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2013-04-02T16:00:00Z","last_updated_date":"2013-04-05T03:30:00Z","reference_number":"EMA/17250/2013","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/perjeta-epar-public-assessment-report_en.pdf"},
    {"id":"8400","name":"VarroMed : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2017-04-10T02:00:00Z","last_updated_date":"2025-10-15T02:00:00Z","reference_number":"EMA/664782/2016","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/varromed-epar-public-assessment-report_en.pdf"},
    {"id":"8453","name":"Entresto : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2015-12-01T01:00:00Z","last_updated_date":"2015-12-01T01:00:00Z","reference_number":"EMA/671279/2015","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/entresto-epar-public-assessment-report_en.pdf"},
    {"id":"8490","name":"Levodopa/Carbidopa/Entacapone Orion : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2011-09-26T02:00:00Z","last_updated_date":"2011-09-26T02:00:00Z","reference_number":"EMA/718241/2011","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/levodopacarbidopaentacapone-orion-epar-public-assessment-report_en.pdf"},
    {"id":"8500","name":"Dropcys : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2016-07-25T02:00:00Z","last_updated_date":"2016-07-25T02:00:00Z","reference_number":"EMA/277124/2016","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/dropcys-epar-public-assessment-report_en.pdf"},
    {"id":"8526","name":"Prevenar 13 : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2010-01-08T01:00:00Z","last_updated_date":"2010-01-08T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/prevenar-13-epar-public-assessment-report_en.pdf"},
    {"id":"8576","name":"Lidocaine/Prilocaine Plethora : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2013-11-25T01:00:00Z","last_updated_date":"2013-11-25T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/lidocaineprilocaine-plethora-epar-public-assessment-report_en.pdf"},
    {"id":"8598","name":"Ceplene : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2008-10-28T01:00:00Z","last_updated_date":"2008-10-28T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/ceplene-epar-public-assessment-report_en.pdf"},
    {"id":"8640","name":"Clopidogrel DURA : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2009-10-14T02:00:00Z","last_updated_date":"2015-07-10T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/clopidogrel-dura-epar-public-assessment-report_en.pdf"},
    {"id":"8695","name":"Procysbi : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2013-10-03T02:00:00Z","last_updated_date":"2013-10-03T02:00:00Z","reference_number":"EMA/375807/2013","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/procysbi-epar-public-assessment-report_en.pdf"},
    {"id":"8719","name":"Pemetrexed Krka : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2018-06-08T12:19:00Z","last_updated_date":"2024-07-30T12:19:00Z","reference_number":"EMA/CHMP/225126/2018","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/pemetrexed-krka-epar-public-assessment-report_en.pdf"},
    {"id":"8748","name":"Maviret : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2017-08-17T02:00:00Z","last_updated_date":"2017-08-17T02:00:00Z","reference_number":"EMA/449689/2017","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/maviret-epar-public-assessment-report_en.pdf"},
    {"id":"8803","name":"Glyxambi : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2016-11-24T01:00:00Z","last_updated_date":"2016-11-24T01:00:00Z","reference_number":"EMA/749639/2016","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/glyxambi-epar-public-assessment-report_en.pdf"},
    {"id":"8881","name":"Porcilis PCV ID : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2015-10-08T02:00:00Z","last_updated_date":"2024-10-14T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/porcilis-pcv-id-epar-public-assessment-report_en.pdf"},
    {"id":"8892","name":"ChondroCelect : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2009-11-17T00:09:21Z","last_updated_date":"2017-01-12T18:20:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/chondrocelect-epar-public-assessment-report_en.pdf"},
    {"id":"8957","name":"Kadcyla : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2013-12-19T01:00:00Z","last_updated_date":"2013-12-19T01:00:00Z","reference_number":"EMA/CHMP/641539/2013","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/kadcyla-epar-public-assessment-report_en.pdf"},
    {"id":"8965","name":"Ivemend : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2008-02-05T01:00:00Z","last_updated_date":"2008-02-05T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/ivemend-epar-public-assessment-report_en.pdf"},
    {"id":"8971","name":"Valdoxan : EPAR - Refusal public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2009-03-26T01:00:00Z","last_updated_date":"2009-03-26T01:00:00Z","reference_number":"EMEA/CHMP/87018/2006","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/valdoxan-epar-refusal-public-assessment-report_en.pdf"},
    {"id":"8983","name":"Orkambi : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2015-12-01T01:00:00Z","last_updated_date":"2018-10-16T01:00:00Z","reference_number":"EMA/667775/2015","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/orkambi-epar-public-assessment-report_en.pdf"},
    {"id":"9021","name":"Kanjinti : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2018-05-30T02:00:00Z","last_updated_date":"2018-05-30T02:00:00Z","reference_number":"EMA/CHMP/261937/2018","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/kanjinti-epar-public-assessment-report_en.pdf"},
    {"id":"9108","name":"Clopidogrel 1A Pharma : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2009-09-08T02:00:00Z","last_updated_date":"2011-02-28T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/clopidogrel-1a-pharma-epar-public-assessment-report_en.pdf"},
    {"id":"9132","name":"Incresync : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2013-10-14T02:00:00Z","last_updated_date":"2013-10-14T02:00:00Z","reference_number":"EMA/CHMP/208477/2013","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/incresync-epar-public-assessment-report_en.pdf"},
    {"id":"9149","name":"Zebinix : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2009-06-03T02:09:21Z","last_updated_date":"2009-06-03T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/zebinix-epar-public-assessment-report_en.pdf"},
    {"id":"9213","name":"Silodyx : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2010-02-22T01:00:00Z","last_updated_date":"2010-02-22T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/silodyx-epar-public-assessment-report_en.pdf"},
    {"id":"9265","name":"Zomarist : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2009-01-12T00:09:21Z","last_updated_date":"2009-01-12T00:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/zomarist-epar-public-assessment-report_en.pdf"},
    {"id":"9325","name":"Semintra : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2013-02-28T01:00:00Z","last_updated_date":"2024-06-25T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/semintra-epar-public-assessment-report_en.pdf"},
    {"id":"9368","name":"Arzerra : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2010-06-14T02:00:00Z","last_updated_date":"2010-06-14T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/arzerra-epar-public-assessment-report_en.pdf"},
    {"id":"9444","name":"Heparesc : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2016-04-04T02:00:00Z","last_updated_date":"2016-04-04T02:00:00Z","reference_number":"EMA/CHMP/746584/2015","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/heparesc-epar-public-assessment-report_en.pdf"},
    {"id":"9455","name":"Selincro : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2013-03-13T11:00:00Z","last_updated_date":"2013-03-13T11:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/selincro-epar-public-assessment-report_en.pdf"},
    {"id":"9487","name":"Ingelvac PCV FLEX : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2017-06-08T17:28:00Z","last_updated_date":"2017-06-08T17:28:00Z","reference_number":"EMA/186905/2017","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/ingelvac-pcv-flex-epar-public-assessment-report_en.pdf"},
    {"id":"9520","name":"Daptomycin Hospira : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2017-04-24T02:00:00Z","last_updated_date":"2017-04-24T02:00:00Z","reference_number":"EMA/109959/2017","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/daptomycin-hospira-epar-public-assessment-report_en.pdf"},
    {"id":"9527","name":"Masipro : EPAR - Refusal public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2018-04-04T12:15:00Z","last_updated_date":"2018-04-04T12:15:00Z","reference_number":"EMA/641255/2017","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/masipro-epar-refusal-public-assessment-report_en.pdf"},
    {"id":"9551","name":"Kalydeco : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2012-08-06T15:30:00Z","last_updated_date":"2012-08-06T15:30:00Z","reference_number":"EMA/473279/2012","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/kalydeco-epar-public-assessment-report_en.pdf"},
    {"id":"9567","name":"Equisolon : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2014-04-28T02:00:00Z","last_updated_date":"2025-09-09T02:00:00Z","reference_number":"EMA/41881/2014","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/equisolon-epar-public-assessment-report_en.pdf"},
    {"id":"9700","name":"Sancuso : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2012-05-08T02:00:00Z","last_updated_date":"2012-05-08T02:00:00Z","reference_number":"EMA/228344/2012","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/sancuso-epar-public-assessment-report_en.pdf"},
    {"id":"9820","name":"Blitzima : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2017-08-17T11:39:00Z","last_updated_date":"2017-08-17T11:39:00Z","reference_number":"EMA/CHMP/421793/2017","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/blitzima-epar-public-assessment-report_en.pdf"},
    {"id":"9825","name":"Entecavir Mylan : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2017-10-10T17:53:00Z","last_updated_date":"2017-10-10T17:53:00Z","reference_number":"EMA/555410/2017","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/entecavir-mylan-epar-public-assessment-report_en.pdf"},
    {"id":"9956","name":"Foclivia : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2009-12-17T01:00:00Z","last_updated_date":"2009-12-17T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/foclivia-epar-public-assessment-report_en.pdf"},
    {"id":"9964","name":"Zoledronic acid Teva Pharma : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2012-08-28T02:00:00Z","last_updated_date":"2018-12-12T02:00:00Z","reference_number":"EMA/534119/2012","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/zoledronic-acid-teva-pharma-epar-public-assessment-report_en.pdf"},
    {"id":"10065","name":"Telmisartan Teva : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2010-03-22T01:00:00Z","last_updated_date":"2010-03-22T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/telmisartan-teva-epar-public-assessment-report_en.pdf"},
    {"id":"10078","name":"Adynovi : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2018-02-16T01:00:00Z","last_updated_date":"2018-02-16T01:00:00Z","reference_number":"EMA/CHMP/782768/2017","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/adynovi-epar-public-assessment-report_en.pdf"},
    {"id":"10089","name":"Bovilis Blue-8 : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2017-12-08T10:51:00Z","last_updated_date":"2024-06-17T10:51:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/bovilis-blue-8-epar-public-assessment-report_en.pdf"},
    {"id":"10097","name":"Accofil : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2014-10-28T01:00:00Z","last_updated_date":"2014-10-28T01:00:00Z","reference_number":"EMA/CHMP/603430/2014","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/accofil-epar-public-assessment-report_en.pdf"},
    {"id":"10102","name":"Contacera : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2012-12-19T01:00:00Z","last_updated_date":"2025-09-04T01:00:00Z","reference_number":"EMA/CVMP/716044/2012","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/contacera-epar-public-assessment-report_en.pdf"},
    {"id":"10137","name":"Oxybee : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2018-03-13T01:00:00Z","last_updated_date":"2025-01-10T01:00:00Z","reference_number":"EMA/602834/2017","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/oxybee-epar-public-assessment-report_en.pdf"},
    {"id":"10251","name":"Rilonacept Regeneron : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2009-11-12T01:00:00Z","last_updated_date":"2009-11-12T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/rilonacept-regeneron-epar-public-assessment-report_en.pdf"},
    {"id":"10264","name":"Letifend : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2016-06-02T02:00:00Z","last_updated_date":"2025-10-09T11:10:00Z","reference_number":"EMA/142471/2016","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/letifend-epar-public-assessment-report_en.pdf"},
    {"id":"10349","name":"Maruxa : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2013-05-21T02:00:00Z","last_updated_date":"2013-05-21T02:00:00Z","reference_number":"EMA/293975/2013","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/maruxa-epar-public-assessment-report_en.pdf"},
    {"id":"10388","name":"Kisplyx : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2016-11-16T12:06:00Z","last_updated_date":"2016-11-16T12:06:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/kisplyx-epar-public-assessment-report_en.pdf"},
    {"id":"10406","name":"Feraccru : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2016-03-18T01:00:00Z","last_updated_date":"2016-03-18T01:00:00Z","reference_number":"EMA/14567/2016","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/feraccru-epar-public-assessment-report_en.pdf"},
    {"id":"10514","name":"Ipreziv : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2011-12-15T01:00:00Z","last_updated_date":"2014-12-19T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/ipreziv-epar-public-assessment-report_en.pdf"},
    {"id":"10520","name":"Bretaris Genuair : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2012-09-19T02:00:00Z","last_updated_date":"2012-09-19T02:00:00Z","reference_number":"EMA/CHMP/303918/2012","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/bretaris-genuair-epar-public-assessment-report_en.pdf"},
    {"id":"10546","name":"Celvapan : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2009-04-08T02:09:21Z","last_updated_date":"2016-12-21T01:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/celvapan-epar-public-assessment-report_en.pdf"},
    {"id":"10549","name":"Pandemrix : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2008-06-03T02:00:00Z","last_updated_date":"2015-10-27T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/pandemrix-epar-public-assessment-report_en.pdf"},
    {"id":"10581","name":"Zydelig : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2014-10-14T02:00:00Z","last_updated_date":"2014-10-14T02:00:00Z","reference_number":"EMEA/CHMP/324336/2014","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/zydelig-epar-public-assessment-report_en.pdf"},
    {"id":"10600","name":"Xydalba : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2015-03-05T01:00:00Z","last_updated_date":"2015-03-05T01:00:00Z","reference_number":"EMA/39820/2015","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/xydalba-epar-public-assessment-report_en.pdf"},
    {"id":"10601","name":"Clopidogrel Teva (hydrogen sulphate) : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2009-08-12T02:09:21Z","last_updated_date":"2010-06-14T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/clopidogrel-teva-hydrogen-sulphate-epar-public-assessment-report_en.pdf"},
    {"id":"10693","name":"Zuprevo : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2011-05-23T02:00:00Z","last_updated_date":"2024-06-28T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/zuprevo-epar-public-assessment-report_en.pdf"},
    {"id":"10786","name":"Ribavirin Teva Pharma B.V. : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2009-07-27T02:00:00Z","last_updated_date":"2021-07-09T19:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/ribavirin-teva-pharma-bv-epar-public-assessment-report_en.pdf"},
    {"id":"10815","name":"Hexyon : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2013-07-12T02:00:00Z","last_updated_date":"2013-07-12T02:00:00Z","reference_number":"EMA/373968/2013","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/hexyon-epar-public-assessment-report_en.pdf"},
    {"id":"10888","name":"Ameluz : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2012-01-09T01:00:00Z","last_updated_date":"2012-01-09T01:00:00Z","reference_number":"EMA/CHMP/484377/2011","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/ameluz-epar-public-assessment-report_en.pdf"},
    {"id":"10936","name":"Desloratadine Actavis : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2012-01-25T01:00:00Z","last_updated_date":"2012-01-25T01:00:00Z","reference_number":"EMA/11666/2012","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/desloratadine-actavis-epar-public-assessment-report_en.pdf"},
    {"id":"10950","name":"Mylotarg : EPAR - Refusal public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2008-04-17T02:00:00Z","last_updated_date":"2008-04-17T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/mylotarg-epar-refusal-public-assessment-report_en.pdf"},
    {"id":"10967","name":"Vylaer Spiromax : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2014-12-05T01:00:00Z","last_updated_date":"2014-12-05T01:00:00Z","reference_number":"EMA/CHMP/706811/2014","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/vylaer-spiromax-epar-public-assessment-report_en.pdf"},
    {"id":"10992","name":"Clopidogrel Hexal : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2009-09-08T02:00:00Z","last_updated_date":"2012-07-26T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/clopidogrel-hexal-epar-public-assessment-report_en.pdf"},
    {"id":"11025","name":"Exviera : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2015-02-12T01:00:00Z","last_updated_date":"2024-10-01T01:00:00Z","reference_number":"EMA/768319/2014","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/exviera-epar-public-assessment-report_en.pdf"},
    {"id":"11074","name":"Rixubis : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2015-02-10T01:00:00Z","last_updated_date":"2015-02-10T01:00:00Z","reference_number":"EMA/702760/2014","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/rixubis-epar-public-assessment-report_en.pdf"},
    {"id":"11077","name":"Pregabalin Mylan Pharma : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2015-07-31T02:00:00Z","last_updated_date":"2022-04-26T02:00:00Z","reference_number":"EMA/CHMP/90102/2015","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/pregabalin-mylan-pharma-epar-public-assessment-report_en.pdf"},
    {"id":"11125","name":"Inhixa : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2016-10-26T02:00:00Z","last_updated_date":"2016-10-26T02:00:00Z","reference_number":"EMA/536977/2016","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/inhixa-epar-public-assessment-report_en.pdf"},
    {"id":"11156","name":"Cometriq : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2014-03-26T13:00:00Z","last_updated_date":"2014-03-26T13:00:00Z","reference_number":"EMA/97103/2014","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/cometriq-epar-public-assessment-report_en.pdf"},
    {"id":"11162","name":"Ovaleap : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2013-10-23T02:00:00Z","last_updated_date":"2013-10-23T02:00:00Z","reference_number":"EMA/CHMP/41467/2013","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/ovaleap-epar-public-assessment-report_en.pdf"},
    {"id":"11187","name":"Eliquis : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2011-06-20T02:00:00Z","last_updated_date":"2011-06-20T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/eliquis-epar-public-assessment-report_en.pdf"},
    {"id":"11267","name":"Thalidomide Celgene : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2008-05-19T02:09:21Z","last_updated_date":"2008-05-19T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/thalidomide-celgene-epar-public-assessment-report_en.pdf"},
    {"id":"11287","name":"Halagon : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2016-12-22T10:36:00Z","last_updated_date":"2025-10-07T12:00:00Z","reference_number":"EMA/664888/2016","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/halagon-epar-public-assessment-report_en.pdf"},
    {"id":"11290","name":"Daxas : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2010-07-28T02:00:00Z","last_updated_date":"2010-07-28T02:00:00Z","reference_number":"EMA/464905/2010","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/daxas-epar-public-assessment-report_en.pdf"},
    {"id":"11334","name":"Thymanax : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2009-06-03T02:09:00Z","last_updated_date":"2023-08-08T16:57:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/thymanax-epar-public-assessment-report_en.pdf"},
    {"id":"11350","name":"Versican Plus DHPPi : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2014-10-20T02:00:00Z","last_updated_date":"2024-12-19T14:30:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/versican-plus-dhppi-epar-public-assessment-report_en.pdf"},
    {"id":"11452","name":"Lartruvo : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2016-11-23T01:00:00Z","last_updated_date":"2016-11-23T01:00:00Z","reference_number":"EMA/CHMP/742133/2016","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/lartruvo-epar-public-assessment-report_en.pdf"},
    {"id":"11540","name":"Kovaltry : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2016-03-07T01:00:00Z","last_updated_date":"2016-03-09T17:40:00Z","reference_number":"EMA/CHMP/40124/2016 Rev. 1","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/kovaltry-epar-public-assessment-report_en.pdf"},
    {"id":"11543","name":"Leflunomide ratiopharm : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2011-01-17T01:00:00Z","last_updated_date":"2011-01-17T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/leflunomide-ratiopharm-epar-public-assessment-report_en.pdf"},
    {"id":"11614","name":"Clopidogrel Acino Pharma : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2009-10-16T02:09:21Z","last_updated_date":"2012-07-26T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/clopidogrel-acino-pharma-epar-public-assessment-report_en.pdf"},
    {"id":"11636","name":"Clopidogrel BGR (previously Zylagren) : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2009-10-14T02:00:00Z","last_updated_date":"2009-10-14T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/clopidogrel-bgr-previously-zylagren-epar-public-assessment-report_en.pdf"},
    {"id":"11658","name":"Holoclar : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2015-03-02T01:00:00Z","last_updated_date":"2015-03-02T01:00:00Z","reference_number":"EMA/25273/2015","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/holoclar-epar-public-assessment-report_en.pdf"},
    {"id":"11698","name":"Incivo : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2011-10-03T02:00:00Z","last_updated_date":"2016-10-06T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/incivo-epar-public-assessment-report_en.pdf"},
    {"id":"11704","name":"Levetiracetam Accord : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2011-10-14T02:00:00Z","last_updated_date":"2011-10-14T02:00:00Z","reference_number":"EMA767403/2011","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/levetiracetam-accord-epar-public-assessment-report_en.pdf"},
    {"id":"11715","name":"Forxiga : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2012-12-07T01:00:00Z","last_updated_date":"2012-12-07T01:00:00Z","reference_number":"EMA/689976/2012","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/forxiga-epar-public-assessment-report_en.pdf"},
    {"id":"11719","name":"Stronghold Plus : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2017-03-09T01:00:00Z","last_updated_date":"2025-07-07T01:00:00Z","reference_number":"EMA/849714/2016","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/stronghold-plus-epar-public-assessment-report_en.pdf"},
    {"id":"11735","name":"Versican Plus Pi/L4R : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2014-10-20T02:00:00Z","last_updated_date":"2024-10-14T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/versican-plus-pi-l4r-epar-public-assessment-report_en.pdf"},
    {"id":"11896","name":"Raplixa : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2015-05-04T02:00:00Z","last_updated_date":"2018-10-10T02:00:00Z","reference_number":"EMA/CHMP/747327/2014","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/raplixa-epar-public-assessment-report_en.pdf"},
    {"id":"11908","name":"Sirturo : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2014-03-14T17:00:00Z","last_updated_date":"2014-03-14T17:00:00Z","reference_number":"EMA/CHMP/329898/2013","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/sirturo-epar-public-assessment-report_en.pdf"},
    {"id":"11952","name":"Darunavir Mylan : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2017-02-03T01:00:00Z","last_updated_date":"2017-02-03T01:00:00Z","reference_number":"EMA/851324/2016","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/darunavir-mylan-epar-public-assessment-report_en.pdf"},
    {"id":"11977","name":"Ristfor : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2010-03-31T02:00:00Z","last_updated_date":"2010-03-31T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/ristfor-epar-public-assessment-report_en.pdf"},
    {"id":"11998","name":"Oncept IL-2 : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2013-07-18T12:00:00Z","last_updated_date":"2025-10-09T12:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/oncept-il-2-epar-public-assessment-report_en.pdf"},
    {"id":"12038","name":"Symtuza : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2017-09-26T17:26:00Z","last_updated_date":"2017-09-26T17:26:00Z","reference_number":"EMA/496527/2017","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/symtuza-epar-public-assessment-report_en.pdf"},
    {"id":"12040","name":"Remsima : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2013-10-04T17:00:00Z","last_updated_date":"2013-10-04T17:00:00Z","reference_number":"EMA/CHMP/589317/2013","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/remsima-epar-public-assessment-report_en.pdf"},
    {"id":"12052","name":"Aimovig : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2018-08-08T02:00:00Z","last_updated_date":"2018-08-08T02:00:00Z","reference_number":"EMA/CHMP/413393/2018","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/aimovig-epar-public-assessment-report_en.pdf"},
    {"id":"12075","name":"Pioglitazone Teva Pharma : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2012-04-11T02:00:00Z","last_updated_date":"2022-08-30T16:49:00Z","reference_number":"EMA/CHMP/844210/2011","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/pioglitazone-teva-pharma-epar-public-assessment-report_en.pdf"},
    {"id":"12104","name":"UpCard : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2015-08-06T02:00:00Z","last_updated_date":"2025-10-15T02:00:00Z","reference_number":"EMA/383273/2015","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/upcard-epar-public-assessment-report_en.pdf"},
    {"id":"12108","name":"Clopidogrel Qualimed : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2009-10-14T02:00:00Z","last_updated_date":"2014-09-08T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/clopidogrel-qualimed-epar-public-assessment-report_en.pdf"},
    {"id":"12143","name":"Pantoloc Control : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2009-06-22T02:00:00Z","last_updated_date":"2022-01-18T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/pantoloc-control-epar-public-assessment-report_en.pdf"},
    {"id":"12171","name":"Oxervate : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2017-07-25T12:47:00Z","last_updated_date":"2017-07-25T12:47:00Z","reference_number":"EMA/351805/2017","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/oxervate-epar-public-assessment-report_en.pdf"},
    {"id":"12173","name":"Nivestim : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2010-06-23T02:00:00Z","last_updated_date":"2010-06-23T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/nivestim-epar-public-assessment-report_en.pdf"},
    {"id":"12203","name":"Clopidogrel Winthrop : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2008-07-24T02:09:21Z","last_updated_date":"2008-07-24T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/clopidogrel-winthrop-epar-public-assessment-report_en.pdf"},
    {"id":"12237","name":"Spectrila : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2016-01-28T01:00:00Z","last_updated_date":"2016-01-28T01:00:00Z","reference_number":"EMA/CHMP/842555/2015 ","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/spectrila-epar-public-assessment-report_en.pdf"},
    {"id":"12264","name":"Stribild : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2013-06-13T02:00:00Z","last_updated_date":"2013-06-13T02:00:00Z","reference_number":"EMA/332263/2013","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/stribild-epar-public-assessment-report_en.pdf"},
    {"id":"12276","name":"Nuwiq : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2014-12-19T01:00:00Z","last_updated_date":"2014-12-19T01:00:00Z","reference_number":"EMA/CHMP/279301/2014","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/nuwiq-epar-public-assessment-report_en.pdf"},
    {"id":"12352","name":"Topotecan Actavis : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2009-08-26T02:00:00Z","last_updated_date":"2010-03-24T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/topotecan-actavis-epar-public-assessment-report_en.pdf"},
    {"id":"12378","name":"Wakix : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2016-04-13T18:00:00Z","last_updated_date":"2016-04-13T18:00:00Z","reference_number":"EMA/828546/2015","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/wakix-epar-public-assessment-report_en.pdf"},
    {"id":"12443","name":"Imrestor : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2016-04-01T02:00:00Z","last_updated_date":"2025-10-08T14:00:00Z","reference_number":"EMA/673811/2015","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/imrestor-epar-public-assessment-report_en.pdf"},
    {"id":"12534","name":"Nerlynx : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2018-09-12T02:00:00Z","last_updated_date":"2018-09-12T02:00:00Z","reference_number":"EMA/CHMP/525204/2018","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/nerlynx-epar-public-assessment-report_en.pdf"},
    {"id":"12571","name":"Iressa : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2009-07-22T02:00:00Z","last_updated_date":"2009-07-22T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/iressa-epar-public-assessment-report_en.pdf"},
    {"id":"12616","name":"Intelence: EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2008-09-04T02:00:00Z","last_updated_date":"2008-09-04T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/intelence-epar-public-assessment-report_en.pdf"},
    {"id":"12660","name":"Nexium Control : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2013-09-19T02:00:00Z","last_updated_date":"2013-09-19T02:00:00Z","reference_number":"EMA/498929/2013","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/nexium-control-epar-public-assessment-report_en.pdf"},
    {"id":"12698","name":"Exforge HCT : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2009-11-12T01:00:00Z","last_updated_date":"2009-11-12T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/exforge-hct-epar-public-assessment-report_en.pdf"},
    {"id":"12739","name":"Bridion : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2008-09-26T02:09:21Z","last_updated_date":"2008-09-26T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/bridion-epar-public-assessment-report_en.pdf"},
    {"id":"12852","name":"Praxbind : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2015-12-01T01:00:00Z","last_updated_date":"2015-12-01T01:00:00Z","reference_number":"EMA/713107/2015","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/praxbind-epar-public-assessment-report_en.pdf"},
    {"id":"12861","name":"Eryseng Parvo : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2014-10-03T02:00:00Z","last_updated_date":"2025-09-09T02:00:00Z","reference_number":"EMA/289490/2014","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/eryseng-parvo-epar-public-assessment-report_en.pdf"},
    {"id":"12999","name":"Fanaptum : EPAR - Refusal public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2018-03-19T01:00:00Z","last_updated_date":"2018-03-19T01:00:00Z","reference_number":"EMA/844865/2017","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/fanaptum-epar-refusal-public-assessment-report_en.pdf"},
    {"id":"13080","name":"Quinsair : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2015-06-12T02:00:00Z","last_updated_date":"2015-07-03T02:00:00Z","reference_number":"EMA/CHMP/676680/2014 Corr. 1","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/quinsair-epar-public-assessment-report_en.pdf"},
    {"id":"13081","name":"Levetiracetam ratiopharm : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2011-09-19T02:00:00Z","last_updated_date":"2011-09-19T02:00:00Z","reference_number":"EMA/CHMP/318321/2011","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/levetiracetam-ratiopharm-epar-public-assessment-report_en.pdf"},
    {"id":"13082","name":"Efavirenz/Emtricitabine/Tenofovir disoproxil Mylan : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2017-11-21T14:29:00Z","last_updated_date":"2017-11-21T14:29:00Z","reference_number":"EMA/CHMP/630402/2017","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/efavirenzemtricitabinetenofovir-disoproxil-mylan-epar-public-assessment-report_en.pdf"},
    {"id":"13102","name":"Broadline : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2014-03-27T01:00:00Z","last_updated_date":"2024-11-07T15:36:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/broadline-epar-public-assessment-report_en.pdf"},
    {"id":"13150","name":"Zoledronic acid Mylan : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2012-09-10T02:00:00Z","last_updated_date":"2012-09-10T02:00:00Z","reference_number":"EMA/550636/2012","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/zoledronic-acid-mylan-epar-public-assessment-report_en.pdf"},
    {"id":"13151","name":"Bemfola : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2014-05-16T02:00:00Z","last_updated_date":"2014-07-22T02:00:00Z","reference_number":"EMA/65507/2013 Rev. 1","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/bemfola-epar-public-assessment-report_en.pdf"},
    {"id":"13210","name":"Glybera : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2012-11-29T01:00:00Z","last_updated_date":"2012-11-29T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/glybera-epar-public-assessment-report_en.pdf"},
    {"id":"13228","name":"Sepioglin : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2012-04-23T02:00:00Z","last_updated_date":"2013-07-18T02:00:00Z","reference_number":"EMA/207581/2012","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/sepioglin-epar-public-assessment-report_en.pdf"},
    {"id":"13434","name":"Esbriet : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2011-03-11T01:00:00Z","last_updated_date":"2011-03-11T01:00:00Z","reference_number":"EMA/CHMP/115147/2011","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/esbriet-epar-public-assessment-report_en.pdf"},
    {"id":"13451","name":"Lamivudine Teva : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2009-11-09T01:00:00Z","last_updated_date":"2009-11-09T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/lamivudine-teva-epar-public-assessment-report_en.pdf"},
    {"id":"13485","name":"Tenkasi: EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2015-05-04T02:00:00Z","last_updated_date":"2015-05-04T02:00:00Z","reference_number":"EMA/CHMP/803704/2015","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/tenkasi-epar-public-assessment-report_en.pdf"},
    {"id":"13522","name":"Pemetrexed Actavis : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2016-01-28T01:00:00Z","last_updated_date":"2016-01-28T01:00:00Z","reference_number":"EMA/819302/2015","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/pemetrexed-actavis-epar-public-assessment-report_en.pdf"},
    {"id":"13546","name":"Copalia HCT : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2009-11-18T00:09:21Z","last_updated_date":"2009-11-18T00:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/copalia-hct-epar-public-assessment-report_en.pdf"},
    {"id":"13622","name":"Humenza : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2010-07-08T02:00:00Z","last_updated_date":"2011-06-30T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/humenza-epar-public-assessment-report_en.pdf"},
    {"id":"13730","name":"Sedadex : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2016-09-12T02:00:00Z","last_updated_date":"2025-10-14T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/sedadex-epar-public-assessment-report_en.pdf"},
    {"id":"13788","name":"Synjardy : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2015-06-12T02:00:00Z","last_updated_date":"2015-06-12T02:00:00Z","reference_number":"EMA/238334/2015","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/synjardy-epar-public-assessment-report_en.pdf"},
    {"id":"13855","name":"Zarzio : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2009-02-16T01:09:21Z","last_updated_date":"2009-02-16T01:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/zarzio-epar-public-assessment-report_en.pdf"},
    {"id":"13905","name":"Vedrop : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2009-08-06T02:00:00Z","last_updated_date":"2009-08-06T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/vedrop-epar-public-assessment-report_en.pdf"},
    {"id":"13944","name":"Prepandrix : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2008-06-03T02:00:00Z","last_updated_date":"2008-06-03T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/prepandrix-epar-public-assessment-report_en.pdf"},
    {"id":"14011","name":"Bortezomib Accord : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2015-07-27T02:00:00Z","last_updated_date":"2015-07-27T02:00:00Z","reference_number":"EMA/449381/2015","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/bortezomib-accord-epar-public-assessment-report_en.pdf"},
    {"id":"14075","name":"Ozempic : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2018-02-21T01:00:00Z","last_updated_date":"2018-02-21T01:00:00Z","reference_number":"EMA/CHMP/715701/2017","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/ozempic-epar-public-assessment-report_en.pdf"},
    {"id":"14077","name":"Cresemba : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2015-10-29T01:00:00Z","last_updated_date":"2015-10-29T01:00:00Z","reference_number":"EMA/596950/2015","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/cresemba-epar-public-assessment-report_en.pdf"},
    {"id":"14082","name":"Xeljanz : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2017-03-31T02:00:00Z","last_updated_date":"2017-03-31T02:00:00Z","reference_number":"EMA/CHMP/853224/2016","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/xeljanz-epar-public-assessment-report_en.pdf"},
    {"id":"14096","name":"Pheburane : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2013-08-08T13:00:00Z","last_updated_date":"2013-08-08T13:00:00Z","reference_number":"EMA/212039/2012","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/pheburane-epar-public-assessment-report_en.pdf"},
    {"id":"14161","name":"Cabometyx  : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2016-10-12T02:00:00Z","last_updated_date":"2016-10-12T02:00:00Z","reference_number":"EMA/664123/2016","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/cabometyx-epar-public-assessment-report_en.pdf"},
    {"id":"14171","name":"Duzallo : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2018-08-24T15:19:00Z","last_updated_date":"2020-08-06T15:19:00Z","reference_number":"EMA/474026/2018","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/duzallo-epar-public-assessment-report_en.pdf"},
    {"id":"14290","name":"Ecoporc Shiga : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2013-05-16T12:00:00Z","last_updated_date":"2013-05-16T12:00:00Z","reference_number":"EMA/125288/2013","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/ecoporc-shiga-epar-public-assessment-report_en.pdf"},
    {"id":"14311","name":"Pregabalin Mylan : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2015-07-31T02:00:00Z","last_updated_date":"2015-07-31T02:00:00Z","reference_number":"EMA/CHMP/90129/2015","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/pregabalin-mylan-epar-public-assessment-report_en.pdf"},
    {"id":"14313","name":"Ibandronic acid Accord : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2012-12-06T01:00:00Z","last_updated_date":"2012-12-06T01:00:00Z","reference_number":"EMA/711044/2012","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/ibandronic-acid-accord-epar-public-assessment-report_en.pdf"},
    {"id":"14424","name":"Genvoya : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2015-12-01T01:00:00Z","last_updated_date":"2015-12-01T01:00:00Z","reference_number":"EMA/688326/2015","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/genvoya-epar-public-assessment-report_en.pdf"},
    {"id":"14465","name":"Stelara : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2009-02-09T01:00:00Z","last_updated_date":"2009-02-09T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/stelara-epar-public-assessment-report_en.pdf"},
    {"id":"14478","name":"Descovy : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2016-06-01T02:00:00Z","last_updated_date":"2016-06-01T02:00:00Z","reference_number":"EMA/192941/2016","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/descovy-epar-public-assessment-report_en.pdf"},
    {"id":"14519","name":"Briviact : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2016-01-25T01:00:00Z","last_updated_date":"2016-01-25T01:00:00Z","reference_number":"EMA/CHMP/822086/2015","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/briviact-epar-public-assessment-report_en.pdf"},
    {"id":"14547","name":"Efficib : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2008-08-06T02:00:00Z","last_updated_date":"2008-08-06T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/efficib-epar-public-assessment-report_en.pdf"},
    {"id":"14549","name":"Xiliarx : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2009-01-09T01:00:00Z","last_updated_date":"2009-01-09T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/xiliarx-epar-public-assessment-report_en.pdf"},
    {"id":"14550","name":"Lymphoseek : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2015-01-08T01:00:00Z","last_updated_date":"2024-08-14T14:13:00Z","reference_number":"EMA/CHMP/264502/2014","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/lymphoseek-epar-public-assessment-report_en.pdf"},
    {"id":"14636","name":"Jardiance : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2014-06-16T02:00:00Z","last_updated_date":"2014-06-16T02:00:00Z","reference_number":"EMA/CHMP/137741/2014","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/jardiance-epar-public-assessment-report_en.pdf"},
    {"id":"14672","name":"Levetiracetam Actavis : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2011-10-18T02:00:00Z","last_updated_date":"2011-10-18T02:00:00Z","reference_number":"EMA/817944/2011","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/levetiracetam-actavis-epar-public-assessment-report_en.pdf"},
    {"id":"14696","name":"Bosulif : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2013-04-09T15:00:00Z","last_updated_date":"2013-04-09T15:00:00Z","reference_number":"EMA/70979/2013","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/bosulif-epar-public-assessment-report_en.pdf"},
    {"id":"14718","name":"Tovanor Breezhaler : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2012-10-17T02:00:00Z","last_updated_date":"2012-10-17T02:00:00Z","reference_number":"EMA/CHMP/508244/2012","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/tovanor-breezhaler-epar-public-assessment-report_en.pdf"},
    {"id":"14748","name":"Jakavi : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2012-10-04T02:00:00Z","last_updated_date":"2012-10-04T02:00:00Z","reference_number":"EMA/465846/2012","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/jakavi-epar-public-assessment-report_en.pdf"},
    {"id":"14762","name":"Kyprolis : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2015-12-01T01:00:00Z","last_updated_date":"2015-12-01T01:00:00Z","reference_number":"EMA/670306/2015","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/kyprolis-epar-public-assessment-report_en.pdf"},
    {"id":"14814","name":"Pramipexole Accord : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2011-10-19T02:00:00Z","last_updated_date":"2024-03-11T02:00:00Z","reference_number":"EMA/816841/2011","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/pramipexole-accord-epar-public-assessment-report_en.pdf"},
    {"id":"14850","name":"Tecfidera : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2014-02-26T01:00:00Z","last_updated_date":"2014-02-26T01:00:00Z","reference_number":"EMA/800904/2013","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/tecfidera-epar-public-assessment-report_en.pdf"},
    {"id":"14875","name":"Kexxtone : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2013-02-13T13:00:00Z","last_updated_date":"2013-02-13T13:00:00Z","reference_number":"EMA/776008/2012","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/kexxtone-epar-public-assessment-report_en.pdf"},
    {"id":"14951","name":"Biograstim : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2008-09-29T02:09:21Z","last_updated_date":"2017-01-19T01:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/biograstim-epar-public-assessment-report_en.pdf"},
    {"id":"14972","name":"Fortekor Plus : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2015-10-08T02:00:00Z","last_updated_date":"2025-09-09T02:00:00Z","reference_number":"EMA/469409/2015","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/fortekor-plus-epar-public-assessment-report_en.pdf"},
    {"id":"14990","name":"Pregabalin Sandoz : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2015-07-16T02:00:00Z","last_updated_date":"2015-07-16T02:00:00Z","reference_number":"EMA/CHMP/102862/2015","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/pregabalin-sandoz-epar-public-assessment-report_en.pdf"},
    {"id":"15033","name":"Clopidogrel Mylan Pharma : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2009-11-09T01:00:00Z","last_updated_date":"2009-11-09T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/clopidogrel-mylan-pharma-epar-public-assessment-report_en.pdf"},
    {"id":"15140","name":"Parsabiv : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2016-11-24T16:26:00Z","last_updated_date":"2016-11-24T16:26:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/parsabiv-epar-public-assessment-report_en.pdf"},
    {"id":"15194","name":"Sycrest : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2010-09-22T02:00:00Z","last_updated_date":"2010-09-22T02:00:00Z","reference_number":"EMA/CHMP/583011/2010","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/sycrest-epar-public-assessment-report_en.pdf"},
    {"id":"15213","name":"Trevaclyn : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2008-07-10T02:09:21Z","last_updated_date":"2008-07-10T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/trevaclyn-epar-public-assessment-report_en.pdf"},
    {"id":"15246","name":"Lamzede : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2018-04-10T17:23:00Z","last_updated_date":"2018-04-10T17:23:00Z","reference_number":"EMA/205473/2018","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/lamzede-epar-public-assessment-report_en.pdf"},
    {"id":"15254","name":"Zeftera : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2010-09-21T02:00:00Z","last_updated_date":"2010-09-22T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/zeftera-epar-public-assessment-report_en.pdf"},
    {"id":"15269","name":"Venclyxto : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2016-12-21T01:00:00Z","last_updated_date":"2016-12-21T01:00:00Z","reference_number":"EMA/725631/2016","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/venclyxto-epar-public-assessment-report_en.pdf"},
    {"id":"15442","name":"Afinitor : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2009-09-02T02:00:00Z","last_updated_date":"2009-09-02T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/afinitor-epar-public-assessment-report_en.pdf"},
    {"id":"15459","name":"Topotecan Hospira : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2010-06-22T02:00:00Z","last_updated_date":"2010-06-22T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/topotecan-hospira-epar-public-assessment-report_en.pdf"},
    {"id":"15470","name":"Pemetrexed Fresenius Kabi : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2016-07-26T02:00:00Z","last_updated_date":"2016-07-26T02:00:00Z","reference_number":"EMA/CHMP/407425/2016","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/pemetrexed-fresenius-kabi-epar-public-assessment-report_en.pdf"},
    {"id":"15473","name":"Abraxane : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2008-02-04T01:00:00Z","last_updated_date":"2008-02-04T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/abraxane-epar-public-assessment-report_en.pdf"},
    {"id":"15537","name":"Tresiba : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2013-02-20T01:00:00Z","last_updated_date":"2013-02-20T01:00:00Z","reference_number":"EMA/CHMP/557821/2012","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/tresiba-epar-public-assessment-report_en.pdf"},
    {"id":"15547","name":"Scintimun : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2010-03-15T01:00:00Z","last_updated_date":"2010-03-15T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/scintimun-epar-public-assessment-report_en.pdf"},
    {"id":"15585","name":"Caprelsa : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2012-03-02T16:15:00Z","last_updated_date":"2012-03-02T16:15:00Z","reference_number":"EMA/128076/2012","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/caprelsa-epar-public-assessment-report_en.pdf"},
    {"id":"15598","name":"Clopidogrel Mylan : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2009-10-14T02:00:00Z","last_updated_date":"2009-10-14T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/clopidogrel-mylan-epar-public-assessment-report_en.pdf"},
    {"id":"15640","name":"Steglatro : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2018-04-05T02:00:00Z","last_updated_date":"2018-04-05T02:00:00Z","reference_number":"EMA/86938/2018","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/steglatro-epar-public-assessment-report_en.pdf"},
    {"id":"15648","name":"Capecitabine Accord : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2012-05-07T02:00:00Z","last_updated_date":"2012-05-07T02:00:00Z","reference_number":"EMA/225644/2012","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/capecitabine-accord-epar-public-assessment-report_en.pdf"},
    {"id":"15670","name":"Repatha : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2015-08-03T02:00:00Z","last_updated_date":"2015-08-03T02:00:00Z","reference_number":"EMA/CHMP/222019/2015","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/repatha-epar-public-assessment-report_en.pdf"},
    {"id":"15786","name":"Cardalis : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2012-08-28T02:00:00Z","last_updated_date":"2024-11-11T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/cardalis-epar-public-assessment-report_en.pdf"},
    {"id":"15788","name":"Mvasi : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2018-01-31T01:00:00Z","last_updated_date":"2018-01-31T01:00:00Z","reference_number":"EMA/798844/2017","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/mvasi-epar-public-assessment-report_en.pdf"},
    {"id":"15789","name":"Erivedge : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2013-07-30T13:30:00Z","last_updated_date":"2013-07-30T13:30:00Z","reference_number":"EMA/297688/2013","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/erivedge-epar-public-assessment-report_en.pdf"},
    {"id":"15817","name":"Tadalafil Lilly : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2017-04-07T17:07:00Z","last_updated_date":"2017-04-07T17:07:00Z","reference_number":"EMA/CHMP/23344/2017","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/tadalafil-lilly-epar-public-assessment-report_en.pdf"},
    {"id":"15930","name":"Ninlaro : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2016-12-07T01:00:00Z","last_updated_date":"2016-12-07T01:00:00Z","reference_number":"EMA/CHMP/594718/2016","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/ninlaro-epar-public-assessment-report_en.pdf"},
    {"id":"15993","name":"Cosentyx : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2015-03-02T01:00:00Z","last_updated_date":"2015-03-02T01:00:00Z","reference_number":"EMA/CHMP/389874/2014","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/cosentyx-epar-public-assessment-report_en.pdf"},
    {"id":"16064","name":"Axumin : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2017-07-06T02:00:00Z","last_updated_date":"2019-06-05T02:00:00Z","reference_number":"EMA/237809/2017 Corr.","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/axumin-epar-public-assessment-report_en.pdf"},
    {"id":"16068","name":"Cinacalcet Mylan : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2015-11-27T01:00:00Z","last_updated_date":"2015-11-27T01:00:00Z","reference_number":"EMA/CHMP/695643/2015","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/cinacalcet-mylan-epar-public-assessment-report_en.pdf"},
    {"id":"16133","name":"Cayston : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2009-10-08T02:00:00Z","last_updated_date":"2009-10-08T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/cayston-epar-public-assessment-report_en.pdf"},
    {"id":"16185","name":"Hizentra : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2011-06-06T02:00:00Z","last_updated_date":"2011-06-06T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/hizentra-epar-public-assessment-report_en.pdf"},
    {"id":"16191","name":"Yervoy  : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2011-07-25T02:00:00Z","last_updated_date":"2011-07-25T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/yervoy-epar-public-assessment-report_en.pdf"},
    {"id":"16201","name":"Lixiana : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2015-07-03T02:00:00Z","last_updated_date":"2015-07-03T02:00:00Z","reference_number":"EMA/321083/2015","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/lixiana-epar-public-assessment-report_en.pdf"},
    {"id":"16326","name":"Hyrimoz : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2018-08-02T02:00:00Z","last_updated_date":"2018-08-02T02:00:00Z","reference_number":"EMA/CHMP/404076/2018","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/hyrimoz-epar-public-assessment-report_en.pdf"},
    {"id":"16469","name":"Sildenafil Actavis : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2009-12-21T01:00:00Z","last_updated_date":"2009-12-21T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/sildenafil-actavis-epar-public-assessment-report_en.pdf"},
    {"id":"16574","name":"Prevomax : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2017-07-06T02:00:00Z","last_updated_date":"2025-10-14T02:00:00Z","reference_number":"EMA/247239/2017","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/prevomax-epar-public-assessment-report_en.pdf"},
    {"id":"16584","name":"Budesonide/Formoterol Teva : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2014-12-04T01:00:00Z","last_updated_date":"2017-01-31T14:38:00Z","reference_number":"EMA/CHMP/707207/2014","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/budesonideformoterol-teva-epar-public-assessment-report_en.pdf"},
    {"id":"16615","name":"ellaOne: EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2009-06-03T02:00:00Z","last_updated_date":"2009-06-03T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/ellaone-epar-public-assessment-report_en.pdf"},
    {"id":"16641","name":"Flixabi : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2016-06-09T02:00:00Z","last_updated_date":"2016-06-09T02:00:00Z","reference_number":"EMA/CHMP/272283/2016","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/flixabi-epar-public-assessment-report_en.pdf"},
    {"id":"16657","name":"Vihuma : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2017-04-12T11:25:00Z","last_updated_date":"2017-04-12T11:25:00Z","reference_number":"EMA/CHMP/814221/2016","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/vihuma-epar-public-assessment-report_en.pdf"},
    {"id":"16705","name":"Leganto : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2011-06-23T02:00:00Z","last_updated_date":"2022-02-18T02:00:00Z","reference_number":"EMA/437167/2011","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/leganto-epar-public-assessment-report_en.pdf"},
    {"id":"16718","name":"Sylvant : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2014-06-19T02:00:00Z","last_updated_date":"2014-06-19T02:00:00Z","reference_number":"EMA/CHMP/258608/2014","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/sylvant-epar-public-assessment-report_en.pdf"},
    {"id":"16800","name":"Revestive : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2012-09-24T02:00:00Z","last_updated_date":"2012-09-24T02:00:00Z","reference_number":"EMA/CHMP/525255/2012","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/revestive-epar-public-assessment-report_en.pdf"},
    {"id":"16903","name":"Veraflox : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2008-01-23T01:00:00Z","last_updated_date":"2008-01-23T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/veraflox-epar-public-assessment-report_en.pdf-0"},
    {"id":"16904","name":"Entyvio : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2014-06-16T02:00:00Z","last_updated_date":"2014-06-16T02:00:00Z","reference_number":"EMA/CHMP/676643/2013","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/entyvio-epar-public-assessment-report_en.pdf"},
    {"id":"16919","name":"Yescarta : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2018-09-10T02:00:00Z","last_updated_date":"2018-09-10T02:00:00Z","reference_number":"EMA/481168/2018","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/yescarta-epar-public-assessment-report_en.pdf"},
    {"id":"16922","name":"Duloxetine Mylan : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2015-06-24T02:00:00Z","last_updated_date":"2015-06-24T02:00:00Z","reference_number":"EMA/CHMP/238550/2015","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/duloxetine-mylan-epar-public-assessment-report_en.pdf"},
    {"id":"16996","name":"Amgevita : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2017-04-06T02:00:00Z","last_updated_date":"2017-04-06T02:00:00Z","reference_number":"EMA/106922/2017","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/amgevita-epar-public-assessment-report_en.pdf"},
    {"id":"17000","name":"Zoledronic acid Teva Generics : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2014-04-30T02:00:00Z","last_updated_date":"2016-08-08T02:00:00Z","reference_number":"EMA/179093/2014","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/zoledronic-acid-teva-generics-epar-public-assessment-report_en.pdf"},
    {"id":"17009","name":"Rekovelle : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2017-01-27T01:00:00Z","last_updated_date":"2017-01-27T01:00:00Z","reference_number":"EMA/11072/2017","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/rekovelle-epar-public-assessment-report_en.pdf"},
    {"id":"17048","name":"Seebri Breezhaler : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2012-10-17T02:00:00Z","last_updated_date":"2012-10-17T02:00:00Z","reference_number":"EMA/CHMP/508029/2012","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/seebri-breezhaler-epar-public-assessment-report_en.pdf"},
    {"id":"17096","name":"Ciambra : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2016-05-03T02:00:00Z","last_updated_date":"2024-10-17T02:00:00Z","reference_number":"EMA/802052/2015","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/ciambra-epar-public-assessment-report_en.pdf"},
    {"id":"17137","name":"Nobivac LeuFel : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2017-11-28T01:00:00Z","last_updated_date":"2025-09-02T01:00:00Z","reference_number":"EMA/602839/2017","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/nobivac-leufel-epar-public-assessment-report_en.pdf"},
    {"id":"17173","name":"Iasibon : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2011-02-03T01:00:00Z","last_updated_date":"2011-02-03T01:00:00Z","reference_number":"EMA/801304/2010","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/iasibon-epar-public-assessment-report_en.pdf"},
    {"id":"17226","name":"Mycophenolate mofetil Teva : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2008-04-08T02:09:21Z","last_updated_date":"2008-04-08T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/mycophenolate-mofetil-teva-epar-public-assessment-report_en.pdf"},
    {"id":"17233","name":"Victrelis: EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2011-08-03T02:00:00Z","last_updated_date":"2018-07-31T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/victrelis-epar-public-assessment-report_en.pdf"},
    {"id":"17263","name":"Cuprymina: EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2012-09-03T02:00:00Z","last_updated_date":"2012-09-03T02:00:00Z","reference_number":"EMA/518790/2012","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/cuprymina-epar-public-assessment-report_en.pdf"},
    {"id":"17264","name":"Abilify Maintena : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2013-11-28T01:00:00Z","last_updated_date":"2013-11-28T01:00:00Z","reference_number":"EMA/737723/2013","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/abilify-maintena-epar-public-assessment-report_en.pdf"},
    {"id":"17271","name":"Masiviera : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2015-01-06T01:00:00Z","last_updated_date":"2015-01-06T01:00:00Z","reference_number":"EMA/CHMP/327108/2014","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/masiviera-epar-public-assessment-report_en.pdf"},
    {"id":"17354","name":"Maci : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2013-07-12T17:10:00Z","last_updated_date":"2018-07-05T17:10:00Z","reference_number":"EMA/25287/2013","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/maci-epar-public-assessment-report_en.pdf"},
    {"id":"17390","name":"Capecitabine Teva : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2012-05-11T02:00:00Z","last_updated_date":"2012-05-11T02:00:00Z","reference_number":"EMA/275974/2012","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/capecitabine-teva-epar-public-assessment-report_en.pdf"},
    {"id":"17395","name":"Apoquel : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2013-10-15T02:00:00Z","last_updated_date":"2024-06-25T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/apoquel-epar-public-assessment-report_en.pdf"},
    {"id":"17473","name":"Xigduo : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2014-02-10T01:00:00Z","last_updated_date":"2014-02-10T01:00:00Z","reference_number":"EMA/620505/2013","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/xigduo-epar-public-assessment-report_en.pdf"},
    {"id":"17520","name":"Reasanz : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2014-09-01T12:00:00Z","last_updated_date":"2014-09-01T12:00:00Z","reference_number":"EMA/303748/2014","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/reasanz-epar-public-assessment-report_en.pdf"},
    {"id":"17525","name":"Onbrez Breezhaler : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2010-01-05T01:00:00Z","last_updated_date":"2010-01-05T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/onbrez-breezhaler-epar-public-assessment-report_en.pdf"},
    {"id":"17545","name":"Matever : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2011-10-14T02:00:00Z","last_updated_date":"2011-10-14T02:00:00Z","reference_number":"EMA/CHMP/323600/2011","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/matever-epar-public-assessment-report_en.pdf"},
    {"id":"17590","name":"Natalizumab Elan Pharma : EPAR - Refusal public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2008-01-25T01:00:00Z","last_updated_date":"2008-01-25T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/natalizumab-elan-pharma-epar-refusal-public-assessment-report_en.pdf"},
    {"id":"17611","name":"Tacforius : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2018-01-26T18:20:00Z","last_updated_date":"2018-01-26T18:20:00Z","reference_number":"EMA/829470/2017","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/tacforius-epar-public-assessment-report_en.pdf"},
    {"id":"17651","name":"Pemetrexed Hospira : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2015-12-01T01:00:00Z","last_updated_date":"2015-12-01T01:00:00Z","reference_number":"EMA/700366/2015","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/pemetrexed-hospira-epar-public-assessment-report_en.pdf"},
    {"id":"17691","name":"Rydapt : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2017-10-25T02:00:00Z","last_updated_date":"2017-10-25T02:00:00Z","reference_number":"EMA/CHMP/516229/2017","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/rydapt-epar-public-assessment-report_en.pdf"},
    {"id":"17693","name":"Zerbaxa : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2015-10-01T02:00:00Z","last_updated_date":"2015-10-01T02:00:00Z","reference_number":"EMA/CHMP/388494/2015","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/zerbaxa-epar-public-assessment-report_en.pdf"},
    {"id":"17733","name":"Olumiant : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2017-03-16T01:00:00Z","last_updated_date":"2017-03-16T01:00:00Z","reference_number":"EMA/13493/2017","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/olumiant-epar-public-assessment-report_en.pdf"},
    {"id":"17735","name":"Mercaptopurine Nova Laboratories : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2012-03-28T02:00:00Z","last_updated_date":"2012-03-28T02:00:00Z","reference_number":"EMA/CHMP/668488/2011","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/mercaptopurine-nova-laboratories-epar-public-assessment-report_en.pdf"},
    {"id":"17767","name":"Instanyl : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2009-07-30T02:00:00Z","last_updated_date":"2009-07-30T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/instanyl-epar-public-assessment-report_en.pdf"},
    {"id":"17865","name":"Zoledronic Acid Hospira : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2012-11-28T01:00:00Z","last_updated_date":"2026-05-12T01:00:00Z","reference_number":"EMA/711812/2012","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/zoledronic-acid-hospira-epar-public-assessment-report_en.pdf"},
    {"id":"17885","name":"Lonsurf : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2016-05-12T02:00:00Z","last_updated_date":"2016-05-12T02:00:00Z","reference_number":"EMA/CHMP/287846/2016","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/lonsurf-epar-public-assessment-report_en.pdf"},
    {"id":"17918","name":"Opsumit : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2014-02-07T01:00:00Z","last_updated_date":"2014-02-07T01:00:00Z","reference_number":"EMA/457699/2013","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/opsumit-epar-public-assessment-report_en.pdf"},
    {"id":"17942","name":"Halaven  : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2011-04-11T02:00:00Z","last_updated_date":"2011-04-11T02:00:00Z","reference_number":"EMA/CHMP/66726/2011","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/halaven-epar-public-assessment-report_en.pdf"},
    {"id":"17965","name":"Ifirmacombi : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2011-03-17T01:00:00Z","last_updated_date":"2011-03-17T01:00:00Z","reference_number":"EMA/99460/2011","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/ifirmacombi-epar-public-assessment-report_en.pdf"},
    {"id":"18048","name":"Conbriza : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2009-05-26T02:00:00Z","last_updated_date":"2009-05-26T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/conbriza-epar-public-assessment-report_en.pdf"},
    {"id":"18085","name":"Trydonis : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2018-05-02T02:00:00Z","last_updated_date":"2018-05-02T02:00:00Z","reference_number":"EMA/155337/2018","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/trydonis-epar-public-assessment-report_en.pdf"},
    {"id":"18090","name":"Rivastigmine 3M Health Care Ltd : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2014-04-14T02:00:00Z","last_updated_date":"2014-09-18T02:00:00Z","reference_number":"EMA/111203/2014","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/rivastigmine-3m-health-care-ltd-epar-public-assessment-report_en.pdf"},
    {"id":"18148","name":"RoActemra : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2009-02-18T01:00:00Z","last_updated_date":"2009-02-18T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/roactemra-epar-public-assessment-report_en.pdf"},
    {"id":"18195","name":"RevitaCAM : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2012-03-14T01:00:00Z","last_updated_date":"2016-05-30T02:00:00Z","reference_number":"EMA/CVMP/37853/2012","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/revitacam-epar-public-assessment-report_en.pdf"},
    {"id":"18208","name":"Granpidam : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2017-01-31T01:00:00Z","last_updated_date":"2017-01-31T01:00:00Z","reference_number":"EMA/645375/2016","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/granpidam-epar-public-assessment-report_en.pdf"},
    {"id":"18212","name":"Prolia : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2010-06-23T02:00:00Z","last_updated_date":"2010-06-23T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/prolia-epar-public-assessment-report_en.pdf"},
    {"id":"18216","name":"Dasselta  : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2011-12-15T01:00:00Z","last_updated_date":"2011-12-15T01:00:00Z","reference_number":"EMA/895265/2011","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/dasselta-epar-public-assessment-report_en.pdf"},
    {"id":"18250","name":"ProZinc : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2013-08-06T02:00:00Z","last_updated_date":"2025-10-14T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/prozinc-epar-public-assessment-report_en.pdf"},
    {"id":"18312","name":"Levetiracetam Teva  : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2011-09-19T02:00:00Z","last_updated_date":"2011-09-19T02:00:00Z","reference_number":"EMA/457042/2011","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/levetiracetam-teva-epar-public-assessment-report_en.pdf"},
    {"id":"18411","name":"Brimica Genuair : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2014-12-05T01:00:00Z","last_updated_date":"2014-12-05T01:00:00Z","reference_number":"EMA/CHMP/717942/2014","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/brimica-genuair-epar-public-assessment-report_en.pdf"},
    {"id":"18446","name":"Brineura : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2017-06-22T14:00:00Z","last_updated_date":"2017-06-22T14:00:00Z","reference_number":"EMA/31226/2017","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/brineura-epar-public-assessment-report_en.pdf"},
    {"id":"18490","name":"Ruconest : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2010-11-08T01:00:00Z","last_updated_date":"2010-11-08T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/ruconest-epar-public-assessment-report_en.pdf"},
    {"id":"18504","name":"Duaklir Genuair : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2014-12-05T01:00:00Z","last_updated_date":"2014-12-05T01:00:00Z","reference_number":"EMA/CHMP/713778/2014","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/duaklir-genuair-epar-public-assessment-report_en.pdf"},
    {"id":"18581","name":"Budesonide/Formoterol Teva Pharma B.V. : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2014-12-05T15:15:00Z","last_updated_date":"2017-01-30T15:15:00Z","reference_number":"EMA/CHMP/707207/2014","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/budesonideformoterol-teva-pharma-bv-epar-public-assessment-report_en.pdf"},
    {"id":"18635","name":"Recocam : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2011-09-26T02:00:00Z","last_updated_date":"2024-06-17T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/recocam-epar-public-assessment-report_en.pdf"},
    {"id":"18784","name":"Plenadren : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2011-11-15T01:00:00Z","last_updated_date":"2011-11-15T01:00:00Z","reference_number":"EMA/CHMP/424438/2011","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/plenadren-epar-public-assessment-report_en.pdf"},
    {"id":"18855","name":"Tybost : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2013-10-24T02:00:00Z","last_updated_date":"2013-10-24T02:00:00Z","reference_number":"EMA/CHMP/609914/2013","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/tybost-epar-public-assessment-report_en.pdf"},
    {"id":"18882","name":"Pregabalin Sandoz GmbH : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2015-07-21T02:00:00Z","last_updated_date":"2023-10-12T02:00:00Z","reference_number":"EMA/CHMP/102870/2015","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/pregabalin-sandoz-gmbh-epar-public-assessment-report_en.pdf"},
    {"id":"18883","name":"Cimalgex : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2011-07-26T02:00:00Z","last_updated_date":"2025-03-17T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/cimalgex-epar-public-assessment-report_en.pdf"},
    {"id":"18908","name":"Zubsolv : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2018-01-12T01:00:00Z","last_updated_date":"2026-01-29T01:00:00Z","reference_number":"EMA/CHMP/12714/2026","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/zubsolv-epar-public-assessment-report_en.pdf"},
    {"id":"18913","name":"Ifirmasta : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2009-04-10T02:00:00Z","last_updated_date":"2009-04-10T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/ifirmasta-epar-public-assessment-report_en.pdf"},
    {"id":"18964","name":"Bortezomib Hospira : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2016-07-29T02:00:00Z","last_updated_date":"2026-04-15T02:00:00Z","reference_number":"EMA/CHMP/421198/2016","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/bortezomib-hospira-epar-public-assessment-report_en.pdf"},
    {"id":"18985","name":"Tolucombi : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2013-04-08T13:00:00Z","last_updated_date":"2013-04-08T13:00:00Z","reference_number":"EMA/84367/2013","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/tolucombi-epar-public-assessment-report_en.pdf"},
    {"id":"19010","name":"Busulfan Fresenius Kabi : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2014-10-15T02:00:00Z","last_updated_date":"2014-10-15T02:00:00Z","reference_number":"EMA/552423/2014","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/busulfan-fresenius-kabi-epar-public-assessment-report_en.pdf"},
    {"id":"19021","name":"Herzuma : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2018-05-17T02:00:00Z","last_updated_date":"2018-05-17T02:00:00Z","reference_number":"EMA/44005/2018","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/herzuma-epar-public-assessment-report_en.pdf"},
    {"id":"19042","name":"Edarbi : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2011-12-15T01:00:00Z","last_updated_date":"2011-12-15T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/edarbi-epar-public-assessment-report_en.pdf"},
    {"id":"19085","name":"Portrazza : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2016-03-04T01:00:00Z","last_updated_date":"2021-07-27T12:12:00Z","reference_number":"EMA/CHMP/15391/2016","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/portrazza-epar-public-assessment-report_en.pdf"},
    {"id":"19110","name":"Irbesartan / Hydrochlorothiazide Teva : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2009-12-16T01:00:00Z","last_updated_date":"2009-12-16T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/irbesartan-hydrochlorothiazide-teva-epar-public-assessment-report_en.pdf"},
    {"id":"19156","name":"Credelio : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2017-05-11T02:00:00Z","last_updated_date":"2024-06-03T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/credelio-epar-public-assessment-report_en.pdf"},
    {"id":"19169","name":"Trelegy Ellipta : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2018-01-12T18:12:00Z","last_updated_date":"2018-01-12T18:12:00Z","reference_number":"EMA/648156/2017","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/trelegy-ellipta-epar-public-assessment-report_en.pdf"},
    {"id":"19172","name":"Sileo : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2015-07-07T02:00:00Z","last_updated_date":"2024-06-21T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/sileo-epar-public-assessment-report_en.pdf"},
    {"id":"19223","name":"Pioglitazone Actavis Group : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2012-04-26T02:00:00Z","last_updated_date":"2022-10-17T02:00:00Z","reference_number":"EMA/207946/2012","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/pioglitazone-actavis-group-epar-public-assessment-report_en.pdf"},
    {"id":"19254","name":"Mycograb : EPAR - Refusal public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2007-10-22T02:00:00Z","last_updated_date":"2007-10-22T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/mycograb-epar-refusal-public-assessment-report_en.pdf"},
    {"id":"19300","name":"Ratiograstim : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2008-09-29T02:00:00Z","last_updated_date":"2008-09-29T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/ratiograstim-epar-public-assessment-report_en.pdf"},
    {"id":"19334","name":"Clopidogrel TAD : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2009-10-15T02:00:00Z","last_updated_date":"2009-10-15T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/clopidogrel-tad-epar-public-assessment-report_en.pdf"},
    {"id":"19405","name":"Taltz : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2016-05-02T02:00:00Z","last_updated_date":"2016-05-02T02:00:00Z","reference_number":"EMA/CHMP/190631/2016","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/taltz-epar-public-assessment-report_en.pdf"},
    {"id":"19421","name":"Docefrez : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2010-07-05T02:00:00Z","last_updated_date":"2012-06-14T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/docefrez-epar-public-assessment-report_en.pdf"},
    {"id":"19472","name":"Fycompa : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2012-08-07T18:00:00Z","last_updated_date":"2012-08-07T18:00:00Z","reference_number":"EMA/424476/2012","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/fycompa-epar-public-assessment-report_en.pdf"},
    {"id":"19500","name":"Zyclara : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2012-09-13T02:00:00Z","last_updated_date":"2012-09-13T02:00:00Z","reference_number":"EMA/525140/2012","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/zyclara-epar-public-assessment-report_en.pdf"},
    {"id":"19513","name":"Kanuma : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2015-09-01T02:00:00Z","last_updated_date":"2015-09-01T02:00:00Z","reference_number":"EMA/514387/2015","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/kanuma-epar-public-assessment-report_en.pdf"},
    {"id":"19536","name":"Lojuxta : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2013-09-03T18:40:00Z","last_updated_date":"2013-09-03T18:40:00Z","reference_number":"EMA/CHMP/274464/2013","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/lojuxta-epar-public-assessment-report_en.pdf"},
    {"id":"19611","name":"Masican : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2014-08-05T02:00:00Z","last_updated_date":"2014-08-05T02:00:00Z","reference_number":"EMA/174182/2014","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/masican-epar-public-assessment-report_en.pdf"},
    {"id":"19620","name":"Insulin lispro Sanofi : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2017-09-22T02:00:00Z","last_updated_date":"2017-09-22T02:00:00Z","reference_number":"EMA/351195/2017","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/insulin-lispro-sanofi-epar-public-assessment-report_en.pdf"},
    {"id":"19680","name":"DuoPlavin : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2010-03-31T02:00:00Z","last_updated_date":"2010-03-31T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/duoplavin-epar-public-assessment-report_en.pdf"},
    {"id":"19681","name":"Efavirenz/Emtricitabine/Tenofovir disoproxil Zentiva : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2017-10-20T02:00:00Z","last_updated_date":"2017-10-20T02:00:00Z","reference_number":"EMA/454542/2017","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/efavirenzemtricitabinetenofovir-disoproxil-zentiva-epar-public-assessment-report_en.pdf"},
    {"id":"19695","name":"Clopidogrel HCS : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2009-10-14T02:00:00Z","last_updated_date":"2009-10-14T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/clopidogrel-hcs-epar-public-assessment-report_en.pdf"},
    {"id":"19729","name":"Ocaliva : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2016-12-19T01:00:00Z","last_updated_date":"2025-01-20T01:00:00Z","reference_number":"EMA/725757/2016","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/ocaliva-epar-public-assessment-report_en.pdf"},
    {"id":"19845","name":"Nimvastid : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2009-06-04T02:09:21Z","last_updated_date":"2009-06-04T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/nimvastid-epar-public-assessment-report_en.pdf"},
    {"id":"19874","name":"Dzuveo : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2018-07-18T17:55:00Z","last_updated_date":"2018-07-18T17:55:00Z","reference_number":"EMA/302958/2018","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/dzuveo-epar-public-assessment-report_en.pdf"},
    {"id":"19911","name":"Rituzena : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2017-08-15T02:00:00Z","last_updated_date":"2017-08-15T02:00:00Z","reference_number":"EMA/CHMP/421811/2017","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/rituzena-epar-public-assessment-report_en.pdf"},
    {"id":"19912","name":"Pregabalin Accord : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2015-09-18T02:00:00Z","last_updated_date":"2015-09-18T02:00:00Z","reference_number":"EMA/CHMP/282380/2015","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/pregabalin-accord-epar-public-assessment-report_en.pdf"},
    {"id":"19932","name":"Dificlir : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2011-12-19T01:00:00Z","last_updated_date":"2011-12-19T01:00:00Z","reference_number":"EMA/857570/2011","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/dificlir-epar-public-assessment-report_en.pdf"},
    {"id":"19967","name":"Onduarp : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2011-12-08T15:00:00Z","last_updated_date":"2014-04-02T16:00:00Z","reference_number":"EMA/891763/2011","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/onduarp-epar-public-assessment-report_en.pdf"},
    {"id":"20048","name":"Ribavirin Teva : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2009-04-17T02:00:00Z","last_updated_date":"2021-07-09T14:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/ribavirin-teva-epar-public-assessment-report_en.pdf"},
    {"id":"20138","name":"Alendronate sodium/colecalciferol MSD : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2009-11-13T01:00:00Z","last_updated_date":"2009-11-13T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/alendronate-sodiumcolecalciferol-msd-epar-public-assessment-report_en.pdf"},
    {"id":"20206","name":"Zinforo : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2012-09-18T02:00:00Z","last_updated_date":"2012-09-18T02:00:00Z","reference_number":"EMA/472628/2012","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/zinforo-epar-public-assessment-report_en.pdf"},
    {"id":"20226","name":"Vepured : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2017-09-18T02:00:00Z","last_updated_date":"2025-10-15T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/vepured-epar-public-assessment-report_en.pdf"},
    {"id":"20232","name":"Alisade : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2008-11-13T01:00:00Z","last_updated_date":"2008-11-13T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/alisade-epar-public-assessment-report_en.pdf"},
    {"id":"20274","name":"Xeljanz : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2013-11-18T12:25:00Z","last_updated_date":"2013-11-18T12:25:00Z","reference_number":"EMA/CHMP/425279/2013","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/xeljanz-epar-public-assessment-report_en.pdf-0"},
    {"id":"20342","name":"Mylotarg : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2018-05-04T18:17:00Z","last_updated_date":"2018-05-04T18:17:00Z","reference_number":"EMA/155284/2018","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/mylotarg-epar-public-assessment-report_en.pdf"},
    {"id":"20397","name":"Praluent : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2015-10-01T02:00:00Z","last_updated_date":"2015-10-01T02:00:00Z","reference_number":"EMA/CHMP/392430/2015","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/praluent-epar-public-assessment-report_en.pdf"},
    {"id":"20418","name":"Nymusa : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2009-07-06T02:09:21Z","last_updated_date":"2009-07-06T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/nymusa-epar-public-assessment-report_en.pdf"},
    {"id":"20477","name":"Rivastigmine Sandoz : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2009-12-21T01:00:00Z","last_updated_date":"2009-12-21T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/rivastigmine-sandoz-epar-public-assessment-report_en.pdf"},
    {"id":"20482","name":"Suliqua : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2017-03-30T02:00:00Z","last_updated_date":"2017-03-30T02:00:00Z","reference_number":"EMA/800280/2016","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/suliqua-epar-public-assessment-report_en.pdf"},
    {"id":"20503","name":"Levetiracetam Actavis Group : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2011-12-14T01:00:00Z","last_updated_date":"2011-12-14T13:15:00Z","reference_number":"EMA/884675/2011","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/levetiracetam-actavis-group-epar-public-assessment-report_en.pdf"},
    {"id":"20517","name":"Obizur : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2015-11-23T01:00:00Z","last_updated_date":"2015-11-23T01:00:00Z","reference_number":"EMA/627966/2015","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/obizur-epar-public-assessment-report_en.pdf"},
    {"id":"20554","name":"Tremfya : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2017-11-30T01:00:00Z","last_updated_date":"2017-11-30T01:00:00Z","reference_number":"EMA/622081/2017","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/tremfya-epar-public-assessment-report_en.pdf"},
    {"id":"20570","name":"Inflectra : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2013-10-04T02:00:00Z","last_updated_date":"2013-10-04T02:00:00Z","reference_number":"EMA/CHMP/589422/2013","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/inflectra-epar-public-assessment-report_en.pdf"},
    {"id":"20606","name":"Ulunar Breezhaler : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2014-05-16T02:00:00Z","last_updated_date":"2014-05-16T02:00:00Z","reference_number":"EMA/CHMP/175185/2014","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/ulunar-breezhaler-epar-public-assessment-report_en.pdf"},
    {"id":"20731","name":"Filgrastim Hexal : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2009-02-17T00:09:21Z","last_updated_date":"2009-02-17T00:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/filgrastim-hexal-epar-public-assessment-report_en.pdf"},
    {"id":"20768","name":"Elocta : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2015-12-10T01:00:00Z","last_updated_date":"2015-12-10T01:00:00Z","reference_number":"EMA/671791/2015","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/elocta-epar-public-assessment-report_en.pdf"},
    {"id":"20853","name":"Myclausen : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2010-10-14T02:00:00Z","last_updated_date":"2010-10-14T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/myclausen-epar-public-assessment-report_en.pdf"},
    {"id":"20958","name":"Flebogammadif : EPAR - Assessment Report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2007-09-13T02:00:00Z","last_updated_date":"2007-09-13T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/flebogammadif-epar-assessment-report_en.pdf"},
    {"id":"20974","name":"Activyl Tick Plus : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2012-01-24T01:00:00Z","last_updated_date":"2022-10-04T09:36:00Z","reference_number":"EMA/899129/2011","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/activyl-tick-plus-epar-public-assessment-report_en.pdf"},
    {"id":"21028","name":"Rasilez HCT : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2009-02-16T01:00:00Z","last_updated_date":"2022-05-20T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/rasilez-hct-epar-public-assessment-report_en.pdf"},
    {"id":"21125","name":"Ivabradine JensonR : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2017-02-08T01:00:00Z","last_updated_date":"2018-12-20T01:00:00Z","reference_number":"EMA/648588/2016","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/ivabradine-jensonr-epar-public-assessment-report_en.pdf"},
    {"id":"21134","name":"HyQvia : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2013-06-03T02:00:00Z","last_updated_date":"2013-06-03T02:00:00Z","reference_number":"EMA/239112/2013","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/hyqvia-epar-public-assessment-report_en.pdf"},
    {"id":"21142","name":"Somac Control: EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2009-06-22T02:00:00Z","last_updated_date":"2009-06-22T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/somac-control-epar-public-assessment-report_en.pdf"},
    {"id":"21160","name":"Gardasil 9 : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2015-07-03T02:00:00Z","last_updated_date":"2015-07-03T02:00:00Z","reference_number":"EMA/CHMP/76591/2015","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/gardasil-9-epar-public-assessment-report_en.pdf"},
    {"id":"21172","name":"Zycortal : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2015-11-13T01:00:00Z","last_updated_date":"2025-10-15T17:20:00Z","reference_number":"EMA/606003/2015","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/zycortal-epar-public-assessment-report_en.pdf"},
    {"id":"21182","name":"Xermelo : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2017-10-20T02:00:00Z","last_updated_date":"2017-10-20T02:00:00Z","reference_number":"EMA/508026/2017","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/xermelo-epar-public-assessment-report_en.pdf"},
    {"id":"21194","name":"Doribax : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2008-08-01T02:00:00Z","last_updated_date":"2014-10-17T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/doribax-epar-public-assessment-report_en.pdf"},
    {"id":"21211","name":"Evarrest : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2013-10-07T02:00:00Z","last_updated_date":"2018-04-03T02:00:00Z","reference_number":"EMA/464286/2013","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/evarrest-epar-public-assessment-report_en.pdf"},
    {"id":"21330","name":"Repaglinide Teva : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2009-10-12T02:00:00Z","last_updated_date":"2009-10-12T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/repaglinide-teva-epar-public-assessment-report_en.pdf"},
    {"id":"21348","name":"Paglitaz : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2012-04-26T02:00:00Z","last_updated_date":"2012-04-26T02:00:00Z","reference_number":"EMA/183894/2012","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/paglitaz-epar-public-assessment-report_en.pdf"},
    {"id":"21395","name":"Bavencio : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2017-10-13T02:00:00Z","last_updated_date":"2017-10-13T02:00:00Z","reference_number":"EMA/496529/2017","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/bavencio-epar-public-assessment-report_en.pdf"},
    {"id":"21441","name":"Exalief : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2009-05-19T02:00:00Z","last_updated_date":"2012-08-16T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/exalief-epar-public-assessment-report_en.pdf"},
    {"id":"21575","name":"Krystexxa : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2013-02-01T13:30:00Z","last_updated_date":"2016-07-22T14:30:00Z","reference_number":"EMA/CHMP/697253/2012","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/krystexxa-epar-public-assessment-report_en.pdf"},
    {"id":"21610","name":"Mepact : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2009-05-06T02:00:00Z","last_updated_date":"2009-05-06T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/mepact-epar-public-assessment-report_en.pdf"},
    {"id":"21624","name":"Vargatef : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2015-01-08T01:00:00Z","last_updated_date":"2015-01-08T01:00:00Z","reference_number":"EMA/CHMP/726072/2014","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/vargatef-epar-public-assessment-report_en.pdf"},
    {"id":"21637","name":"Zoledronic acid Actavis : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2012-05-07T02:00:00Z","last_updated_date":"2026-05-12T02:00:00Z","reference_number":"EMA/225612/2012","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/zoledronic-acid-actavis-epar-public-assessment-report_en.pdf"},
    {"id":"21720","name":"Kynamro : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2013-06-17T02:00:00Z","last_updated_date":"2013-06-17T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/kynamro-epar-public-assessment-report_en.pdf"},
    {"id":"21786","name":"ImmunoGam : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2010-05-07T02:00:00Z","last_updated_date":"2011-01-26T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/immunogam-epar-public-assessment-report_en.pdf"},
    {"id":"21793","name":"Pantecta Control : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2009-06-22T02:00:00Z","last_updated_date":"2016-11-15T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/pantecta-control-epar-public-assessment-report_en.pdf"},
    {"id":"21860","name":"Gilenya : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2011-03-30T02:00:00Z","last_updated_date":"2011-03-30T02:00:00Z","reference_number":"EMA/108602/2011","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/gilenya-epar-public-assessment-report_en.pdf"},
    {"id":"21889","name":"Jylamvo : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2017-04-19T02:00:00Z","last_updated_date":"2017-04-19T02:00:00Z","reference_number":"EMA/78284/2017","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/jylamvo-epar-public-assessment-report_en.pdf"},
    {"id":"21917","name":"Panacur AquaSol : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2011-12-16T01:00:00Z","last_updated_date":"2011-12-16T01:00:00Z","reference_number":"EMA/834185/2011","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/panacur-aquasol-epar-public-assessment-report_en.pdf"},
    {"id":"21928","name":"Novaquin : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2015-10-08T02:00:00Z","last_updated_date":"2025-10-09T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/novaquin-epar-public-assessment-report_en.pdf"},
    {"id":"21979","name":"Keytruda : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2015-07-30T02:00:00Z","last_updated_date":"2017-10-13T02:00:00Z","reference_number":"EMA/444458/2015 Rev. 1","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/keytruda-epar-public-assessment-report_en.pdf"},
    {"id":"22010","name":"Pumarix : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2011-04-05T02:00:00Z","last_updated_date":"2015-03-17T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/pumarix-epar-public-assessment-report_en.pdf"},
    {"id":"22018","name":"Mirvaso : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2014-03-14T01:00:00Z","last_updated_date":"2014-03-14T01:00:00Z","reference_number":"EMA/CHMP/115246/2014","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/mirvaso-epar-public-assessment-report_en.pdf"},
    {"id":"22221","name":"Pramipexole Teva : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2009-03-10T01:00:00Z","last_updated_date":"2009-03-10T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/pramipexole-teva-epar-public-assessment-report_en.pdf"},
    {"id":"22258","name":"DuoResp Spiromax : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2014-05-20T02:00:00Z","last_updated_date":"2014-05-20T02:00:00Z","reference_number":"EMA/CHMP/175692/2014","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/duoresp-spiromax-epar-public-assessment-report_en.pdf"},
    {"id":"22280","name":"Varuby : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2017-05-31T15:33:00Z","last_updated_date":"2020-03-02T15:33:00Z","reference_number":"EMA/239011/2017","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/varuby-epar-public-assessment-report_en.pdf"},
    {"id":"22290","name":"Simponi : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2009-10-20T02:00:00Z","last_updated_date":"2009-10-20T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/simponi-epar-public-assessment-report_en.pdf"},
    {"id":"22319","name":"Rivastigmine Teva : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2009-05-13T02:00:00Z","last_updated_date":"2012-09-27T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/rivastigmine-teva-epar-public-assessment-report_en.pdf"},
    {"id":"22378","name":"Olanzapine Glenmark Europe : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2010-01-29T01:00:00Z","last_updated_date":"2010-01-29T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/olanzapine-glenmark-europe-epar-public-assessment-report_en.pdf"},
    {"id":"22417","name":"Ibrance : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2016-11-25T01:00:00Z","last_updated_date":"2016-11-25T01:00:00Z","reference_number":"EMA/652627/2016","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/ibrance-epar-public-assessment-report_en.pdf"},
    {"id":"22465","name":"Aflunov : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2011-01-24T01:00:00Z","last_updated_date":"2011-01-24T01:00:00Z","reference_number":"EMA/639703/2010","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/aflunov-epar-public-assessment-report_en.pdf"},
    {"id":"22512","name":"Ravicti : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2015-12-18T01:00:00Z","last_updated_date":"2015-12-18T01:00:00Z","reference_number":"EMA/676925/2015","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/ravicti-epar-public-assessment-report_en.pdf"},
    {"id":"22526","name":"Atazanavir Mylan : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2017-01-31T01:00:00Z","last_updated_date":"2017-01-31T01:00:00Z","reference_number":"EMA/503216/2016","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/atazanavir-mylan-epar-public-assessment-report_en.pdf"},
    {"id":"22574","name":"Unituxin : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2015-09-01T02:00:00Z","last_updated_date":"2017-04-28T02:00:00Z","reference_number":"EMA/CHMP/408316/2015","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/unituxin-epar-public-assessment-report_en.pdf"},
    {"id":"22636","name":"Votubia : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2011-09-19T02:00:00Z","last_updated_date":"2011-09-19T02:00:00Z","reference_number":"EMA/646111/2011","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/votubia-epar-public-assessment-report_en.pdf"},
    {"id":"22650","name":"Suvaxyn PRRS MLV : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2017-09-21T02:00:00Z","last_updated_date":"2024-10-17T09:51:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/suvaxyn-prrs-mlv-epar-public-assessment-report_en.pdf"},
    {"id":"22653","name":"Benlysta   : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2011-08-09T02:00:00Z","last_updated_date":"2011-08-09T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/benlysta-epar-public-assessment-report_en.pdf"},
    {"id":"22676","name":"Cyltezo : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2017-11-17T15:04:00Z","last_updated_date":"2017-11-17T15:04:00Z","reference_number":"EMA/CHMP/750187/2017","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/cyltezo-epar-public-assessment-report_en.pdf"},
    {"id":"22682","name":"Pemetrexed Accord : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2016-01-29T01:00:00Z","last_updated_date":"2016-01-29T01:00:00Z","reference_number":"EMA/CHMP/828561/2015","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/pemetrexed-accord-epar-public-assessment-report_en.pdf"},
    {"id":"22686","name":"Volibris : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2008-04-29T02:00:00Z","last_updated_date":"2008-04-29T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/volibris-epar-public-assessment-report_en.pdf"},
    {"id":"22718","name":"Xtandi : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2013-07-02T02:00:00Z","last_updated_date":"2013-07-02T02:00:00Z","reference_number":"EMA/CHMP/383457/2013","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/xtandi-epar-public-assessment-report_en.pdf"},
    {"id":"22753","name":"Daliresp : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2011-03-11T01:00:00Z","last_updated_date":"2018-02-06T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/daliresp-epar-public-assessment-report_en.pdf"},
    {"id":"22870","name":"Bortezomib Sun : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2016-08-04T02:00:00Z","last_updated_date":"2016-08-04T02:00:00Z","reference_number":"EMA/CHMP/449636/2016","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/bortezomib-sun-epar-public-assessment-report_en.pdf"},
    {"id":"22872","name":"Elebrato Ellipta : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2018-01-25T01:00:00Z","last_updated_date":"2018-01-25T01:00:00Z","reference_number":"EMA/25056/2018","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/elebrato-ellipta-epar-public-assessment-report_en.pdf"},
    {"id":"22947","name":"Tenofovir disoproxil Zentiva : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2017-03-13T01:00:00Z","last_updated_date":"2017-03-13T01:00:00Z","reference_number":"EMA/532453/2016","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/tenofovir-disoproxil-zentiva-epar-public-assessment-report_en.pdf"},
    {"id":"23011","name":"Galliprant : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2018-02-06T01:00:00Z","last_updated_date":"2025-10-07T11:40:00Z","reference_number":"EMA/747932/2017","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/galliprant-epar-public-assessment-report_en.pdf"},
    {"id":"23050","name":"Respreeza : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2015-09-16T17:30:00Z","last_updated_date":"2015-09-16T17:30:00Z","reference_number":"EMA/CHMP/76739/2015","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/respreeza-epar-public-assessment-report_en.pdf"},
    {"id":"23066","name":"Verkazia : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2018-07-12T02:00:00Z","last_updated_date":"2018-07-12T02:00:00Z","reference_number":"EMA/505143/2017","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/verkazia-epar-public-assessment-report_en.pdf"},
    {"id":"23090","name":"Reagila : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2017-09-18T02:00:00Z","last_updated_date":"2017-09-18T02:00:00Z","reference_number":"EMA/CHMP/353055/2017","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/reagila-epar-public-assessment-report_en.pdf"},
    {"id":"23136","name":"Sildenafil Teva : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2009-12-08T01:00:00Z","last_updated_date":"2009-12-08T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/sildenafil-teva-epar-public-assessment-report_en.pdf"},
    {"id":"23213","name":"Nerventra : EPAR - Refusal public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2014-09-01T02:00:00Z","last_updated_date":"2014-09-01T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/nerventra-epar-refusal-public-assessment-report_en.pdf"},
    {"id":"23236","name":"Tredaptive : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2008-07-11T02:09:21Z","last_updated_date":"2008-07-11T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/tredaptive-epar-public-assessment-report_en.pdf"},
    {"id":"23257","name":"Multaq : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2009-12-16T01:00:00Z","last_updated_date":"2009-12-16T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/multaq-epar-public-assessment-report_en.pdf"},
    {"id":"23264","name":"Imbruvica : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2014-11-25T01:00:00Z","last_updated_date":"2014-11-25T01:00:00Z","reference_number":"EMA/CHMP/645137/2014","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/imbruvica-epar-public-assessment-report_en.pdf"},
    {"id":"23291","name":"Synflorix : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2009-05-12T02:00:00Z","last_updated_date":"2009-05-12T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/synflorix-epar-public-assessment-report_en.pdf"},
    {"id":"23347","name":"Ionsys : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2015-11-30T01:00:00Z","last_updated_date":"2018-11-06T01:00:00Z","reference_number":"EMA/801150/2015","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/ionsys-epar-public-assessment-report_en.pdf"},
    {"id":"23419","name":"Riximyo : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2017-07-28T18:52:00Z","last_updated_date":"2017-07-28T18:52:00Z","reference_number":"EMA/440905/2017","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/riximyo-epar-public-assessment-report_en.pdf"},
    {"id":"23539","name":"Cimzia : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2009-10-22T02:00:00Z","last_updated_date":"2009-10-22T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/cimzia-epar-public-assessment-report_en.pdf"},
    {"id":"23546","name":"Fampyra : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2011-08-04T02:00:00Z","last_updated_date":"2011-08-04T02:00:00Z","reference_number":"EMA/555661/2011","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/fampyra-epar-public-assessment-report_en.pdf"},
    {"id":"23560","name":"Lodipressin : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2015-07-17T14:00:00Z","last_updated_date":"2015-07-17T14:00:00Z","reference_number":"EMA/310823/2015","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/lodipressin-epar-public-assessment-report_en.pdf"},
    {"id":"23581","name":"Clopidogrel Acino : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2009-09-09T02:09:21Z","last_updated_date":"2009-09-09T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/clopidogrel-acino-epar-public-assessment-report_en.pdf"},
    {"id":"23648","name":"Ixiaro : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2009-05-06T02:00:00Z","last_updated_date":"2009-05-06T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/ixiaro-epar-public-assessment-report_en.pdf"},
    {"id":"23714","name":"Samsca : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2009-08-18T02:09:21Z","last_updated_date":"2009-08-18T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/samsca-epar-public-assessment-report_en.pdf"},
    {"id":"23728","name":"Fiasp : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2017-02-03T17:16:00Z","last_updated_date":"2017-02-03T17:16:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/fiasp-epar-public-assessment-report_en.pdf"},
    {"id":"23807","name":"Rasagiline ratiopharm : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2015-03-02T01:00:00Z","last_updated_date":"2015-03-02T01:00:00Z","reference_number":"EMA/CHMP/684236/2014","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/rasagiline-ratiopharm-epar-public-assessment-report_en.pdf"},
    {"id":"23837","name":"Rhucin : EPAR - Refusal public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2008-06-27T02:00:00Z","last_updated_date":"2008-06-27T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/rhucin-epar-refusal-public-assessment-report_en.pdf"},
    {"id":"23853","name":"Cotellic : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2015-12-10T01:00:00Z","last_updated_date":"2015-12-10T01:00:00Z","reference_number":"EMA/685908/2015","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/cotellic-epar-public-assessment-report_en.pdf"},
    {"id":"23873","name":"Ranexa : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2008-07-31T02:00:00Z","last_updated_date":"2008-07-31T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/ranexa-epar-public-assessment-report_en.pdf"},
    {"id":"23895","name":"Imraldi : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2017-08-31T11:42:00Z","last_updated_date":"2017-08-31T11:42:00Z","reference_number":"EMA/CHMP/559383/2017","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/imraldi-epar-public-assessment-report_en.pdf"},
    {"id":"23913","name":"Pioglitazone Teva : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2012-04-10T18:30:00Z","last_updated_date":"2023-05-04T18:30:00Z","reference_number":"EMEA/CHMP/844031/2011","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/pioglitazone-teva-epar-public-assessment-report_en.pdf"},
    {"id":"23975","name":"Clopidogrel HCS : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2010-11-16T01:00:00Z","last_updated_date":"2010-11-16T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/clopidogrel-hcs-epar-public-assessment-report_en.pdf-0"},
    {"id":"24004","name":"EnCyzix : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2018-04-20T02:00:00Z","last_updated_date":"2018-04-20T02:00:00Z","reference_number":"EMA/88321/2018","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/encyzix-epar-public-assessment-report_en.pdf"},
    {"id":"24024","name":"Balaxur : EPAR - Refusal public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2013-03-11T01:00:00Z","last_updated_date":"2013-03-11T01:00:00Z","reference_number":"EMA/817438/2012","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/balaxur-epar-refusal-public-assessment-report_en.pdf"},
    {"id":"24038","name":"Arepanrix : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2010-04-26T02:00:00Z","last_updated_date":"2011-10-25T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/arepanrix-epar-public-assessment-report_en.pdf"},
    {"id":"24043","name":"Ofev : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2015-02-13T01:00:00Z","last_updated_date":"2015-02-13T01:00:00Z","reference_number":"EMA/76777/2015","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/ofev-epar-public-assessment-report_en.pdf"},
    {"id":"24118","name":"Omidria : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2015-09-01T02:00:00Z","last_updated_date":"2015-09-01T02:00:00Z","reference_number":"EMA/CHMP/289528/2015","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/omidria-epar-public-assessment-report_en.pdf"},
    {"id":"24159","name":"Nucala : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2015-12-03T01:00:00Z","last_updated_date":"2016-01-12T16:30:00Z","reference_number":"EMA/CHMP/672504/2015 Rev. 1","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/nucala-epar-public-assessment-report_en.pdf"},
    {"id":"24185","name":"Amyvid : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2013-01-23T01:00:00Z","last_updated_date":"2013-01-23T01:00:00Z","reference_number":"EMA/30808/2013","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/amyvid-epar-public-assessment-report_en.pdf"},
    {"id":"24194","name":"Tafinlar : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2013-09-18T02:00:00Z","last_updated_date":"2013-09-18T02:00:00Z","reference_number":"EMA/CHMP/242419/2013","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/tafinlar-epar-public-assessment-report_en.pdf"},
    {"id":"24244","name":"Repso : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2011-03-28T02:00:00Z","last_updated_date":"2011-03-28T02:00:00Z","reference_number":"EMA/79461/2011","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/repso-epar-public-assessment-report_en.pdf"},
    {"id":"24337","name":"Empliciti : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2016-05-19T02:00:00Z","last_updated_date":"2016-05-19T02:00:00Z","reference_number":"EMA/129497/2015","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/empliciti-epar-public-assessment-report_en.pdf"},
    {"id":"24373","name":"Sumatriptan Galpharm : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2012-02-16T12:00:00Z","last_updated_date":"2012-02-16T12:00:00Z","reference_number":"EMA/40740/2012","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/sumatriptan-galpharm-epar-public-assessment-report_en.pdf"},
    {"id":"24383","name":"Clopidogrel Teva Generics B.V. : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2010-11-16T01:00:00Z","last_updated_date":"2014-05-12T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/clopidogrel-teva-generics-bv-epar-public-assessment-report_en.pdf"},
    {"id":"24435","name":"Kengrexal : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2015-06-12T02:00:00Z","last_updated_date":"2015-08-27T02:00:00Z","reference_number":"EMA/CHMP/85523/2015","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/kengrexal-epar-public-assessment-report_en.pdf"},
    {"id":"24439","name":"Porcilis PCV M Hyo : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2014-11-14T01:00:00Z","last_updated_date":"2014-11-14T01:00:00Z","reference_number":"EMA/559030/2014","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/porcilis-pcv-m-hyo-epar-public-assessment-report_en.pdf"},
    {"id":"24489","name":"Tookad : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2017-11-29T01:00:00Z","last_updated_date":"2017-11-29T01:00:00Z","reference_number":"EMA/644309/2017","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/tookad-epar-public-assessment-report_en.pdf"},
    {"id":"24620","name":"Dacogen : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2012-10-16T02:00:00Z","last_updated_date":"2012-10-16T02:00:00Z","reference_number":"EMA/620205/2012","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/dacogen-epar-public-assessment-report_en.pdf"},
    {"id":"24626","name":"Kinzalkomb-H-C-415-A31-0084 : EPAR - Assessment Report - Article 31","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2014-10-03T02:00:00Z","last_updated_date":"2014-10-03T02:00:00Z","reference_number":"EMA/PRAC/294920/2014","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/kinzalkomb-h-c-415-a31-0084-epar-assessment-report-article-31_en.pdf"},
    {"id":"24638","name":"Eylea : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2012-12-05T01:00:00Z","last_updated_date":"2013-02-21T15:20:00Z","reference_number":"EMA/646256/2012 corr","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/eylea-epar-public-assessment-report_en.pdf"},
    {"id":"24664","name":"Potactasol : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2011-01-17T01:00:00Z","last_updated_date":"2011-01-17T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/potactasol-epar-public-assessment-report_en.pdf"},
    {"id":"24769","name":"Osurnia : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2014-08-15T02:00:00Z","last_updated_date":"2025-10-09T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/osurnia-epar-public-assessment-report_en.pdf"},
    {"id":"24818","name":"Eperzan : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2014-04-10T02:00:00Z","last_updated_date":"2019-02-20T02:00:00Z","reference_number":"EMA/CHMP/705417/2013","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/eperzan-epar-public-assessment-report_en.pdf"},
    {"id":"24823","name":"Pioglitazone Accord : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2012-04-26T02:00:00Z","last_updated_date":"2012-04-26T02:00:00Z","reference_number":"EMA/CHMP/46573/2012","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/pioglitazone-accord-epar-public-assessment-report_en.pdf"},
    {"id":"24887","name":"Tivicay : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2014-02-05T01:00:00Z","last_updated_date":"2014-02-05T01:00:00Z","reference_number":"EMA/CHMP/772068/2013","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/tivicay-epar-public-assessment-report_en.pdf"},
    {"id":"24954","name":"Oprymea : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2008-09-23T02:09:21Z","last_updated_date":"2008-09-23T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/oprymea-epar-public-assessment-report_en.pdf"},
    {"id":"25008","name":"Olazax Disperzi : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2010-01-29T01:00:00Z","last_updated_date":"2010-01-29T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/olazax-disperzi-epar-public-assessment-report_en.pdf"},
    {"id":"25066","name":"Fertavid : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2009-04-08T02:09:00Z","last_updated_date":"2020-06-23T02:09:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/fertavid-epar-public-assessment-report_en.pdf"},
    {"id":"25081","name":"Afstyla : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2017-03-30T11:24:00Z","last_updated_date":"2017-03-30T11:24:00Z","reference_number":"EMA/CHMP/699390/2016","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/afstyla-epar-public-assessment-report_en.pdf"},
    {"id":"25095","name":"Airexar Spiromax : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2016-09-05T02:00:00Z","last_updated_date":"2016-09-05T02:00:00Z","reference_number":"EMA/486131/2016","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/airexar-spiromax-epar-public-assessment-report_en.pdf"},
    {"id":"25135","name":"Withdrawal assessment report for Alendronic Acid/Colecalciferol Mylan","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2017-02-02T12:10:00Z","last_updated_date":"2017-02-02T12:10:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/withdrawal-assessment-report-alendronic-acid-colecalciferol-mylan_en.pdf"},
    {"id":"25148","name":"Nobilis IB Primo QX : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2014-11-04T01:00:00Z","last_updated_date":"2025-10-09T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/nobilis-ib-primo-qx-epar-public-assessment-report_en.pdf"},
    {"id":"25189","name":"Scenesse : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2015-02-12T01:00:00Z","last_updated_date":"2015-06-15T17:20:00Z","reference_number":"EMA/CHMP/709396/2014 Rev. 1","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/scenesse-epar-public-assessment-report_en.pdf"},
    {"id":"25234","name":"Exzolt : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2017-10-20T12:19:00Z","last_updated_date":"2024-06-25T12:19:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/exzolt-epar-public-assessment-report_en.pdf"},
    {"id":"25283","name":"Biktarvy : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2018-06-22T02:00:00Z","last_updated_date":"2018-06-22T02:00:00Z","reference_number":"EMA/293559/2018","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/biktarvy-epar-public-assessment-report_en.pdf"},
    {"id":"25362","name":"Moventig : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2014-12-17T01:00:00Z","last_updated_date":"2014-12-17T01:00:00Z","reference_number":"EMA/CHMP/738815/2014","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/moventig-epar-public-assessment-report_en.pdf"},
    {"id":"25382","name":"Myalepta : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2018-08-06T02:00:00Z","last_updated_date":"2018-08-06T02:00:00Z","reference_number":"EMA/435156/2018","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/myalepta-epar-public-assessment-report_en.pdf"},
    {"id":"25431","name":"Veltassa : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2017-08-01T02:00:00Z","last_updated_date":"2017-08-01T02:00:00Z","reference_number":"EMA/CHMP/424270/2017","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/veltassa-epar-public-assessment-report_en.pdf"},
    {"id":"25446","name":"Azarga : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2009-01-08T01:00:00Z","last_updated_date":"2009-01-08T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/azarga-epar-public-assessment-report_en.pdf"},
    {"id":"25511","name":"Fotivda : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2017-11-22T01:00:00Z","last_updated_date":"2017-11-22T01:00:00Z","reference_number":"EMA/CHMP/437168/2017","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/fotivda-epar-public-assessment-report_en.pdf"},
    {"id":"25577","name":"Bovela : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2015-02-17T01:00:00Z","last_updated_date":"2024-11-07T15:18:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/bovela-epar-public-assessment-report_en.pdf"},
    {"id":"25583","name":"Adempas : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2014-04-10T02:00:00Z","last_updated_date":"2014-04-10T02:00:00Z","reference_number":"EMA/CHMP/734750/2013","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/adempas-epar-public-assessment-report_en.pdf"},
    {"id":"25587","name":"Desloratadine ratiopharm : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2012-02-07T01:00:00Z","last_updated_date":"2012-02-07T01:00:00Z","reference_number":"EMA/41222/2012","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/desloratadine-ratiopharm-epar-public-assessment-report_en.pdf"},
    {"id":"25593","name":"Bexsero : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2012-01-28T01:00:00Z","last_updated_date":"2012-01-28T01:00:00Z","reference_number":"EMA/790069/2012","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/bexsero-epar-public-assessment-report_en.pdf"},
    {"id":"25616","name":"Grepid : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2009-08-05T02:09:21Z","last_updated_date":"2009-08-05T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/grepid-epar-public-assessment-report_en.pdf"},
    {"id":"25635","name":"Enyglid : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2009-10-19T02:00:00Z","last_updated_date":"2009-10-19T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/enyglid-epar-public-assessment-report_en.pdf"},
    {"id":"25709","name":"Clevor : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2018-05-16T02:00:00Z","last_updated_date":"2025-09-03T02:00:00Z","reference_number":"EMA/101046/2018","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/clevor-epar-public-assessment-report_en.pdf"},
    {"id":"25737","name":"Coliprotec F4/F18 : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2017-02-06T01:00:00Z","last_updated_date":"2025-09-04T01:00:00Z","reference_number":"EMA/746591/2016","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/coliprotec-f4-f18-epar-public-assessment-report_en.pdf"},
    {"id":"25823","name":"Repaglinide Krka : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2009-11-16T01:00:00Z","last_updated_date":"2009-11-16T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/repaglinide-krka-epar-public-assessment-report_en.pdf"},
    {"id":"25825","name":"Erelzi : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2017-06-29T02:00:00Z","last_updated_date":"2017-06-29T02:00:00Z","reference_number":"EMA/CHMP/302222/2017","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/erelzi-epar-public-assessment-report_en.pdf"},
    {"id":"25842","name":"Rasitrio : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2011-12-19T01:00:00Z","last_updated_date":"2011-12-19T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/rasitrio-epar-public-assessment-report_en.pdf"},
    {"id":"25900","name":"Eravac : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2016-10-20T02:00:00Z","last_updated_date":"2025-09-02T02:00:00Z","reference_number":"EMA/485590/2016","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/eravac-epar-public-assessment-report_en.pdf"},
    {"id":"25954","name":"Kuvan : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2009-04-10T02:00:00Z","last_updated_date":"2009-04-10T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/kuvan-epar-public-assessment-report_en.pdf"},
    {"id":"25993","name":"Milnacipran Pierre Fabre Medicament : EPAR - Refusal public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2010-04-26T02:00:00Z","last_updated_date":"2010-04-26T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/milnacipran-pierre-fabre-medicament-epar-refusal-public-assessment-report_en.pdf"},
    {"id":"26018","name":"Riluzole Zentiva : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2012-05-23T02:00:00Z","last_updated_date":"2012-05-23T02:00:00Z","reference_number":"EMA/241210/2012","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/riluzole-zentiva-epar-public-assessment-report_en.pdf"},
    {"id":"26032","name":"Nobivac L4 : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2013-01-29T01:00:00Z","last_updated_date":"2024-12-19T14:30:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/nobivac-l4-epar-public-assessment-report_en.pdf"},
    {"id":"26095","name":"Ultibro Breezhaler : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2013-10-03T02:00:00Z","last_updated_date":"2013-10-03T02:00:00Z","reference_number":"EMA/CHMP/296722/2013","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/ultibro-breezhaler-epar-public-assessment-report_en.pdf"},
    {"id":"26317","name":"Fluenz Tetra : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2013-12-17T01:00:00Z","last_updated_date":"2025-08-14T01:00:00Z","reference_number":"EMA/586629/2013","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/fluenz-tetra-epar-public-assessment-report_en.pdf"},
    {"id":"26343","name":"Semglee : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2018-05-23T02:00:00Z","last_updated_date":"2018-05-23T02:00:00Z","reference_number":"EMA/119474/2018","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/semglee-epar-public-assessment-report_en.pdf"},
    {"id":"26347","name":"Tasermity : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2015-04-09T02:00:00Z","last_updated_date":"2018-03-27T02:00:00Z","reference_number":"EMA/CHMP/68384/2015","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/tasermity-epar-public-assessment-report_en.pdf"},
    {"id":"26452","name":"Viekirax : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2015-03-09T01:00:00Z","last_updated_date":"2024-10-02T01:00:00Z","reference_number":"EMA/768346/2014","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/viekirax-epar-public-assessment-report_en.pdf"},
    {"id":"26488","name":"Versican Plus L4 : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2014-10-20T02:00:00Z","last_updated_date":"2014-10-20T02:00:00Z","reference_number":"EMA/316861/2014","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/versican-plus-l4-epar-public-assessment-report_en.pdf"},
    {"id":"26509","name":"Sovrima : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2009-07-09T02:00:00Z","last_updated_date":"2009-07-09T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/sovrima-epar-public-assessment-report_en.pdf"},
    {"id":"26650","name":"Docetaxel Hospira UK Limited : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2015-09-17T02:00:00Z","last_updated_date":"2019-10-15T02:00:00Z","reference_number":"EMA/CHMP/289489/2015","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/docetaxel-hospira-uk-limited-epar-public-assessment-report_en.pdf"},
    {"id":"26671","name":"Renvela : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2009-06-23T02:00:00Z","last_updated_date":"2009-06-23T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/renvela-epar-public-assessment-report_en.pdf"},
    {"id":"26697","name":"Ucedane : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2017-06-30T02:00:00Z","last_updated_date":"2017-06-30T02:00:00Z","reference_number":"EMA/CHMP/404487/2017","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/ucedane-epar-public-assessment-report_en.pdf"},
    {"id":"26730","name":"Versican Plus DHPPi/L4 : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2014-08-12T02:00:00Z","last_updated_date":"2024-12-19T14:30:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/versican-plus-dhppi-l4-epar-public-assessment-report_en.pdf"},
    {"id":"26755","name":"Irbesartan Teva : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2009-11-16T01:00:00Z","last_updated_date":"2009-11-16T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/irbesartan-teva-epar-public-assessment-report_en.pdf"},
    {"id":"26766","name":"Brinavess : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2010-09-28T02:00:00Z","last_updated_date":"2010-09-28T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/brinavess-epar-public-assessment-report_en.pdf"},
    {"id":"26772","name":"Clopidogrel ratiopharm GmbH : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2009-09-08T02:00:00Z","last_updated_date":"2009-09-08T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/clopidogrel-ratiopharm-gmbh-epar-public-assessment-report_en.pdf"},
    {"id":"26800","name":"Gazyvaro : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2014-08-20T02:00:00Z","last_updated_date":"2014-08-20T02:00:00Z","reference_number":"EMA/CHMP/231450/2014","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/gazyvaro-epar-public-assessment-report_en.pdf"},
    {"id":"26843","name":"Entacapone Teva : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2011-03-03T01:00:00Z","last_updated_date":"2011-03-03T01:00:00Z","reference_number":"EMA/52316/2011","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/entacapone-teva-epar-public-assessment-report_en.pdf"},
    {"id":"26850","name":"Invokana : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2013-11-29T01:00:00Z","last_updated_date":"2013-11-29T01:00:00Z","reference_number":"EMA/374133/2013","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/invokana-epar-public-assessment-report_en.pdf"},
    {"id":"26867","name":"Firdapse : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2010-01-28T01:00:00Z","last_updated_date":"2010-01-28T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/firdapse-epar-public-assessment-report_en.pdf"},
    {"id":"26868","name":"Provenge : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2013-10-03T02:00:00Z","last_updated_date":"2015-05-19T02:00:00Z","reference_number":"EMA/440011/2013","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/provenge-epar-public-assessment-report_en.pdf"},
    {"id":"26912","name":"Benepali : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2016-01-28T13:20:00Z","last_updated_date":"2016-01-28T13:20:00Z","reference_number":"EMA/CHMP/819219/2015","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/benepali-epar-public-assessment-report_en.pdf"},
    {"id":"26925","name":"BindRen : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2013-02-21T01:00:00Z","last_updated_date":"2015-04-01T02:00:00Z","reference_number":"EMA/CHMP/169525/2012","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/bindren-epar-public-assessment-report_en.pdf"},
    {"id":"26945","name":"Velphoro : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2014-10-13T02:00:00Z","last_updated_date":"2014-10-13T02:00:00Z","reference_number":"EMA/567960/2014","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/velphoro-epar-public-assessment-report_en.pdf"},
    {"id":"26948","name":"Dexdor : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2011-10-04T02:00:00Z","last_updated_date":"2011-10-04T02:00:00Z","reference_number":"EMA/789509/2011","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/dexdor-epar-public-assessment-report_en.pdf"},
    {"id":"26963","name":"BiResp Spiromax : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2014-05-19T02:00:00Z","last_updated_date":"2014-05-19T02:00:00Z","reference_number":"EMA/CHMP/175684/2014","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/biresp-spiromax-epar-public-assessment-report_en.pdf"},
    {"id":"26980","name":"Natpar : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2017-04-26T18:22:00Z","last_updated_date":"2017-04-26T18:22:00Z","reference_number":"EMA/180882/2017","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/natpar-epar-public-assessment-report_en.pdf"},
    {"id":"27037","name":"Imatinib Teva : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2013-01-17T01:00:00Z","last_updated_date":"2013-01-17T01:00:00Z","reference_number":"EMA/CHMP/593709/2012","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/imatinib-teva-epar-public-assessment-report_en.pdf"},
    {"id":"27044","name":"Chenodeoxycholic acid sigma-tau : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2017-05-05T02:00:00Z","last_updated_date":"2017-05-05T02:00:00Z","reference_number":"EMA/650359/2016","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/chenodeoxycholic-acid-sigma-tau-epar-public-assessment-report_en.pdf"},
    {"id":"27162","name":"Imatinib Teva B.V. : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2018-03-21T01:00:00Z","last_updated_date":"2018-10-09T01:00:00Z","reference_number":"EMA/652456/2017","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/imatinib-teva-bv-epar-public-assessment-report_en.pdf"},
    {"id":"27295","name":"Pemetrexed medac : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2015-12-09T01:00:00Z","last_updated_date":"2015-12-09T01:00:00Z","reference_number":"EMA/671085/2015","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/pemetrexed-medac-epar-public-assessment-report_en.pdf"},
    {"id":"27321","name":"Prasugrel Mylan : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2018-05-24T02:00:00Z","last_updated_date":"2018-05-24T02:00:00Z","reference_number":"EMA/243820/2018","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/prasugrel-mylan-epar-public-assessment-report_en.pdf"},
    {"id":"27331","name":"Tadalafil Lilly : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2008-10-16T02:00:00Z","last_updated_date":"2008-10-16T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/tadalafil-lilly-epar-public-assessment-report_en.pdf-0"},
    {"id":"27339","name":"Eryseng : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2014-10-02T02:00:00Z","last_updated_date":"2025-09-09T02:00:00Z","reference_number":"EMA/289511/2014","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/eryseng-epar-public-assessment-report_en.pdf"},
    {"id":"27407","name":"Xofigo : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2013-11-28T01:00:00Z","last_updated_date":"2013-11-28T01:00:00Z","reference_number":"EMA/CHMP/578779/2013","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/xofigo-epar-public-assessment-report_en.pdf"},
    {"id":"27473","name":"Lenvima : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2015-06-25T02:00:00Z","last_updated_date":"2015-06-25T02:00:00Z","reference_number":"EMA/250082/2015","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/lenvima-epar-public-assessment-report_en.pdf"},
    {"id":"27486","name":"Olanzapine Glenmark : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2010-01-29T01:00:00Z","last_updated_date":"2010-01-29T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/olanzapine-glenmark-epar-public-assessment-report_en.pdf"},
    {"id":"27539","name":"Numient : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2015-11-25T01:00:00Z","last_updated_date":"2015-11-25T01:00:00Z","reference_number":"EMA/CHMP/672104/2015","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/numient-epar-public-assessment-report_en.pdf"},
    {"id":"27544","name":"Human IGG1 monoclonal antibody specific for human interleukin-1 alpha XBiotech : EPAR - Refusal public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2017-11-13T01:00:00Z","last_updated_date":"2017-11-13T01:00:00Z","reference_number":"EMA/CHMP/552293/2017","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/human-igg1-monoclonal-antibody-specific-human-interleukin-1-alpha-xbiotech-epar-refusal-public-assessment-report_en.pdf"},
    {"id":"27558","name":"Zykadia : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2015-06-04T02:00:00Z","last_updated_date":"2015-06-04T02:00:00Z","reference_number":"EMA/170114/2015","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/zykadia-epar-public-assessment-report_en.pdf"},
    {"id":"27614","name":"Rixathon : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2017-07-28T16:56:00Z","last_updated_date":"2017-07-28T16:56:00Z","reference_number":"EMA/303207/2017","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/rixathon-epar-public-assessment-report_en.pdf"},
    {"id":"27683","name":"Olanzapine Mylan : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2008-10-16T02:09:21Z","last_updated_date":"2008-10-16T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/olanzapine-mylan-epar-public-assessment-report_en.pdf"},
    {"id":"27724","name":"Sprimeo HCT : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2011-09-07T02:00:00Z","last_updated_date":"2012-08-28T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/sprimeo-hct-epar-public-assessment-report_en.pdf"},
    {"id":"27725","name":"Vosevi : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2017-09-22T02:00:00Z","last_updated_date":"2017-09-22T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/vosevi-epar-public-assessment-report_en.pdf"},
    {"id":"27745","name":"Rasagiline Mylan : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2016-04-29T02:00:00Z","last_updated_date":"2016-04-29T02:00:00Z","reference_number":"EMA/282791/2016","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/rasagiline-mylan-epar-public-assessment-report_en.pdf"},
    {"id":"27750","name":"Tadalafil Mylan : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2014-12-19T01:00:00Z","last_updated_date":"2014-12-19T01:00:00Z","reference_number":"EMA/707959/2014","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/tadalafil-mylan-epar-public-assessment-report_en.pdf"},
    {"id":"27851","name":"Memantine LEK : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2013-04-29T02:00:00Z","last_updated_date":"2024-10-23T02:00:00Z","reference_number":"EMA/227468/2013","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/memantine-lek-epar-public-assessment-report_en.pdf"},
    {"id":"27877","name":"EndolucinBeta : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2016-07-14T19:00:00Z","last_updated_date":"2016-07-14T19:00:00Z","reference_number":"EMA/CHMP/404078/2016","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/endolucinbeta-epar-public-assessment-report_en.pdf"},
    {"id":"28007","name":"Lyxumia  : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2013-03-14T17:30:00Z","last_updated_date":"2026-02-05T17:30:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/lyxumia-epar-public-assessment-report_en.pdf"},
    {"id":"28049","name":"Dinutuximab beta Apeiron : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2017-05-15T02:00:00Z","last_updated_date":"2017-05-15T02:00:00Z","reference_number":"EMA/263814/2017","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/dinutuximab-beta-apeiron-epar-public-assessment-report_en.pdf"},
    {"id":"28085","name":"Evalon : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2016-05-13T02:00:00Z","last_updated_date":"2025-09-09T17:54:00Z","reference_number":"EMA/142422/2016-Rev.1","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/evalon-epar-public-assessment-report_en.pdf"},
    {"id":"28110","name":"Kisqali : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2017-08-31T02:00:00Z","last_updated_date":"2017-08-31T02:00:00Z","reference_number":"EMA/CHMP/506968/2017","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/kisqali-epar-public-assessment-report_en.pdf"},
    {"id":"28131","name":"Clynav : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2017-07-20T02:00:00Z","last_updated_date":"2025-09-04T02:00:00Z","reference_number":"EMA/293169/2016","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/clynav-epar-public-assessment-report_en.pdf"},
    {"id":"28244","name":"Impulsor : EPAR - Refusal public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2010-04-26T02:00:00Z","last_updated_date":"2010-04-26T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/impulsor-epar-refusal-public-assessment-report_en.pdf"},
    {"id":"28249","name":"Porcilis ColiClos : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2013-06-13T15:30:00Z","last_updated_date":"2024-11-05T17:49:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/porcilis-coliclos-epar-public-assessment-report_en.pdf"},
    {"id":"28281","name":"Zelnorm : EPAR - Refusal public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2007-10-22T02:09:21Z","last_updated_date":"2007-10-22T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/zelnorm-epar-refusal-public-assessment-report_en.pdf"},
    {"id":"28340","name":"Edistride : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2015-12-10T01:00:00Z","last_updated_date":"2015-12-10T01:00:00Z","reference_number":"EMA/679678/2015","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/edistride-epar-public-assessment-report_en.pdf"},
    {"id":"28362","name":"Twynsta-H-C-1224-A31-0017 : EPAR - Assessment Report - Article 31","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2014-10-03T02:00:00Z","last_updated_date":"2014-10-03T02:00:00Z","reference_number":"EMA/PRAC/294920/2014","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/twynsta-h-c-1224-a31-0017-epar-assessment-report-article-31_en.pdf"},
    {"id":"28378","name":"Vizarsin : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2009-10-12T02:00:00Z","last_updated_date":"2009-10-12T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/vizarsin-epar-public-assessment-report_en.pdf"},
    {"id":"28394","name":"Adcetris : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2012-11-22T11:00:00Z","last_updated_date":"2012-11-22T11:00:00Z","reference_number":"EMA/702390/2012","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/adcetris-epar-public-assessment-report_en.pdf"},
    {"id":"28456","name":"Zytiga : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2011-09-23T02:00:00Z","last_updated_date":"2011-09-23T11:35:00Z","reference_number":"EMA/CHMP/542871/2011","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/zytiga-epar-public-assessment-report_en.pdf"},
    {"id":"28458","name":"Zessly : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2018-05-30T12:03:00Z","last_updated_date":"2018-05-30T12:03:00Z","reference_number":"EMA/223369/2018","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/zessly-epar-public-assessment-report_en.pdf"},
    {"id":"28499","name":"Triumeq : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2014-10-15T02:00:00Z","last_updated_date":"2014-10-15T02:00:00Z","reference_number":"EMA/580654/2014","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/triumeq-epar-public-assessment-report_en.pdf"},
    {"id":"28507","name":"Solumarv : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2016-02-16T01:00:00Z","last_updated_date":"2016-02-16T01:00:00Z","reference_number":"EMA/596513/2015","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/solumarv-epar-public-assessment-report_en.pdf"},
    {"id":"28527","name":"Teysuno : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2011-03-30T02:00:00Z","last_updated_date":"2011-03-30T02:00:00Z","reference_number":"EMA/CHMP/831565/2010","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/teysuno-epar-public-assessment-report_en.pdf"},
    {"id":"28553","name":"Voriconazole Accord : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2013-06-07T11:00:00Z","last_updated_date":"2013-06-07T11:00:00Z","reference_number":"EMA/CHMP/151290/2013","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/voriconazole-accord-epar-public-assessment-report_en.pdf"},
    {"id":"28558","name":"Pregabalin Zentiva k.s. : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2017-03-06T01:00:00Z","last_updated_date":"2023-03-20T01:00:00Z","reference_number":"EMA/14344/2017","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/pregabalin-zentiva-ks-epar-public-assessment-report_en.pdf"},
    {"id":"28602","name":"Yellox : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2011-06-14T02:00:00Z","last_updated_date":"2011-06-14T02:00:00Z","reference_number":"EMA/431843/2011","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/yellox-epar-public-assessment-report_en.pdf"},
    {"id":"28610","name":"Zyllt : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2009-10-14T02:09:21Z","last_updated_date":"2009-10-14T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/zyllt-epar-public-assessment-report_en.pdf"},
    {"id":"28616","name":"Amglidia : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2018-06-08T16:01:00Z","last_updated_date":"2018-06-08T16:01:00Z","reference_number":"EMA/153558/2018","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/amglidia-epar-public-assessment-report_en.pdf"},
    {"id":"28661","name":"Senshio : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2015-02-17T01:00:00Z","last_updated_date":"2015-02-17T01:00:00Z","reference_number":"EMA/78875/2015","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/senshio-epar-public-assessment-report_en.pdf"},
    {"id":"28667","name":"Lemtrada : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2013-09-25T02:00:00Z","last_updated_date":"2013-09-25T02:00:00Z","reference_number":"EMA/563018/2013","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/lemtrada-epar-public-assessment-report_en.pdf"},
    {"id":"28676","name":"Signifor : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2012-06-01T02:00:00Z","last_updated_date":"2012-06-01T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/signifor-epar-public-assessment-report_en.pdf"},
    {"id":"28686","name":"Resolor : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2009-11-17T01:00:00Z","last_updated_date":"2009-11-17T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/resolor-epar-public-assessment-report_en.pdf"},
    {"id":"28702","name":"Jorveza : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2018-01-18T01:00:00Z","last_updated_date":"2018-01-18T01:00:00Z","reference_number":"EMA/774645/2017","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/jorveza-epar-public-assessment-report_en.pdf"},
    {"id":"28724","name":"Rezolsta : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2014-12-12T01:00:00Z","last_updated_date":"2014-12-12T01:00:00Z","reference_number":"EMA/669488/2014 Corr.","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/rezolsta-epar-public-assessment-report_en.pdf"},
    {"id":"28780","name":"Stayveer : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2013-07-02T18:30:00Z","last_updated_date":"2013-07-02T18:30:00Z","reference_number":"EMA/CHMP/294640/2013","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/stayveer-epar-public-assessment-report_en.pdf"},
    {"id":"28804","name":"Imlygic : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2016-02-05T01:00:00Z","last_updated_date":"2019-12-03T16:00:00Z","reference_number":"EMA/734400/2015 corr. 1","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/imlygic-epar-public-assessment-report_en.pdf"},
    {"id":"28810","name":"Pandemic influenza vaccine H5N1 MedImmune : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2016-06-02T02:00:00Z","last_updated_date":"2016-06-02T02:00:00Z","reference_number":"EMA/CHMP/323530/2016","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/pandemic-influenza-vaccine-h5n1-medimmune-epar-public-assessment-report_en.pdf"},
    {"id":"28814","name":"Docetaxel Mylan : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2012-02-17T16:55:00Z","last_updated_date":"2015-03-12T16:55:00Z","reference_number":"EMA/40836/2012","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/docetaxel-mylan-epar-public-assessment-report_en.pdf"},
    {"id":"28857","name":"Aerivio Spiromax : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2016-09-02T02:00:00Z","last_updated_date":"2020-01-15T02:00:00Z","reference_number":"EMA/486136/2016","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/aerivio-spiromax-epar-public-assessment-report_en.pdf"},
    {"id":"28882","name":"Istodax : EPAR - Refusal public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2013-03-14T01:00:00Z","last_updated_date":"2013-03-14T01:00:00Z","reference_number":"EMA/CHMP/27767/2013","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/istodax-epar-refusal-public-assessment-report_en.pdf"},
    {"id":"28941","name":"Fexeric : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2015-10-02T02:00:00Z","last_updated_date":"2015-10-02T02:00:00Z","reference_number":"EMA/CHMP/535898/2015","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/fexeric-epar-public-assessment-report_en.pdf"},
    {"id":"29091","name":"Latuda : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2014-04-08T16:00:00Z","last_updated_date":"2014-04-08T16:00:00Z","reference_number":"EMA/113836/2014","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/latuda-epar-public-assessment-report_en.pdf"},
    {"id":"29094","name":"Akynzeo : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2015-06-23T02:00:00Z","last_updated_date":"2015-06-23T02:00:00Z","reference_number":"EMA/236963/2015","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/akynzeo-epar-public-assessment-report_en.pdf"},
    {"id":"29098","name":"Trazimera : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2018-08-16T02:00:00Z","last_updated_date":"2018-08-16T02:00:00Z","reference_number":"EMA/414095/2018","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/trazimera-epar-public-assessment-report_en.pdf"},
    {"id":"29216","name":"Sevelamer carbonate Zentiva : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2015-03-13T01:00:00Z","last_updated_date":"2015-03-13T01:00:00Z","reference_number":"EMA/CHMP/473530/2014","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/sevelamer-carbonate-zentiva-epar-public-assessment-report_en.pdf"},
    {"id":"29245","name":"Levodopa/Carbidopa/Entacapone Sandoz : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2013-11-29T01:00:00Z","last_updated_date":"2013-11-29T01:00:00Z","reference_number":"EMA/CHMP/707244/2013","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/levodopacarbidopaentacapone-sandoz-epar-public-assessment-report_en.pdf"},
    {"id":"29247","name":"Menveo : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2010-05-04T02:00:00Z","last_updated_date":"2010-05-04T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/menveo-epar-public-assessment-report_en.pdf"},
    {"id":"29268","name":"Zavicefta : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2016-07-14T02:00:00Z","last_updated_date":"2016-07-14T02:00:00Z","reference_number":"EMA/CHMP/377887/2016","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/zavicefta-epar-public-assessment-report_en.pdf"},
    {"id":"29278","name":"Suvaxyn Circo+MH RTU : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2015-12-22T01:00:00Z","last_updated_date":"2025-10-14T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/suvaxyn-circomh-rtu-epar-public-assessment-report_en.pdf"},
    {"id":"29291","name":"Otezla : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2015-02-16T01:00:00Z","last_updated_date":"2015-02-16T01:00:00Z","reference_number":"EMA/CHMP/476353/2014","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/otezla-epar-public-assessment-report_en.pdf"},
    {"id":"29295","name":"Levetiracetam Sun : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2012-01-17T01:00:00Z","last_updated_date":"2012-01-17T01:00:00Z","reference_number":"EMA/CHMP/657653/2011","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/levetiracetam-sun-epar-public-assessment-report_en.pdf"},
    {"id":"29335","name":"Capecitabine Medac : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2012-11-29T01:00:00Z","last_updated_date":"2012-11-29T01:00:00Z","reference_number":"EMA/711212/2012","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/capecitabine-medac-epar-public-assessment-report_en.pdf"},
    {"id":"29348","name":"Efavirenz/Emtricitabine/Tenofovir disoproxil Krka : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2018-02-20T01:00:00Z","last_updated_date":"2018-02-20T01:00:00Z","reference_number":"EMA/846772/2017","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/efavirenzemtricitabinetenofovir-disoproxil-krka-epar-public-assessment-report_en.pdf"},
    {"id":"29437","name":"Spedra : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2013-07-03T17:15:00Z","last_updated_date":"2013-07-03T17:15:00Z","reference_number":"EMA/321885/2013","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/spedra-epar-public-assessment-report_en.pdf"},
    {"id":"29560","name":"Trulicity : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2014-12-19T01:00:00Z","last_updated_date":"2014-12-19T01:00:00Z","reference_number":"EMA/CHMP/524604/2014","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/trulicity-epar-public-assessment-report_en.pdf"},
    {"id":"29664","name":"Aripiprazole Accord : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2015-11-27T01:00:00Z","last_updated_date":"2015-11-27T01:00:00Z","reference_number":"EMA/CHMP/523618/2015","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/aripiprazole-accord-epar-public-assessment-report_en.pdf"},
    {"id":"29715","name":"Tenofovir disoproxil Mylan : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2016-12-19T12:29:00Z","last_updated_date":"2016-12-19T12:29:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/tenofovir-disoproxil-mylan-epar-public-assessment-report_en.pdf"},
    {"id":"29789","name":"Filgrastim ratiopharm : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2008-09-30T02:00:00Z","last_updated_date":"2011-07-20T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/filgrastim-ratiopharm-epar-public-assessment-report_en.pdf"},
    {"id":"29841","name":"Kyntheum : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2017-08-03T02:00:00Z","last_updated_date":"2017-08-03T02:00:00Z","reference_number":"EMA/381484/2017","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/kyntheum-epar-public-assessment-report_en.pdf"},
    {"id":"29852","name":"Trajenta : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2011-10-06T02:00:00Z","last_updated_date":"2011-10-06T02:00:00Z","reference_number":"EMA/604444/2011","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/trajenta-epar-public-assessment-report_en.pdf"},
    {"id":"29877","name":"Plegridy : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2014-07-31T02:00:00Z","last_updated_date":"2016-01-27T01:00:00Z","reference_number":"EMA/339024/2014","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/plegridy-epar-public-assessment-report_en.pdf"},
    {"id":"29909","name":"Topotecan Teva : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2009-10-06T02:00:00Z","last_updated_date":"2009-10-06T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/topotecan-teva-epar-public-assessment-report_en.pdf"},
    {"id":"29980","name":"Velmetia : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2008-08-06T02:00:00Z","last_updated_date":"2008-08-06T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/velmetia-epar-public-assessment-report_en.pdf"},
    {"id":"29985","name":"Laventair : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2014-06-13T02:00:00Z","last_updated_date":"2014-06-13T02:00:00Z","reference_number":"EMA/CHMP/163506/2014","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/laventair-epar-public-assessment-report_en.pdf"},
    {"id":"30048","name":"Adlumiz : EPAR - Refusal public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2017-11-30T12:20:00Z","last_updated_date":"2017-11-30T12:20:00Z","reference_number":"EMA/647868/2017","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/adlumiz-epar-refusal-public-assessment-report_en.pdf"},
    {"id":"30068","name":"Vectra Felis : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2014-06-27T02:00:00Z","last_updated_date":"2025-10-15T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/vectra-felis-epar-public-assessment-report_en.pdf"},
    {"id":"30097","name":"Memantine ratiopharm : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2013-06-20T02:00:00Z","last_updated_date":"2013-06-20T02:00:00Z","reference_number":"EMA/328117/2013","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/memantine-ratiopharm-epar-public-assessment-report_en.pdf"},
    {"id":"30132","name":"Nevirapine Teva : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2009-12-14T01:00:00Z","last_updated_date":"2023-03-21T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/nevirapine-teva-epar-public-assessment-report_en.pdf"},
    {"id":"30144","name":"Nitisinone MendeliKABS : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2017-10-05T02:00:00Z","last_updated_date":"2023-06-14T02:00:00Z","reference_number":"EMA/CHMP/502860/2017","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/nitisinone-mendelikabs-epar-public-assessment-report_en.pdf"},
    {"id":"30161","name":"Pemetrexed Hospira UK Limited : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2017-05-30T02:00:00Z","last_updated_date":"2021-07-28T02:00:00Z","reference_number":"EMA/CHMP/270680/2017","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/pemetrexed-hospira-uk-limited-epar-public-assessment-report_en.pdf"},
    {"id":"30173","name":"Hirobriz Breezhaler : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2010-01-05T01:00:00Z","last_updated_date":"2010-01-05T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/hirobriz-breezhaler-epar-public-assessment-report_en.pdf"},
    {"id":"30188","name":"Vizamyl : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2014-09-17T02:00:00Z","last_updated_date":"2014-09-17T02:00:00Z","reference_number":"EMA/546752/2014","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/vizamyl-epar-public-assessment-report_en.pdf"},
    {"id":"30260","name":"Nobivac Myxo-RHD : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2011-09-26T02:00:00Z","last_updated_date":"2023-09-12T13:32:00Z","reference_number":"EMA/646849/2011 Rev. 1","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/nobivac-myxo-rhd-epar-public-assessment-report_en.pdf"},
    {"id":"30305","name":"Nemdatine : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2013-04-30T02:00:00Z","last_updated_date":"2013-04-30T02:00:00Z","reference_number":"EMA/228869/2013","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/nemdatine-epar-public-assessment-report_en.pdf"},
    {"id":"30330","name":"Zopya : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2009-10-14T02:00:00Z","last_updated_date":"2009-10-14T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/zopya-epar-public-assessment-report_en.pdf"},
    {"id":"30351","name":"Docetaxel Teva Pharma : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2011-02-03T01:00:00Z","last_updated_date":"2014-01-29T01:00:00Z","reference_number":"EMA/32518/2011","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/docetaxel-teva-pharma-epar-public-assessment-report_en.pdf"},
    {"id":"30382","name":"Izba : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2014-03-17T15:00:00Z","last_updated_date":"2014-03-17T15:00:00Z","reference_number":"EMA/13480/2014","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/izba-epar-public-assessment-report_en.pdf"},
    {"id":"30406","name":"Imatinib Accord : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2013-07-10T02:00:00Z","last_updated_date":"2013-07-10T02:00:00Z","reference_number":"EMA/389694/2013","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/imatinib-accord-epar-public-assessment-report_en.pdf"},
    {"id":"30422","name":"Sialanar : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2016-09-29T02:00:00Z","last_updated_date":"2016-09-29T02:00:00Z","reference_number":"EMA/555265/2016","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/sialanar-epar-public-assessment-report_en.pdf"},
    {"id":"30435","name":"Memantine Mylan : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2013-04-29T02:00:00Z","last_updated_date":"2013-04-29T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/memantine-mylan-epar-public-assessment-report_en.pdf"},
    {"id":"30488","name":"Dutrebis : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2015-04-21T02:00:00Z","last_updated_date":"2017-04-27T02:00:00Z","reference_number":"EMA/154027/2015","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/dutrebis-epar-public-assessment-report_en.pdf"},
    {"id":"30505","name":"Topotecan Eagle : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2012-01-12T01:00:00Z","last_updated_date":"2014-11-14T01:00:00Z","reference_number":"EMA/1352/2012","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/topotecan-eagle-epar-public-assessment-report_en.pdf"},
    {"id":"30532","name":"Zulvac SBV : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2015-03-02T01:00:00Z","last_updated_date":"2025-10-15T16:50:00Z","reference_number":"EMA/786089/2014","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/zulvac-sbv-epar-public-assessment-report_en.pdf"},
    {"id":"30534","name":"Telmisartan Teva Pharma : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2011-10-18T02:00:00Z","last_updated_date":"2011-10-18T02:00:00Z","reference_number":"EMA/777686/2011","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/telmisartan-teva-pharma-epar-public-assessment-report_en.pdf"},
    {"id":"30614","name":"Cuprior : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2017-10-03T19:00:00Z","last_updated_date":"2017-10-03T19:00:00Z","reference_number":"EMA/308946/2017","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/cuprior-epar-public-assessment-report_en.pdf"},
    {"id":"30672","name":"Vibativ   : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2011-09-28T13:00:00Z","last_updated_date":"2018-05-16T13:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/vibativ-epar-public-assessment-report_en.pdf"},
    {"id":"30682","name":"Strensiq : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2015-09-28T02:00:00Z","last_updated_date":"2015-09-28T02:00:00Z","reference_number":"EMA/CHMP/383178/2015","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/strensiq-epar-public-assessment-report_en.pdf"},
    {"id":"30731","name":"Elelyso : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2012-11-23T01:00:00Z","last_updated_date":"2012-11-23T01:00:00Z","reference_number":"EMA/CHMP/399615/2012","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/elelyso-epar-public-assessment-report_en.pdf"},
    {"id":"30732","name":"Myfenax : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2008-04-08T02:00:00Z","last_updated_date":"2008-04-08T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/myfenax-epar-public-assessment-report_en.pdf"},
    {"id":"30767","name":"Lamivudine Teva Pharma B.V. : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2009-12-16T01:00:00Z","last_updated_date":"2009-12-16T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/lamivudine-teva-pharma-bv-epar-public-assessment-report_en.pdf"},
    {"id":"30781","name":"Docetaxel Accord : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2012-06-11T02:00:00Z","last_updated_date":"2012-06-11T02:00:00Z","reference_number":"EMA/339179/2012","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/docetaxel-accord-epar-public-assessment-report_en.pdf"},
    {"id":"30824","name":"Twynsta : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2010-10-19T02:00:00Z","last_updated_date":"2010-10-19T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/twynsta-epar-public-assessment-report_en.pdf"},
    {"id":"30903","name":"Cerdelga : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2015-02-13T01:00:00Z","last_updated_date":"2015-02-13T01:00:00Z","reference_number":"EMA/57549/2015","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/cerdelga-epar-public-assessment-report_en.pdf"},
    {"id":"30943","name":"Hefiya : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2018-08-06T16:44:00Z","last_updated_date":"2018-08-06T16:44:00Z","reference_number":"EMA/CHMP/520007/2018","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/hefiya-epar-public-assessment-report_en.pdf"},
    {"id":"30953","name":"Bydureon : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2011-07-05T02:00:00Z","last_updated_date":"2022-08-01T10:48:00Z","reference_number":"EMA/CHMP/644257/2022","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/bydureon-epar-public-assessment-report_en.pdf"},
    {"id":"30995","name":"Alkindi : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2018-03-01T01:00:00Z","last_updated_date":"2018-03-01T01:00:00Z","reference_number":"EMA/4145/2018","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/alkindi-epar-public-assessment-report_en.pdf"},
    {"id":"31079","name":"Zontivity : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2015-03-02T11:30:00Z","last_updated_date":"2017-09-20T12:30:00Z","reference_number":"EMA/CHMP/85159/2015","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/zontivity-epar-public-assessment-report_en.pdf"},
    {"id":"31139","name":"Pelzont : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2008-07-10T02:00:00Z","last_updated_date":"2008-07-10T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/pelzont-epar-public-assessment-report_en.pdf"},
    {"id":"31224","name":"Vaxelis : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2016-02-26T01:00:00Z","last_updated_date":"2016-02-26T01:00:00Z","reference_number":"EMA/CHMP/72003/2016","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/vaxelis-epar-public-assessment-report_en.pdf"},
    {"id":"31249","name":"Rolufta : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2017-03-23T01:00:00Z","last_updated_date":"2017-03-23T01:00:00Z","reference_number":"EMA/CHMP/148961/2017","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/rolufta-epar-public-assessment-report_en.pdf"},
    {"id":"31334","name":"Zejula : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2017-11-27T01:00:00Z","last_updated_date":"2017-11-27T01:00:00Z","reference_number":"EMA/648982/2017","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/zejula-epar-public-assessment-report_en.pdf"},
    {"id":"31337","name":"Rivastigmine Actavis : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2011-07-11T02:00:00Z","last_updated_date":"2011-07-11T02:00:00Z","reference_number":"EMA/454217/2011","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/rivastigmine-actavis-epar-public-assessment-report_en.pdf"},
    {"id":"31347","name":"Pomalidomide Celgene : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2013-08-13T02:00:00Z","last_updated_date":"2013-08-13T02:00:00Z","reference_number":"EMA/CHMP/427059/2013","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/pomalidomide-celgene-epar-public-assessment-report_en.pdf"},
    {"id":"31359","name":"Memantine Accord : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2013-12-16T01:00:00Z","last_updated_date":"2013-12-16T01:00:00Z","reference_number":"EMA/610378/2013","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/memantine-accord-epar-public-assessment-report_en.pdf"},
    {"id":"31385","name":"Odomzo : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2015-09-02T02:00:00Z","last_updated_date":"2015-09-02T02:00:00Z","reference_number":"EMA/472165/2015","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/odomzo-epar-public-assessment-report_en.pdf"},
    {"id":"31438","name":"Proteq West Nile : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2011-08-15T02:00:00Z","last_updated_date":"2011-08-15T02:00:00Z","reference_number":"EMA/541960/2011","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/proteq-west-nile-epar-public-assessment-report_en.pdf"},
    {"id":"31448","name":"Zurampic : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2016-03-09T01:00:00Z","last_updated_date":"2016-03-09T01:00:00Z","reference_number":"EMA/6459/2016","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/zurampic-epar-public-assessment-report_en.pdf"},
    {"id":"31495","name":"Ristaben : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2010-03-29T02:00:00Z","last_updated_date":"2010-03-29T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/ristaben-epar-public-assessment-report_en.pdf"},
    {"id":"31521","name":"Cinqaero : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2016-09-02T02:00:00Z","last_updated_date":"2016-09-02T02:00:00Z","reference_number":"EMA/CHMP/481610/2016","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/cinqaero-epar-public-assessment-report_en.pdf"},
    {"id":"31553","name":"Firazyr : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2008-07-21T02:00:00Z","last_updated_date":"2008-07-21T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/firazyr-epar-public-assessment-report_en.pdf"},
    {"id":"31597","name":"Clopidogrel Krka : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2009-10-20T02:00:00Z","last_updated_date":"2009-10-20T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/clopidogrel-krka-epar-public-assessment-report_en.pdf"},
    {"id":"31598","name":"Betmiga : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2013-01-15T18:00:00Z","last_updated_date":"2013-01-15T18:00:00Z","reference_number":"EMA/706651/2012","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/betmiga-epar-public-assessment-report_en.pdf"},
    {"id":"31641","name":"Yargesa : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2017-04-10T18:57:00Z","last_updated_date":"2017-04-10T18:57:00Z","reference_number":"EMA/103540/2017","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/yargesa-epar-public-assessment-report_en.pdf"},
    {"id":"31650","name":"Xalkori : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2012-11-14T01:00:00Z","last_updated_date":"2012-11-14T01:00:00Z","reference_number":"EMA/CHMP/497137/2012","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/xalkori-epar-public-assessment-report_en.pdf"},
    {"id":"31678","name":"Efavirenz Teva : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2012-01-27T01:00:00Z","last_updated_date":"2012-01-27T01:00:00Z","reference_number":"EMA/916997/2011","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/efavirenz-teva-epar-public-assessment-report_en.pdf"},
    {"id":"31759","name":"Hetlioz : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2015-07-22T02:00:00Z","last_updated_date":"2015-07-22T02:00:00Z","reference_number":"EMA/CHMP/601383/2014","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/hetlioz-epar-public-assessment-report_en.pdf"},
    {"id":"31846","name":"Docetaxel Teva : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2010-02-11T01:00:00Z","last_updated_date":"2021-12-14T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/docetaxel-teva-epar-public-assessment-report_en.pdf"},
    {"id":"31912","name":"Focetria : EPAR - Assessment Report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2009-10-01T02:00:00Z","last_updated_date":"2009-10-01T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/focetria-epar-assessment-report_en.pdf"},
    {"id":"31925","name":"Entecavir Accord : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2018-01-26T16:41:00Z","last_updated_date":"2018-01-26T16:41:00Z","reference_number":"EMA/520001/2017","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/entecavir-accord-epar-public-assessment-report_en.pdf"},
    {"id":"31947","name":"Mepsevii : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2018-08-28T02:00:00Z","last_updated_date":"2018-08-28T02:00:00Z","reference_number":"EMA/480950/2018","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/mepsevii-epar-public-assessment-report_en.pdf"},
    {"id":"31964","name":"Temozolomide Sun : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2011-08-02T02:00:00Z","last_updated_date":"2011-08-02T02:00:00Z","reference_number":"EMA/555661/2011","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/temozolomide-sun-epar-public-assessment-report_en.pdf"},
    {"id":"31991","name":"Cholib : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2013-09-18T02:00:00Z","last_updated_date":"2013-09-18T02:00:00Z","reference_number":"EMA/CHMP/308856/2013","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/cholib-epar-public-assessment-report_en.pdf"},
    {"id":"32043","name":"Vectormune ND : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2015-10-12T02:00:00Z","last_updated_date":"2024-02-15T15:43:00Z","reference_number":"EMA/469665/2015","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/vectormune-nd-epar-public-assessment-report_en.pdf"},
    {"id":"32063","name":"Olysio : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2014-06-04T02:00:00Z","last_updated_date":"2018-05-23T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/olysio-epar-public-assessment-report_en.pdf"},
    {"id":"32064","name":"Suvaxyn Circo : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2018-04-20T11:47:00Z","last_updated_date":"2025-10-14T11:47:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/suvaxyn-circo-epar-public-assessment-report_en.pdf"},
    {"id":"32113","name":"Javlor : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2009-10-08T02:09:21Z","last_updated_date":"2009-10-08T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/javlor-epar-public-assessment-report_en.pdf"},
    {"id":"32132","name":"Ioa : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2012-01-23T01:00:00Z","last_updated_date":"2014-08-28T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/ioa-epar-public-assessment-report_en.pdf"},
    {"id":"32134","name":"Qsiva : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2013-06-13T12:10:00Z","last_updated_date":"2013-06-13T12:10:00Z","reference_number":"EMA/CHMP/108692/2013","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/qsiva-epar-public-assessment-report_en.pdf"},
    {"id":"32180","name":"Fluenz  : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2011-03-17T01:00:00Z","last_updated_date":"2014-12-03T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/fluenz-epar-public-assessment-report_en.pdf"},
    {"id":"32294","name":"Zonisamide Mylan : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2016-04-06T02:00:00Z","last_updated_date":"2016-04-06T02:00:00Z","reference_number":"EMA/170957/2016","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/zonisamide-mylan-epar-public-assessment-report_en.pdf"},
    {"id":"32349","name":"Ikervis : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2015-05-07T02:00:00Z","last_updated_date":"2015-05-07T02:00:00Z","reference_number":"EMA/CHMP/473489/2014","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/ikervis-epar-public-assessment-report_en.pdf"},
    {"id":"32374","name":"Daklinza : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2014-09-15T02:00:00Z","last_updated_date":"2014-09-15T02:00:00Z","reference_number":"EMA/419836/2014","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/daklinza-epar-public-assessment-report_en.pdf"},
    {"id":"32417","name":"Vantobra : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2015-03-19T01:00:00Z","last_updated_date":"2019-03-29T01:00:00Z","reference_number":"EMA/86872/2015","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/vantobra-epar-public-assessment-report_en.pdf"},
    {"id":"32426","name":"Clopidogrel Teva Pharma B.V. : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2011-06-30T02:00:00Z","last_updated_date":"2015-02-03T01:00:00Z","reference_number":"WC500108104.pdf","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/clopidogrel-teva-pharma-bv-epar-public-assessment-report_en.pdf"},
    {"id":"32446","name":"Terrosa : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2017-03-16T01:00:00Z","last_updated_date":"2017-03-16T01:00:00Z","reference_number":"EMA/84371/2017","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/terrosa-epar-public-assessment-report_en.pdf"},
    {"id":"32482","name":"Tadalafil Generics : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2017-01-26T01:00:00Z","last_updated_date":"2017-01-26T01:00:00Z","reference_number":"EMA/803097/2016","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/tadalafil-generics-epar-public-assessment-report_en.pdf"},
    {"id":"32689","name":"Raxone : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2015-09-17T02:00:00Z","last_updated_date":"2015-09-17T02:00:00Z","reference_number":"EMA/480039/2015","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/raxone-epar-public-assessment-report_en.pdf"},
    {"id":"32741","name":"Pandemic Influenza Vaccine H5N1 Baxter : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2009-12-17T01:00:00Z","last_updated_date":"2023-09-13T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/pandemic-influenza-vaccine-h5n1-baxter-epar-public-assessment-report_en.pdf"},
    {"id":"32744","name":"Actelsar HCT : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2013-03-26T14:00:00Z","last_updated_date":"2013-03-26T14:00:00Z","reference_number":"EMA/163479/2013","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/actelsar-hct-epar-public-assessment-report_en.pdf"},
    {"id":"32768","name":"Telmisartan Actavis : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2010-10-20T02:00:00Z","last_updated_date":"2010-10-20T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/telmisartan-actavis-epar-public-assessment-report_en.pdf"},
    {"id":"32806","name":"Ulipristal Acetate Gedeon Richter : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2018-09-06T02:00:00Z","last_updated_date":"2021-07-02T02:00:00Z","reference_number":"EMA/483416/2018","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/ulipristal-acetate-gedeon-richter-epar-public-assessment-report_en.pdf"},
    {"id":"32842","name":"Anagrelide Mylan : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2018-02-27T01:00:00Z","last_updated_date":"2018-02-27T01:00:00Z","reference_number":"EMA/63484/2018","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/anagrelide-mylan-epar-public-assessment-report_en.pdf"},
    {"id":"32899","name":"Intuniv : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2015-10-06T02:00:00Z","last_updated_date":"2015-10-06T02:00:00Z","reference_number":"EMA/CHMP/534329/2015","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/intuniv-epar-public-assessment-report_en.pdf"},
    {"id":"32924","name":"Envarsus : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2014-07-31T02:00:00Z","last_updated_date":"2014-07-31T02:00:00Z","reference_number":"EMA/CHMP/81205/2014","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/envarsus-epar-public-assessment-report_en.pdf"},
    {"id":"32959","name":"Ebymect : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2015-11-23T01:00:00Z","last_updated_date":"2015-11-23T01:00:00Z","reference_number":"EMA/679419/2015","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/ebymect-epar-public-assessment-report_en.pdf"},
    {"id":"33008","name":"Palonosetron Hospira : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2016-04-21T02:00:00Z","last_updated_date":"2022-04-08T02:00:00Z","reference_number":"EMA/215640/2016","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/palonosetron-hospira-epar-public-assessment-report_en.pdf"},
    {"id":"33036","name":"Eviplera : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2011-12-12T01:00:00Z","last_updated_date":"2011-12-12T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/eviplera-epar-public-assessment-report_en.pdf"},
    {"id":"33077","name":"Ribavirin BioPartners : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2010-04-26T02:00:00Z","last_updated_date":"2013-05-06T12:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/ribavirin-biopartners-epar-public-assessment-report_en.pdf"},
    {"id":"33105","name":"Episalvan : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2016-02-05T01:00:00Z","last_updated_date":"2022-07-15T13:42:00Z","reference_number":"EMA/833320/2015","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/episalvan-epar-public-assessment-report_en.pdf"},
    {"id":"33115","name":"Imvanex : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2013-08-16T02:00:00Z","last_updated_date":"2013-08-16T02:00:00Z","reference_number":"EMA/369203/2013","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/imvanex-epar-public-assessment-report_en.pdf"},
    {"id":"33117","name":"Ristempa : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2015-04-16T02:00:00Z","last_updated_date":"2018-03-07T01:00:00Z","reference_number":"EMA/187414/2015","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/ristempa-epar-public-assessment-report_en.pdf"},
    {"id":"33138","name":"Qutenza : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2009-06-09T02:00:00Z","last_updated_date":"2009-06-09T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/qutenza-epar-public-assessment-report_en.pdf"},
    {"id":"33149","name":"Firmagon : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2009-03-04T01:00:00Z","last_updated_date":"2009-03-04T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/firmagon-epar-public-assessment-report_en.pdf"},
    {"id":"33162","name":"Riprazo HCT  : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2011-09-29T02:00:00Z","last_updated_date":"2012-09-20T02:00:00Z","reference_number":"EMA/745107/2011","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/riprazo-hct-epar-public-assessment-report_en.pdf"},
    {"id":"33169","name":"Trobalt : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2011-04-05T02:00:00Z","last_updated_date":"2018-11-19T02:00:00Z","reference_number":"EMA/CHMP/207154/2011","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/trobalt-epar-public-assessment-report_en.pdf"},
    {"id":"33221","name":"Halimatoz : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2018-08-03T02:00:00Z","last_updated_date":"2021-01-29T12:00:00Z","reference_number":"EMA/CHMP/519681/2018","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/halimatoz-epar-public-assessment-report_en.pdf"},
    {"id":"33262","name":"Ivabradine Zentiva : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2017-02-08T01:00:00Z","last_updated_date":"2017-02-08T01:00:00Z","reference_number":"EMA/73167/2017","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/ivabradine-zentiva-epar-public-assessment-report_en.pdf"},
    {"id":"33318","name":"Lacosamide Accord : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2017-09-27T02:00:00Z","last_updated_date":"2017-09-27T02:00:00Z","reference_number":"EMA/518597/2017","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/lacosamide-accord-epar-public-assessment-report_en.pdf"},
    {"id":"33331","name":"Docetaxel Kabi : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2012-06-18T02:00:00Z","last_updated_date":"2012-06-18T02:00:00Z","reference_number":"EMA/305675/2012","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/docetaxel-kabi-epar-public-assessment-report_en.pdf"},
    {"id":"33350","name":"Voncento : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2013-10-04T02:00:00Z","last_updated_date":"2013-10-04T12:30:00Z","reference_number":"EMA/404213/2013","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/voncento-epar-public-assessment-report_en.pdf"},
    {"id":"33356","name":"Tevagrastim : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2008-09-29T02:09:21Z","last_updated_date":"2008-09-29T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/tevagrastim-epar-public-assessment-report_en.pdf"},
    {"id":"33366","name":"Besponsa : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2017-07-13T12:11:00Z","last_updated_date":"2017-12-12T11:11:00Z","reference_number":"EMA/289046/2017","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/besponsa-epar-public-assessment-report_en.pdf"},
    {"id":"33433","name":"Rabitec : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2017-12-18T01:00:00Z","last_updated_date":"2025-10-20T09:15:00Z","reference_number":"EMA/666973/2017","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/rabitec-epar-public-assessment-report_en.pdf"},
    {"id":"33450","name":"Farydak : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2015-09-11T02:00:00Z","last_updated_date":"2015-09-11T02:00:00Z","reference_number":"EMA/CHMP/496296/2015 Rev. 1","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/farydak-epar-public-assessment-report_en.pdf"},
    {"id":"33610","name":"Possia : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2011-01-07T01:00:00Z","last_updated_date":"2011-01-07T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/possia-epar-public-assessment-report_en.pdf"},
    {"id":"33626","name":"Sabervel : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2012-04-23T02:00:00Z","last_updated_date":"2012-04-23T02:00:00Z","reference_number":"EMA/225623/2012","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/sabervel-epar-public-assessment-report_en.pdf"},
    {"id":"33642","name":"Tesavel : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2008-02-14T00:09:21Z","last_updated_date":"2008-02-14T00:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/tesavel-epar-public-assessment-report_en.pdf"},
    {"id":"33701","name":"Fasenra : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2018-03-08T01:00:00Z","last_updated_date":"2018-03-08T01:00:00Z","reference_number":"EMA/780390/2017","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/fasenra-epar-public-assessment-report_en.pdf"},
    {"id":"33739","name":"Strimvelis : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2016-06-08T02:00:00Z","last_updated_date":"2017-10-05T02:00:00Z","reference_number":"EMA/CHMP/323455/2016","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/strimvelis-epar-public-assessment-report_en.pdf"},
    {"id":"33774","name":"Votrient : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2010-07-08T02:00:00Z","last_updated_date":"2010-07-08T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/votrient-epar-public-assessment-report_en.pdf"},
    {"id":"33892","name":"Ledaga : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2017-03-16T14:45:00Z","last_updated_date":"2017-03-16T14:45:00Z","reference_number":"EMA/CHMP/13156/2017","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/ledaga-epar-public-assessment-report_en.pdf"},
    {"id":"33954","name":"Pravafenix  : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2011-05-17T02:00:00Z","last_updated_date":"2011-05-17T02:00:00Z","reference_number":"EMA/79515/2011","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/pravafenix-epar-public-assessment-report_en.pdf"},
    {"id":"33981","name":"Zalmoxis : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2016-09-05T02:00:00Z","last_updated_date":"2016-09-05T02:00:00Z","reference_number":"EMA/CHMP/589978/2016","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/zalmoxis-epar-public-assessment-report_en.pdf"},
    {"id":"34007","name":"Clopidogrel Acino Pharma GmbH : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2009-10-16T02:09:21Z","last_updated_date":"2012-07-26T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/clopidogrel-acino-pharma-gmbh-epar-public-assessment-report_en.pdf"},
    {"id":"34086","name":"Revinty Ellipta : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2014-06-17T02:00:00Z","last_updated_date":"2014-06-17T02:00:00Z","reference_number":"EMA/CHMP/175905/2014","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/revinty-ellipta-epar-public-assessment-report_en.pdf"},
    {"id":"34179","name":"Evicel : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2008-12-09T01:00:00Z","last_updated_date":"2024-08-02T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/evicel-epar-public-assessment-report_en.pdf"},
    {"id":"34203","name":"Alpheon : EPAR - Refusal public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2007-10-22T02:00:00Z","last_updated_date":"2007-10-22T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/alpheon-epar-refusal-public-assessment-report_en.pdf"},
    {"id":"34271","name":"Xgeva : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2011-08-15T02:00:00Z","last_updated_date":"2011-08-15T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/xgeva-epar-public-assessment-report_en.pdf"},
    {"id":"34324","name":"Evotaz : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2015-08-10T02:00:00Z","last_updated_date":"2015-08-10T02:00:00Z","reference_number":"EMA/517796/2015","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/evotaz-epar-public-assessment-report_en.pdf"},
    {"id":"34351","name":"Innovax-ND-IBD : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2017-09-21T11:48:00Z","last_updated_date":"2017-09-21T11:48:00Z","reference_number":"EMA/377164/2017","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/innovax-nd-ibd-epar-public-assessment-report_en.pdf"},
    {"id":"34364","name":"Amgevita : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2017-04-05T02:00:00Z","last_updated_date":"2017-04-05T02:00:00Z","reference_number":"EMA/106922/2017","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/amgevita-epar-public-assessment-report_en.pdf-0"},
    {"id":"34497","name":"Zelboraf : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2012-03-19T13:00:00Z","last_updated_date":"2012-03-19T13:00:00Z","reference_number":"EMA/200986/2012","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/zelboraf-epar-public-assessment-report_en.pdf"},
    {"id":"34525","name":"Jevtana : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2011-04-05T02:00:00Z","last_updated_date":"2012-04-13T16:30:00Z","reference_number":"EMA/CHMP/66633/2011","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/jevtana-epar-public-assessment-report_en.pdf"},
    {"id":"34628","name":"Cimzia : EPAR - Refusal public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2008-05-23T02:00:00Z","last_updated_date":"2008-05-23T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/cimzia-epar-refusal-public-assessment-report_en.pdf"},
    {"id":"34632","name":"Trumenba : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2017-06-06T02:00:00Z","last_updated_date":"2017-06-06T02:00:00Z","reference_number":"EMA/CHMP/232746/2017","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/trumenba-epar-public-assessment-report_en.pdf"},
    {"id":"34643","name":"Ocrevus : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2018-01-11T01:00:00Z","last_updated_date":"2018-01-11T01:00:00Z","reference_number":"EMA/790835/2017","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/ocrevus-epar-public-assessment-report_en.pdf"},
    {"id":"34718","name":"Temozolomide Sandoz : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2010-03-26T01:00:00Z","last_updated_date":"2023-02-27T16:51:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/temozolomide-sandoz-epar-public-assessment-report_en.pdf"},
    {"id":"34754","name":"Darunavir Krka d.d. : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2018-01-25T01:00:00Z","last_updated_date":"2023-02-03T01:00:00Z","reference_number":"EMA/786962/2017","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/darunavir-krka-dd-epar-public-assessment-report_en.pdf"},
    {"id":"34815","name":"Lonquex : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2013-09-02T02:00:00Z","last_updated_date":"2013-09-02T02:00:00Z","reference_number":"EMA/371234/2013","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/lonquex-epar-public-assessment-report_en.pdf"},
    {"id":"34832","name":"SomaKit TOC : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2017-02-20T11:26:00Z","last_updated_date":"2017-02-20T11:26:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/somakit-toc-epar-public-assessment-report_en.pdf"},
    {"id":"34945","name":"Zepatier : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2016-07-28T02:00:00Z","last_updated_date":"2016-07-28T02:00:00Z","reference_number":"EMA/419807/2016","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/zepatier-epar-public-assessment-report_en.pdf"},
    {"id":"34976","name":"Aripiprazole Sandoz : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2015-09-25T02:00:00Z","last_updated_date":"2015-09-25T02:00:00Z","reference_number":"EMA/CHMP/512637/2015","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/aripiprazole-sandoz-epar-public-assessment-report_en.pdf"},
    {"id":"34995","name":"Coliprotec F4 : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2015-03-20T01:00:00Z","last_updated_date":"2015-03-20T01:00:00Z","reference_number":"EMA/39171/2015","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/coliprotec-f4-epar-public-assessment-report_en.pdf"},
    {"id":"35111","name":"Alprolix : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2016-05-25T02:00:00Z","last_updated_date":"2016-05-25T02:00:00Z","reference_number":"EMA/CHMP/196953/2016","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/alprolix-epar-public-assessment-report_en.pdf"},
    {"id":"35162","name":"Duloxetine Boehringer Ingelheim : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2008-10-28T01:00:00Z","last_updated_date":"2008-10-28T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/duloxetine-boehringer-ingelheim-epar-public-assessment-report_en.pdf"},
    {"id":"35175","name":"Alsitek : EPAR - Refusal public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2018-07-31T02:00:00Z","last_updated_date":"2018-07-31T02:00:00Z","reference_number":"EMA/406203/2018","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/alsitek-epar-refusal-public-assessment-report_en.pdf"},
    {"id":"35184","name":"Cinryze : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2011-07-15T02:00:00Z","last_updated_date":"2011-07-15T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/cinryze-epar-public-assessment-report_en.pdf"},
    {"id":"35222","name":"Vidaza : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2009-01-23T01:00:00Z","last_updated_date":"2009-01-23T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/vidaza-epar-public-assessment-report_en.pdf"},
    {"id":"35265","name":"Leflunomide medac : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2010-08-05T02:00:00Z","last_updated_date":"2010-08-05T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/leflunomide-medac-epar-public-assessment-report_en.pdf"},
    {"id":"35286","name":"Incruse : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2014-05-22T02:00:00Z","last_updated_date":"2014-05-22T02:00:00Z","reference_number":"EMA/175100/2014","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/incruse-epar-public-assessment-report_en.pdf"},
    {"id":"35316","name":"VeraSeal : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2018-01-17T18:11:00Z","last_updated_date":"2018-01-17T18:11:00Z","reference_number":"EMA/734511/2017","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/veraseal-epar-public-assessment-report_en.pdf"},
    {"id":"35337","name":"Versican Plus Pi : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2014-10-20T02:00:00Z","last_updated_date":"2014-10-20T02:00:00Z","reference_number":"EMA/283495/2014","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/versican-plus-pi-epar-public-assessment-report_en.pdf"},
    {"id":"35354","name":"Ozurdex : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2010-08-05T02:00:00Z","last_updated_date":"2010-08-05T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/ozurdex-epar-public-assessment-report_en.pdf"},
    {"id":"35358","name":"Rubraca : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2018-05-31T02:00:00Z","last_updated_date":"2018-05-31T02:00:00Z","reference_number":"EMA/CHMP/238139/2018","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/rubraca-epar-public-assessment-report_en.pdf"},
    {"id":"35375","name":"Ilaris : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2009-11-12T01:00:00Z","last_updated_date":"2009-11-12T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/ilaris-epar-public-assessment-report_en.pdf"},
    {"id":"35399","name":"Zinplava : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2017-03-08T01:00:00Z","last_updated_date":"2017-03-08T01:00:00Z","reference_number":"EMA/853812/2016","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/zinplava-epar-public-assessment-report_en.pdf"},
    {"id":"35413","name":"Iblias : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2016-03-09T01:00:00Z","last_updated_date":"2016-03-09T01:00:00Z","reference_number":"EMA/CHMP/71742/2016","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/iblias-epar-public-assessment-report_en.pdf"},
    {"id":"35427","name":"Capecitabine SUN : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2013-07-05T02:00:00Z","last_updated_date":"2016-12-22T01:00:00Z","reference_number":"EMA/370014/2013","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/capecitabine-sun-epar-public-assessment-report_en.pdf"},
    {"id":"35429","name":"Vyndaqel : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2011-11-18T01:00:00Z","last_updated_date":"2011-11-18T01:00:00Z","reference_number":"EMA/815723/2011","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/vyndaqel-epar-public-assessment-report_en.pdf"},
    {"id":"35479","name":"Imatinib medac : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2013-10-23T02:00:00Z","last_updated_date":"2013-10-23T02:00:00Z","reference_number":"EMA/622006/2013","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/imatinib-medac-epar-public-assessment-report_en.pdf"},
    {"id":"35579","name":"Tegsedi : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2018-08-06T02:00:00Z","last_updated_date":"2018-08-06T02:00:00Z","reference_number":"EMA/411876/2018","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/tegsedi-epar-public-assessment-report_en.pdf"},
    {"id":"35662","name":"Pantozol Control : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2009-06-22T02:00:00Z","last_updated_date":"2009-06-22T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/pantozol-control-epar-public-assessment-report_en.pdf"},
    {"id":"35672","name":"Epclusa : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2016-07-28T02:00:00Z","last_updated_date":"2016-07-28T02:00:00Z","reference_number":"EMA/399285/2016","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/epclusa-epar-public-assessment-report_en.pdf"},
    {"id":"35682","name":"Aubagio : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2013-09-06T02:00:00Z","last_updated_date":"2013-09-06T02:00:00Z","reference_number":"EMA/529295/2013","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/aubagio-epar-public-assessment-report_en.pdf"},
    {"id":"35785","name":"Urorec : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2010-02-22T01:00:00Z","last_updated_date":"2010-02-22T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/urorec-epar-public-assessment-report_en.pdf"},
    {"id":"35808","name":"Dafiro HCT : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2009-11-12T01:00:00Z","last_updated_date":"2009-11-12T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/dafiro-hct-epar-public-assessment-report_en.pdf"},
    {"id":"35838","name":"Movymia : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2017-03-16T10:48:00Z","last_updated_date":"2017-03-16T10:48:00Z","reference_number":"EMA/88527/2017","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/movymia-epar-public-assessment-report_en.pdf"},
    {"id":"35909","name":"Brilique : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2011-01-07T01:00:00Z","last_updated_date":"2011-01-07T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/brilique-epar-public-assessment-report_en.pdf"},
    {"id":"36053","name":"Vokanamet : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2014-05-15T02:00:00Z","last_updated_date":"2014-05-15T02:00:00Z","reference_number":"EMA/179391/2014","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/vokanamet-epar-public-assessment-report_en.pdf"},
    {"id":"36068","name":"Opgenra : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2009-03-04T00:09:21Z","last_updated_date":"2016-07-15T01:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/opgenra-epar-public-assessment-report_en.pdf"},
    {"id":"36095","name":"Extavia : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2008-06-05T02:00:00Z","last_updated_date":"2025-04-30T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/extavia-epar-public-assessment-report_en.pdf"},
    {"id":"36108","name":"Vimpat : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2008-09-17T02:00:00Z","last_updated_date":"2008-09-17T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/vimpat-epar-public-assessment-report_en.pdf"},
    {"id":"36130","name":"Fulvestrant Mylan : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2018-02-02T17:58:00Z","last_updated_date":"2018-02-02T17:58:00Z","reference_number":"EMA/CHMP/810299/2017","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/fulvestrant-mylan-epar-public-assessment-report_en.pdf"},
    {"id":"36269","name":"Miglustat Gen.Orph : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2017-11-23T01:00:00Z","last_updated_date":"2017-11-23T01:00:00Z","reference_number":"EMA/658246/2017","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/miglustat-genorph-epar-public-assessment-report_en.pdf"},
    {"id":"36301","name":"Buccolam : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2011-09-19T02:00:00Z","last_updated_date":"2011-09-19T02:00:00Z","reference_number":"EMA/662938/2011","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/buccolam-epar-public-assessment-report_en.pdf"},
    {"id":"36342","name":"Vimizim : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2014-06-26T02:00:00Z","last_updated_date":"2014-06-26T02:00:00Z","reference_number":"EMA/357933/2014","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/vimizim-epar-public-assessment-report_en.pdf"},
    {"id":"36375","name":"Clopidogrel ratiopharm : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2009-10-16T02:00:00Z","last_updated_date":"2013-12-12T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/clopidogrel-ratiopharm-epar-public-assessment-report_en.pdf"},
    {"id":"36396","name":"NexGard : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2013-03-27T01:00:00Z","last_updated_date":"2024-06-13T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/nexgard-epar-public-assessment-report_en.pdf"},
    {"id":"36470","name":"Adenuric : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2008-05-28T02:00:00Z","last_updated_date":"2008-05-28T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/adenuric-epar-public-assessment-report_en.pdf"},
    {"id":"36517","name":"Victoza : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2009-07-09T02:00:00Z","last_updated_date":"2009-07-09T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/victoza-epar-public-assessment-report_en.pdf"},
    {"id":"36561","name":"Emtricitabine / Tenofovir disoproxil Mylan : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2017-02-03T01:00:00Z","last_updated_date":"2017-02-03T01:00:00Z","reference_number":"EMA/CHMP/636453/2016","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/emtricitabine-tenofovir-disoproxil-mylan-epar-public-assessment-report_en.pdf"},
    {"id":"36600","name":"Grastofil : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2013-11-11T01:00:00Z","last_updated_date":"2013-11-11T01:00:00Z","reference_number":"EMEA/CHMP/303037/2013","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/grastofil-epar-public-assessment-report_en.pdf"},
    {"id":"36606","name":"Defitelio : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2013-10-25T02:00:00Z","last_updated_date":"2013-10-25T02:00:00Z","reference_number":"EMA/CHMP/824715/2012","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/defitelio-epar-public-assessment-report_en.pdf"},
    {"id":"36609","name":"Trimbow : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2017-08-09T02:00:00Z","last_updated_date":"2017-08-09T02:00:00Z","reference_number":"EMA/CHMP/289952/2017","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/trimbow-epar-public-assessment-report_en.pdf"},
    {"id":"36625","name":"Removab : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2009-05-12T02:00:00Z","last_updated_date":"2017-07-12T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/removab-epar-public-assessment-report_en.pdf"},
    {"id":"36640","name":"Lifmior : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2017-03-13T14:28:00Z","last_updated_date":"2020-02-20T12:09:00Z","reference_number":"EMA/114647/2016","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/lifmior-epar-public-assessment-report_en.pdf"},
    {"id":"36644","name":"Palonosetron Accord : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2016-06-08T02:00:00Z","last_updated_date":"2016-06-08T02:00:00Z","reference_number":"EMA/287566/2016","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/palonosetron-accord-epar-public-assessment-report_en.pdf"},
    {"id":"36691","name":"Efient : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2009-03-13T01:00:00Z","last_updated_date":"2009-03-13T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/efient-epar-public-assessment-report_en.pdf"},
    {"id":"36771","name":"Tolura : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2010-06-22T02:00:00Z","last_updated_date":"2010-06-22T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/tolura-epar-public-assessment-report_en.pdf"},
    {"id":"36789","name":"Zutectra : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2010-02-12T01:00:00Z","last_updated_date":"2010-02-12T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/zutectra-epar-public-assessment-report_en.pdf"},
    {"id":"36832","name":"Entacapone Orion : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2011-08-31T02:00:00Z","last_updated_date":"2011-08-31T02:00:00Z","reference_number":"EMA/533485/2011","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/entacapone-orion-epar-public-assessment-report_en.pdf"},
    {"id":"36885","name":"Prevymis : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2018-01-17T01:00:00Z","last_updated_date":"2018-01-17T01:00:00Z","reference_number":"EMA/CHMP/490007/2017","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/prevymis-epar-public-assessment-report_en.pdf"},
    {"id":"36922","name":"Elmiron : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2017-06-20T02:00:00Z","last_updated_date":"2017-06-20T02:00:00Z","reference_number":"EMA/287422/2017","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/elmiron-epar-public-assessment-report_en.pdf"},
    {"id":"36967","name":"Nimenrix : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2012-05-24T02:00:00Z","last_updated_date":"2012-05-24T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/nimenrix-epar-public-assessment-report_en.pdf"},
    {"id":"37031","name":"TruScient : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2011-12-20T01:00:00Z","last_updated_date":"2015-02-03T01:00:00Z","reference_number":"EMA/847913/2011","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/truscient-epar-public-assessment-report_en.pdf"},
    {"id":"37074","name":"Ivabradine Anpharm : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2015-09-21T02:00:00Z","last_updated_date":"2015-09-21T02:00:00Z","reference_number":"EMA/CHMP/594878/2015","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/ivabradine-anpharm-epar-public-assessment-report_en.pdf"},
    {"id":"37116","name":"Skilarence : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2017-07-11T12:42:00Z","last_updated_date":"2017-07-11T12:42:00Z","reference_number":"EMA/412737/2017","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/skilarence-epar-public-assessment-report_en.pdf"},
    {"id":"37168","name":"Mavenclad : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2017-09-08T02:00:00Z","last_updated_date":"2017-09-08T02:00:00Z","reference_number":"EMA/435731/2017","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/mavenclad-epar-public-assessment-report_en.pdf"},
    {"id":"37184","name":"Kevzara : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2017-06-29T02:00:00Z","last_updated_date":"2017-06-29T02:00:00Z","reference_number":"EMA/292840/2017","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/kevzara-epar-public-assessment-report_en.pdf"},
    {"id":"37193","name":"Zaltrap : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2013-03-07T01:00:00Z","last_updated_date":"2013-03-07T01:00:00Z","reference_number":"EMA/755420/2012","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/zaltrap-epar-public-assessment-report_en.pdf"},
    {"id":"37197","name":"Olazax : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2010-01-29T01:00:00Z","last_updated_date":"2010-01-29T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/olazax-epar-public-assessment-report_en.pdf"},
    {"id":"37276","name":"Icandra : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2008-12-23T01:00:00Z","last_updated_date":"2008-12-23T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/icandra-epar-public-assessment-report_en.pdf"},
    {"id":"37286","name":"Nivolumab BMS : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2015-07-27T02:00:00Z","last_updated_date":"2016-01-14T01:00:00Z","reference_number":"EMA/CHMP/392114/2015","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/nivolumab-bms-epar-public-assessment-report_en.pdf"},
    {"id":"37287","name":"Pexion : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2013-03-26T01:00:00Z","last_updated_date":"2025-10-09T01:00:00Z","reference_number":"EMA/808597/2012","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/pexion-epar-public-assessment-report_en.pdf"},
    {"id":"37293","name":"Elonva : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2010-02-26T01:00:00Z","last_updated_date":"2010-02-26T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/elonva-epar-public-assessment-report_en.pdf"},
    {"id":"37396","name":"Duavive : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2015-01-30T01:00:00Z","last_updated_date":"2015-01-30T01:00:00Z","reference_number":"EMA/CHMP/383987/2014","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/duavive-epar-public-assessment-report_en.pdf"},
    {"id":"37523","name":"Emtricitabine/Tenofovir disoproxil Krka d.d. : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2017-06-09T02:00:00Z","last_updated_date":"2017-06-09T02:00:00Z","reference_number":"EMA/CHMP/236203/2017","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/emtricitabinetenofovir-disoproxil-krka-dd-epar-public-assessment-report_en.pdf"},
    {"id":"37764","name":"Sovaldi : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2014-02-05T01:00:00Z","last_updated_date":"2014-02-05T01:00:00Z","reference_number":"EMA/CHMP/688774/2013","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/sovaldi-epar-public-assessment-report_en.pdf"},
    {"id":"37793","name":"Jentadueto : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2012-08-16T02:00:00Z","last_updated_date":"2012-08-16T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/jentadueto-epar-public-assessment-report_en.pdf"},
    {"id":"37808","name":"Intanza : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2009-04-07T02:00:00Z","last_updated_date":"2018-09-04T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/intanza-epar-public-assessment-report_en.pdf"},
    {"id":"37811","name":"Jetrea : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2013-04-18T13:30:00Z","last_updated_date":"2025-06-19T13:30:00Z","reference_number":"EMA/CHMP/74766/2013","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/jetrea-epar-public-assessment-report_en.pdf"},
    {"id":"37907","name":"Zoely : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2011-10-06T02:00:00Z","last_updated_date":"2011-10-06T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/zoely-epar-public-assessment-report_en.pdf"},
    {"id":"37911","name":"Respiporc FLUpan H1N1 : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2017-06-20T02:00:00Z","last_updated_date":"2025-10-14T02:00:00Z","reference_number":"EMA/186254/2017","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/respiporc-flupan-h1n1-epar-public-assessment-report_en.pdf"},
    {"id":"37963","name":"Eurartesim : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2011-11-28T01:00:00Z","last_updated_date":"2011-11-28T01:00:00Z","reference_number":"EMA/739355/2011","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/eurartesim-epar-public-assessment-report_en.pdf"},
    {"id":"38114","name":"Revolade : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2010-04-29T02:00:00Z","last_updated_date":"2010-05-18T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/revolade-epar-public-assessment-report_en.pdf"},
    {"id":"38147","name":"Fungitraxx : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2014-04-29T02:00:00Z","last_updated_date":"2025-09-09T02:00:00Z","reference_number":"EMA/41548/2014","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/fungitraxx-epar-public-assessment-report_en.pdf"},
    {"id":"38189","name":"Somatropin Biopartners : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2013-09-09T02:00:00Z","last_updated_date":"2013-09-09T02:00:00Z","reference_number":"EMA/CHMP/229458/2013","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/somatropin-biopartners-epar-public-assessment-report_en.pdf"},
    {"id":"38195","name":"Simbrinza : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2014-07-31T02:00:00Z","last_updated_date":"2014-07-31T02:00:00Z","reference_number":"EMA/366328/2014","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/simbrinza-epar-public-assessment-report_en.pdf"},
    {"id":"38316","name":"Xeplion : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2011-03-14T01:00:00Z","last_updated_date":"2011-03-14T01:00:00Z","reference_number":"EMA/60983/2011","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/xeplion-epar-public-assessment-report_en.pdf"},
    {"id":"38412","name":"Desloratadine Teva : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2011-12-08T01:00:00Z","last_updated_date":"2011-12-08T01:00:00Z","reference_number":"EMA/CHMP/654268/2011","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/desloratadine-teva-epar-public-assessment-report_en.pdf"},
    {"id":"38489","name":"Pioglitazone Actavis : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2012-04-26T02:00:00Z","last_updated_date":"2012-04-26T02:00:00Z","reference_number":"EMA/210151/2012","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/pioglitazone-actavis-epar-public-assessment-report_en.pdf"},
    {"id":"38493","name":"Harvoni : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2014-12-04T01:00:00Z","last_updated_date":"2014-12-04T01:00:00Z","reference_number":"EMA/702742/2014","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/harvoni-epar-public-assessment-report_en.pdf"},
    {"id":"38498","name":"Versican Plus DHPPi/L4R : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2014-08-11T02:00:00Z","last_updated_date":"2024-10-14T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/versican-plus-dhppi-l4r-epar-public-assessment-report_en.pdf"},
    {"id":"38514","name":"Intrarosa : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2018-02-14T12:00:00Z","last_updated_date":"2018-02-14T12:00:00Z","reference_number":"EMA/793337/2017","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/intrarosa-epar-public-assessment-report_en.pdf"},
    {"id":"38519","name":"Rienso : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2012-07-06T02:00:00Z","last_updated_date":"2015-07-13T02:00:00Z","reference_number":"EMA/CHMP/221776/2012","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/rienso-epar-public-assessment-report_en.pdf"},
    {"id":"38530","name":"Picato : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2012-11-29T01:00:00Z","last_updated_date":"2020-03-04T01:00:00Z","reference_number":"EMA/650464/2012","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/picato-epar-public-assessment-report_en.pdf"},
    {"id":"38710","name":"Carmustine Obvius : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2018-08-20T02:00:00Z","last_updated_date":"2018-08-20T02:00:00Z","reference_number":"EMA/CHMP/88371/2018","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/carmustine-obvius-epar-public-assessment-report_en.pdf"},
    {"id":"38715","name":"Crysvita : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2018-03-12T01:00:00Z","last_updated_date":"2018-03-12T01:00:00Z","reference_number":"EMA/148319/2018","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/crysvita-epar-public-assessment-report_en.pdf"},
    {"id":"38809","name":"Clopidogrel ratiopharm : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2015-03-11T01:00:00Z","last_updated_date":"2015-03-11T01:00:00Z","reference_number":"EMA/63392/2015","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/clopidogrel-ratiopharm-epar-public-assessment-report_en.pdf-0"},
    {"id":"38827","name":"Nuedexta : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2013-07-02T02:00:00Z","last_updated_date":"2013-07-02T02:00:00Z","reference_number":"EMA/CHMP/80029/2013","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/nuedexta-epar-public-assessment-report_en.pdf"},
    {"id":"38912","name":"Zoledronic acid Teva : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2012-08-24T02:00:00Z","last_updated_date":"2012-08-24T02:00:00Z","reference_number":"EMA/534108/2012","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/zoledronic-acid-teva-epar-public-assessment-report_en.pdf"},
    {"id":"38971","name":"Glubrava-H-A31-1432 : EPAR - Public assessment report - Article 31","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2017-01-17T16:42:00Z","last_updated_date":"2022-10-18T16:42:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/glubrava-h-a31-1432-epar-public-assessment-report-article-31_en.pdf"},
    {"id":"39030","name":"Janumet : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2008-08-06T02:09:21Z","last_updated_date":"2008-08-06T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/janumet-epar-public-assessment-report_en.pdf"},
    {"id":"39056","name":"Alofisel : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2018-04-04T02:00:00Z","last_updated_date":"2025-01-21T02:00:00Z","reference_number":"EMA/CHMP/64055/2018","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/alofisel-epar-public-assessment-report_en.pdf"},
    {"id":"39123","name":"Eporatio : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2009-12-16T01:00:00Z","last_updated_date":"2009-12-16T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/eporatio-epar-public-assessment-report_en.pdf"},
    {"id":"39151","name":"Temozolomide Hospira : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2010-03-26T01:00:00Z","last_updated_date":"2010-03-26T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/temozolomide-hospira-epar-public-assessment-report_en.pdf"},
    {"id":"39172","name":"Vemlidy : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2017-03-10T01:00:00Z","last_updated_date":"2017-03-10T01:00:00Z","reference_number":"EMA/793580/2016","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/vemlidy-epar-public-assessment-report_en.pdf"},
    {"id":"39249","name":"Eptifibatide Accord : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2016-01-18T01:00:00Z","last_updated_date":"2016-01-18T01:00:00Z","reference_number":"EMA/851528/2015","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/eptifibatide-accord-epar-public-assessment-report_en.pdf"},
    {"id":"39307","name":"Sivextro : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2015-03-26T01:00:00Z","last_updated_date":"2015-03-26T01:00:00Z","reference_number":"EMA/83337/2015","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/sivextro-epar-public-assessment-report_en.pdf"},
    {"id":"39379","name":"Hexacima : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2013-07-12T02:00:00Z","last_updated_date":"2013-07-12T02:00:00Z","reference_number":"EMA/373868/2013","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/hexacima-epar-public-assessment-report_en.pdf"},
    {"id":"39436","name":"CaniLeish : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2011-04-06T02:00:00Z","last_updated_date":"2023-10-24T13:13:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/canileish-epar-public-assessment-report_en.pdf"},
    {"id":"39467","name":"NovoEight : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2013-12-09T01:00:00Z","last_updated_date":"2013-12-09T01:00:00Z","reference_number":"EMA/612026/2013","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/novoeight-epar-public-assessment-report_en.pdf"},
    {"id":"39525","name":"Vipdomet : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2013-10-14T02:00:00Z","last_updated_date":"2013-10-14T02:00:00Z","reference_number":"EMA/CHMP/207158/2013","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/vipdomet-epar-public-assessment-report_en.pdf"},
    {"id":"39635","name":"Juluca : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2018-05-24T17:58:00Z","last_updated_date":"2018-05-24T17:58:00Z","reference_number":"EMA/243517/2018","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/juluca-epar-public-assessment-report_en.pdf"},
    {"id":"39657","name":"Ebilfumin : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2014-06-06T02:00:00Z","last_updated_date":"2014-06-06T02:00:00Z","reference_number":"EMA/260303/2014","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/ebilfumin-epar-public-assessment-report_en.pdf"},
    {"id":"39676","name":"Emtricitabine/Tenofovir disoproxil Krka : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2017-04-04T02:00:00Z","last_updated_date":"2017-04-04T02:00:00Z","reference_number":"EMA/CHMP/522913/2016","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/emtricitabine-tenofovir-disoproxil-krka-epar-public-assessment-report_en.pdf"},
    {"id":"39850","name":"Neofordex : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2016-04-01T02:00:00Z","last_updated_date":"2016-04-01T02:00:00Z","reference_number":"EMA/CHMP/6613/2016","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/neofordex-epar-public-assessment-report_en.pdf"},
    {"id":"39895","name":"Ibandronic Acid Teva : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2010-10-13T02:00:00Z","last_updated_date":"2010-10-13T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/ibandronic-acid-teva-epar-public-assessment-report_en.pdf"},
    {"id":"39944","name":"Recuvyra : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2011-10-12T02:00:00Z","last_updated_date":"2017-07-12T02:00:00Z","reference_number":"EMA/399540/2011","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/recuvyra-epar-public-assessment-report_en.pdf"},
    {"id":"40074","name":"Lympreva : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2015-07-17T18:20:00Z","last_updated_date":"2015-07-17T18:20:00Z","reference_number":"EMA/314727/2015","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/lympreva-epar-public-assessment-report_en.pdf"},
    {"id":"40077","name":"Relistor : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2008-07-10T02:00:00Z","last_updated_date":"2008-07-10T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/relistor-epar-public-assessment-report_en.pdf"},
    {"id":"40081","name":"Maci : EPAR - Public assessment report : Article-20 procedure","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2014-12-17T01:00:00Z","last_updated_date":"2018-07-05T02:00:00Z","reference_number":"EMA/671958/2014","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/maci-epar-public-assessment-report-article-20-procedure_en.pdf"},
    {"id":"40138","name":"Para-aminosalicylic acid Lucane : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2014-05-12T02:00:00Z","last_updated_date":"2026-01-05T02:00:00Z","reference_number":"EMA/18511/2014","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/para-aminosalicylic-acid-lucane-epar-public-assessment-report_en.pdf"},
    {"id":"40166","name":"Lopinavir/Ritonavir Mylan : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2016-02-09T01:00:00Z","last_updated_date":"2016-02-09T01:00:00Z","reference_number":"EMA/828552/2015","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/lopinavirritonavir-mylan-epar-public-assessment-report_en.pdf"},
    {"id":"40173","name":"Zeleris : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2017-05-30T02:00:00Z","last_updated_date":"2024-10-03T02:00:00Z","reference_number":"EMA/186838/2017","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/zeleris-epar-public-assessment-report_en.pdf"},
    {"id":"40289","name":"Thymanax : EPAR - Refusal public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2007-10-22T02:00:00Z","last_updated_date":"2007-10-22T02:00:00Z","reference_number":"EMEA/37021/2007 - update","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/thymanax-epar-refusal-public-assessment-report_en.pdf"},
    {"id":"40353","name":"Giotrif : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2013-10-16T12:00:00Z","last_updated_date":"2013-10-16T12:00:00Z","reference_number":"EMA/491185/2013","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/giotrif-epar-public-assessment-report_en.pdf"},
    {"id":"40355","name":"Nyxoid : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2017-12-12T01:00:00Z","last_updated_date":"2017-12-12T01:00:00Z","reference_number":"EMA/CHMP/690823/2017","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/nyxoid-epar-public-assessment-report_en.pdf"},
    {"id":"40414","name":"Leflunomide Teva : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2011-03-21T01:00:00Z","last_updated_date":"2014-03-18T01:00:00Z","reference_number":"EMA/79144/2011","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/leflunomide-teva-epar-public-assessment-report_en.pdf"},
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    {"id":"40592","name":"Pradaxa : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2008-04-23T02:00:00Z","last_updated_date":"2008-04-23T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/pradaxa-epar-public-assessment-report_en.pdf"},
    {"id":"40610","name":"Uptravi : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2016-05-26T02:00:00Z","last_updated_date":"2016-05-26T02:00:00Z","reference_number":"EMA/272184/2016","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/uptravi-epar-public-assessment-report_en.pdf"},
    {"id":"40696","name":"Capecitabine Krka : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2012-05-07T02:00:00Z","last_updated_date":"2012-05-07T02:00:00Z","reference_number":"EMA/199988/2012","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/capecitabine-krka-epar-public-assessment-report_en.pdf"},
    {"id":"40711","name":"Cepedex : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2016-12-22T01:00:00Z","last_updated_date":"2024-11-11T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/cepedex-epar-public-assessment-report_en.pdf"},
    {"id":"40731","name":"Darzalex : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2016-05-27T02:00:00Z","last_updated_date":"2016-05-27T02:00:00Z","reference_number":"EMA/278085/2016","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/darzalex-epar-public-assessment-report_en.pdf"},
    {"id":"40734","name":"Fablyn : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2009-03-23T00:09:21Z","last_updated_date":"2012-06-22T01:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/fablyn-epar-public-assessment-report_en.pdf"},
    {"id":"40742","name":"Mycamine : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2008-05-08T02:09:21Z","last_updated_date":"2008-05-08T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/mycamine-epar-public-assessment-report_en.pdf"},
    {"id":"40760","name":"Imprida HCT : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2009-11-12T01:00:00Z","last_updated_date":"2012-10-29T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/imprida-hct-epar-public-assessment-report_en.pdf"},
    {"id":"40764","name":"Ritonavir Mylan : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2017-11-20T01:00:00Z","last_updated_date":"2017-11-20T01:00:00Z","reference_number":"EMA/CHMP/749789/2017","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/ritonavir-mylan-epar-public-assessment-report_en.pdf"},
    {"id":"40810","name":"Kolbam  : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2015-12-09T01:00:00Z","last_updated_date":"2020-07-15T01:00:00Z","reference_number":"EMA/689761/2015","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/kolbam-epar-public-assessment-report_en.pdf"},
    {"id":"40848","name":"Nplate : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2009-02-13T00:09:21Z","last_updated_date":"2009-02-13T00:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/nplate-epar-public-assessment-report_en.pdf"},
    {"id":"40866","name":"Tyverb : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2008-06-26T02:09:21Z","last_updated_date":"2008-06-26T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/tyverb-epar-public-assessment-report_en.pdf"},
    {"id":"40892","name":"Xiapex : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2011-03-14T01:00:00Z","last_updated_date":"2020-03-02T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/xiapex-epar-public-assessment-report_en.pdf"},
    {"id":"40909","name":"Constella : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2012-11-30T01:00:00Z","last_updated_date":"2012-11-30T01:00:00Z","reference_number":"EMA/CHMP/60979/2012","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/constella-epar-public-assessment-report_en.pdf"},
    {"id":"40912","name":"Truberzi : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2016-09-29T02:00:00Z","last_updated_date":"2021-02-25T02:00:00Z","reference_number":"EMA/549473/2016","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/truberzi-epar-public-assessment-report_en.pdf"},
    {"id":"40967","name":"Idelvion : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2016-05-27T02:00:00Z","last_updated_date":"2016-05-27T02:00:00Z","reference_number":"EMA/CHMP/213825/2016","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/idelvion-epar-public-assessment-report_en.pdf"},
    {"id":"41057","name":"Imatinib Actavis : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2013-05-06T02:00:00Z","last_updated_date":"2022-07-05T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/imatinib-actavis-epar-public-assessment-report_en.pdf"},
    {"id":"41061","name":"Opdivo : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2015-07-16T02:00:00Z","last_updated_date":"2015-07-16T02:00:00Z","reference_number":"EMA/CHMP/76688/2015","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/opdivo-epar-public-assessment-report_en.pdf"},
    {"id":"41101","name":"Jalra : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2009-01-09T00:09:21Z","last_updated_date":"2009-01-09T00:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/jalra-epar-public-assessment-report_en.pdf"},
    {"id":"41243","name":"Lynparza : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2015-01-09T01:00:00Z","last_updated_date":"2015-01-09T01:00:00Z","reference_number":"EMA/CHMP/789139/2014","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/lynparza-epar-public-assessment-report_en.pdf"},
    {"id":"41271","name":"Cyramza : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2015-01-22T01:00:00Z","last_updated_date":"2015-01-22T01:00:00Z","reference_number":"EMA/CHMP/305462/2014","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/cyramza-epar-public-assessment-report_en.pdf"},
    {"id":"41367","name":"Bravecto : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2014-03-26T01:00:00Z","last_updated_date":"2024-06-03T11:30:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/bravecto-epar-public-assessment-report_en.pdf"},
    {"id":"41392","name":"Controloc Control : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2009-06-22T02:09:21Z","last_updated_date":"2009-06-22T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/controloc-control-epar-public-assessment-report_en.pdf","translations":{"bg":"https://www.ema.europa.eu/bg/documents/assessment-report/controloc-control-epar-public-assessment-report_bg.pdf","es":"https://www.ema.europa.eu/es/documents/assessment-report/controloc-control-epar-public-assessment-report_es.pdf","cs":"https://www.ema.europa.eu/cs/documents/assessment-report/controloc-control-epar-public-assessment-report_cs.pdf","da":"https://www.ema.europa.eu/da/documents/assessment-report/controloc-control-epar-public-assessment-report_da.pdf","de":"https://www.ema.europa.eu/de/documents/assessment-report/controloc-control-epar-public-assessment-report_de.pdf","et":"https://www.ema.europa.eu/et/documents/assessment-report/controloc-control-epar-public-assessment-report_et.pdf","el":"https://www.ema.europa.eu/el/documents/assessment-report/controloc-control-epar-public-assessment-report_el.pdf","fr":"https://www.ema.europa.eu/fr/documents/assessment-report/controloc-control-epar-public-assessment-report_fr.pdf","it":"https://www.ema.europa.eu/it/documents/assessment-report/controloc-control-epar-public-assessment-report_it.pdf","lv":"https://www.ema.europa.eu/lv/documents/assessment-report/controloc-control-epar-public-assessment-report_lv.pdf","lt":"https://www.ema.europa.eu/lt/documents/assessment-report/controloc-control-epar-public-assessment-report_lt.pdf","hu":"https://www.ema.europa.eu/hu/documents/assessment-report/controloc-control-epar-public-assessment-report_hu.pdf","mt":"https://www.ema.europa.eu/mt/documents/assessment-report/controloc-control-epar-public-assessment-report_mt.pdf","nl":"https://www.ema.europa.eu/nl/documents/assessment-report/controloc-control-epar-public-assessment-report_nl.pdf","pl":"https://www.ema.europa.eu/pl/documents/assessment-report/controloc-control-epar-public-assessment-report_pl.pdf","pt":"https://www.ema.europa.eu/pt/documents/assessment-report/controloc-control-epar-public-assessment-report_pt.pdf","ro":"https://www.ema.europa.eu/ro/documents/assessment-report/controloc-control-epar-public-assessment-report_ro.pdf","sk":"https://www.ema.europa.eu/sk/documents/assessment-report/controloc-control-epar-public-assessment-report_sk.pdf","sl":"https://www.ema.europa.eu/sl/documents/assessment-report/controloc-control-epar-public-assessment-report_sl.pdf","fi":"https://www.ema.europa.eu/fi/documents/assessment-report/controloc-control-epar-public-assessment-report_fi.pdf","sv":"https://www.ema.europa.eu/sv/documents/assessment-report/controloc-control-epar-public-assessment-report_sv.pdf"}},
    {"id":"41394","name":"Mekinist : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2014-07-09T02:00:00Z","last_updated_date":"2014-07-09T02:00:00Z","reference_number":"EMA/CHMP/258608/2014","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/mekinist-epar-public-assessment-report_en.pdf"},
    {"id":"41448","name":"Komboglyze : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2011-12-16T01:00:00Z","last_updated_date":"2011-12-16T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/komboglyze-epar-public-assessment-report_en.pdf"},
    {"id":"41490","name":"Xoterna Breezhaler : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2013-10-04T14:00:00Z","last_updated_date":"2013-10-04T14:00:00Z","reference_number":"EMA/CHMP/456924/2013","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/xoterna-breezhaler-epar-public-assessment-report_en.pdf"},
    {"id":"41492","name":"Ubac : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2018-08-14T17:25:00Z","last_updated_date":"2025-10-14T17:25:00Z","reference_number":"EMA/368039/2018","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/ubac-epar-public-assessment-report_en.pdf"},
    {"id":"41497","name":"Rapiscan : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2010-09-28T02:00:00Z","last_updated_date":"2010-09-28T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/rapiscan-epar-public-assessment-report_en.pdf"},
    {"id":"41512","name":"Cablivi : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2018-09-10T11:27:00Z","last_updated_date":"2018-09-10T11:27:00Z","reference_number":"EMA/490172/2018","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/cablivi-epar-public-assessment-report_en.pdf"},
    {"id":"41531","name":"Hemlibra : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2018-03-01T16:30:00Z","last_updated_date":"2018-03-01T16:30:00Z","reference_number":"EMA/88475/2018","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/hemlibra-epar-public-assessment-report_en.pdf"},
    {"id":"41536","name":"Vitekta : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2013-11-26T01:00:00Z","last_updated_date":"2017-05-29T02:00:00Z","reference_number":"EMA/701401/2013","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/vitekta-epar-public-assessment-report_en.pdf"},
    {"id":"41537","name":"Prepandemic influenza vaccine (H5N1) (surface antigen, inactivated, adjuvanted) Novartis Vaccines and Diagnostics : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2011-01-24T01:00:00Z","last_updated_date":"2011-01-24T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/prepandemic-influenza-vaccine-h5n1-surface-antigen-inactivated-adjuvanted-novartis-vaccines-and-diagnostics-epar-public-assessment-report_en.pdf"},
    {"id":"41539","name":"Amlodipine  / Valsartan Mylan  : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2016-04-06T02:00:00Z","last_updated_date":"2016-04-06T02:00:00Z","reference_number":"EMA/CHMP/182030/2016","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/amlodipine-valsartan-mylan-epar-public-assessment-report_en.pdf"},
    {"id":"41560","name":"Relvar Ellipta : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2013-12-10T01:00:00Z","last_updated_date":"2013-12-10T01:00:00Z","reference_number":"EMA/282960/2013","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/relvar-ellipta-epar-public-assessment-report_en.pdf"},
    {"id":"41562","name":"Tagrisso : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2016-02-17T11:00:00Z","last_updated_date":"2016-02-17T11:00:00Z","reference_number":"EMA/CHMP/15445/20165","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/tagrisso-epar-public-assessment-report_en.pdf"},
    {"id":"41567","name":"Saxenda : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2015-04-16T02:00:00Z","last_updated_date":"2015-04-16T02:00:00Z","reference_number":"EMA/143005/2015","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/saxenda-epar-public-assessment-report_en.pdf"},
    {"id":"41580","name":"Atosiban SUN : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2013-08-07T02:00:00Z","last_updated_date":"2013-08-07T02:00:00Z","reference_number":"EMA/476499/2013","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/atosiban-sun-epar-public-assessment-report_en.pdf"},
    {"id":"41661","name":"MiPet Easecto : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2018-02-23T01:00:00Z","last_updated_date":"2024-06-11T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/mipet-easecto-epar-public-assessment-report_en.pdf"},
    {"id":"41717","name":"Valdoxan : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2009-03-17T01:00:00Z","last_updated_date":"2009-03-17T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/valdoxan-epar-public-assessment-report_en.pdf"},
    {"id":"41725","name":"DuoCover : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2010-03-31T02:00:00Z","last_updated_date":"2010-03-31T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/duocover-epar-public-assessment-report_en.pdf"},
    {"id":"41839","name":"Stivarga : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2013-09-12T02:00:00Z","last_updated_date":"2013-09-12T02:00:00Z","reference_number":"EMA/CHMP/403683/2013","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/stivarga-epar-public-assessment-report_en.pdf"},
    {"id":"41858","name":"Lusduna : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2017-01-12T01:00:00Z","last_updated_date":"2019-01-22T13:00:00Z","reference_number":"EMA/813309/2016","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/lusduna-epar-public-assessment-report_en.pdf"},
    {"id":"41890","name":"Alpivab : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2018-04-25T15:58:00Z","last_updated_date":"2020-12-09T15:58:00Z","reference_number":"EMA/CHMP/148367/2018","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/alpivab-epar-public-assessment-report_en.pdf"},
    {"id":"41895","name":"Thorinane : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2016-10-26T02:00:00Z","last_updated_date":"2019-10-24T02:00:00Z","reference_number":"EMA/536972/2016","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/thorinane-epar-public-assessment-report_en.pdf"},
    {"id":"41896","name":"Segluromet : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2018-04-05T02:00:00Z","last_updated_date":"2018-04-05T02:00:00Z","reference_number":"EMA/86928/2018","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/segluromet-epar-public-assessment-report_en.pdf"},
    {"id":"41897","name":"Hemangiol : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2014-05-19T02:00:00Z","last_updated_date":"2014-05-19T02:00:00Z","reference_number":"EMA/CHMP/8171/2014","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/hemangiol-epar-public-assessment-report_en.pdf"},
    {"id":"41901","name":"Mysimba : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2015-04-15T02:00:00Z","last_updated_date":"2015-04-15T02:00:00Z","reference_number":"EMA/805547/2015","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/mysimba-epar-public-assessment-report_en.pdf"},
    {"id":"41909","name":"Neparvis : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2016-06-13T02:00:00Z","last_updated_date":"2016-06-13T02:00:00Z","reference_number":"EMA/255018/2016","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/neparvis-epar-public-assessment-report_en.pdf"},
    {"id":"41993","name":"Suvaxyn CSF Marker : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2015-04-17T02:00:00Z","last_updated_date":"2025-09-02T02:00:00Z","reference_number":"EMA/786291/2014","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/suvaxyn-csf-marker-epar-public-assessment-report_en.pdf"},
    {"id":"42050","name":"Kymriah : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2018-09-19T02:00:00Z","last_updated_date":"2018-09-19T02:00:00Z","reference_number":"EMA/485563/2018","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/kymriah-epar-public-assessment-report_en.pdf"},
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    {"id":"42121","name":"Hulio : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2018-09-21T02:00:00Z","last_updated_date":"2018-09-21T02:00:00Z","reference_number":"EMA/541826/2018","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/hulio-epar-public-assessment-report_en.pdf"},
    {"id":"42147","name":"Hydrocortisone aceponate Ecuphar (previously Cortacare) : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2018-09-28T14:47:00Z","last_updated_date":"2025-10-07T15:45:00Z","reference_number":"EMA/426890/2018","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/hydrocortisone-aceponate-ecuphar-previously-cortacare-epar-public-assessment-report_en.pdf"},
    {"id":"42189","name":"Spinraza : EPAR - Public Assessment Report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2017-06-21T18:27:00Z","last_updated_date":"2017-06-21T18:27:00Z","reference_number":"EMA/289068/2017","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/spinraza-epar-public-assessment-report_en.pdf-0"},
    {"id":"42211","name":"Deferiprone Lipomed : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2018-10-05T15:28:00Z","last_updated_date":"2018-10-05T15:28:00Z","reference_number":"EMA/535221/2018","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/deferiprone-lipomed-epar-public-assessment-report_en.pdf"},
    {"id":"42233","name":"Xerava : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2018-10-08T15:12:00Z","last_updated_date":"2018-10-08T15:12:00Z","reference_number":"EMA/540193/2018","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/xerava-epar-public-assessment-report_en.pdf"},
    {"id":"42247","name":"Ilumetri : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2018-10-09T17:06:00Z","last_updated_date":"2018-10-09T17:06:00Z","reference_number":"EMA/CHMP/664213/2018","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/ilumetri-epar-public-assessment-report_en.pdf"},
    {"id":"42267","name":"Gefitinib Mylan : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2018-10-10T13:58:00Z","last_updated_date":"2024-10-17T11:14:00Z","reference_number":"EMA/587444/2018","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/gefitinib-mylan-epar-public-assessment-report_en.pdf"},
    {"id":"42280","name":"Slenyto : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2018-10-10T16:43:00Z","last_updated_date":"2018-10-10T16:43:00Z","reference_number":"EMA/556280/2018","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/slenyto-epar-public-assessment-report_en.pdf"},
    {"id":"42308","name":"Mektovi : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2018-10-12T12:41:00Z","last_updated_date":"2018-10-12T12:41:00Z","reference_number":"EMA/CHMP/554701/2018","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/mektovi-epar-public-assessment-report_en.pdf"},
    {"id":"42313","name":"Braftovi : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2018-10-12T12:59:00Z","last_updated_date":"2018-10-12T12:59:00Z","reference_number":"EMA/CHMP/554696/2018","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/braftovi-epar-public-assessment-report_en.pdf"},
    {"id":"42324","name":"Kigabeq : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2018-10-12T14:56:00Z","last_updated_date":"2018-10-12T14:56:00Z","reference_number":"EMA/549064/2018","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/kigabeq-epar-public-assessment-report_en.pdf"},
    {"id":"42330","name":"Lenalidomide Accord : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2018-10-12T15:34:00Z","last_updated_date":"2018-10-12T15:34:00Z","reference_number":"EMA/CHMP/563114/2018","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/lenalidomide-accord-epar-public-assessment-report_en.pdf"},
    {"id":"42417","name":"Udenyca : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2018-10-23T12:02:00Z","last_updated_date":"2018-10-23T12:02:00Z","reference_number":"EMA/552721/2018","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/udenyca-epar-public-assessment-report_en.pdf"},
    {"id":"42441","name":"Pelgraz : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2018-10-26T15:11:00Z","last_updated_date":"2018-10-26T15:11:00Z","reference_number":"EMA/595848/2018","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/pelgraz-epar-public-assessment-report_en.pdf"},
    {"id":"42448","name":"Vyxeos : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2018-10-26T17:20:00Z","last_updated_date":"2018-10-26T17:20:00Z","reference_number":"EMA/665588/2022","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/vyxeos-epar-public-assessment-report_en.pdf"},
    {"id":"42476","name":"Verzenios : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2018-10-29T18:24:00Z","last_updated_date":"2018-10-29T18:24:00Z","reference_number":"EMA/551438/2018","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/verzenios-epar-public-assessment-report_en.pdf"},
    {"id":"42479","name":"Verzenios : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2018-10-29T18:24:00Z","last_updated_date":"2018-10-29T18:24:00Z","reference_number":"EMA/551438/2018","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/verzenios-epar-public-assessment-report_en.pdf-0"},
    {"id":"42500","name":"Onpattro : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2018-10-30T15:19:00Z","last_updated_date":"2018-10-30T15:19:00Z","reference_number":"EMA/554262/2018","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/onpattro-epar-public-assessment-report_en.pdf"},
    {"id":"42738","name":"Symkevi : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2018-11-22T10:05:00Z","last_updated_date":"2018-11-22T10:05:00Z","reference_number":"EMA/CHMP/567306/2018","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/symkevi-epar-public-assessment-report_en.pdf"},
    {"id":"42788","name":"Rxulti : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2018-11-26T13:22:00Z","last_updated_date":"2018-11-26T13:22:00Z","reference_number":"EMN556923/2018","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/rxulti-epar-public-assessment-report_en.pdf"},
    {"id":"42793","name":"Alunbrig : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2018-11-26T15:09:00Z","last_updated_date":"2018-11-26T15:09:00Z","reference_number":"EMA/696925/2018","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/alunbrig-epar-public-assessment-report_en.pdf"},
    {"id":"42903","name":"Fulphila : Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2018-12-03T11:44:00Z","last_updated_date":"2018-12-03T11:44:00Z","reference_number":"EMA/724003/2018","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/fulphila-public-assessment-report_en.pdf"},
    {"id":"42908","name":"Pelmeg : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2018-12-03T12:42:00Z","last_updated_date":"2018-12-03T12:42:00Z","reference_number":"EMA/703393/2018","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/pelmeg-epar-public-assessment-report_en.pdf"},
    {"id":"42924","name":"Apealea : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2018-12-05T16:17:00Z","last_updated_date":"2024-03-06T16:12:00Z","reference_number":"EMA/CHMP/785964/2018","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/apealea-epar-public-assessment-report_en.pdf"},
    {"id":"43021","name":"Exondys : EPAR - Refusal public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2018-12-12T17:25:00Z","last_updated_date":"2018-12-12T17:25:00Z","reference_number":"EMA/691796/2018","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/exondys-epar-refusal-public-assessment-report_en.pdf"},
    {"id":"43105","name":"Takhzyro : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2018-12-17T15:27:00Z","last_updated_date":"2018-12-17T15:27:00Z","reference_number":"EMA/794314/2018","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/takhzyro-epar-public-assessment-report_en.pdf"},
    {"id":"43119","name":"Buvidal : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2018-12-18T11:09:00Z","last_updated_date":"2018-12-18T11:09:00Z","reference_number":"EMA/693347/2018","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/buvidal-epar-public-assessment-report_en.pdf"},
    {"id":"43133","name":"Vabomere : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2018-12-18T16:00:00Z","last_updated_date":"2018-12-18T16:00:00Z","reference_number":"EMA/CHMP/700663/2018","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/vabomere-epar-public-assessment-report_en.pdf"},
    {"id":"43147","name":"Dengvaxia : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2018-12-18T17:40:00Z","last_updated_date":"2025-12-04T12:00:00Z","reference_number":"EMA/791273/2018","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/dengvaxia-epar-public-assessment-report_en.pdf"},
    {"id":"43198","name":"Public statement on Ivabradine JensonR: Withdrawal of the marketing authorisation in the European Union","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2018-12-20T14:40:00Z","last_updated_date":"2018-12-20T14:40:00Z","reference_number":"EMA/875585/2018","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/public-statement-ivabradine-jensonr-withdrawal-marketing-authorisation-european-union_en.pdf"},
    {"id":"43202","name":"Flucelvax Tetra : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2018-12-20T15:33:00Z","last_updated_date":"2026-02-27T08:00:00Z","reference_number":"EMA/814746/2018","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/flucelvax-tetra-epar-public-assessment-report_en.pdf"},
    {"id":"43255","name":"Ogivri : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2019-01-09T10:09:00Z","last_updated_date":"2019-01-09T10:09:00Z","reference_number":"EMA/810499/2018","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/ogivri-epar-public-assessment-report_en.pdf"},
    {"id":"43270","name":"Pifeltro : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2019-01-10T12:15:00Z","last_updated_date":"2019-01-10T12:15:00Z","reference_number":"EMA/821709/2018","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/pifeltro-epar-public-assessment-report_en.pdf"},
    {"id":"43302","name":"Delstrigo : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2019-01-10T15:58:00Z","last_updated_date":"2019-01-10T15:58:00Z","reference_number":"EMA/874672/2018","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/delstrigo-epar-public-assessment-report_en.pdf"},
    {"id":"43337","name":"Luxturna : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2019-01-11T12:01:00Z","last_updated_date":"2019-01-11T12:01:00Z","reference_number":"EMA/CHMP/700911/2018","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/luxturna-epar-public-assessment-report_en.pdf"},
    {"id":"43377","name":"Ziextenzo : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2019-01-16T17:04:00Z","last_updated_date":"2019-01-16T17:04:00Z","reference_number":"EMA/CHMP/706001/2018","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/ziextenzo-epar-public-assessment-report_en.pdf"},
    {"id":"43438","name":"Silodosin Recordati : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2019-01-22T12:40:00Z","last_updated_date":"2019-01-22T12:40:00Z","reference_number":"EMA/CHMP/845183/2018","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/silodosin-recordati-epar-public-assessment-report_en.pdf"},
    {"id":"43492","name":"Poteligeo : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2019-01-28T11:00:00Z","last_updated_date":"2019-01-28T11:00:00Z","reference_number":"EMA/698539/2018","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/poteligeo-epar-public-assessment-report_en.pdf"},
    {"id":"43506","name":"Jivi : Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2019-01-28T12:38:00Z","last_updated_date":"2019-01-28T12:38:00Z","reference_number":"EMA/698571/2018","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/jivi-public-assessment-report_en.pdf"},
    {"id":"43617","name":"Namuscla : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2019-02-01T18:01:00Z","last_updated_date":"2019-02-01T18:01:00Z","reference_number":"EMA/831802/2018","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/namuscla-epar-public-assessment-report_en.pdf"},
    {"id":"43640","name":"Bevespi Aerosphere : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2019-02-05T15:39:00Z","last_updated_date":"2019-02-05T15:39:00Z","reference_number":"EMA/778350/2018","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/bevespi-aerosphere-epar-public-assessment-report_en.pdf"},
    {"id":"43666","name":"Isemid : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2019-02-07T13:59:00Z","last_updated_date":"2025-10-08T11:11:11Z","reference_number":"EMA/802659/2018","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/isemid-epar-public-assessment-report_en.pdf"},
    {"id":"43678","name":"Syvazul BTV : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2019-02-08T11:08:00Z","last_updated_date":"2025-09-02T11:11:11Z","reference_number":"EMA/802733/2018","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/syvazul-btv-epar-public-assessment-report_en.pdf"},
    {"id":"43729","name":"Eladynos : EPAR - Refusal public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2019-02-14T15:07:00Z","last_updated_date":"2019-02-14T15:07:00Z","reference_number":"EMA/CHMP/581111/2018","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/eladynos-epar-refusal-public-assessment-report_en.pdf"},
    {"id":"43733","name":"Emgality : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2019-02-14T17:32:00Z","last_updated_date":"2019-02-14T17:32:00Z","reference_number":"EMA/708631/2018","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/emgality-epar-public-assessment-report_en.pdf"},
    {"id":"43840","name":"Public statement on Eperzan: Withdrawal of the marketing authorisation in the European Union","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2019-02-20T16:35:00Z","last_updated_date":"2019-02-20T16:35:00Z","reference_number":"EMA/824408/2018","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/public-statement-eperzan-withdrawal-marketing-authorisation-european-union_en.pdf"},
    {"id":"43906","name":"Ghryvelin (previously Macimorelin Aeterna Zentaris) : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2019-02-26T09:40:00Z","last_updated_date":"2019-02-26T09:40:00Z","reference_number":"EMA/CHMP/845216/2018","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/ghryvelin-previously-macimorelin-aeterna-zentaris-epar-public-assessment-report_en.pdf"},
    {"id":"43952","name":"Kriptazen : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2019-03-01T10:11:00Z","last_updated_date":"2025-10-09T11:00:00Z","reference_number":"EMA/867848/2018","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/kriptazen-epar-public-assessment-report_en.pdf"},
    {"id":"43968","name":"Evant : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2019-03-01T16:51:00Z","last_updated_date":"2025-09-09T11:11:11Z","reference_number":"EMA/861413/2018","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/evant-epar-public-assessment-report_en.pdf"},
    {"id":"43972","name":"Rizmoic : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2019-03-01T17:31:00Z","last_updated_date":"2019-03-01T17:31:00Z","reference_number":"EMA/466/2019","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/rizmoic-epar-public-assessment-report_en.pdf"},
    {"id":"44035","name":"Lusutrombopag Shionogi : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2019-03-14T16:07:00Z","last_updated_date":"2019-03-14T16:07:00Z","reference_number":"EMA/CHMP/817852/2018","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/lusutrombopag-shionogi-epar-public-assessment-report_en.pdf"},
    {"id":"44082","name":"Longrange : EPAR - Refusal public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2019-03-21T09:45:00Z","last_updated_date":"2019-03-21T09:45:00Z","reference_number":"EMA/804461/2018","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/longrange-epar-refusal-public-assessment-report_en.pdf"},
    {"id":"44085","name":"Erleada : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2019-03-21T14:27:00Z","last_updated_date":"2019-03-21T14:27:00Z","reference_number":"EMA/879617/2018","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/erleada-epar-public-assessment-report_en.pdf"},
    {"id":"44157","name":"Febuxostat Krka : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2019-03-29T15:55:00Z","last_updated_date":"2019-03-29T15:55:00Z","reference_number":"EMA/123663/2019","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/febuxostat-krka-epar-public-assessment-report_en.pdf"},
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    {"id":"44539","name":"Waylivra : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2019-05-20T10:48:00Z","last_updated_date":"2019-05-20T10:48:00Z","reference_number":"EMA/180717/2019","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/waylivra-epar-public-assessment-report_en.pdf"},
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    {"id":"44878","name":"Doptelet : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2019-06-25T12:35:00Z","last_updated_date":"2019-06-25T12:35:00Z","reference_number":"EMA/CHMP/322871/2019","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/doptelet-epar-public-assessment-report_en.pdf"},
    {"id":"44901","name":"Skyrizi : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2019-06-26T17:19:00Z","last_updated_date":"2019-06-26T17:19:00Z","reference_number":"EMA/191996/2019","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/skyrizi-epar-public-assessment-report_en.pdf"},
    {"id":"44917","name":"Ondexxya : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2019-06-27T15:54:00Z","last_updated_date":"2019-06-27T15:54:00Z","reference_number":"EMA/347546/2019","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/ondexxya-epar-public-assessment-report_en.pdf"},
    {"id":"44934","name":"Grasustek : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2019-06-28T10:05:00Z","last_updated_date":"2019-06-28T10:05:00Z","reference_number":"EMA/CHMP/323149/2019","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/grasustek-epar-public-assessment-report_en.pdf"},
    {"id":"44958","name":"Esperoct : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2019-06-28T14:52:00Z","last_updated_date":"2019-06-28T14:52:00Z","reference_number":"EMA/CHMP/352302/2019","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/esperoct-epar-public-assessment-report_en.pdf"},
    {"id":"44980","name":"Sixmo : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2019-07-02T15:26:00Z","last_updated_date":"2025-08-14T18:15:43Z","reference_number":"EMA/CHMP/266482/2019","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/sixmo-epar-public-assessment-report_en.pdf"},
    {"id":"45001","name":"Libtayo : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2019-07-05T14:52:00Z","last_updated_date":"2019-07-05T14:52:00Z","reference_number":"EMA/CHMP/368468/2019","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/libtayo-epar-public-assessment-report_en.pdf"},
    {"id":"45007","name":"Talzenna : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2019-07-08T10:28:00Z","last_updated_date":"2019-07-08T10:28:00Z","reference_number":"EMA/270498/2019","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/talzenna-epar-public-assessment-report_en.pdf"},
    {"id":"45018","name":"Xromi : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2019-07-08T16:39:00Z","last_updated_date":"2019-07-08T16:39:00Z","reference_number":"EMA/CHMP/170631/2019","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/xromi-epar-public-assessment-report_en.pdf"},
    {"id":"45033","name":"Ultomiris : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2019-07-10T15:23:00Z","last_updated_date":"2019-07-10T15:23:00Z","reference_number":"EMA/CHMP/220699/2019","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/ultomiris-epar-public-assessment-report_en.pdf"},
    {"id":"45058","name":"Ambrisentan Mylan : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2019-07-15T10:14:00Z","last_updated_date":"2019-07-15T10:14:00Z","reference_number":"EMA/CHMP/294468/2019","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/ambrisentan-mylan-epar-public-assessment-report_en.pdf"},
    {"id":"45110","name":"Trecondi : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2019-07-22T12:24:00Z","last_updated_date":"2019-07-22T12:24:00Z","reference_number":"EMA/903773/2019","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/trecondi-epar-public-assessment-report_en.pdf"},
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    {"id":"45144","name":"Cufence : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2019-07-29T11:53:00Z","last_updated_date":"2019-07-29T11:53:00Z","reference_number":"EMA/330602/2019","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/cufence-epar-public-assessment-report_en.pdf"},
    {"id":"45159","name":"LysaKare : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2019-07-30T15:03:00Z","last_updated_date":"2019-07-30T15:03:00Z","reference_number":"EMA/CHMP/363968/2019","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/lysakare-epar-public-assessment-report_en.pdf"},
    {"id":"45165","name":"Nasym : EPAR - Public Assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2019-07-31T13:56:00Z","last_updated_date":"2025-10-09T15:15:00Z","reference_number":"EMA/290800/2019","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/nasym-epar-public-assessment-report_en.pdf"},
    {"id":"45187","name":"Evicto : Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2019-08-01T14:20:00Z","last_updated_date":"2024-06-25T16:45:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/evicto-public-assessment-report_en.pdf"},
    {"id":"45243","name":"Striascan : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2019-08-02T11:27:00Z","last_updated_date":"2019-08-02T11:27:00Z","reference_number":"EMA/280752/2019","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/striascan-epar-public-assessment-report_en.pdf"},
    {"id":"45254","name":"Azacitidine Celgene : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2019-08-14T10:13:00Z","last_updated_date":"2021-08-04T17:33:00Z","reference_number":"EMA/CHMP/445484/2019","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/azacitidine-celgene-epar-public-assessment-report_en.pdf"},
    {"id":"45326","name":"Doxolipad : EPAR - Refusal public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2019-08-26T11:27:00Z","last_updated_date":"2019-08-26T11:27:00Z","reference_number":"EMA/398153/2019","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/doxolipad-epar-refusal-public-assessment-report_en.pdf"},
    {"id":"45335","name":"Posaconazole AHCL : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2019-08-28T09:25:00Z","last_updated_date":"2019-08-28T09:25:00Z","reference_number":"EMA/354180/2019","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/posaconazole-ahcl-epar-public-assessment-report_en.pdf"},
    {"id":"45342","name":"Posaconazole Accord : EPAR - Assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2019-08-28T11:23:00Z","last_updated_date":"2019-08-28T11:23:00Z","reference_number":"EMA/354142/2019","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/posaconazole-accord-epar-assessment-report_en.pdf"},
    {"id":"45380","name":"Dovato : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2019-09-04T11:29:00Z","last_updated_date":"2019-09-04T11:29:00Z","reference_number":"EMA/267082/2019","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/dovato-epar-public-assessment-report_en.pdf"},
    {"id":"45411","name":"HorStem: EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2019-09-10T16:51:00Z","last_updated_date":"2024-02-19T17:14:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/horstem-epar-public-assessment-report_en.pdf","translations":{"bg":"https://www.ema.europa.eu/bg/documents/assessment-report/horstem-epar-public-assessment-report_bg.pdf","es":"https://www.ema.europa.eu/es/documents/assessment-report/horstem-epar-public-assessment-report_es.pdf","cs":"https://www.ema.europa.eu/cs/documents/assessment-report/horstem-epar-public-assessment-report_cs.pdf","da":"https://www.ema.europa.eu/da/documents/assessment-report/horstem-epar-public-assessment-report_da.pdf","de":"https://www.ema.europa.eu/de/documents/assessment-report/horstem-epar-public-assessment-report_de.pdf","et":"https://www.ema.europa.eu/et/documents/assessment-report/horstem-epar-public-assessment-report_et.pdf","el":"https://www.ema.europa.eu/el/documents/assessment-report/horstem-epar-public-assessment-report_el.pdf","fr":"https://www.ema.europa.eu/fr/documents/assessment-report/horstem-epar-public-assessment-report_fr.pdf","ga":"https://www.ema.europa.eu/ga/documents/assessment-report/horstem-epar-public-assessment-report_ga.pdf","hr":"https://www.ema.europa.eu/hr/documents/assessment-report/horstem-epar-public-assessment-report_hr.pdf","it":"https://www.ema.europa.eu/it/documents/assessment-report/horstem-epar-public-assessment-report_it.pdf","lv":"https://www.ema.europa.eu/lv/documents/assessment-report/horstem-epar-public-assessment-report_lv.pdf","lt":"https://www.ema.europa.eu/lt/documents/assessment-report/horstem-epar-public-assessment-report_lt.pdf","hu":"https://www.ema.europa.eu/hu/documents/assessment-report/horstem-epar-public-assessment-report_hu.pdf","mt":"https://www.ema.europa.eu/mt/documents/assessment-report/horstem-epar-public-assessment-report_mt.pdf","nl":"https://www.ema.europa.eu/nl/documents/assessment-report/horstem-epar-public-assessment-report_nl.pdf","pl":"https://www.ema.europa.eu/pl/documents/assessment-report/horstem-epar-public-assessment-report_pl.pdf","pt":"https://www.ema.europa.eu/pt/documents/assessment-report/horstem-epar-public-assessment-report_pt.pdf","ro":"https://www.ema.europa.eu/ro/documents/assessment-report/horstem-epar-public-assessment-report_ro.pdf","sk":"https://www.ema.europa.eu/sk/documents/assessment-report/horstem-epar-public-assessment-report_sk.pdf","sl":"https://www.ema.europa.eu/sl/documents/assessment-report/horstem-epar-public-assessment-report_sl.pdf","fi":"https://www.ema.europa.eu/fi/documents/assessment-report/horstem-epar-public-assessment-report_fi.pdf","sv":"https://www.ema.europa.eu/sv/documents/assessment-report/horstem-epar-public-assessment-report_sv.pdf","is":"https://www.ema.europa.eu/is/documents/assessment-report/horstem-epar-public-assessment-report_is.pdf","no":"https://www.ema.europa.eu/no/documents/assessment-report/horstem-epar-public-assessment-report_no.pdf"}},
    {"id":"45427","name":"Horse Allo 20 : EPAR - Refusal public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2019-09-12T14:10:00Z","last_updated_date":"2019-09-12T14:10:00Z","reference_number":"EMA/805150/2018","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/horse-allo-20-epar-refusal-public-assessment-report_en.pdf"},
    {"id":"45440","name":"Lacosamide UCB : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2019-09-12T17:19:00Z","last_updated_date":"2019-09-12T17:19:00Z","reference_number":"EMA/CHMP/441053/2019","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/lacosamide-ucb-epar-public-assessment-report_en.pdf"},
    {"id":"45510","name":"Temybric Ellipta : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2019-09-23T15:41:00Z","last_updated_date":"2022-11-24T15:31:00Z","reference_number":"EMA/299628/2019","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/temybric-ellipta-epar-public-assessment-report_en.pdf"},
    {"id":"45539","name":"Inbrija : EPAR - Public assessmente report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2019-09-30T15:00:00Z","last_updated_date":"2019-09-30T15:00:00Z","reference_number":"EMA/CHMP/450567/2019","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/inbrija-epar-public-assessmente-report_en.pdf"},
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    {"id":"46396","name":"Mirataz : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2020-01-08T12:56:00Z","last_updated_date":"2025-10-09T14:40:00Z","reference_number":"EMA/562416/2019","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/mirataz-epar-public-assessment-report_en.pdf"},
    {"id":"46400","name":"Neptra : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2020-01-09T09:20:00Z","last_updated_date":"2025-10-09T12:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/neptra-epar-public-assessment-report_en.pdf"},
    {"id":"46510","name":"Mayzent : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2020-01-23T15:53:00Z","last_updated_date":"2020-01-23T15:53:00Z","reference_number":"EMA/CHMP/652767/2019","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/mayzent-epar-public-assessment-report_en.pdf"},
    {"id":"46577","name":"Polivy : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2020-01-27T13:57:00Z","last_updated_date":"2020-01-27T13:57:00Z","reference_number":"EMA/CHMP/690748/2019","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/polivy-epar-public-assessment-report_en.pdf"},
    {"id":"46684","name":"Baqsimi : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2020-02-06T13:13:00Z","last_updated_date":"2020-02-06T13:13:00Z","reference_number":"EMA/CHMP/602404/2019  ","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/baqsimi-epar-public-assessment-report_en.pdf"},
    {"id":"46706","name":"Imfinzi : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2018-10-30T14:38:00Z","last_updated_date":"2020-02-11T11:11:11Z","reference_number":"EMA/CHMP/548232/2018","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/imfinzi-epar-public-assessment-report_en.pdf"},
    {"id":"46713","name":"Tavlesse : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2020-02-11T16:04:00Z","last_updated_date":"2020-02-11T16:04:00Z","reference_number":"EMA/CHMP/654949/2019","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/tavlesse-epar-public-assessment-report_en.pdf"},
    {"id":"46718","name":"Stelfonta : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2020-02-11T16:04:00Z","last_updated_date":"2025-10-14T12:22:22Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/stelfonta-epar-public-assessment-report_en.pdf"},
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    {"id":"46780","name":"Beovu : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2020-02-18T10:52:00Z","last_updated_date":"2020-02-18T10:52:00Z","reference_number":"EMA/23630/2020","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/beovu-epar-public-assessment-report_en.pdf"},
    {"id":"46798","name":"Isturisa : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2020-02-18T16:02:00Z","last_updated_date":"2020-12-17T10:35:00Z","reference_number":"EMA/653461/2019 Corr.2","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/isturisa-epar-public-assessment-report_en.pdf"},
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    {"id":"46825","name":"Azacitidine Accord : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2020-02-21T14:31:00Z","last_updated_date":"2020-02-21T14:31:00Z","reference_number":"EMA/CHMP/22245/2020","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/azacitidine-accord-epar-public-assessment-report_en.pdf"},
    {"id":"46843","name":"Evenity : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2020-02-24T17:02:00Z","last_updated_date":"2020-02-24T17:02:00Z","reference_number":"EMA/26554/2020","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/evenity-epar-public-assessment-report_en.pdf"},
    {"id":"46883","name":"Recarbrio : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2020-02-26T15:22:00Z","last_updated_date":"2020-02-26T15:22:00Z","reference_number":"EMA/7621/2020","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/recarbrio-epar-public-assessment-report_en.pdf"},
    {"id":"46889","name":"Aservo EquiHaler : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2020-02-28T09:05:00Z","last_updated_date":"2024-06-28T18:41:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/aservo-equihaler-epar-public-assessment-report_en.pdf"},
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    {"id":"46974","name":"Givlaari : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2020-03-09T14:02:00Z","last_updated_date":"2020-03-09T14:02:00Z","reference_number":"EMA/CHMP/70703/2020","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/givlaari-epar-public-assessment-report_en.pdf"},
    {"id":"47269","name":"Azacitidine betapharm : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2020-04-01T14:06:00Z","last_updated_date":"2020-04-01T14:06:00Z","reference_number":"EMA/CHMP/91461/2020 ","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/azacitidine-betapharm-epar-public-assessment-report_en.pdf"},
    {"id":"47328","name":"Nubeqa : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2020-04-03T13:25:00Z","last_updated_date":"2020-04-03T13:25:00Z","reference_number":"EMA/84124/2020","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/nubeqa-epar-public-assessment-report_en.pdf"},
    {"id":"47347","name":"Azacitidine Mylan : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2020-04-06T09:36:00Z","last_updated_date":"2020-04-06T09:36:00Z","reference_number":"EMA/CHMP/36881/2020","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/azacitidine-mylan-epar-public-assessment-report_en.pdf"},
    {"id":"47363","name":"Ruxience : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2020-04-07T11:24:00Z","last_updated_date":"2020-04-07T11:24:00Z","reference_number":"EMA/CHMP/155201/2020 ","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/ruxience-epar-public-assessment-report_en.pdf"},
    {"id":"47372","name":"Budesonide/Formoterol Teva Pharma B.V. : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2020-04-07T14:32:00Z","last_updated_date":"2020-04-07T14:32:00Z","reference_number":"EMA/83618/2020","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/budesonideformoterol-teva-pharma-bv-epar-public-assessment-report_en.pdf-0"},
    {"id":"47381","name":"Vaxchora : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2020-04-08T14:42:00Z","last_updated_date":"2020-04-08T14:42:00Z","reference_number":"EMA/82271/2020 ","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/vaxchora-epar-public-assessment-report_en.pdf"},
    {"id":"47391","name":"Trepulmix : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2020-04-08T17:31:00Z","last_updated_date":"2020-04-08T17:31:00Z","reference_number":"EMA/CHMP/86002/2020","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/trepulmix-epar-public-assessment-report_en.pdf"},
    {"id":"47411","name":"Cinacalcet Accordpharma : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2020-04-15T13:56:00Z","last_updated_date":"2020-04-15T13:56:00Z","reference_number":"EMA/92635/2020","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/cinacalcet-accordpharma-epar-public-assessment-report_en.pdf"},
    {"id":"47419","name":"Liumjev : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2020-04-16T16:42:00Z","last_updated_date":"2020-04-16T16:42:00Z","reference_number":"EMA/86760/2020","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/liumjev-epar-public-assessment-report_en.pdf"},
    {"id":"47427","name":"Arsenic trioxide Mylan : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2020-04-17T10:48:00Z","last_updated_date":"2025-05-06T11:22:00Z","reference_number":"EMA/CHMP/638190/2019","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/arsenic-trioxide-mylan-epar-public-assessment-report_en.pdf"},
    {"id":"47453","name":"Staquis : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2020-04-22T11:43:00Z","last_updated_date":"2022-02-08T14:14:00Z","reference_number":"EMA/88816/2020","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/staquis-epar-public-assessment-report_en.pdf"},
    {"id":"47476","name":"Nustendi : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2020-04-24T10:18:00Z","last_updated_date":"2020-04-24T10:18:00Z","reference_number":"EMA/CHMP/86205/2020 ","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/nustendi-epar-public-assessment-report_en.pdf"},
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    {"id":"47832","name":"Fluad Tetra : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2020-05-29T16:32:00Z","last_updated_date":"2026-02-26T16:00:00Z","reference_number":"EMA/200444/2020","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/fluad-tetra-epar-public-assessment-report_en.pdf"},
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    {"id":"48158","name":"Tulaven : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2020-06-26T11:33:00Z","last_updated_date":"2025-10-14T11:11:11Z","reference_number":"EMA/94834/2020","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/tulaven-epar-public-assessment-report_en.pdf"},
    {"id":"48166","name":"Tulissin : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2020-06-26T12:20:00Z","last_updated_date":"2025-10-14T11:11:01Z","reference_number":"EMA/94821/2020","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/tulissin-epar-public-assessment-report_en.pdf"},
    {"id":"48216","name":"Fingolimod Accord : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2020-07-03T11:28:00Z","last_updated_date":"2020-07-03T11:28:00Z","reference_number":"EMA/CHMP/267804/2020","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/fingolimod-accord-epar-public-assessment-report_en.pdf"},
    {"id":"48231","name":"Veklury : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2020-07-06T11:30:00Z","last_updated_date":"2020-07-06T11:30:00Z","reference_number":"EMA/357513/2020","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/veklury-epar-public-assessment-report_en.pdf"},
    {"id":"48248","name":"Paliperidone Janssen-Cilag International : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2020-07-07T15:02:00Z","last_updated_date":"2020-07-07T15:02:00Z","reference_number":"EMA/358737/2020","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/paliperidone-janssen-cilag-international-epar-public-assessment-report_en.pdf"},
    {"id":"48253","name":"Insulin aspart Sanofi : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2020-07-07T16:31:00Z","last_updated_date":"2020-07-07T16:31:00Z","reference_number":"EMA/CHMP/269410/2020","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/insulin-aspart-sanofi-epar-public-assessment-report_en.pdf"},
    {"id":"48266","name":"Reblozyl  : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2020-07-08T16:57:00Z","last_updated_date":"2020-07-08T16:57:00Z","reference_number":"EMA/270924/2020","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/reblozyl-epar-public-assessment-report_en.pdf"},
    {"id":"48274","name":"Faslodex : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2020-07-10T09:35:00Z","last_updated_date":"2020-07-10T09:35:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/faslodex-epar-public-assessment-report_en.pdf"},
    {"id":"48279","name":"Daurismo : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2020-07-10T10:57:00Z","last_updated_date":"2020-07-10T10:57:00Z","reference_number":"EMA/CHMP/284008/2020","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/daurismo-epar-public-assessment-report_en.pdf"},
    {"id":"48350","name":"Enerzair Breezhaler : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2020-07-21T14:58:00Z","last_updated_date":"2020-07-21T14:58:00Z","reference_number":"EMA/271332/2020","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/enerzair-breezhaler-epar-public-assessment-report_en.pdf"},
    {"id":"48360","name":"Mvabea : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2020-07-23T10:00:00Z","last_updated_date":"2020-11-24T16:42:00Z","reference_number":"EMA/323668/2020","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/mvabea-epar-public-assessment-report_en.pdf"},
    {"id":"48367","name":"Zabdeno : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2020-07-23T10:27:00Z","last_updated_date":"2020-07-23T10:27:00Z","reference_number":"EMA/323670/2020","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/zabdeno-epar-public-assessment-report_en.pdf"},
    {"id":"48435","name":"Zercepac : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2020-07-28T10:26:00Z","last_updated_date":"2020-07-28T10:26:00Z","reference_number":"EMA/327248/2020","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/zercepac-epar-public-assessment-report_en.pdf"},
    {"id":"48506","name":"Piqray : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2020-07-30T17:16:00Z","last_updated_date":"2020-07-30T17:16:00Z","reference_number":"EMA/CHMP/321881/2020","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/piqray-epar-public-assessment-report_en.pdf"},
    {"id":"48561","name":"Apixaban Accord : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2020-08-06T16:27:00Z","last_updated_date":"2020-08-06T16:27:00Z","reference_number":"EMA/322602/2020","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/apixaban-accord-epar-public-assessment-report_en.pdf"},
    {"id":"48566","name":"Xenleta : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2020-08-06T17:13:00Z","last_updated_date":"2020-08-06T17:13:00Z","reference_number":"EMA/325848/2020","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/xenleta-epar-public-assessment-report_en.pdf"},
    {"id":"48576","name":"Pretomanid FGK : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2020-08-11T09:37:00Z","last_updated_date":"2020-08-11T09:37:00Z","reference_number":"EMA/200048/2020","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/pretomanid-fgk-epar-public-assessment-report_en.pdf"},
    {"id":"48596","name":"Hepcludex : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2020-08-12T14:40:00Z","last_updated_date":"2020-08-12T14:40:00Z","reference_number":"EMA/326446/2020","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/hepcludex-epar-public-assessment-report_en.pdf"},
    {"id":"48692","name":"Methylthioninium chloride Cosmo : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2020-08-26T10:28:00Z","last_updated_date":"2020-08-26T10:28:00Z","reference_number":"EMA/CHMP/424242/2020","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/methylthioninium-chloride-cosmo-epar-public-assessment-report_en.pdf"},
    {"id":"48700","name":"Lydaxx : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2020-08-27T10:15:00Z","last_updated_date":"2025-10-09T12:22:02Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/lydaxx-epar-public-assessment-report_en.pdf"},
    {"id":"48705","name":"Gencebok : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2020-08-27T11:38:00Z","last_updated_date":"2020-08-27T11:38:00Z","reference_number":"EMA/372967/2020","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/gencebok-epar-public-assessment-report_en.pdf"},
    {"id":"48713","name":"Idefirix : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2020-08-28T11:05:00Z","last_updated_date":"2020-08-28T11:05:00Z","reference_number":"EMA/372587/2020 Rev 1","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/idefirix-epar-public-assessment-report_en.pdf"},
    {"id":"48736","name":"Zimbus Breezhaler : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2020-09-02T16:14:00Z","last_updated_date":"2020-09-02T16:14:00Z","reference_number":"EMA/271341/2020","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/zimbus-breezhaler-epar-public-assessment-report_en.pdf"},
    {"id":"48740","name":"Aybintio : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2020-09-02T17:19:00Z","last_updated_date":"2020-09-02T17:19:00Z","reference_number":"EMA/380645/2020","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/aybintio-epar-public-assessment-report_en.pdf"},
    {"id":"48748","name":"Vectormune FP ILT + AE : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2020-09-03T11:08:00Z","last_updated_date":"2025-10-15T12:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/vectormune-fp-ilt-ae-epar-public-assessment-report_en.pdf"},
    {"id":"48800","name":"Rozlytrek: EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2020-09-11T15:10:00Z","last_updated_date":"2020-09-11T15:10:00Z","reference_number":"EMA/379739/2020","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/rozlytrek-epar-public-assessment-report_en.pdf"},
    {"id":"48833","name":"Blenrep : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2020-09-17T09:51:00Z","last_updated_date":"2024-03-13T12:28:00Z","reference_number":"EMA/CHMP/414341/2020 Corr.","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/blenrep-epar-public-assessment-report_en.pdf"},
    {"id":"48897","name":"Jyseleca : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2020-09-28T10:43:00Z","last_updated_date":"2020-09-28T10:43:00Z","reference_number":"EMA/424374/2020","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/jyseleca-epar-public-assessment-report_en.pdf"},
    {"id":"48908","name":"Kaftrio : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2020-09-29T11:13:00Z","last_updated_date":"2020-09-29T11:13:00Z","reference_number":"EMA/385871/2020 Rev.1 ","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/kaftrio-epar-public-assessment-report_en.pdf"},
    {"id":"48914","name":"Ayvakyt : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2020-09-30T18:01:00Z","last_updated_date":"2020-09-30T18:01:00Z","reference_number":"EMA/451735/2020","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/ayvakyt-epar-public-assessment-report_en.pdf"},
    {"id":"48930","name":"Arsenic trioxide medac : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2020-10-01T14:37:00Z","last_updated_date":"2020-10-01T14:37:00Z","reference_number":"EMA/CHMP/411838/2020","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/arsenic-trioxide-medac-epar-public-assessment-report_en.pdf"},
    {"id":"48934","name":"Fampridine Accord : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2020-10-02T11:21:00Z","last_updated_date":"2020-10-02T11:21:00Z","reference_number":"EMA/CHMP/432671/2020","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/fampridine-accord-epar-public-assessment-report_en.pdf"},
    {"id":"48959","name":"Zynrelef : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2020-10-06T17:58:00Z","last_updated_date":"2023-11-22T12:00:00Z","reference_number":"EMA/CHMP/450646/2020","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/zynrelef-epar-public-assessment-report_en.pdf"},
    {"id":"48988","name":"Equidacent : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2020-10-12T09:35:00Z","last_updated_date":"2021-11-25T16:47:00Z","reference_number":"EMA/427966/2020","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/equidacent-epar-public-assessment-report_en.pdf"},
    {"id":"49147","name":"Cabazitaxel Accord : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2020-10-28T15:10:00Z","last_updated_date":"2020-10-28T15:10:00Z","reference_number":"EMA/267872/2020","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/cabazitaxel-accord-epar-public-assessment-report_en.pdf"},
    {"id":"49216","name":"Calquence : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2020-11-11T17:34:00Z","last_updated_date":"2020-11-11T17:34:00Z","reference_number":"EMA/CHMP/458179/2020","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/calquence-epar-public-assessment-report_en.pdf"},
    {"id":"49277","name":"Arikayce liposomal : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2020-11-18T16:24:00Z","last_updated_date":"2020-11-18T16:24:00Z","reference_number":"EMA/473660/2020","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/arikayce-liposomal-epar-public-assessment-report_en.pdf"},
    {"id":"49324","name":"Nyvepria : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2020-11-23T17:11:00Z","last_updated_date":"2020-11-23T17:11:00Z","reference_number":"EMA/CHMP/603684/2020","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/nyvepria-epar-public-assessment-report_en.pdf"},
    {"id":"49329","name":"Adakveo : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2020-11-24T11:24:00Z","last_updated_date":"2023-08-21T14:02:00Z","reference_number":"EMA/427120/2020","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/adakveo-epar-public-assessment-report_en.pdf"},
    {"id":"49336","name":"Rivaroxaban Accord : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2020-11-24T12:08:00Z","last_updated_date":"2020-11-24T12:08:00Z","reference_number":"EMA/550657/2020","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/rivaroxaban-accord-epar-public-assessment-report_en.pdf"},
    {"id":"49357","name":"Oxlumo : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2020-11-25T14:16:00Z","last_updated_date":"2020-11-25T14:16:00Z","reference_number":"EMA/568312/2020","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/oxlumo-epar-public-assessment-report_en.pdf"},
    {"id":"49365","name":"Supemtek : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2020-11-25T15:39:00Z","last_updated_date":"2020-11-25T15:39:00Z","reference_number":"EMA/522939/2020","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/supemtek-epar-public-assessment-report_en.pdf"},
    {"id":"49370","name":"Phelinun : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2020-11-25T16:26:00Z","last_updated_date":"2020-11-25T16:26:00Z","reference_number":"EMA/CHMP/624882/2020","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/phelinun-epar-public-assessment-report_en.pdf"},
    {"id":"49385","name":"MenQuadfi : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2020-11-27T09:24:00Z","last_updated_date":"2020-11-27T09:24:00Z","reference_number":"EMA/522942/2020","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/menquadfi-epar-public-assessment-report_en.pdf"},
    {"id":"49391","name":"Obiltoxaximab SFL : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2020-11-27T11:48:00Z","last_updated_date":"2024-09-09T12:12:00Z","reference_number":"EMA/524933/2020","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/obiltoxaximab-sfl-epar-public-assessment-report_en.pdf"},
    {"id":"49495","name":"Tulinovet : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2020-12-09T16:23:00Z","last_updated_date":"2025-10-14T11:11:01Z","reference_number":"EMA/457567/2020","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/tulinovet-epar-public-assessment-report_en.pdf"},
    {"id":"49529","name":"Exparel liposomal : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2020-12-10T17:17:00Z","last_updated_date":"2020-12-10T17:17:00Z","reference_number":"EMA/CHMP/528272/2020","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/exparel-liposomal-epar-public-assessment-report_en.pdf"},
    {"id":"49602","name":"Increxxa : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2020-12-17T10:04:00Z","last_updated_date":"2025-10-08T14:00:00Z","reference_number":"EMA/457503/2020","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/increxxa-epar-public-assessment-report_en.pdf"},
    {"id":"49645","name":"Turalio : EPAR - Refusal public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2020-12-18T09:48:00Z","last_updated_date":"2020-12-18T09:48:00Z","reference_number":"EMA/CHMP/431740/2020","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/turalio-epar-refusal-public-assessment-report_en.pdf"},
    {"id":"49646","name":"Turalio : EPAR - Refusal public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2020-12-18T09:48:00Z","last_updated_date":"2020-12-18T09:48:00Z","reference_number":"EMA/CHMP/431740/2020","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/turalio-epar-refusal-public-assessment-report_en.pdf-0"},
    {"id":"49667","name":"Palforzia : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2020-12-21T13:33:00Z","last_updated_date":"2020-12-21T13:33:00Z","reference_number":"EMA/583336/2020","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/palforzia-epar-public-assessment-report_en.pdf"},
    {"id":"49676","name":"Libmeldy : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2020-12-22T11:08:00Z","last_updated_date":"2020-12-22T11:08:00Z","reference_number":"EMA/584450/2020","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/libmeldy-epar-public-assessment-report_en.pdf"},
    {"id":"49695","name":"Comirnaty : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2020-12-23T22:35:00Z","last_updated_date":"2023-10-23T12:57:00Z","reference_number":"EMA/707383/2020 Corr.2","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/comirnaty-epar-public-assessment-report_en.pdf"},
    {"id":"49706","name":"Rekambys : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2021-01-04T14:49:00Z","last_updated_date":"2021-01-04T14:49:00Z","reference_number":"EMA/CHMP/455298/2020","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/rekambys-epar-public-assessment-report_en.pdf"},
    {"id":"49714","name":"Vocabria : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2021-01-05T11:53:00Z","last_updated_date":"2021-01-05T11:53:00Z","reference_number":"EMA/586324/2020","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/vocabria-epar-public-assessment-report_en.pdf"},
    {"id":"49718","name":"Trixeo Aerosphere : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2021-01-05T14:54:00Z","last_updated_date":"2021-01-05T14:54:00Z","reference_number":"EMA/582495/2020","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/trixeo-aerosphere-epar-public-assessment-report_en.pdf"},
    {"id":"49733","name":"Livogiva : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2021-01-06T12:44:00Z","last_updated_date":"2021-01-06T12:44:00Z","reference_number":"EMA/CHMP/379175/2020","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/livogiva-epar-public-assessment-report_en.pdf"},
    {"id":"49738","name":"Leqvio : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2021-01-06T15:19:00Z","last_updated_date":"2021-01-06T15:19:00Z","reference_number":"EMA/696912/2020","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/leqvio-epar-public-assessment-report_en.pdf"},
    {"id":"49748","name":"Lenalidomide Mylan : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2021-01-07T16:02:00Z","last_updated_date":"2021-01-07T16:02:00Z","reference_number":"EMA/CHMP/583241/2020","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/lenalidomide-mylan-epar-public-assessment-report_en.pdf"},
    {"id":"49754","name":"Fintepla : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2021-01-08T10:51:00Z","last_updated_date":"2021-04-29T11:46:00Z","reference_number":"EMA/639853/2020 Corr.","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/fintepla-epar-public-assessment-report_en.pdf"},
    {"id":"49799","name":"Phesgo : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2021-01-13T15:36:00Z","last_updated_date":"2021-01-13T15:36:00Z","reference_number":"EMA/CHMP/646782/2020","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/phesgo-epar-public-assessment-report_en.pdf"},
    {"id":"49825","name":"Qutavina : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2021-01-18T15:02:00Z","last_updated_date":"2021-01-18T15:02:00Z","reference_number":"EMA/CHMP/379170/2020","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/qutavina-epar-public-assessment-report_en.pdf"},
    {"id":"49849","name":"Spikevax (previously COVID-19 Vaccine Moderna) : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2021-01-20T18:10:00Z","last_updated_date":"2021-01-20T18:10:00Z","reference_number":"EMA/15689/2021","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/spikevax-previously-covid-19-vaccine-moderna-epar-public-assessment-report_en.pdf"},
    {"id":"49871","name":"Roclanda : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2021-01-21T10:37:00Z","last_updated_date":"2021-01-21T10:37:00Z","reference_number":"EMA/CHMP/637805/2020","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/roclanda-epar-public-assessment-report_en.pdf"},
    {"id":"49898","name":"Xofluza : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2021-01-22T11:50:00Z","last_updated_date":"2021-01-22T11:50:00Z","reference_number":"EMA/CHMP/537088/2020","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/xofluza-epar-public-assessment-report_en.pdf"},
    {"id":"49927","name":"Elzonris : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2021-01-25T10:40:00Z","last_updated_date":"2021-01-25T10:40:00Z","reference_number":"EMA/CHMP/24699/2021","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/elzonris-epar-public-assessment-report_en.pdf"},
    {"id":"49936","name":"Tecartus : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2021-01-25T15:58:00Z","last_updated_date":"2021-01-25T15:58:00Z","reference_number":"EMA/588798/2020","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/tecartus-epar-public-assessment-report_en.pdf"},
    {"id":"50057","name":"Innovax-ND-ILT : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2021-02-03T16:50:00Z","last_updated_date":"2024-10-11T10:31:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/innovax-nd-ilt-epar-public-assessment-report_en.pdf"},
    {"id":"50107","name":"Enhertu : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2021-02-08T17:22:00Z","last_updated_date":"2021-02-08T17:22:00Z","reference_number":"EMA/CHMP/636117/2022","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/enhertu-epar-public-assessment-report_en.pdf"},
    {"id":"50110","name":"Clopidogrel / Acetylsalicylic acid Mylan : EPAR  - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2020-01-24T17:40:00Z","last_updated_date":"2020-01-24T17:40:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/clopidogrel-acetylsalicylic-acid-mylan-epar-public-assessment-report_en.pdf"},
    {"id":"50137","name":"Luveris : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2000-07-27T14:29:00Z","last_updated_date":"2000-07-27T14:29:00Z","reference_number":"CPMP/1390/00","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/luveris-epar-public-assessment-report_en.pdf"},
    {"id":"50158","name":"Rukobia : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2021-02-12T14:29:00Z","last_updated_date":"2021-02-12T14:29:00Z","reference_number":"EMA/702367/2020","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/rukobia-epar-public-assessment-report_en.pdf"},
    {"id":"50182","name":"Targretin : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2021-02-16T10:24:00Z","last_updated_date":"2021-02-16T10:24:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/targretin-epar-public-assessment-report_en.pdf"},
    {"id":"50200","name":"Enzepi : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2021-02-17T12:09:00Z","last_updated_date":"2021-02-17T12:09:00Z","reference_number":"EMA/340098/2016","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/enzepi-epar-public-assessment-report_en.pdf-0"},
    {"id":"50208","name":"Mhyosphere PCV ID : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2021-02-17T17:40:00Z","last_updated_date":"2025-03-14T11:11:11Z","reference_number":"EMA/457772/2020","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/mhyosphere-pcv-id-epar-public-assessment-report_en.pdf"},
    {"id":"50212","name":"Vaxzevria (previously COVID-19 Vaccine AstraZeneca) : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2021-02-18T09:48:00Z","last_updated_date":"2024-05-07T11:00:00Z","reference_number":"EMA/94907/2021","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/vaxzevria-previously-covid-19-vaccine-astrazeneca-epar-public-assessment-report_en.pdf"},
    {"id":"50217","name":"Lenalidomide Krka d.d. : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2021-02-18T12:18:00Z","last_updated_date":"2023-07-10T15:15:00Z","reference_number":"EMA/CHMP/3809/2021","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/lenalidomide-krka-dd-epar-public-assessment-report_en.pdf"},
    {"id":"50223","name":"Lenalidomide Krka d.d. Novo mesto : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2021-02-18T13:00:00Z","last_updated_date":"2021-02-18T13:00:00Z","reference_number":"EMA/CHMP/3824/2021","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/lenalidomide-krka-dd-novo-mesto-epar-public-assessment-report_en.pdf"},
    {"id":"50227","name":"Lenalidomide Krka : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2021-02-18T14:20:00Z","last_updated_date":"2021-02-18T14:20:00Z","reference_number":"EMA/CHMP/3806/2021","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/lenalidomide-krka-epar-public-assessment-report_en.pdf"},
    {"id":"50241","name":"Tukysa : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2021-02-18T16:04:00Z","last_updated_date":"2021-02-18T16:04:00Z","reference_number":"EMA/78409/2021","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/tukysa-epar-public-assessment-report_en.pdf"},
    {"id":"50298","name":"Yuflyma : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2021-02-26T16:07:00Z","last_updated_date":"2021-02-26T16:07:00Z","reference_number":"EMA/47907/2021","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/yuflyma-epar-public-assessment-report_en.pdf"},
    {"id":"50305","name":"Ogluo : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2021-02-26T16:54:00Z","last_updated_date":"2021-02-26T16:54:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/ogluo-epar-public-assessment-report_en.pdf"},
    {"id":"50323","name":"Heplisav B : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2021-03-01T13:40:00Z","last_updated_date":"2021-03-01T13:40:00Z","reference_number":"EMA/1767/2021","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/heplisav-b-epar-public-assessment-report_en.pdf"},
    {"id":"50374","name":"Inrebic : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2021-03-03T09:22:00Z","last_updated_date":"2021-06-09T09:29:00Z","reference_number":"EMA/705612/2020","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/inrebic-epar-public-assessment-report_en.pdf"},
    {"id":"50471","name":"Onbevzi : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2021-03-05T16:48:00Z","last_updated_date":"2024-10-24T14:40:00Z","reference_number":"EMA/117409/2021","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/onbevzi-epar-public-assessment-report_en.pdf"},
    {"id":"50491","name":"Lumoxiti : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2021-03-09T09:13:00Z","last_updated_date":"2021-08-11T16:37:00Z","reference_number":"EMA/CHMP/36661/2021","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/lumoxiti-epar-public-assessment-report_en.pdf"},
    {"id":"50549","name":"Rexxolide : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2021-03-12T15:25:00Z","last_updated_date":"2025-10-14T11:11:01Z","reference_number":"EMA/557847/2020","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/rexxolide-epar-public-assessment-report_en.pdf"},
    {"id":"50580","name":"Kixelle : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2021-03-16T14:17:00Z","last_updated_date":"2021-03-16T14:17:00Z","reference_number":"EMA/64677/2021","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/kixelle-epar-public-assessment-report_en.pdf"},
    {"id":"50646","name":"COVID-19 Vaccine Janssen : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2021-03-19T20:04:00Z","last_updated_date":"2024-08-09T12:05:00Z","reference_number":"EMA/158424/2021","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/covid-19-vaccine-janssen-epar-public-assessment-report_en.pdf"},
    {"id":"50673","name":"Gamifant : EPAR - Refusal public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2021-03-23T11:00:00Z","last_updated_date":"2021-03-23T11:00:00Z","reference_number":"EMA/656530/2020","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/gamifant-epar-refusal-public-assessment-report_en.pdf"},
    {"id":"50767","name":"Sunitinib Accord : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2021-04-06T17:37:00Z","last_updated_date":"2021-04-06T17:37:00Z","reference_number":"EMA/CHMP/2430/2021","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/sunitinib-accord-epar-public-assessment-report_en.pdf"},
    {"id":"50807","name":"Ontozry : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2021-04-13T15:38:00Z","last_updated_date":"2021-04-13T15:38:00Z","reference_number":"EMA/CHMP/160820/2021","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/ontozry-epar-public-assessment-report_en.pdf"},
    {"id":"50812","name":"Seffalair Spiromax : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2021-04-13T16:36:00Z","last_updated_date":"2021-04-13T16:36:00Z","reference_number":"EMA/99377/2021","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/seffalair-spiromax-epar-public-assessment-report_en.pdf"},
    {"id":"50820","name":"BroPair Spiromax : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2021-04-14T11:11:00Z","last_updated_date":"2025-06-30T16:10:00Z","reference_number":"EMA/CHMP/21349/2021","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/bropair-spiromax-epar-public-assessment-report_en.pdf"},
    {"id":"50831","name":"Enteroporc Coli : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2021-04-14T12:50:00Z","last_updated_date":"2024-05-31T15:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/enteroporc-coli-epar-public-assessment-report_en.pdf"},
    {"id":"50839","name":"Vazkepa : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2021-04-14T17:11:00Z","last_updated_date":"2021-04-14T17:11:00Z","reference_number":"EMA/145271/2021","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/vazkepa-epar-public-assessment-report_en.pdf"},
    {"id":"50860","name":"Sogroya : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2021-04-15T14:10:00Z","last_updated_date":"2021-04-15T14:10:00Z","reference_number":"EMA/95144/2021","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/sogroya-epar-public-assessment-report_en.pdf"},
    {"id":"50867","name":"Oyavas : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2021-04-15T15:07:00Z","last_updated_date":"2021-05-06T11:28:00Z","reference_number":"EMA/197736/2021 Corr.","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/oyavas-epar-public-assessment-report_en.pdf"},
    {"id":"50875","name":"Prevexxion RN+HVT+IBD : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2021-04-15T16:56:00Z","last_updated_date":"2024-12-02T11:11:11Z","reference_number":"EMA/321394/2020","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/prevexxion-rnhvtibd-epar-public-assessment-report_en.pdf"},
    {"id":"50891","name":"Kesimpta : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2021-04-16T15:31:00Z","last_updated_date":"2021-04-16T15:31:00Z","reference_number":"EMA/160608/2021","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/kesimpta-epar-public-assessment-report_en.pdf"},
    {"id":"50896","name":"Prevexxion RN : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2021-04-16T17:05:00Z","last_updated_date":"2025-03-14T11:11:11Z","reference_number":"EMA/321289/2020","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/prevexxion-rn-epar-public-assessment-report_en.pdf"},
    {"id":"50914","name":"NexGard Combo : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2021-04-20T09:41:00Z","last_updated_date":"2024-10-03T12:00:00Z","reference_number":"EMA/640861/2020","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/nexgard-combo-epar-public-assessment-report_en.pdf"},
    {"id":"50921","name":"Byfavo : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2021-04-20T17:29:00Z","last_updated_date":"2021-04-20T17:29:00Z","reference_number":"EMA/160756/2021 ","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/byfavo-epar-public-assessment-report_en.pdf"},
    {"id":"50974","name":"Retsevmo : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2021-04-23T16:08:00Z","last_updated_date":"2021-04-23T16:08:00Z","reference_number":"EMA/9037/2021","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/retsevmo-epar-public-assessment-report_en.pdf"},
    {"id":"50985","name":"Alymsys : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2021-04-26T10:23:00Z","last_updated_date":"2021-04-26T10:23:00Z","reference_number":"EMA/112177/2021","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/alymsys-epar-public-assessment-report_en.pdf"},
    {"id":"51021","name":"Thiotepa Riemser : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2021-04-30T11:24:00Z","last_updated_date":"2021-04-30T11:24:00Z","reference_number":"EMA/129214/2021","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/thiotepa-riemser-epar-public-assessment-report_en.pdf"},
    {"id":"51033","name":"Sibnayal : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2021-05-03T09:28:00Z","last_updated_date":"2021-05-03T09:28:00Z","reference_number":"EMA/1419/2021","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/sibnayal-epar-public-assessment-report_en.pdf"},
    {"id":"51041","name":"Jemperli : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2021-05-03T12:00:00Z","last_updated_date":"2021-05-03T12:00:00Z","reference_number":"EMA/176464/2021","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/jemperli-epar-public-assessment-report_en.pdf"},
    {"id":"51051","name":"Pemazyre : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2021-05-04T09:10:00Z","last_updated_date":"2021-05-04T09:10:00Z","reference_number":"EMA/CHMP/105411/2021 ","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/pemazyre-epar-public-assessment-report_en.pdf"},
    {"id":"51058","name":"Evrysdi : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2021-05-04T11:36:00Z","last_updated_date":"2021-05-04T11:36:00Z","reference_number":"EMA/216061/2021","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/evrysdi-epar-public-assessment-report_en.pdf"},
    {"id":"51067","name":"Abiraterone Accord : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2021-05-05T10:17:00Z","last_updated_date":"2021-05-05T10:17:00Z","reference_number":"EMA/174959/2021","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/abiraterone-accord-epar-public-assessment-report_en.pdf"},
    {"id":"51095","name":"Kaftrio : EPAR - Assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2021-05-06T11:50:00Z","last_updated_date":"2021-05-06T11:50:00Z","reference_number":"EMA/206350/2021","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/kaftrio-epar-assessment-report_en.pdf"},
    {"id":"51100","name":"Librela : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2021-05-06T14:37:00Z","last_updated_date":"2024-05-31T14:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/librela-epar-public-assessment-report_en.pdf"},
    {"id":"51111","name":"OvuGel : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2021-05-07T14:51:00Z","last_updated_date":"2025-10-09T12:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/ovugel-epar-public-assessment-report_en.pdf"},
    {"id":"51281","name":"Nexpovio : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2021-05-27T14:34:00Z","last_updated_date":"2021-05-27T14:34:00Z","reference_number":"EMA/CHMP/95252/2021","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/nexpovio-epar-public-assessment-report_en.pdf"},
    {"id":"51298","name":"Orladeyo : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2021-06-01T10:26:00Z","last_updated_date":"2021-06-01T10:26:00Z","reference_number":"EMA/153239/2021","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/orladeyo-epar-public-assessment-report_en.pdf"},
    {"id":"51308","name":"Copiktra : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2021-05-31T14:07:00Z","last_updated_date":"2026-04-09T11:14:00Z","reference_number":"EMA/CHMP/236249/2021","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/copiktra-epar-public-assessment-report_en.pdf"},
    {"id":"51331","name":"Lydisilka : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2021-06-02T11:11:00Z","last_updated_date":"2021-06-02T11:11:00Z","reference_number":"EMA/212535/2021","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/lydisilka-epar-public-assessment-report_en.pdf"},
    {"id":"51336","name":"Drovelis : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2021-06-02T11:11:00Z","last_updated_date":"2021-06-02T11:11:00Z","reference_number":"EMA/212533/2021","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/drovelis-epar-public-assessment-report_en.pdf"},
    {"id":"51344","name":"Ponvory : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2021-06-02T13:28:00Z","last_updated_date":"2021-06-02T13:28:00Z","reference_number":"EMA/CHMP/206970/2021","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/ponvory-epar-public-assessment-report_en.pdf"},
    {"id":"51427","name":"Efmody : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2021-06-14T12:02:00Z","last_updated_date":"2021-06-14T12:02:00Z","reference_number":"EMA/CHMP/233437/2021","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/efmody-epar-public-assessment-report_en.pdf"},
    {"id":"51526","name":"Adtralza : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2021-06-22T09:47:00Z","last_updated_date":"2021-06-22T09:47:00Z","reference_number":"EMA/266138/2021","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/adtralza-epar-public-assessment-report_en.pdf"},
    {"id":"51551","name":"Jayempi : EPAR - Public assessment report ","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2021-06-23T09:43:00Z","last_updated_date":"2021-06-23T09:43:00Z","reference_number":"EMA/303143/2021","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/jayempi-epar-public-assessment-report_en.pdf"},
    {"id":"51620","name":"Solensia : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2021-06-25T14:59:00Z","last_updated_date":"2024-10-24T10:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/solensia-epar-public-assessment-report_en.pdf"},
    {"id":"51653","name":"Onureg : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2021-06-28T15:14:00Z","last_updated_date":"2021-06-28T15:14:00Z","reference_number":"EMA/308711/2021","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/onureg-epar-public-assessment-report_en.pdf"},
    {"id":"51670","name":"Enspryng : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2021-06-30T10:00:00Z","last_updated_date":"2021-06-30T10:00:00Z","reference_number":"EMA/CHMP/265568/2021","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/enspryng-epar-public-assessment-report_en.pdf"},
    {"id":"51710","name":"Celsunax : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2021-07-01T09:08:00Z","last_updated_date":"2021-07-01T09:08:00Z","reference_number":"EMA/323721/2021","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/celsunax-epar-public-assessment-report_en.pdf"},
    {"id":"51947","name":"Daxocox : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2021-07-16T13:31:00Z","last_updated_date":"2025-09-02T11:11:11Z","reference_number":"EMA/160329/2021","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/daxocox-epar-public-assessment-report_en.pdf"},
    {"id":"51985","name":"Klisyri : EPAR - Assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2021-07-21T11:17:00Z","last_updated_date":"2021-07-21T11:17:00Z","reference_number":"EMA/397273/2021","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/klisyri-epar-assessment-report_en.pdf"},
    {"id":"52007","name":"Imcivree : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2021-07-22T10:34:00Z","last_updated_date":"2021-07-22T10:34:00Z","reference_number":"EMA/CHMP/319064/2021","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/imcivree-epar-public-assessment-report_en.pdf"},
    {"id":"52095","name":"Verquvo : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2021-07-27T10:48:00Z","last_updated_date":"2021-07-27T10:48:00Z","reference_number":"EMA/394228/2021","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/verquvo-epar-public-assessment-report_en.pdf"},
    {"id":"52102","name":"Skysona : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2021-07-27T15:34:00Z","last_updated_date":"2022-04-04T12:48:00Z","reference_number":"EMA/332184/2021","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/skysona-epar-public-assessment-report_en.pdf"},
    {"id":"52128","name":"Bylvay : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2021-07-28T16:12:00Z","last_updated_date":"2021-07-28T16:12:00Z","reference_number":"EMA/319560/2021","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/bylvay-epar-public-assessment-report_en.pdf"},
    {"id":"52138","name":"Ryeqo : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2021-07-29T09:19:00Z","last_updated_date":"2021-07-29T09:19:00Z","reference_number":"EMA/CHMP/127692/2021","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/ryeqo-epar-public-assessment-report_en.pdf"},
    {"id":"52191","name":"Credelio Plus : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2021-08-04T11:45:00Z","last_updated_date":"2024-06-11T15:44:00Z","reference_number":"EMA/160155/2021","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/credelio-plus-epar-public-assessment-report_en.pdf"},
    {"id":"52247","name":"Enteroporc Coli AC : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2021-08-20T08:54:00Z","last_updated_date":"2025-09-05T11:11:11Z","reference_number":"Enteroporc Coli AC : EPAR","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/enteroporc-coli-ac-epar-public-assessment-report_en.pdf"},
    {"id":"52253","name":"Nobivac DP Plus : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2021-08-23T09:36:00Z","last_updated_date":"2024-11-05T16:00:00Z","reference_number":"EMA/565735/2020","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/nobivac-dp-plus-epar-public-assessment-report_en.pdf"},
    {"id":"52258","name":"Bimzelx : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2021-08-24T09:17:00Z","last_updated_date":"2021-08-24T09:17:00Z","reference_number":"EMA/393532/2021","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/bimzelx-epar-public-assessment-report_en.pdf"},
    {"id":"52265","name":"Evrenzo : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2021-08-24T16:55:00Z","last_updated_date":"2021-08-24T16:55:00Z","reference_number":"EMA/CHMP/393136/2021","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/evrenzo-epar-public-assessment-report_en.pdf"},
    {"id":"52275","name":"Abecma : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2021-08-25T15:57:00Z","last_updated_date":"2021-08-25T15:57:00Z","reference_number":"EMA/409800/20212021","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/abecma-epar-public-assessment-report_en.pdf"},
    {"id":"52281","name":"Abiraterone Mylan : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2021-08-26T09:16:00Z","last_updated_date":"2021-08-26T09:16:00Z","reference_number":"EMA/444189/2021","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/abiraterone-mylan-epar-public-assessment-report_en.pdf"},
    {"id":"52288","name":"Abevmy : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2021-08-27T10:00:00Z","last_updated_date":"2021-08-27T10:00:00Z","reference_number":"EMA/176217/2021","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/abevmy-epar-public-assessment-report_en.pdf"},
    {"id":"52308","name":"Fingolimod Mylan : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2021-08-31T15:50:00Z","last_updated_date":"2021-08-31T15:50:00Z","reference_number":"EMA/CHMP/386085/2021","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/fingolimod-mylan-epar-public-assessment-report_en.pdf"},
    {"id":"52348","name":"Icatibant Accord : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2021-09-06T15:43:00Z","last_updated_date":"2021-09-06T15:43:00Z","reference_number":"EMA/306744/2021","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/icatibant-accord-epar-public-assessment-report_en.pdf"},
    {"id":"52369","name":"Byooviz : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2021-09-08T14:42:00Z","last_updated_date":"2021-09-08T14:42:00Z","reference_number":"EMA/446448/2021","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/byooviz-epar-public-assessment-report_en.pdf"},
    {"id":"52381","name":"Minjuvi : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2021-09-08T15:06:00Z","last_updated_date":"2021-09-08T15:06:00Z","reference_number":"EMA/426468/2021","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/minjuvi-epar-public-assessment-report_en.pdf"},
    {"id":"52404","name":"Voxzogo : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2021-09-09T15:46:00Z","last_updated_date":"2021-09-09T15:46:00Z","reference_number":"EMA/397108/2021","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/voxzogo-epar-public-assessment-report_en.pdf"},
    {"id":"52416","name":"Vectormune FP ILT : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2021-09-10T08:55:00Z","last_updated_date":"2024-05-27T14:34:00Z","reference_number":"EMA/565679/2020","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/vectormune-fp-ilt-epar-public-assessment-report_en.pdf"},
    {"id":"52527","name":"CircoMax Myco : EPAR - CVMP assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2021-09-20T17:13:00Z","last_updated_date":"2021-09-20T17:13:00Z","reference_number":"EMA/549226/2020","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/circomax-myco-epar-cvmp-assessment-report_en.pdf"},
    {"id":"52532","name":"Ultifend ND IBD : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2021-09-21T14:30:00Z","last_updated_date":"2025-10-15T11:11:01Z","reference_number":"EMA/160757/2021","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/ultifend-nd-ibd-epar-public-assessment-report_en.pdf"},
    {"id":"52703","name":"Imatinib Koanaa : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2021-10-01T15:40:00Z","last_updated_date":"2023-10-19T10:41:00Z","reference_number":"EMA/CHMP/444756/2021","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/imatinib-koanaa-epar-public-assessment-report_en.pdf"},
    {"id":"52808","name":"Fatrovax RHD : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2021-10-12T11:12:00Z","last_updated_date":"2025-09-09T11:11:11Z","reference_number":"EMA/364135/2021","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/fatrovax-rhd-epar-public-assessment-report_en.pdf"},
    {"id":"52817","name":"Bonqat : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2021-10-12T16:16:00Z","last_updated_date":"2024-06-17T14:37:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/bonqat-epar-public-assessment-report_en.pdf"},
    {"id":"52827","name":"Koselugo : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2021-10-13T10:52:00Z","last_updated_date":"2021-10-13T10:52:00Z","reference_number":"EMA/549867/2021","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/koselugo-epar-public-assessment-report_en.pdf"},
    {"id":"52834","name":"Tessie : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2021-10-13T15:13:00Z","last_updated_date":"2024-04-11T10:33:00Z","reference_number":"EMA/364178/2021","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/tessie-epar-public-assessment-report_en.pdf"},
    {"id":"52845","name":"Ozawade : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2021-10-14T13:31:00Z","last_updated_date":"2021-10-14T13:31:00Z","reference_number":"EMA/375687/2021","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/ozawade-epar-public-assessment-report_en.pdf"},
    {"id":"52918","name":"Strangvac : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2021-10-27T11:48:00Z","last_updated_date":"2021-10-27T11:48:00Z","reference_number":"EMA/364209/2021","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/strangvac-epar-public-assessment-report_en.pdf"},
    {"id":"53167","name":"Ronapreve : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2021-11-19T09:12:00Z","last_updated_date":"2026-01-23T17:40:00Z","reference_number":"EMA/680189/2021","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/ronapreve-epar-public-assessment-report_en.pdf"},
    {"id":"53199","name":"Sugammadex Mylan : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2021-11-22T15:20:00Z","last_updated_date":"2021-11-22T15:20:00Z","reference_number":"EMA/CHMP/555625/2021","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/sugammadex-mylan-epar-public-assessment-report_en.pdf"},
    {"id":"53223","name":"Qinlock : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2021-11-23T10:08:00Z","last_updated_date":"2021-11-23T15:39:00Z","reference_number":"EMA/CHMP/555164/2021","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/qinlock-epar-public-assessment-report_en.pdf"},
    {"id":"53243","name":"Abiraterone Krka : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2021-11-23T13:42:00Z","last_updated_date":"2021-11-23T13:42:00Z","reference_number":"EMA/653711/2021","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/abiraterone-krka-epar-public-assessment-report_en.pdf"},
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    {"id":"53263","name":"Trodelvy : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2021-11-24T14:32:00Z","last_updated_date":"2021-11-24T14:32:00Z","reference_number":"EMA/623887/2021","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/trodelvy-epar-public-assessment-report_en.pdf"},
    {"id":"53313","name":"Rivaroxaban Mylan : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2021-11-29T13:32:00Z","last_updated_date":"2021-11-29T13:32:00Z","reference_number":"EMA/560715/2021","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/rivaroxaban-mylan-epar-public-assessment-report_en.pdf"},
    {"id":"53341","name":"Regkirona : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2021-11-30T15:05:00Z","last_updated_date":"2025-04-24T12:06:00Z","reference_number":"EMA/679271/2021","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/regkirona-epar-public-assessment-report_en.pdf"},
    {"id":"53434","name":"Gavreto : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2021-12-09T11:03:00Z","last_updated_date":"2025-01-17T16:20:02Z","reference_number":"EMA/CHMP/41191/2021","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/gavreto-epar-public-assessment-report_en.pdf"},
    {"id":"53496","name":"Lextemy : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2021-12-14T14:05:00Z","last_updated_date":"2021-12-14T14:05:00Z","reference_number":"EMA/CHMP/680012/2021","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/lextemy-epar-public-assessment-report_en.pdf"},
    {"id":"53520","name":"Brukinsa : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2021-12-15T09:32:00Z","last_updated_date":"2021-12-15T09:32:00Z","reference_number":"EMA/627600/2021","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/brukinsa-epar-public-assessment-report_en.pdf"},
    {"id":"53546","name":"Aspaveli : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2021-12-16T10:18:00Z","last_updated_date":"2021-12-16T10:18:00Z","reference_number":"EMA/CHMP/629737/2021","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/aspaveli-epar-public-assessment-report_en.pdf"},
    {"id":"53594","name":"Cibinqo : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2021-12-17T15:05:00Z","last_updated_date":"2021-12-17T15:05:00Z","reference_number":"EMA/647846/2021","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/cibinqo-epar-public-assessment-report_en.pdf"},
    {"id":"53624","name":"Artesunate Amivas : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2022-01-04T09:20:00Z","last_updated_date":"2022-01-13T11:13:00Z","reference_number":"EMA/584728/2021","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/artesunate-amivas-epar-public-assessment-report_en.pdf"},
    {"id":"53648","name":"Xevudy : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2022-01-07T10:54:00Z","last_updated_date":"2026-03-04T11:02:00Z","reference_number":"EMA/CHMP/694191/2021","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/xevudy-epar-public-assessment-report_en.pdf"},
    {"id":"53653","name":"Nuvaxovid : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2022-01-07T17:28:00Z","last_updated_date":"2022-01-07T17:28:00Z","reference_number":"EMA/783213/2021","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/nuvaxovid-epar-public-assessment-report_en.pdf"},
    {"id":"53743","name":"Sitagliptin SUN : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2022-01-17T09:43:00Z","last_updated_date":"2022-01-17T09:43:00Z","reference_number":"EMA/611380/2021","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/sitagliptin-sun-epar-public-assessment-report_en.pdf"},
    {"id":"53775","name":"Vaxneuvance : EPAR - Public Assessment Report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2022-01-17T17:36:00Z","last_updated_date":"2022-01-17T17:36:00Z","reference_number":"EMA/620380/2021","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/vaxneuvance-epar-public-assessment-report_en.pdf"},
    {"id":"53790","name":"Hukyndra : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2022-01-18T09:22:00Z","last_updated_date":"2022-01-18T09:22:00Z","reference_number":"EMA/555939/2021","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/hukyndra-epar-public-assessment-report_en.pdf"},
    {"id":"53795","name":"Libmyris : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2022-01-18T09:55:00Z","last_updated_date":"2022-01-18T09:55:00Z","reference_number":"EMA/771818/2021","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/libmyris-epar-public-assessment-report_en.pdf"},
    {"id":"53838","name":"Nouryant : EPAR - Refusal public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2022-01-19T16:16:00Z","last_updated_date":"2022-01-19T16:16:00Z","reference_number":"EMA/CHMP/446813/2021","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/nouryant-epar-refusal-public-assessment-report_en.pdf"},
    {"id":"53843","name":"Voraxaze : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2022-01-20T09:37:00Z","last_updated_date":"2022-01-20T09:37:00Z","reference_number":"EMA/CHMP/751047/2021","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/voraxaze-epar-public-assessment-report_en.pdf"},
    {"id":"53884","name":"Suiseng Diff/A : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2022-01-24T09:43:00Z","last_updated_date":"2025-10-14T17:10:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/suiseng-diff-epar-public-assessment-report_en.pdf"},
    {"id":"53888","name":"Imoxat : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2022-01-24T10:31:00Z","last_updated_date":"2025-10-07T16:10:00Z","reference_number":"EMA/576114/2021","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/imoxat-epar-public-assessment-report_en.pdf"},
    {"id":"53941","name":"Tavneos : EPAR - Public Assessment Report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2022-01-27T10:21:00Z","last_updated_date":"2023-07-20T15:29:00Z","reference_number":"EMA/708044/2021 Corr","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/tavneos-epar-public-assessment-report_en.pdf"},
    {"id":"54005","name":"Tecovirimat SIGA : EPAR - Public Assessment Report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2022-01-28T12:08:00Z","last_updated_date":"2022-01-28T12:08:00Z","reference_number":"EMA/703119/2021","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/tecovirimat-siga-epar-public-assessment-report_en.pdf"},
    {"id":"54046","name":"Rybrevant : EPAR - Public Assessment Report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2022-02-01T16:05:00Z","last_updated_date":"2022-02-01T16:05:00Z","reference_number":"EMA/629045/2021","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/rybrevant-epar-public-assessment-report_en.pdf"},
    {"id":"54067","name":"Riltrava Aerosphere : EPAR - Public Assessment Report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2022-02-04T09:08:00Z","last_updated_date":"2022-02-04T09:08:00Z","reference_number":"EMA/622167/2021","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/riltrava-aerosphere-epar-public-assessment-report_en.pdf"},
    {"id":"54072","name":"Lonapegsomatropin Ascendis Pharma : EPAR - Public Assessment Report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2022-02-04T12:33:00Z","last_updated_date":"2022-03-16T12:33:00Z","reference_number":"EMA/706519/2021","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/lonapegsomatropin-ascendis-pharma-epar-public-assessment-report_en.pdf"},
    {"id":"54169","name":"Vyepti : EPAR - Public Assessment Report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2022-02-15T11:21:00Z","last_updated_date":"2022-02-15T11:21:00Z","reference_number":"EMA/9446/2022","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/vyepti-epar-public-assessment-report_en.pdf"},
    {"id":"54181","name":"Raylumis : EPAR - Refusal public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2022-02-15T15:05:00Z","last_updated_date":"2022-02-15T15:05:00Z","reference_number":"EMA/CHMP/556162/2021","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/raylumis-epar-refusal-public-assessment-report_en.pdf"},
    {"id":"54224","name":"Paxlovid : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2022-02-18T14:36:00Z","last_updated_date":"2022-02-24T13:39:00Z","reference_number":"EMA/95110/2022 Rev. 1","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/paxlovid-epar-public-assessment-report_en.pdf"},
    {"id":"54239","name":"Saphnelo : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2022-02-21T14:22:00Z","last_updated_date":"2022-02-21T14:22:00Z","reference_number":"EMA/4079/2022","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/saphnelo-epar-public-assessment-report_en.pdf"},
    {"id":"54316","name":"Okedi : EPAR - Public Assessment Report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2022-03-01T15:12:00Z","last_updated_date":"2022-03-01T15:12:00Z","reference_number":"EMA/CHMP/11233/2022 rev.1","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/okedi-epar-public-assessment-report_en.pdf"},
    {"id":"54345","name":"Apexxnar : EPAR - Public Assessment Report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2022-03-02T17:40:00Z","last_updated_date":"2022-03-02T17:40:00Z","reference_number":"EMA/12384/2022","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/apexxnar-epar-public-assessment-report_en.pdf"},
    {"id":"54360","name":"Ontilyv : EPAR - Public Assessment Report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2022-03-07T10:30:00Z","last_updated_date":"2025-03-28T15:50:00Z","reference_number":"EMA/129900/2022","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/ontilyv-epar-public-assessment-report_en.pdf"},
    {"id":"54394","name":"Sitagliptin / Metformin hydrochloride Mylan : EPAR - Public Assessment Report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2022-03-08T12:42:00Z","last_updated_date":"2022-03-08T12:42:00Z","reference_number":"EMA/27581/2022","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/sitagliptin-metformin-hydrochloride-mylan-epar-public-assessment-report_en.pdf"},
    {"id":"54406","name":"Felpreva : EPAR - Public Assessment Report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2022-03-09T16:20:00Z","last_updated_date":"2025-09-09T11:11:11Z","reference_number":"EMA/532968/2021","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/felpreva-epar-public-assessment-report_en.pdf"},
    {"id":"54415","name":"Wegovy : EPAR - Public Assessment Report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2022-03-10T17:20:00Z","last_updated_date":"2022-03-10T17:20:00Z","reference_number":"EMA/112307/2022","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/wegovy-epar-public-assessment-report_en.pdf"},
    {"id":"54417","name":"Ngenla : EPAR - Public Assessment Report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2022-03-11T09:35:00Z","last_updated_date":"2022-03-11T09:35:00Z","reference_number":"EMA/15620/2022","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/ngenla-epar-public-assessment-report_en.pdf"},
    {"id":"54429","name":"Kerendia : EPAR - Public Assessment Report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2022-03-11T15:05:00Z","last_updated_date":"2022-03-11T15:05:00Z","reference_number":"EMA/78746/2022","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/kerendia-epar-public-assessment-report_en.pdf"},
    {"id":"54464","name":"Zenalpha : EPAR - Public Assessment Report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2022-03-15T10:59:00Z","last_updated_date":"2025-10-15T14:10:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/zenalpha-epar-public-assessment-report_en.pdf"},
    {"id":"54497","name":"Sapropterin Dipharma : EPAR - Public Assessment Report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2022-03-16T17:42:00Z","last_updated_date":"2022-03-16T17:42:00Z","reference_number":"EMA/2232/2022","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/sapropterin-dipharma-epar-public-assessment-report_en.pdf"},
    {"id":"54506","name":"Oxbryta : EPAR - Public Assessment Report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2022-03-17T13:45:00Z","last_updated_date":"2022-03-17T13:45:00Z","reference_number":"EMA/102184/2022","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/oxbryta-epar-public-assessment-report_en.pdf"},
    {"id":"54617","name":"Dasatinib Accordpharma : EPAR - Public Assessment Report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2022-03-30T10:04:00Z","last_updated_date":"2023-03-30T11:53:00Z","reference_number":"EMA/117327/2022","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/dasatinib-accordpharma-epar-public-assessment-report_en.pdf"},
    {"id":"54622","name":"Dasatinib Accord : EPAR - Public Assessment Report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2022-03-30T10:30:00Z","last_updated_date":"2023-03-30T09:14:00Z","reference_number":"EMA/116969/2022","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/dasatinib-accord-epar-public-assessment-report_en.pdf"},
    {"id":"54642","name":"Lumykras : EPAR - Public Assessment Report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2022-03-31T15:28:00Z","last_updated_date":"2022-03-31T15:28:00Z","reference_number":"EMA/706135/2021","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/lumykras-epar-public-assessment-report_en.pdf"},
    {"id":"54658","name":"Stimufend : EPAR - Public Assessment Report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2022-04-04T10:05:00Z","last_updated_date":"2022-04-04T10:05:00Z","reference_number":"EMA/98697/2022","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/stimufend-epar-public-assessment-report_en.pdf"},
    {"id":"54710","name":"Breyanzi : EPAR - Public Assessment Report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2022-04-08T15:32:00Z","last_updated_date":"2022-04-08T15:32:00Z","reference_number":"EMA/134759/2022","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/breyanzi-epar-public-assessment-report_en.pdf"},
    {"id":"54801","name":"Kimmtrak : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2022-04-22T11:05:00Z","last_updated_date":"2022-04-22T11:05:00Z","reference_number":"EMA/206916/2022","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/kimmtrak-epar-public-assessment-report_en.pdf"},
    {"id":"54842","name":"Kapruvia : EPAR - Public Assessment Report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2022-04-28T09:41:00Z","last_updated_date":"2022-04-28T09:41:00Z","reference_number":"EMA/152430/2022","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/kapruvia-epar-public-assessment-report_en.pdf"},
    {"id":"54858","name":"Evusheld : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2022-04-28T14:30:00Z","last_updated_date":"2025-10-14T12:22:22Z","reference_number":"EMA/205600/2022","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/evusheld-epar-public-assessment-report_en.pdf"},
    {"id":"54888","name":"Quviviq : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2022-05-03T16:53:00Z","last_updated_date":"2022-05-03T16:53:00Z","reference_number":"EMA/187589/2022","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/quviviq-epar-public-assessment-report_en.pdf"},
    {"id":"54897","name":"Tepmetko : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2022-05-05T09:15:00Z","last_updated_date":"2022-05-05T09:15:00Z","reference_number":"EMA/36625/2022","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/tepmetko-epar-public-assessment-report_en.pdf"},
    {"id":"54905","name":"Padcev : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2022-05-05T17:17:00Z","last_updated_date":"2022-05-05T17:17:00Z","reference_number":"EMA/249357/2022","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/padcev-epar-public-assessment-report_en.pdf"},
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    {"id":"54949","name":"Vydura : EPAR - Public Assessment Report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2022-05-11T16:12:00Z","last_updated_date":"2022-05-11T16:12:00Z","reference_number":"EMA/CHMP/172260/2022","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/vydura-epar-public-assessment-report_en.pdf"},
    {"id":"54991","name":"PreHevbri : EPAR - Public Assessment Report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2022-02-25T15:36:00Z","last_updated_date":"2025-01-10T17:21:00Z","reference_number":"EMA/CHMP/86102/2022","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/prehevbri-epar-public-assessment-report_en.pdf"},
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    {"id":"55069","name":"Dimethyl fumarate Mylan : EPAR - Public Assessment Report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2023-12-22T10:55:00Z","last_updated_date":"2023-12-22T10:55:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/dimethyl-fumarate-mylan-epar-public-assessment-report_en.pdf"},
    {"id":"55074","name":"Dimethyl fumarate Neuraxpharm : EPAR - Public Assessment Report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2022-05-24T11:22:00Z","last_updated_date":"2023-12-22T14:25:00Z","reference_number":"EMA/CHMP/153578/2022","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/dimethyl-fumarate-neuraxpharm-epar-public-assessment-report_en.pdf"},
    {"id":"55079","name":"Dimethyl fumarate Polpharma : EPAR - Public Assessment Report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2023-12-22T12:02:00Z","last_updated_date":"2023-12-22T12:02:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/dimethyl-fumarate-polpharma-epar-public-assessment-report_en.pdf"},
    {"id":"55086","name":"Amifampridine Serb : EPAR - Public Assessment Report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2022-05-24T15:21:00Z","last_updated_date":"2022-05-24T15:21:00Z","reference_number":"EMA/216122/2022","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/amifampridine-serb-epar-public-assessment-report_en.pdf"},
    {"id":"55243","name":"Truvelog Mix 30 : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2022-06-15T09:24:00Z","last_updated_date":"2026-05-07T12:44:00Z","reference_number":"EMA/165165/2022","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/truvelog-mix-30-epar-public-assessment-report_en.pdf"},
    {"id":"55279","name":"Vildagliptin / Metformin hydrochloride Accord : EPAR - Public Assessment Report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2022-06-17T12:24:00Z","last_updated_date":"2022-06-17T12:24:00Z","reference_number":"EMA/246681/2022","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/vildagliptin-metformin-hydrochloride-accord-epar-public-assessment-report_en.pdf"},
    {"id":"55287","name":"Carvykti : EPAR - Public Assessment Report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2022-06-17T16:08:00Z","last_updated_date":"2022-06-17T16:08:00Z","reference_number":"EMA/594558/2022","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/carvykti-epar-public-assessment-report_en.pdf"},
    {"id":"55296","name":"Camcevi : EPAR - Public Assessment Report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2022-06-20T11:16:00Z","last_updated_date":"2022-06-20T11:16:00Z","reference_number":"EMA/567396/2022","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/camcevi-epar-public-assessment-report_en.pdf"},
    {"id":"55298","name":"Sondelbay : EPAR - Public Assessment Report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2022-06-20T11:40:00Z","last_updated_date":"2022-06-20T11:40:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/sondelbay-epar-public-assessment-report_en.pdf"},
    {"id":"55304","name":"Zolsketil pegylated liposomal : EPAR - Public Assessment Report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2022-06-20T16:19:00Z","last_updated_date":"2022-06-20T16:19:00Z","reference_number":"EMA/CHMP/212114/2022","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/zolsketil-pegylated-liposomal-epar-public-assessment-report_en.pdf"},
    {"id":"55332","name":"Lunsumio : EPAR - Public Assessment Report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2022-06-23T13:52:00Z","last_updated_date":"2022-06-23T13:52:00Z","reference_number":"EMA/CHMP/63179/2022","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/lunsumio-epar-public-assessment-report_en.pdf"},
    {"id":"55399","name":"Pirfenidone AET : EPAR - Public Assessment Report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2022-06-28T16:45:00Z","last_updated_date":"2022-06-28T16:45:00Z","reference_number":"EMA/609423/2022 ","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/pirfenidone-aet-epar-public-assessment-report_en.pdf"},
    {"id":"55417","name":"Inpremzia : EPAR - Public Assessment Report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2022-06-30T12:23:00Z","last_updated_date":"2023-04-20T12:20:00Z","reference_number":"EMA/127616/2022","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/inpremzia-epar-public-assessment-report_en.pdf"},
    {"id":"55441","name":"Yselty : EPAR - Public Assessment Report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2022-07-01T15:17:00Z","last_updated_date":"2022-07-01T15:17:00Z","reference_number":"EMA/13882/2022","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/yselty-epar-public-assessment-report_en.pdf"},
    {"id":"55447","name":"Filsuvez : EPAR - Public Assessment Report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2022-07-04T12:10:00Z","last_updated_date":"2022-07-04T12:10:00Z","reference_number":"EMA/260035/2022","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/filsuvez-epar-public-assessment-report_en.pdf"},
    {"id":"55467","name":"Sitagliptin Accord : EPAR - Public Assessment Report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2022-07-05T16:28:00Z","last_updated_date":"2022-07-05T16:28:00Z","reference_number":"EMA/128895/2022","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/sitagliptin-accord-epar-public-assessment-report_en.pdf"},
    {"id":"55505","name":"COVID-19 Vaccine (inactivated, adjuvanted) Valneva : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2022-07-08T13:39:00Z","last_updated_date":"2023-12-01T12:00:00Z","reference_number":"EMA/627695/2022","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/covid-19-vaccine-inactivated-adjuvanted-valneva-epar-public-assessment-report_en.pdf"},
    {"id":"55602","name":"Ganirelix Gedeon Richter : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2022-07-20T11:01:00Z","last_updated_date":"2022-07-20T11:01:00Z","reference_number":"EMA/588110/2022","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/ganirelix-gedeon-richter-epar-public-assessment-report_en.pdf"},
    {"id":"55617","name":"Sugammadex Fresenius Kabi : EPAR - Public Assessment Report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2022-07-21T14:43:00Z","last_updated_date":"2022-07-21T14:43:00Z","reference_number":"EMA/612933/2022","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/sugammadex-fresenius-kabi-epar-public-assessment-report_en.pdf"},
    {"id":"55699","name":"Xenpozyme : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2022-07-27T14:47:00Z","last_updated_date":"2022-07-27T14:47:00Z","reference_number":"EMA/571472/2022","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/xenpozyme-epar-public-assessment-report_en.pdf"},
    {"id":"55705","name":"Nexviadyme : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2022-07-27T16:37:00Z","last_updated_date":"2022-07-27T16:37:00Z","reference_number":"EMA/708926/2021","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/nexviadyme-epar-public-assessment-report_en.pdf"},
    {"id":"55725","name":"Amversio : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2022-07-28T15:34:00Z","last_updated_date":"2022-07-28T15:34:00Z","reference_number":"EMA/203554/2022","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/amversio-epar-public-assessment-report_en.pdf"},
    {"id":"55754","name":"Zokinvy : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2022-08-01T16:15:00Z","last_updated_date":"2022-12-13T16:10:00Z","reference_number":"EMA/656670/2022 Rev.1","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/zokinvy-epar-public-assessment-report_en.pdf"},
    {"id":"55778","name":"Sitagliptin / Metformin hydrochloride Accord : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2022-08-03T16:16:00Z","last_updated_date":"2025-11-13T09:44:44Z","reference_number":"EMA/568807/2022","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/sitagliptin-metformin-hydrochloride-accord-epar-public-assessment-report_en.pdf"},
    {"id":"55802","name":"Upstaza : EPAR - Public Assessment Report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2022-08-09T11:08:00Z","last_updated_date":"2022-08-09T11:08:00Z","reference_number":"EMA/CHMP/571076/2022","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/upstaza-epar-public-assessment-report_en.pdf"},
    {"id":"55857","name":"Pepaxti : EPAR - Public Assessment Report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2022-08-22T14:27:00Z","last_updated_date":"2022-09-06T15:14:00Z","reference_number":"EMA/638305/2022","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/pepaxti-epar-public-assessment-report_en.pdf"},
    {"id":"55866","name":"Kinpeygo : EPAR - Public Assessment Report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2022-08-23T11:12:00Z","last_updated_date":"2022-08-23T11:12:00Z","reference_number":"EMA/570757/2022","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/kinpeygo-epar-public-assessment-report_en.pdf"},
    {"id":"55876","name":"Sunlenca : EPAR - Public Assessment Report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2022-08-25T14:48:00Z","last_updated_date":"2022-08-25T14:48:00Z","reference_number":"EMA/657007/2022","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/sunlenca-epar-public-assessment-report_en.pdf"},
    {"id":"56001","name":"Roctavian : EPAR - Public Assessment Report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2022-09-06T15:43:00Z","last_updated_date":"2022-09-06T15:43:00Z","reference_number":"EMA/685615/2022","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/roctavian-epar-public-assessment-report_en.pdf"},
    {"id":"56011","name":"Scemblix : EPAR - Public Assessment Report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2022-09-07T12:41:00Z","last_updated_date":"2022-09-07T12:41:00Z","reference_number":"EMA/CHMP/634238/2022","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/scemblix-epar-public-assessment-report_en.pdf"},
    {"id":"56016","name":"Vegzelma : EPAR - Public Assessment Report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2022-09-07T15:36:00Z","last_updated_date":"2022-09-07T15:36:00Z","reference_number":"EMA/CHMP/636045/2022","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/vegzelma-epar-public-assessment-report_en.pdf"},
    {"id":"56063","name":"Vyvgart : EPAR - Public Assessment Report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2022-09-12T10:59:00Z","last_updated_date":"2022-09-12T10:59:00Z","reference_number":"EMA/641081/2022","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/vyvgart-epar-public-assessment-report_en.pdf"},
    {"id":"56133","name":"Opdualag : EPAR - Public Assessment Report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2022-09-20T15:53:00Z","last_updated_date":"2022-09-20T15:53:00Z","reference_number":"EMA/720884/2022","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/opdualag-epar-public-assessment-report_en.pdf"},
    {"id":"56145","name":"Lupkynis : EPAR - Public Assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2022-09-20T15:50:00Z","last_updated_date":"2022-09-20T15:50:00Z","reference_number":"EMA/681286/2022","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/lupkynis-epar-public-assessment-report_en.pdf"},
    {"id":"56152","name":"Tabrecta : EPAR - Public Assessment Report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2022-09-21T10:36:00Z","last_updated_date":"2022-09-21T10:36:00Z","reference_number":"EMA/272390/2022","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/tabrecta-epar-public-assessment-report_en.pdf"},
    {"id":"56156","name":"Illuzyce : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2022-09-21T11:20:00Z","last_updated_date":"2022-09-21T11:20:00Z","reference_number":"EMA/689220/2022","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/illuzyce-epar-public-assessment-report_en.pdf"},
    {"id":"56161","name":"Tezspire : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2022-09-21T11:59:00Z","last_updated_date":"2025-09-18T11:58:12Z","reference_number":"EMA/682391/2022","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/tezspire-epar-public-assessment-report_en.pdf"},
    {"id":"56258","name":"Nulibry : EPAR - Public Assessment Report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2022-09-29T15:34:00Z","last_updated_date":"2022-09-29T15:34:00Z","reference_number":"EMA/677145/2022","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/nulibry-epar-public-assessment-report_en.pdf"},
    {"id":"56290","name":"Rayvow : EPAR - Public Assessment Report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2022-10-03T14:49:00Z","last_updated_date":"2022-10-03T14:49:00Z","reference_number":"EMA/622555/2022","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/rayvow-epar-public-assessment-report_en.pdf"},
    {"id":"56309","name":"Ranivisio : EPAR - Public Assessment Report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2022-10-04T11:54:00Z","last_updated_date":"2022-10-04T11:54:00Z","reference_number":"EMA/640346/2022","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/ranivisio-epar-public-assessment-report_en.pdf"},
    {"id":"56370","name":"Amvuttra : EPAR - Public Assessment Report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2022-10-12T12:35:00Z","last_updated_date":"2022-10-12T12:35:00Z","reference_number":"EMA/CHMP/689555/2022","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/amvuttra-epar-public-assessment-report_en.pdf"},
    {"id":"56388","name":"Tecvayli : EPAR - Public Assessment Report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2022-10-13T11:38:00Z","last_updated_date":"2022-10-13T11:38:00Z","reference_number":"EMA/789141/2022","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/tecvayli-epar-public-assessment-report_en.pdf"},
    {"id":"56394","name":"Vabysmo : EPAR - Public Assessment Report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2022-10-13T11:58:00Z","last_updated_date":"2022-10-13T11:58:00Z","reference_number":"EMA/687844/2022","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/vabysmo-epar-public-assessment-report_en.pdf"},
    {"id":"56446","name":"Thalidomide Lipomed : EPAR - Public Assessment Report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2022-10-20T14:14:00Z","last_updated_date":"2022-10-20T14:14:00Z","reference_number":"EMA/773068/2022","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/thalidomide-lipomed-epar-public-assessment-report_en.pdf"},
    {"id":"56620","name":"Teriflunomide Accord : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2022-11-14T16:19:00Z","last_updated_date":"2022-11-14T16:19:00Z","reference_number":"EMA/CHMP/805980/2022","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/teriflunomide-accord-epar-public-assessment-report_en.pdf"},
    {"id":"56630","name":"Beyfortus : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2022-11-15T15:42:00Z","last_updated_date":"2022-11-15T15:42:00Z","reference_number":"EMA/786523/2022","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/beyfortus-epar-public-assessment-report_en.pdf"},
    {"id":"56698","name":"Enjaymo : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2022-11-17T17:06:00Z","last_updated_date":"2022-11-17T17:06:00Z","reference_number":"EMA/863061/2022","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/enjaymo-epar-public-assessment-report_en.pdf"},
    {"id":"56725","name":"Ertapenem SUN : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2022-11-21T14:55:00Z","last_updated_date":"2022-11-21T14:55:00Z","reference_number":"EMA/569175/2022","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/ertapenem-sun-epar-public-assessment-report_en.pdf"},
    {"id":"56737","name":"Teriflunomide Mylan : EPAR - Public Assessment Report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2022-11-22T10:56:00Z","last_updated_date":"2022-11-22T10:56:00Z","reference_number":"EMA/CHMP/792181/2022","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/teriflunomide-mylan-epar-public-assessment-report_en.pdf"},
    {"id":"56759","name":"Melatonin Neurim : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2022-11-23T13:06:00Z","last_updated_date":"2022-11-23T13:06:00Z","reference_number":"EMA/847216/2022","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/melatonin-neurim-epar-public-assessment-report_en.pdf"},
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    {"id":"56787","name":"Sorafenib Accord : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2022-11-25T09:51:00Z","last_updated_date":"2022-11-25T09:51:00Z","reference_number":"EMA/834802/2022","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/sorafenib-accord-epar-public-assessment-report_en.pdf"},
    {"id":"56809","name":"Ximluci : EPAR - Public Assessment Report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2022-11-28T10:43:00Z","last_updated_date":"2022-11-28T10:43:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/ximluci-epar-public-assessment-report_en.pdf"},
    {"id":"56828","name":"Cevenfacta : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2022-11-29T10:50:00Z","last_updated_date":"2022-11-29T10:50:00Z","reference_number":"EMA/CHMP/577398/2022","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/cevenfacta-epar-public-assessment-report_en.pdf"},
    {"id":"56840","name":"VidPrevtyn Beta : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2022-11-30T14:17:00Z","last_updated_date":"2024-03-20T13:28:00Z","reference_number":"EMA/893684/2022","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/vidprevtyn-beta-epar-public-assessment-report_en.pdf"},
    {"id":"56875","name":"Pyrukynd : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2022-12-05T10:56:00Z","last_updated_date":"2022-12-05T10:56:00Z","reference_number":"EMA/792328/2022","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/pyrukynd-epar-public-assessment-report_en.pdf"},
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    {"id":"57115","name":"Dimethyl fumarate Teva: EPAR - Public Assessment Report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2022-12-21T16:49:00Z","last_updated_date":"2023-12-22T14:51:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/dimethyl-fumarate-teva-epar-public-assessment-report_en.pdf"},
    {"id":"57121","name":"Pluvicto : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2022-12-21T17:44:00Z","last_updated_date":"2022-12-21T17:44:00Z","reference_number":"EMA/871459/2022","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/pluvicto-epar-public-assessment-report_en.pdf"},
    {"id":"57125","name":"Locametz: EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2022-12-21T17:39:00Z","last_updated_date":"2025-05-22T14:37:30Z","reference_number":"EMA/871509/2022","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/locametz-epar-public-assessment-report_en.pdf"},
    {"id":"57143","name":"Mycapssa: EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2022-12-22T13:00:00Z","last_updated_date":"2025-03-21T10:50:00Z","reference_number":"EMA/796198/2022","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/mycapssa-epar-public-assessment-report_en.pdf"},
    {"id":"57153","name":"Eladynos : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2022-12-22T17:35:00Z","last_updated_date":"2022-12-22T17:35:00Z","reference_number":"EMA/857958/2022","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/eladynos-epar-public-assessment-report_en.pdf"},
    {"id":"57223","name":"Ebvallo : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2023-01-11T15:23:00Z","last_updated_date":"2023-01-11T15:23:00Z","reference_number":"EMA/858618/2022","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/ebvallo-epar-public-assessment-report_en.pdf"},
    {"id":"57291","name":"Sugammadex Amomed : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2023-01-13T16:31:00Z","last_updated_date":"2023-01-13T16:31:00Z","reference_number":"EMA/CHMP/906354/2022","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/sugammadex-amomed-epar-public-assessment-report_en.pdf"},
    {"id":"57314","name":"Pirfenidone Viatris : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2023-01-17T17:13:00Z","last_updated_date":"2023-01-17T17:13:00Z","reference_number":"EMA/907420/2022","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/pirfenidone-viatris-epar-public-assessment-report_en.pdf"},
    {"id":"57334","name":"Pemetrexed Baxter : EPAR - Public Assessment Report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2023-01-19T13:02:00Z","last_updated_date":"2023-01-19T13:02:00Z","reference_number":"EMA/CHMP/251833/2022","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/pemetrexed-baxter-epar-public-assessment-report_en.pdf"},
    {"id":"57403","name":"Zynlonta : EPAR - Public Assessment Report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2023-01-26T13:56:00Z","last_updated_date":"2023-01-26T13:56:00Z","reference_number":"EMA/CHMP/834750/2022","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/zynlonta-epar-public-assessment-report_en.pdf"},
    {"id":"57481","name":"Celdoxome pegylated liposomal : EPAR - Public Assessment Report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2023-01-31T13:20:00Z","last_updated_date":"2025-11-27T09:36:00Z","reference_number":"EMA/685994/2022","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/celdoxome-pegylated-liposomal-epar-public-assessment-report_en.pdf"},
    {"id":"57504","name":"Ceprotin : EPAR - Assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2023-02-02T11:51:00Z","last_updated_date":"2023-02-02T11:51:00Z","reference_number":"EMA/913542/2022","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/ceprotin-epar-assessment-report_en.pdf"},
    {"id":"57531","name":"Plerixafor Accord : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2023-02-06T13:54:00Z","last_updated_date":"2023-02-06T13:54:00Z","reference_number":"EMA/889120/2022","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/plerixafor-accord-epar-public-assessment-report_en.pdf"},
    {"id":"57577","name":"Spevigo : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2023-02-08T15:43:00Z","last_updated_date":"2023-02-08T15:43:00Z","reference_number":"EMA/50357/2023","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/spevigo-epar-public-assessment-report_en.pdf"},
    {"id":"57789","name":"Dimethyl fumarate Accord : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2023-02-22T12:39:00Z","last_updated_date":"2023-12-22T12:51:00Z","reference_number":"EMA/CHMP/2411/2023","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/dimethyl-fumarate-accord-epar-public-assessment-report_en.pdf"},
    {"id":"57837","name":"Hemgenix : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2023-02-28T12:28:00Z","last_updated_date":"2023-02-28T12:28:00Z","reference_number":"EMA/46569/2023","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/hemgenix-epar-public-assessment-report_en.pdf"},
    {"id":"57866","name":"Imjudo : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2023-03-02T15:58:00Z","last_updated_date":"2023-03-02T15:58:00Z","reference_number":"EMA/CHMP/17771/2023","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/imjudo-epar-public-assessment-report_en.pdf"},
    {"id":"57942","name":"Kauliv : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2023-03-07T15:51:00Z","last_updated_date":"2023-03-07T15:51:00Z","reference_number":"EMA/923811/2022","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/kauliv-epar-public-assessment-report_en.pdf"},
    {"id":"58265","name":"Sotyktu : EPAR - Public Assessment Report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2023-03-31T17:20:00Z","last_updated_date":"2023-03-31T17:20:00Z","reference_number":"EMA/68815/2023","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/sotyktu-epar-public-assessment-report_en.pdf"},
    {"id":"58276","name":"Tremelimumab AstraZeneca : EPAR - Public Assessment Report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2023-04-04T10:14:00Z","last_updated_date":"2024-08-22T10:43:00Z","reference_number":"EMA/42903/2023","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/tremelimumab-astrazeneca-epar-public-assessment-report_en.pdf"},
    {"id":"58281","name":"Dapagliflozin Viatris : EPAR - Public Assessment Report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2023-04-04T16:41:00Z","last_updated_date":"2023-04-04T16:41:00Z","reference_number":"EMA/68353/2023","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/dapagliflozin-viatris-epar-public-assessment-report_en.pdf"},
    {"id":"58486","name":"Opzelura : EPAR - Public Assessment Report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2023-04-20T14:58:00Z","last_updated_date":"2023-04-20T14:58:00Z","reference_number":"EMA/135534/2023","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/opzelura-epar-public-assessment-report_en.pdf"},
    {"id":"58597","name":"Elfabrio : EPAR - Public Assessment Report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2023-05-08T15:03:00Z","last_updated_date":"2023-05-08T15:03:00Z","reference_number":"EMA/58745/2023","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/elfabrio-epar-public-assessment-report_en.pdf"},
    {"id":"58654","name":"Tibsovo : EPAR - Public Assessment Report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2023-05-12T12:15:00Z","last_updated_date":"2023-05-12T12:15:00Z","reference_number":"EMA/173654/2023","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/tibsovo-epar-public-assessment-report_en.pdf"},
    {"id":"58690","name":"Bekemv : EPAR - Public Assessment Report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2023-05-15T15:42:00Z","last_updated_date":"2023-05-15T15:42:00Z","reference_number":"EMA/114622/2023","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/bekemv-epar-public-assessment-report_en.pdf"},
    {"id":"58705","name":"Pombiliti : EPAR - Public Assessment Report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2023-05-16T15:41:00Z","last_updated_date":"2025-01-24T12:01:00Z","reference_number":"EMA/CHMP/794395/2022","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/pombiliti-epar-public-assessment-report_en.pdf"},
    {"id":"58823","name":"Epysqli : EPAR - Public Assessment Report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2023-05-31T11:06:00Z","last_updated_date":"2023-05-31T11:06:00Z","reference_number":"EMA/203468/2023","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/epysqli-epar-public-assessment-report_en.pdf"},
    {"id":"58831","name":"Dabigatran Etexilate Accord : EPAR - Public Assessment Report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2023-05-31T13:47:00Z","last_updated_date":"2023-05-31T13:47:00Z","reference_number":"EMA/182457/2023","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/dabigatran-etexilate-accord-epar-public-assessment-report_en.pdf"},
    {"id":"58835","name":"Vafseo: EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2023-05-31T14:09:00Z","last_updated_date":"2023-05-31T14:09:00Z","reference_number":"EMA/130457/2023","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/vafseo-epar-public-assessment-report_en.pdf"},
    {"id":"58848","name":"Pedmarqsi : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2023-06-02T08:59:00Z","last_updated_date":"2023-06-02T08:59:00Z","reference_number":"EMA/196210/2023","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/pedmarqsi-epar-public-assessment-report_en.pdf"},
    {"id":"58855","name":"Akeega : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2023-06-02T10:12:00Z","last_updated_date":"2023-06-02T10:12:00Z","reference_number":"EMA/126335/2023","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/akeega-epar-public-assessment-report_en.pdf"},
    {"id":"58869","name":"Lacosamide Adroiq : EPAR - Public Assessment Report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2023-06-05T10:30:00Z","last_updated_date":"2023-06-05T10:30:00Z","reference_number":"EMA/216528/2023","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/lacosamide-adroiq-epar-public-assessment-report_en.pdf"},
    {"id":"58888","name":"Omvoh : EPAR - Public Assessment Report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2023-06-08T12:13:00Z","last_updated_date":"2023-06-08T12:13:00Z","reference_number":"EMA/197960/2023","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/omvoh-epar-public-assessment-report_en.pdf"},
    {"id":"58899","name":"Hyftor : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2023-06-08T17:14:00Z","last_updated_date":"2023-06-08T17:14:00Z","reference_number":"EMA/CHMP/844737/2022","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/hyftor-epar-public-assessment-report_en.pdf"},
    {"id":"58938","name":"Omblastys : EPAR - Refusal public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2023-06-14T12:21:00Z","last_updated_date":"2023-06-14T12:21:00Z","reference_number":"EMA/CHMP/3393/2023","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/omblastys-epar-refusal-public-assessment-report_en.pdf"},
    {"id":"58959","name":"Bimervax : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2023-06-15T13:15:00Z","last_updated_date":"2023-06-15T13:15:00Z","reference_number":"EMA/175278/2023","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/bimervax-epar-public-assessment-report_en.pdf"},
    {"id":"58972","name":"Sugammadex Adroiq : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2023-06-16T10:18:00Z","last_updated_date":"2023-06-16T10:18:00Z","reference_number":"EMA/CHMP/177188/2023","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/sugammadex-adroiq-epar-public-assessment-report_en.pdf"},
    {"id":"58977","name":"Arexvy : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2023-06-16T11:00:00Z","last_updated_date":"2023-06-16T11:00:00Z","reference_number":"EMA/227054/2023","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/arexvy-epar-public-assessment-report_en.pdf"},
    {"id":"59299","name":"Opfolda : EPAR - Public Assessment Report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2023-07-07T12:55:00Z","last_updated_date":"2023-07-07T12:55:00Z","reference_number":"EMA/CHMP/794405/2022","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/opfolda-epar-public-assessment-report_en.pdf"},
    {"id":"59349","name":"Briumvi : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2023-07-13T14:17:00Z","last_updated_date":"2024-02-07T10:14:00Z","reference_number":"EMA/173313/2023","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/briumvi-epar-public-assessment-report_en.pdf"},
    {"id":"59379","name":"Columvi : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2023-07-18T11:54:00Z","last_updated_date":"2023-07-18T11:54:00Z","reference_number":"EMA/228393/2023","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/columvi-epar-public-assessment-report_en.pdf"},
    {"id":"59385","name":"Lytgobi : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2023-07-18T12:36:00Z","last_updated_date":"2023-07-18T12:36:00Z","reference_number":"EMA/218116/2023","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/lytgobi-epar-public-assessment-report_en.pdf"},
    {"id":"59396","name":"Sugammadex Piramal : EPAR - Public Assessment Report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2023-07-18T17:30:00Z","last_updated_date":"2023-07-18T17:30:00Z","reference_number":"EMA/228402/2023","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/sugammadex-piramal-epar-public-assessment-report_en.pdf"},
    {"id":"59476","name":"Camzyos : EPAR - Public Assessment Report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2023-07-24T15:49:00Z","last_updated_date":"2023-07-24T15:49:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/camzyos-epar-public-assessment-report_en.pdf"},
    {"id":"59481","name":"Qaialdo : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2023-07-25T11:56:00Z","last_updated_date":"2023-07-25T11:56:00Z","reference_number":"EMA/175439/2023","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/qaialdo-epar-public-assessment-report_en.pdf"},
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    {"id":"59632","name":"Aquipta : EPAR - Public Assessment Report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2023-08-25T10:50:00Z","last_updated_date":"2023-08-25T10:50:00Z","reference_number":"EMA/CHMP/326142/2023","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/aquipta-epar-public-assessment-report_en.pdf"},
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    {"id":"60081","name":"Apretude : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2023-09-20T16:00:00Z","last_updated_date":"2023-09-20T16:00:00Z","reference_number":"EMA/360205/2023","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/apretude-epar-public-assessment-report_en.pdf"},
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    {"id":"60191","name":"Tyruko : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2023-09-28T08:54:00Z","last_updated_date":"2023-09-28T08:54:00Z","reference_number":"EMA/359152/2023","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/tyruko-epar-public-assessment-report_en.pdf"},
    {"id":"60218","name":"Lyfnua : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2023-09-29T15:18:00Z","last_updated_date":"2023-10-10T17:10:00Z","reference_number":"EMA/357321/2023 Corr.1","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/lyfnua-epar-public-assessment-report_en.pdf"},
    {"id":"60223","name":"Tyenne : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2023-10-02T13:15:00Z","last_updated_date":"2023-10-02T13:15:00Z","reference_number":"EMA/365561/2023","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/tyenne-epar-public-assessment-report_en.pdf"},
    {"id":"60229","name":"Tevimbra : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2023-10-02T15:36:00Z","last_updated_date":"2023-10-02T15:36:00Z","reference_number":"EMA/CHMP/359838/2023","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/tevimbra-epar-public-assessment-report_en.pdf"},
    {"id":"60242","name":"Yesafili : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2023-10-03T13:35:00Z","last_updated_date":"2023-10-03T13:35:00Z","reference_number":"EMA/359132/2023","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/yesafili-epar-public-assessment-report_en.pdf"},
    {"id":"60259","name":"Enrylaze : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2023-10-05T08:57:00Z","last_updated_date":"2023-10-05T08:57:00Z","reference_number":"EMA/429470/2023","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/enrylaze-epar-public-assessment-report_en.pdf"},
    {"id":"60264","name":"Tepkinly : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2023-10-05T09:28:00Z","last_updated_date":"2023-10-05T09:28:00Z","reference_number":"EMA/CHMP/419797/2023","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/tepkinly-epar-public-assessment-report_en.pdf"},
    {"id":"60294","name":"Orserdu : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2023-10-09T10:54:00Z","last_updated_date":"2023-10-09T10:54:00Z","reference_number":"EMA/CHMP/358130/2023","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/orserdu-epar-public-assessment-report_en.pdf"},
    {"id":"60549","name":"Trifexis : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2013-10-17T02:00:00Z","last_updated_date":"2018-10-08T02:00:00Z","reference_number":"EMA/481078/2013","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/trifexis-epar-public-assessment-report_en.pdf"},
    {"id":"60558","name":"Pemetrexed Lilly : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2015-10-02T02:00:00Z","last_updated_date":"2021-11-26T02:00:00Z","reference_number":"EMA/CHMP/448343/2015","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/pemetrexed-lilly-epar-public-assessment-report_en.pdf"},
    {"id":"60567","name":"Refixia : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2017-08-02T18:00:00Z","last_updated_date":"2017-08-02T18:00:00Z","reference_number":"EMA/346525/2017","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/refixia-epar-public-assessment-report_en.pdf"},
    {"id":"60587","name":"Dexxience : EPAR - Refusal public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2018-10-09T15:50:00Z","last_updated_date":"2018-10-09T15:50:00Z","reference_number":"EMA/548301/2018","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/dexxience-epar-refusal-public-assessment-report_en.pdf"},
    {"id":"60727","name":"Sitagliptin/Metformin hydrochloride Sun : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2023-07-17T12:06:00Z","last_updated_date":"2023-07-17T12:06:00Z","reference_number":"EMA/290005/2023","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/sitagliptin-metformin-hydrochloride-sun-epar-public-assessment-report_en.pdf"},
    {"id":"60800","name":"Degarelix Accord : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2023-11-08T10:08:00Z","last_updated_date":"2023-11-08T10:08:00Z","reference_number":"EMA/380123/2023","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/degarelix-accord-epar-public-assessment-report_en.pdf"},
    {"id":"60853","name":"Zoonotic Influenza Vaccine Seqirus: EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2023-11-10T11:59:00Z","last_updated_date":"2023-11-10T11:59:00Z","reference_number":"EMEA/H/C/006375","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/zoonotic-influenza-vaccine-seqirus-epar-public-assessment-report_en.pdf"},
    {"id":"60927","name":"Ebglyss : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2023-11-20T16:33:27Z","last_updated_date":"2023-11-20T16:33:27Z","reference_number":"EMA/453942/2023","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/ebglyss-epar-public-assessment-report_en.pdf"},
    {"id":"60942","name":"Jaypirca : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2023-11-20T15:27:05Z","last_updated_date":"2023-11-20T15:27:05Z","reference_number":"EMA/308908/2023","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/jaypirca-epar-public-assessment-report_en.pdf"},
    {"id":"60952","name":"Vanflyta : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2023-11-21T11:27:13Z","last_updated_date":"2023-11-21T11:27:13Z","reference_number":"EMA/443555/2023","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/vanflyta-epar-public-assessment-report_en.pdf"},
    {"id":"60958","name":"Aqumeldi : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2023-11-22T14:33:44Z","last_updated_date":"2023-11-22T14:33:44Z","reference_number":"EMA/481595/2023","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/aqumeldi-epar-public-assessment-report_en.pdf"},
    {"id":"60973","name":"Herwenda : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2023-11-23T10:53:20Z","last_updated_date":"2023-11-23T10:53:20Z","reference_number":"EMA/514898/2023","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/herwenda-epar-public-assessment-report_en.pdf"},
    {"id":"61085","name":"Inaqovi : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2023-11-30T16:11:11Z","last_updated_date":"2023-11-30T16:11:11Z","reference_number":"EMA/CHMP/402324/2023","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/inaqovi-epar-public-assessment-report_en.pdf"},
    {"id":"61245","name":"Finlee : EPAR - Public Assessment Report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2023-12-05T14:02:25Z","last_updated_date":"2023-12-05T14:02:25Z","reference_number":"EMA/443504/2023","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/finlee-epar-public-assessment-report_en.pdf"},
    {"id":"61265","name":"Yorvipath : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2023-12-06T09:39:41Z","last_updated_date":"2023-12-06T09:39:41Z","reference_number":"EMA/439682/2023","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/yorvipath-epar-public-assessment-report_en.pdf"},
    {"id":"61334","name":"Zilbrysq : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2023-12-08T11:34:24Z","last_updated_date":"2023-12-08T11:34:24Z","reference_number":"EMA/CHMP/439661/2023","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/zilbrysq-epar-public-assessment-report_en.pdf"},
    {"id":"61363","name":"Catiolanze : EPAR - Public Assessment Report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2023-12-11T16:31:56Z","last_updated_date":"2023-12-11T16:31:56Z","reference_number":"EMA/CHMP/448508/2023","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/catiolanze-epar-public-assessment-report_en.pdf"},
    {"id":"61508","name":"Veoza : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2023-12-20T15:12:12Z","last_updated_date":"2023-12-20T15:12:12Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/veoza-epar-public-assessment-report_en.pdf"},
    {"id":"61612","name":"Loargys : EPAR - Public Assessment Report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2023-12-22T16:46:23Z","last_updated_date":"2023-12-22T16:46:23Z","reference_number":"EMA/485896/2023","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/loargys-epar-public-assessment-report_en.pdf"},
    {"id":"61629","name":"Agamree : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2024-01-04T14:31:27Z","last_updated_date":"2024-01-04T14:31:27Z","reference_number":"EMA/CHMP/487504/2023","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/agamree-epar-public-assessment-report_en.pdf"},
    {"id":"61799","name":"Spexotras : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2024-01-17T14:34:12Z","last_updated_date":"2024-01-17T14:34:12Z","reference_number":"EMA/542043/2023","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/spexotras-epar-public-assessment-report_en.pdf"},
    {"id":"61870","name":"Rezzayo : EPAR - Public Assessment Report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2024-01-24T13:59:26Z","last_updated_date":"2024-01-24T13:59:26Z","reference_number":"EMA/487522/2023","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/rezzayo-epar-public-assessment-report_en.pdf"},
    {"id":"61885","name":"Elrexfio : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2024-01-25T11:42:19Z","last_updated_date":"2024-01-25T11:42:19Z","reference_number":"EMA/544323/2023","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/elrexfio-epar-public-assessment-report_en.pdf"},
    {"id":"61965","name":"Rimmyrah : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2024-01-31T11:15:58Z","last_updated_date":"2024-01-31T11:15:58Z","reference_number":"EMA/CHMP/536323/2023","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/rimmyrah-epar-public-assessment-report_en.pdf"},
    {"id":"61972","name":"Albrioza : EPAR - Refusal public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2024-02-01T13:40:17Z","last_updated_date":"2024-02-20T13:48:00Z","reference_number":"EMA/CHMP/487533/2023","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/albrioza-epar-refusal-public-assessment-report_en.pdf"},
    {"id":"62026","name":"Uzprovo : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2024-02-07T16:02:09Z","last_updated_date":"2024-02-07T16:02:09Z","reference_number":"EMA/549260/2023","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/uzprovo-epar-public-assessment-report_en.pdf"},
    {"id":"62038","name":"Omjjara : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2024-02-08T11:28:07Z","last_updated_date":"2024-02-08T11:28:07Z","reference_number":"EMA/548646/2023","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/omjjara-epar-public-assessment-report_en.pdf"},
    {"id":"62044","name":"Elucirem : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2024-02-08T12:03:03Z","last_updated_date":"2024-02-08T12:03:03Z","reference_number":"EMA/CHMP/488512/2023","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/elucirem-epar-public-assessment-report_en.pdf"},
    {"id":"62096","name":"Vueway : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2024-02-13T11:41:51Z","last_updated_date":"2024-02-13T11:41:51Z","reference_number":"EMA/CHMP/577756/2023","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/vueway-epar-public-assessment-report_en.pdf"},
    {"id":"62179","name":"Mevlyq : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2024-02-15T12:31:34Z","last_updated_date":"2024-02-15T12:31:34Z","reference_number":"EMA/504544/2023","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/mevlyq-epar-public-assessment-report_en.pdf"},
    {"id":"62232","name":"Velsipity : EPAR - Public Assessment Report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2024-02-21T10:29:33Z","last_updated_date":"2024-02-21T10:29:33Z","reference_number":"EMA/6733/2024","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/velsipity-epar-public-assessment-report_en.pdf"},
    {"id":"62261","name":"Azacitidine Kabi: EPAR - Public assessment report ","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2024-02-22T14:57:02Z","last_updated_date":"2024-02-22T14:57:02Z","reference_number":"EMA/71813/2024","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/azacitidine-kabi-epar-public-assessment-report_en.pdf"},
    {"id":"62297","name":"Skyclarys : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2024-02-26T12:22:51Z","last_updated_date":"2024-02-26T12:22:51Z","reference_number":"EMA/43636/2024","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/skyclarys-epar-public-assessment-report_en.pdf"},
    {"id":"62304","name":"Rystiggo : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2024-02-26T14:43:33Z","last_updated_date":"2024-02-26T14:43:33Z","reference_number":"EMA/CHMP/535512/2023","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/rystiggo-epar-public-assessment-report_en.pdf"},
    {"id":"62313","name":"Naveruclif : EPAR - Public Assessment Report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2024-02-27T15:06:09Z","last_updated_date":"2024-02-27T15:06:09Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/naveruclif-epar-public-assessment-report_en.pdf"},
    {"id":"62337","name":"Casgevy : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2024-02-28T13:01:00Z","last_updated_date":"2024-02-28T13:01:00Z","reference_number":"EMA/6332/2024","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/casgevy-epar-public-assessment-report_en.pdf"},
    {"id":"62552","name":"Ibuprofen Gen.Orph : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2024-03-12T13:01:23Z","last_updated_date":"2024-03-12T13:01:23Z","reference_number":"EMA/586586/2023","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/ibuprofen-genorph-epar-public-assessment-report_en.pdf"},
    {"id":"62566","name":"Pomalidomide Viatris : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2024-03-12T16:05:04Z","last_updated_date":"2024-03-12T16:05:04Z","reference_number":"EMA/21354/2024","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/pomalidomide-viatris-epar-public-assessment-report_en.pdf"},
    {"id":"62592","name":"Krazati : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2024-03-13T11:28:47Z","last_updated_date":"2024-03-13T11:28:47Z","reference_number":"EMA/552099/2023","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/krazati-epar-public-assessment-report_en.pdf"},
    {"id":"62674","name":"Dabigatran Etexilate Leon Farma : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2024-03-21T12:25:14Z","last_updated_date":"2024-03-21T12:25:14Z","reference_number":"EMA/12212/2024","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/dabigatran-etexilate-leon-farma-epar-public-assessment-report_en.pdf"},
    {"id":"62713","name":"Trevicta : EPAR - Public Assessment Report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2024-03-22T14:57:19Z","last_updated_date":"2024-03-22T14:57:19Z","reference_number":"EMA/664603/2014","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/trevicta-epar-public-assessment-report_en.pdf"},
    {"id":"62719","name":"Exblifep : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2024-03-22T16:33:20Z","last_updated_date":"2024-03-22T16:33:20Z","reference_number":"EMA/63929/2024","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/exblifep-epar-public-assessment-report_en.pdf"},
    {"id":"63031","name":"Nintedanib Accord : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2024-04-22T10:36:14Z","last_updated_date":"2024-04-22T10:36:14Z","reference_number":"EMA/108684/2024","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/nintedanib-accord-epar-public-assessment-report_en.pdf"},
    {"id":"63061","name":"Niapelf : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2024-04-25T09:00:00Z","last_updated_date":"2024-04-25T09:00:00Z","reference_number":"EMA/100717/2024","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/niapelf-epar-public-assessment-report_en.pdf"},
    {"id":"63125","name":"Zynyz : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2024-05-02T09:30:00Z","last_updated_date":"2024-05-02T09:30:00Z","reference_number":"EMA/122634/2024","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/zynyz-epar-public-assessment-report_en.pdf"},
    {"id":"63139","name":"Celldemic : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2024-05-02T13:09:00Z","last_updated_date":"2024-05-02T13:09:00Z","reference_number":"EMA/108198/2024","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/celldemic-epar-public-assessment-report_en.pdf"},
    {"id":"63145","name":"Incellipan : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2024-05-02T14:15:00Z","last_updated_date":"2024-05-02T14:15:00Z","reference_number":"EMA/108199/2024","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/incellipan-epar-public-assessment-report_en.pdf"},
    {"id":"63182","name":"Emblaveo : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2024-05-07T09:43:00Z","last_updated_date":"2024-05-07T09:43:00Z","reference_number":"EMA/147600/2024","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/emblaveo-epar-public-assessment-report_en.pdf"},
    {"id":"63204","name":"Ryzneuta : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2024-05-13T15:53:12Z","last_updated_date":"2024-05-13T15:53:12Z","reference_number":"EMA/62813/2024","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/ryzneuta-epar-public-assessment-report_en.pdf"},
    {"id":"63260","name":"Voydeya : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2024-05-17T14:40:00Z","last_updated_date":"2024-05-17T14:40:00Z","reference_number":"EMA/107893/2024","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/voydeya-epar-public-assessment-report_en.pdf"},
    {"id":"63278","name":"Apremilast Accord : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2024-05-21T11:08:00Z","last_updated_date":"2024-05-21T11:08:00Z","reference_number":"EMA/96125/2024","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/apremilast-accord-epar-public-assessment-report_en.pdf"},
    {"id":"63310","name":"Tizveni : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2024-05-23T15:01:00Z","last_updated_date":"2024-08-02T11:28:00Z","reference_number":"EMA/116407/2024","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/tizveni-epar-public-assessment-report_en.pdf"},
    {"id":"63349","name":"Filspari : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2024-05-28T15:32:00Z","last_updated_date":"2024-05-28T15:32:00Z","reference_number":"EMA/106429/2024","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/filspari-epar-public-assessment-report_en.pdf"},
    {"id":"63362","name":"Omlyclo : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2024-05-29T11:40:00Z","last_updated_date":"2024-05-29T11:40:00Z","reference_number":"EMA/153515/2024","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/omlyclo-epar-public-assessment-report_en.pdf"},
    {"id":"63444","name":"Lytenava : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2024-05-31T15:56:00Z","last_updated_date":"2024-05-31T15:56:00Z","reference_number":"EMA/146883/2024","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/lytenava-epar-public-assessment-report_en.pdf"},
    {"id":"63456","name":"Awiqli : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2024-06-03T12:57:00Z","last_updated_date":"2024-06-03T12:57:00Z","reference_number":"EMA/146690/2024","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/awiqli-epar-public-assessment-report_en.pdf"},
    {"id":"63511","name":"Jubbonti : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2024-06-06T11:22:00Z","last_updated_date":"2024-06-06T11:22:00Z","reference_number":"EMA/169039/2024","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/jubbonti-epar-public-assessment-report_en.pdf"},
    {"id":"63563","name":"Pyzchiva : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2024-06-11T12:45:00Z","last_updated_date":"2024-06-11T12:45:00Z","reference_number":"EMA/106045/2024","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/pyzchiva-epar-public-assessment-report_en.pdf"},
    {"id":"63604","name":"Fabhalta : Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2024-06-14T11:11:01Z","last_updated_date":"2024-06-14T11:11:01Z","reference_number":"EMA/170439/2024","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/fabhalta-public-assessment-report_en.pdf"},
    {"id":"63609","name":"Qalsody : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2024-06-14T12:21:22Z","last_updated_date":"2024-06-14T12:21:22Z","reference_number":"EMA/276404/2024","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/qalsody-epar-public-assessment-report_en.pdf"},
    {"id":"63650","name":"Wyost : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2024-06-17T13:05:00Z","last_updated_date":"2024-06-17T13:05:00Z","reference_number":"EMA/169040/2024","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/wyost-epar-public-assessment-report_en.pdf"},
    {"id":"63682","name":"Neoatricon : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2024-06-19T11:50:00Z","last_updated_date":"2024-06-19T11:50:00Z","reference_number":"EMA/260885/2024","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/neoatricon-epar-public-assessment-report_en.pdf"},
    {"id":"63759","name":"Fluenz : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2024-06-26T14:33:00Z","last_updated_date":"2024-06-26T14:33:00Z","reference_number":"EMA/259848/2024","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/fluenz-epar-public-assessment-report_en.pdf-0"},
    {"id":"63827","name":"Agilus - EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2024-07-01T15:08:00Z","last_updated_date":"2024-07-01T15:08:00Z","reference_number":"EMA/150697/2024","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/agilus-epar-public-assessment-report_en.pdf"},
    {"id":"63937","name":"Obgemsa : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2024-07-05T15:57:00Z","last_updated_date":"2024-07-05T15:57:00Z","reference_number":"EMA/226759/2024","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/obgemsa-epar-public-assessment-report_en.pdf"},
    {"id":"63968","name":"Eribulin Baxter : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2024-07-09T14:14:00Z","last_updated_date":"2024-07-09T14:14:00Z","reference_number":"EMA/229035/2024","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/eribulin-baxter-epar-public-assessment-report_en.pdf"},
    {"id":"64007","name":"Fruzaqla : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2024-07-10T17:30:00Z","last_updated_date":"2024-07-10T17:30:00Z","reference_number":"EMA/CHMP/462300/2023","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/fruzaqla-epar-public-assessment-report_en.pdf"},
    {"id":"64012","name":"Tofidence : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2024-07-10T11:11:01Z","last_updated_date":"2024-07-10T11:11:01Z","reference_number":"EMA/230842/2024","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/tofidence-epar-public-assessment-report_en.pdf"},
    {"id":"64020","name":"Dimethyl fumarate Neuraxpharm : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2024-07-11T11:11:01Z","last_updated_date":"2024-07-11T11:11:01Z","reference_number":"EMA/321710/2024","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/dimethyl-fumarate-neuraxpharm-epar-public-assessment-report_en.pdf-0"},
    {"id":"64026","name":"Truqap : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2024-07-11T11:11:01Z","last_updated_date":"2024-07-11T11:11:01Z","reference_number":"EMA/236868/2024","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/truqap-epar-public-assessment-report_en.pdf"},
    {"id":"64043","name":"Dimethyl fumarate Accord : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2024-07-11T11:11:01Z","last_updated_date":"2024-07-11T11:11:01Z","reference_number":"EMA/146707/2024","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/dimethyl-fumarate-accord-epar-public-assessment-report_en.pdf-0"},
    {"id":"64051","name":"Dimethyl fumarate Mylan : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2024-07-11T11:11:01Z","last_updated_date":"2024-07-11T11:11:01Z","reference_number":"EMA/CHMP/144685/2024","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/dimethyl-fumarate-mylan-epar-public-assessment-report_en.pdf-0"},
    {"id":"64075","name":"Altuvoct : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2024-07-12T11:11:01Z","last_updated_date":"2024-07-12T11:11:01Z","reference_number":"EMA/459190/2024 Corr.1","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/altuvoct-epar-public-assessment-report_en.pdf"},
    {"id":"64196","name":"Wezenla : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2024-07-18T11:15:00Z","last_updated_date":"2024-07-18T11:15:00Z","reference_number":"EMA/228742/2024","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/wezenla-epar-public-assessment-report_en.pdf"},
    {"id":"64202","name":"Ixchiq : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2024-07-18T11:44:00Z","last_updated_date":"2024-07-18T11:44:00Z","reference_number":"EMA/292025/2024","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/ixchiq-epar-public-assessment-report_en.pdf"},
    {"id":"64296","name":"Jeraygo : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2024-07-24T11:11:01Z","last_updated_date":"2024-07-24T11:11:01Z","reference_number":"EMA/256238/2024","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/jeraygo-epar-public-assessment-report_en.pdf-0"},
    {"id":"64456","name":"Durveqtix : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2024-08-01T09:32:56Z","last_updated_date":"2025-06-04T11:45:00Z","reference_number":"EMA/323453/2024","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/durveqtix-epar-public-assessment-report_en.pdf"},
    {"id":"64461","name":"Dasatinib Accord Healthcare : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2024-08-01T09:56:26Z","last_updated_date":"2024-08-01T09:56:26Z","reference_number":"EMA/313181/2024","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/dasatinib-accord-healthcare-epar-public-assessment-report_en.pdf"},
    {"id":"64467","name":"Pomalidomide Krka : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2024-08-01T10:26:16Z","last_updated_date":"2024-08-01T10:26:16Z","reference_number":"EMA/341648/2024","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/pomalidomide-krka-epar-public-assessment-report_en.pdf"},
    {"id":"64473","name":"Pomalidomide Zentiva : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2024-08-01T11:00:53Z","last_updated_date":"2024-08-01T11:00:53Z","reference_number":"EMA/290725/2024","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/pomalidomide-zentiva-epar-public-assessment-report_en.pdf"},
    {"id":"64490","name":"Apexelsin : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2024-08-02T12:34:22Z","last_updated_date":"2024-08-02T12:34:22Z","reference_number":"EMA/283170/2024","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/apexelsin-epar-public-assessment-report_en.pdf"},
    {"id":"64499","name":"Pomalidomide Accord : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2024-08-02T15:41:21Z","last_updated_date":"2024-08-02T15:41:21Z","reference_number":"EMA/341688/2024","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/pomalidomide-accord-epar-public-assessment-report_en.pdf"},
    {"id":"64530","name":"Adzynma : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2024-08-07T12:55:16Z","last_updated_date":"2025-11-04T15:08:00Z","reference_number":"EMA/352066/2024 Corr.1","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/adzynma-epar-public-assessment-report_en.pdf"},
    {"id":"64542","name":"Avzivi : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2024-08-08T14:06:18Z","last_updated_date":"2024-08-08T14:06:18Z","reference_number":"EMA/285021/2024 ","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/avzivi-epar-public-assessment-report_en.pdf"},
    {"id":"64619","name":"GalliaPharm : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2024-08-22T13:54:27Z","last_updated_date":"2024-08-22T13:54:27Z","reference_number":"EMA/285852/2024","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/galliapharm-epar-public-assessment-report_en.pdf"},
    {"id":"64624","name":"Zegalogue : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2024-08-23T15:18:56Z","last_updated_date":"2024-08-23T15:18:56Z","reference_number":"EMA/281112/2024","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/zegalogue-epar-public-assessment-report_en.pdf"},
    {"id":"64656","name":"Balversa : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2024-08-29T13:35:20Z","last_updated_date":"2024-08-29T13:35:20Z","reference_number":"EMA/336561/2024","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/balversa-epar-public-assessment-report_en.pdf"},
    {"id":"64668","name":"Piasky : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2024-08-30T11:28:05Z","last_updated_date":"2024-08-30T11:28:05Z","reference_number":"EMA/332145/2024","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/piasky-epar-public-assessment-report_en.pdf"},
    {"id":"64720","name":"Eurneffy : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2024-09-05T13:26:30Z","last_updated_date":"2024-09-05T13:26:30Z","reference_number":"EMA/328958/2024","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/eurneffy-epar-public-assessment-report_en.pdf"},
    {"id":"64730","name":"mResvia : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2024-09-06T09:39:33Z","last_updated_date":"2024-09-06T09:39:33Z","reference_number":"EMA/329706/2024","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/mresvia-epar-public-assessment-report_en.pdf"},
    {"id":"64792","name":"Steqeyma : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2024-09-11T12:56:00Z","last_updated_date":"2024-09-11T12:56:00Z","reference_number":"EMA/328491/2024","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/steqeyma-epar-public-assessment-report_en.pdf"},
    {"id":"64801","name":"Nilotinib Accord : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2024-09-11T15:55:00Z","last_updated_date":"2024-09-11T15:55:00Z","reference_number":"EMA/325502/2024","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/nilotinib-accord-epar-public-assessment-report_en.pdf"},
    {"id":"64853","name":"Tauvid : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2024-09-13T14:45:00Z","last_updated_date":"2024-09-13T14:45:00Z","reference_number":"EMA/CHMP/287487/2024","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/tauvid-epar-public-assessment-report_en.pdf"},
    {"id":"64977","name":"Iqirvo : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2024-09-20T12:28:00Z","last_updated_date":"2024-09-20T12:28:00Z","reference_number":"EMA/372188/2024","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/iqirvo-epar-public-assessment-report_en.pdf"},
    {"id":"64991","name":"Kayfanda : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2024-09-23T11:50:00Z","last_updated_date":"2024-09-23T11:50:00Z","reference_number":"EMA/372096/2024","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/kayfanda-epar-public-assessment-report_en.pdf"},
    {"id":"64998","name":"Vyloy : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2024-09-23T15:32:00Z","last_updated_date":"2024-09-23T15:32:00Z","reference_number":"EMA/378968/2024","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/vyloy-epar-public-assessment-report_en.pdf"},
    {"id":"65011","name":"Anzupgo : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2024-09-24T12:31:00Z","last_updated_date":"2024-09-24T12:31:00Z","reference_number":"EMA/372390/2024","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/anzupgo-epar-public-assessment-report_en.pdf"},
    {"id":"65016","name":"Eksunbi : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2024-09-24T13:00:00Z","last_updated_date":"2025-09-08T16:02:00Z","reference_number":"EMA/371773/2024","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/eksunbi-epar-public-assessment-report_en.pdf"},
    {"id":"65021","name":"Loqtorzi : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2024-09-24T13:20:00Z","last_updated_date":"2024-09-24T13:20:00Z","reference_number":"EMA/CHMP/372271/2024","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/loqtorzi-epar-public-assessment-report_en.pdf"},
    {"id":"65031","name":"Winrevair : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2024-09-25T11:27:00Z","last_updated_date":"2024-09-25T11:27:00Z","reference_number":"EMA/330301/2024","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/winrevair-epar-public-assessment-report_en.pdf"},
    {"id":"65041","name":"Tuznue : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2024-09-25T15:36:00Z","last_updated_date":"2024-09-25T15:36:00Z","reference_number":"EMA/CHMP/367870/2024","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/tuznue-epar-public-assessment-report_en.pdf"},
    {"id":"65061","name":"Imcivree : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2024-09-30T15:48:00Z","last_updated_date":"2024-09-30T15:48:00Z","reference_number":"EMA/402097/2024","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/imcivree-epar-public-assessment-report_en.pdf-0"},
    {"id":"65107","name":"Axitinib Accord : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2024-10-02T08:59:00Z","last_updated_date":"2024-10-02T08:59:00Z","reference_number":"EMA/372021/2024","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/axitinib-accord-epar-public-assessment-report_en.pdf"},
    {"id":"65115","name":"Otulfi : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2024-10-02T14:12:00Z","last_updated_date":"2024-10-02T14:12:00Z","reference_number":"EMA/378457/2024","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/otulfi-epar-public-assessment-report_en.pdf"},
    {"id":"65196","name":"Fymskina : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2024-10-07T09:09:24Z","last_updated_date":"2024-10-07T09:09:24Z","reference_number":"EMA/378464/2024","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/fymskina-epar-public-assessment-report_en.pdf"},
    {"id":"65207","name":"Yuvanci : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2024-10-07T10:50:00Z","last_updated_date":"2024-10-07T10:50:00Z","reference_number":"EMA/CHMP/332056/2024","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/yuvanci-epar-public-assessment-report_en.pdf"},
    {"id":"65257","name":"Enzalutamide Viatris : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2024-10-09T15:04:00Z","last_updated_date":"2024-10-09T15:04:00Z","reference_number":"EMA/338096/2024","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/enzalutamide-viatris-epar-public-assessment-report_en.pdf"},
    {"id":"65467","name":"Akantior : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2024-10-29T09:30:36Z","last_updated_date":"2024-10-29T09:30:36Z","reference_number":"EMA/286425/2024","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/akantior-epar-public-assessment-report_en.pdf"},
    {"id":"65473","name":"Ranibizumab Midas : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2024-10-29T09:52:31Z","last_updated_date":"2024-10-29T09:52:31Z","reference_number":"EMA/371818/2024","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/ranibizumab-midas-epar-public-assessment-report_en.pdf"},
    {"id":"65542","name":"Cejemly : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2024-11-05T09:24:46Z","last_updated_date":"2024-11-05T09:24:46Z","reference_number":"EMA/380155/2024","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/cejemly-epar-public-assessment-report_en.pdf"},
    {"id":"65574","name":"Vevizye : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2024-11-08T12:02:19Z","last_updated_date":"2024-11-08T12:02:19Z","reference_number":"EMA/439518/2024","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/vevizye-epar-public-assessment-report_en.pdf"},
    {"id":"65717","name":"Ordspono : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2024-11-19T16:20:35Z","last_updated_date":"2024-11-19T16:20:35Z","reference_number":"EMA/518269/2024","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/ordspono-epar-public-assessment-report_en.pdf"},
    {"id":"65723","name":"Nezglyal : EPAR - Refusal public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2024-11-20T11:57:24Z","last_updated_date":"2024-11-20T11:57:24Z","reference_number":"EMA/CHMP/301934/2024","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/nezglyal-epar-refusal-public-assessment-report_en.pdf"},
    {"id":"65854","name":"Pomalidomide Teva : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2024-11-28T09:55:23Z","last_updated_date":"2024-11-28T09:55:23Z","reference_number":"EMA/518385/2024","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/pomalidomide-teva-epar-public-assessment-report_en.pdf"},
    {"id":"65872","name":"Flucelvax : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2024-11-28T15:09:42Z","last_updated_date":"2024-11-28T15:09:42Z","reference_number":"EMA/511525/2024","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/flucelvax-epar-public-assessment-report_en.pdf"},
    {"id":"65920","name":"Fluad : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2024-12-03T12:14:05Z","last_updated_date":"2024-12-03T12:14:05Z","reference_number":"EMA/511487/2024","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/fluad-epar-public-assessment-report_en.pdf"},
    {"id":"65971","name":"Theralugand : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2024-12-05T12:46:05Z","last_updated_date":"2024-12-05T12:46:05Z","reference_number":"EMA/468008/2024","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/theralugand-epar-public-assessment-report_en.pdf"},
    {"id":"66039","name":"Opuviz: EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2024-12-10T11:09:28Z","last_updated_date":"2024-12-10T11:09:28Z","reference_number":"EMA/466892/2024","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/opuviz-epar-public-assessment-report_en.pdf"},
    {"id":"66066","name":"Elahere : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2024-12-11T10:57:08Z","last_updated_date":"2024-12-11T10:57:08Z","reference_number":"EMA/473768/2024","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/elahere-epar-public-assessment-report_en.pdf"},
    {"id":"66081","name":"Penbraya : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2024-12-12T11:10:55Z","last_updated_date":"2025-02-05T12:46:00Z","reference_number":"EMA/464092/2024","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/penbraya-epar-public-assessment-report_en.pdf"},
    {"id":"66164","name":"Durysta: Withdrawal assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2024-12-17T09:49:26Z","last_updated_date":"2024-12-17T09:49:26Z","reference_number":"EMA/CHMP/457051/2024","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/durysta-withdrawal-assessment-report_en.pdf"},
    {"id":"66201","name":"Absimky : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2024-12-18T13:21:48Z","last_updated_date":"2025-12-18T12:06:00Z","reference_number":"EMA/511029/2024","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/absimky-epar-public-assessment-report_en.pdf"},
    {"id":"66206","name":"Hympavzi : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2024-12-18T14:09:28Z","last_updated_date":"2024-12-18T14:09:28Z","reference_number":"EMA/464842/2024","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/hympavzi-epar-public-assessment-report_en.pdf"},
    {"id":"66212","name":"Imuldosa : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2024-12-18T14:33:14Z","last_updated_date":"2024-12-18T14:33:14Z","reference_number":"EMA/592044/2024","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/imuldosa-epar-public-assessment-report_en.pdf"},
    {"id":"66217","name":"Epixram: EPAR - Withdrawal assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2024-12-19T09:40:40Z","last_updated_date":"2024-12-19T09:40:40Z","reference_number":"EMA/CHMP/469993/2024","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/epixram-epar-withdrawal-assessment-report_en.pdf"},
    {"id":"66366","name":"Alhemo : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2025-01-17T15:57:26Z","last_updated_date":"2025-01-17T15:57:26Z","reference_number":"EMA/511415/2024","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/alhemo-epar-public-assessment-report_en.pdf"},
    {"id":"66380","name":"Afqlir : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2025-01-20T15:18:47Z","last_updated_date":"2025-01-20T15:18:47Z","reference_number":"EMA/466863/2024","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/afqlir-epar-public-assessment-report_en.pdf"},
    {"id":"66391","name":"Eltrombopag Viatris : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2025-01-21T10:30:09Z","last_updated_date":"2025-01-21T10:30:09Z","reference_number":"EMA/510859/2024","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/eltrombopag-viatris-epar-public-assessment-report_en.pdf"},
    {"id":"66415","name":"Masitinib AB Science : EPAR - Refusal public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2025-01-22T14:09:58Z","last_updated_date":"2025-01-22T14:09:58Z","reference_number":"EMA/CHMP/514389/2024","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/masitinib-ab-science-epar-refusal-public-assessment-report_en.pdf"},
    {"id":"66462","name":"Ahzantive : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2025-01-24T16:53:25Z","last_updated_date":"2025-01-24T16:53:25Z","reference_number":"EMA/CHMP/565845/2024","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/ahzantive-epar-public-assessment-report_en.pdf"},
    {"id":"66493","name":"Augtyro : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2025-01-28T17:02:40Z","last_updated_date":"2025-01-28T17:02:40Z","reference_number":"EMA/567599/2024","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/augtyro-epar-public-assessment-report_en.pdf"},
    {"id":"66572","name":"Gohibic : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2025-02-03T12:13:38Z","last_updated_date":"2025-02-03T12:13:38Z","reference_number":"EMA/564703/2024","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/gohibic-epar-public-assessment-report_en.pdf"},
    {"id":"66655","name":"Ituxredi : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2025-02-10T16:18:18Z","last_updated_date":"2025-02-10T16:18:18Z","reference_number":"EMA/565284/2024","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/ituxredi-epar-public-assessment-report_en.pdf"},
    {"id":"66665","name":"Hetronifly : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2025-02-11T10:27:45Z","last_updated_date":"2025-02-11T10:27:45Z","reference_number":"EMA/465512/2024","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/hetronifly-epar-public-assessment-report_en.pdf"},
    {"id":"66674","name":"Korjuny : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2025-02-11T12:35:54Z","last_updated_date":"2025-02-11T12:35:54Z","reference_number":"EMA/551738/2024","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/korjuny-epar-public-assessment-report_en.pdf"},
    {"id":"66863","name":"Siiltibcy : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2025-02-19T09:24:22Z","last_updated_date":"2025-02-19T09:24:22Z","reference_number":"EMA/509248/2024","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/siiltibcy-epar-public-assessment-report_en.pdf"},
    {"id":"66868","name":"Nemluvio : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2025-02-19T09:43:33Z","last_updated_date":"2025-02-19T09:43:33Z","reference_number":"EMA/CHMP/487280/2024","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/nemluvio-epar-public-assessment-report_en.pdf"},
    {"id":"66901","name":"Yesintek : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2025-02-20T12:02:53Z","last_updated_date":"2025-02-20T12:02:53Z","reference_number":"EMA/820/2025","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/yesintek-epar-public-assessment-report_en.pdf"},
    {"id":"66932","name":"Kavigale : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2025-02-24T15:21:15Z","last_updated_date":"2025-02-24T15:21:15Z","reference_number":"EMA/8692/2025 corr.1","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/kavigale-epar-public-assessment-report_en.pdf"},
    {"id":"66947","name":"Seladelpar Gilead : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2025-02-25T13:55:37Z","last_updated_date":"2025-02-25T13:55:37Z","reference_number":"EMA/12861/2025","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/seladelpar-gilead-epar-public-assessment-report_en.pdf"},
    {"id":"66999","name":"Kostaive: EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2025-02-26T14:57:47Z","last_updated_date":"2025-02-26T14:57:47Z","reference_number":"EMA/18711/2025 corr.1","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/kostaive-epar-public-assessment-report_en.pdf"},
    {"id":"67010","name":"Welireg : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2025-02-27T13:30:42Z","last_updated_date":"2025-05-14T11:20:00Z","reference_number":"EMA/18425/2025","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/welireg-epar-public-assessment-report_en.pdf"},
    {"id":"67077","name":"Beyonttra : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2025-03-03T14:28:10Z","last_updated_date":"2025-03-03T14:28:10Z","reference_number":"EMA/66885/2025","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/beyonttra-epar-public-assessment-report_en.pdf"},
    {"id":"67085","name":"Obodence : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2025-03-03T15:30:10Z","last_updated_date":"2025-03-03T15:30:10Z","reference_number":"EMA/560515/2024","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/obodence-epar-public-assessment-report_en.pdf"},
    {"id":"67095","name":"Baiama : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2025-03-04T13:20:27Z","last_updated_date":"2025-03-04T13:20:27Z","reference_number":"EMA/CHMP/564859/2024","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/baiama-epar-public-assessment-report_en.pdf"},
    {"id":"67136","name":"Emcitate : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2025-03-11T10:58:19Z","last_updated_date":"2025-03-11T10:58:19Z","reference_number":"EMA/586378/2024","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/emcitate-epar-public-assessment-report_en.pdf"},
    {"id":"67174","name":"Zefylti : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2025-03-10T15:22:29Z","last_updated_date":"2025-03-10T15:22:29Z","reference_number":"EMA/1684/2025","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/zefylti-epar-public-assessment-report_en.pdf"},
    {"id":"67192","name":"Andembry : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2025-03-11T14:58:42Z","last_updated_date":"2025-03-11T14:58:42Z","reference_number":"EMA/15345/2025","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/andembry-epar-public-assessment-report_en.pdf"},
    {"id":"67196","name":"Paxneury : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2025-03-11T15:26:37Z","last_updated_date":"2025-03-11T15:26:37Z","reference_number":"EMA/CHMP/14178/2025","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/paxneury-epar-public-assessment-report_en.pdf"},
    {"id":"67202","name":"Rytelo : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2025-03-11T15:57:22Z","last_updated_date":"2025-03-11T15:57:22Z","reference_number":"EMA/13310/2025","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/rytelo-epar-public-assessment-report_en.pdf"},
    {"id":"67228","name":"Wainzua : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2025-03-12T11:17:20Z","last_updated_date":"2025-03-12T11:17:20Z","reference_number":"EMA/CHMP/515905/2024","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/wainzua-epar-public-assessment-report_en.pdf"},
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    {"id":"67617","name":"Osenvelt : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2025-04-03T12:50:36Z","last_updated_date":"2025-04-03T12:50:36Z","reference_number":"EMA/51220/2025","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/osenvelt-epar-public-assessment-report_en.pdf"},
    {"id":"67639","name":"Avtozma : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2025-04-04T13:25:59Z","last_updated_date":"2025-04-04T13:25:59Z","reference_number":"EMA/10943/2025","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/avtozma-epar-public-assessment-report_en.pdf"},
    {"id":"67648","name":"Stoboclo : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2025-04-04T15:28:24Z","last_updated_date":"2025-04-04T15:28:24Z","reference_number":"EMA/51238/2025","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/stoboclo-epar-public-assessment-report_en.pdf"},
    {"id":"67665","name":"Tivdak : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2025-04-07T12:25:05Z","last_updated_date":"2025-04-07T12:25:05Z","reference_number":"EMA/59170/2025","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/tivdak-epar-public-assessment-report_en.pdf"},
    {"id":"67724","name":"Pavblu : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2025-04-10T09:48:25Z","last_updated_date":"2025-04-10T09:48:25Z","reference_number":"EMA/90425/2025","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/pavblu-epar-public-assessment-report_en.pdf"},
    {"id":"67802","name":"Capvaxive : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2025-04-14T16:46:56Z","last_updated_date":"2025-04-14T16:46:56Z","reference_number":"EMA/68123/2025","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/capvaxive-epar-public-assessment-report_en.pdf"},
    {"id":"67887","name":"Dyrupeg : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2025-04-16T16:47:37Z","last_updated_date":"2025-04-16T16:47:37Z","reference_number":"EMA/57953/2025","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/dyrupeg-epar-public-assessment-report_en.pdf"},
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    {"id":"68064","name":"Lynozyfic : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2025-05-02T13:20:40Z","last_updated_date":"2025-05-02T13:20:40Z","reference_number":"EMA/141656/2025","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/lynozyfic-epar-public-assessment-report_en.pdf"},
    {"id":"68098","name":"Leqembi - EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2025-05-05T16:21:38Z","last_updated_date":"2025-05-05T16:21:38Z","reference_number":"EMA/CHMP/573107/2024","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/leqembi-epar-public-assessment-report_en.pdf"},
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    {"id":"68250","name":"Datroway : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2025-05-13T10:04:53Z","last_updated_date":"2025-05-13T10:04:53Z","reference_number":"EMA/CHMP/78522/2025","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/datroway-epar-public-assessment-report_en.pdf"},
    {"id":"68315","name":"Deqsiga : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2025-05-16T11:10:54Z","last_updated_date":"2025-05-16T11:10:54Z","reference_number":"EMA/157144/2025","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/deqsiga-epar-public-assessment-report_en.pdf"},
    {"id":"68638","name":"Qoyvolma : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2025-06-10T12:34:24Z","last_updated_date":"2025-06-10T12:34:24Z","reference_number":"EMA/130000/2025","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/qoyvolma-epar-public-assessment-report_en.pdf"},
    {"id":"68773","name":"Xbryk : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2025-06-16T15:17:20Z","last_updated_date":"2025-06-16T15:17:20Z","reference_number":"EMA/560527/2024","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/xbryk-epar-public-assessment-report_en.pdf"},
    {"id":"69087","name":"Ziihera : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2025-07-03T10:54:39Z","last_updated_date":"2025-07-03T10:54:39Z","reference_number":"EMA/169374/2025","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/ziihera-epar-public-assessment-report_en.pdf"},
    {"id":"69109","name":"Oczyesa : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2025-07-04T13:25:38Z","last_updated_date":"2025-07-04T13:25:38Z","reference_number":"EMA/164079/2025","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/oczyesa-epar-public-assessment-report_en.pdf"},
    {"id":"69197","name":"Duvyzat : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2025-07-09T15:40:20Z","last_updated_date":"2025-07-09T15:40:20Z","reference_number":"EMA/CHMP/176222/2025","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/duvyzat-epar-public-assessment-report_en.pdf"},
    {"id":"69269","name":"Tepezza : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2025-07-14T15:55:10Z","last_updated_date":"2025-07-14T15:55:10Z","reference_number":"EMA/175329/2025","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/tepezza-epar-public-assessment-report_en.pdf"},
    {"id":"69292","name":"Trabectedin Accord : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2025-07-15T11:58:23Z","last_updated_date":"2025-07-15T11:58:23Z","reference_number":"EMA/97108/2025","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/trabectedin-accord-epar-public-assessment-report_en.pdf"},
    {"id":"69532","name":"Jubereq : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2025-07-28T13:05:33Z","last_updated_date":"2025-07-28T13:05:33Z","reference_number":"EMA/131555/2025","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/jubereq-epar-public-assessment-report_en.pdf"},
    {"id":"69540","name":"Sephience : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2025-07-28T14:25:50Z","last_updated_date":"2025-07-28T14:25:50Z","reference_number":"EMA/167549/2025","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/sephience-epar-public-assessment-report_en.pdf"},
    {"id":"69549","name":"Osvyrti : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2025-07-28T15:31:36Z","last_updated_date":"2025-07-28T15:31:36Z","reference_number":"EMA/131611/2025","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/osvyrti-epar-public-assessment-report_en.pdf"},
    {"id":"69626","name":"Blenrep : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2025-08-01T15:07:17Z","last_updated_date":"2025-08-01T15:07:17Z","reference_number":"EMA/240108/2025 ","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/blenrep-epar-public-assessment-report_en.pdf-0"},
    {"id":"69663","name":"Emtricitabine / Tenofovir alafenamide Viatris : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2025-08-05T12:04:14Z","last_updated_date":"2025-08-05T12:04:14Z","reference_number":"EMA/192996/2025","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/emtricitabine-tenofovir-alafenamide-viatris-epar-public-assessment-report_en.pdf"},
    {"id":"69718","name":"Dazublys: EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2025-08-12T17:43:07Z","last_updated_date":"2025-08-12T17:43:07Z","reference_number":"EMA/CHMP/86926/2025","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/dazublys-epar-public-assessment-report_en.pdf"},
    {"id":"69772","name":"Aucatzyl: EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2025-08-19T15:32:52Z","last_updated_date":"2025-08-19T15:32:52Z","reference_number":"EMA/197444/2025","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/aucatzyl-epar-public-assessment-report_en.pdf"},
    {"id":"69779","name":"Usymro: EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2025-08-19T19:41:50Z","last_updated_date":"2025-08-19T19:41:50Z","reference_number":"EMA/135976/2025","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/usymro-epar-public-assessment-report_en.pdf"},
    {"id":"69785","name":"Ezmekly: EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2025-08-20T11:12:30Z","last_updated_date":"2025-08-20T11:12:30Z","reference_number":"EMA/CHMP/86925/2025","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/ezmekly-epar-public-assessment-report_en.pdf"},
    {"id":"69825","name":"Vevzuo: EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2025-08-21T14:54:53Z","last_updated_date":"2025-08-21T14:54:53Z","reference_number":"EMA/164555/2025","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/vevzuo-epar-public-assessment-report_en.pdf"},
    {"id":"69841","name":"Vimkunya : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2025-08-22T10:23:22Z","last_updated_date":"2025-08-22T10:23:22Z","reference_number":"EMA/59925/2025","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/vimkunya-epar-public-assessment-report_en.pdf"},
    {"id":"69876","name":"Itovebi : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2025-08-27T16:28:51Z","last_updated_date":"2025-08-27T16:28:51Z","reference_number":"EMA/CHMP/122122/2025","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/itovebi-epar-public-assessment-report_en.pdf"},
    {"id":"69901","name":"Attrogy : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2025-08-28T16:31:53Z","last_updated_date":"2025-08-28T16:31:53Z","reference_number":"EMA/161582/2025","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/attrogy-epar-public-assessment-report_en.pdf"},
    {"id":"69932","name":"Yeytuo : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2025-09-03T09:59:11Z","last_updated_date":"2025-09-03T09:59:11Z","reference_number":"EMA/265754/2025","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/yeytuo-epar-public-assessment-report_en.pdf"},
    {"id":"69938","name":"Junod : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2025-09-03T10:46:31Z","last_updated_date":"2025-09-03T10:46:31Z","reference_number":"EMA/165403/2025","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/junod-epar-public-assessment-report_en.pdf"},
    {"id":"69961","name":"Nintedanib Viatris : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2025-09-05T08:59:10Z","last_updated_date":"2025-09-05T08:59:10Z","reference_number":"EMA/212977/2025","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/nintedanib-viatris-epar-public-assessment-report_en.pdf"},
    {"id":"69974","name":"Zemcelpro : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2025-09-05T15:11:14Z","last_updated_date":"2025-09-05T15:11:14Z","reference_number":"EMA/232925/2025","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/zemcelpro-epar-public-assessment-report_en.pdf"},
    {"id":"70006","name":"Yaxwer : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2025-09-08T16:41:38Z","last_updated_date":"2025-09-08T16:41:38Z","reference_number":"EMA/165411/2025","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/yaxwer-epar-public-assessment-report_en.pdf"},
    {"id":"70060","name":"Ryjunea : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2025-09-11T09:23:06Z","last_updated_date":"2025-09-11T09:23:06Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/ryjunea-epar-public-assessment-report_en.pdf"},
    {"id":"70099","name":"Riulvy : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2025-09-16T17:14:45Z","last_updated_date":"2025-09-16T17:14:45Z","reference_number":"EMA/221770/2025","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/riulvy-epar-public-assessment-report_en.pdf"},
    {"id":"70207","name":"Romvimza : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2025-09-22T11:58:38Z","last_updated_date":"2025-09-22T11:58:38Z","reference_number":"EMA/CHMP/139482/2025","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/romvimza-epar-public-assessment-report_en.pdf"},
    {"id":"70230","name":"Alyftrek : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2025-09-23T14:05:54Z","last_updated_date":"2025-09-23T14:05:54Z","reference_number":"EMA/160870/2025","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/alyftrek-epar-public-assessment-report_en.pdf"},
    {"id":"70263","name":"Emtricitabine / Rilpivirine / Tenofovir Alafenamide Viatris : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2025-09-25T09:46:42Z","last_updated_date":"2025-09-25T09:46:42Z","reference_number":"EMA/CHMP/200896/2025","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/emtricitabine-rilpivirine-tenofovir-alafenamide-viatris-epar-public-assessment-report_en.pdf"},
    {"id":"70298","name":"Voranigo : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2025-09-26T14:42:26Z","last_updated_date":"2025-09-26T14:42:26Z","reference_number":"EMA/271829/2025","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/voranigo-epar-public-assessment-report_en.pdf"},
    {"id":"70326","name":"Zurzuvae : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2025-09-29T15:39:31Z","last_updated_date":"2025-09-29T15:39:31Z","reference_number":"EMA/264858/2025","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/zurzuvae-epar-public-assessment-report_en.pdf"},
    {"id":"70342","name":"Usrenty : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2025-09-30T09:33:56Z","last_updated_date":"2025-09-30T09:33:56Z","reference_number":"EMA/268909/2025","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/usrenty-epar-public-assessment-report_en.pdf"},
    {"id":"70370","name":"Maapliv : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2025-09-30T14:52:56Z","last_updated_date":"2025-09-30T14:52:56Z","reference_number":"EMA/200492/2025","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/maapliv-epar-public-assessment-report_en.pdf"},
    {"id":"70417","name":"Vivlipeg : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2025-10-02T15:52:54Z","last_updated_date":"2025-11-03T14:28:53Z","reference_number":"EMA/CMHP/212241/2025","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/vivlipeg-epar-public-assessment-report_en.pdf"},
    {"id":"70438","name":"Ogsiveo : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2025-10-03T11:59:13Z","last_updated_date":"2025-10-03T11:59:13Z","reference_number":"EMA/CHMP/82481/2025","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/ogsiveo-epar-public-assessment-report_en.pdf"},
    {"id":"70486","name":"Ekterly : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2025-10-08T08:53:20Z","last_updated_date":"2025-10-08T08:53:20Z","reference_number":"EMA/266036/2025","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/ekterly-epar-public-assessment-report_en.pdf"},
    {"id":"70504","name":"Zadenvi : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2025-10-09T11:34:12Z","last_updated_date":"2025-10-09T11:34:12Z","reference_number":"EMA/165387/2025","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/zadenvi-epar-public-assessment-report_en.pdf"},
    {"id":"70521","name":"Denbrayce : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2025-10-09T16:58:45Z","last_updated_date":"2025-10-09T16:58:45Z","reference_number":"EMA/CHMP/165386/2025","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/denbrayce-epar-public-assessment-report_en.pdf"},
    {"id":"70532","name":"Syfovre : EPAR - Refusal public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2025-08-14T18:06:24Z","last_updated_date":"2025-10-10T18:25:00Z","reference_number":"EMA/CHMP/196327/2025 Corr.","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/syfovre-epar-refusal-public-assessment-report_en.pdf"},
    {"id":"70642","name":"Mynzepli : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2025-10-17T14:58:56Z","last_updated_date":"2025-10-17T14:58:56Z","reference_number":"EMA/CHMP/203339/2025","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/mynzepli-epar-public-assessment-report_en.pdf"},
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    {"id":"70690","name":"Elevidys : EPAR - Refusal public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2025-10-20T16:34:19Z","last_updated_date":"2025-10-20T16:34:19Z","reference_number":"EMA/CHMP/CAT/213364/2025","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/elevidys-epar-refusal-public-assessment-report_en.pdf"},
    {"id":"70776","name":"Rolcya : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2025-10-23T09:27:22Z","last_updated_date":"2025-10-23T09:27:22Z","reference_number":"EMA/198412/2025","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/rolcya-epar-public-assessment-report_en.pdf"},
    {"id":"70833","name":"Bilprevda : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2025-10-27T09:58:04Z","last_updated_date":"2025-10-27T09:58:04Z","reference_number":"EMA/CHMP/228042/2025","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/bilprevda-epar-public-assessment-report_en.pdf"},
    {"id":"70841","name":"Bildyos : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2025-10-27T10:22:18Z","last_updated_date":"2025-10-27T10:22:18Z","reference_number":"EMA/CHMP/228090/2025","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/bildyos-epar-public-assessment-report_en.pdf"},
    {"id":"70876","name":"Kisunla : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2025-10-28T12:34:31Z","last_updated_date":"2025-10-28T12:34:31Z","reference_number":"EMA/298973/2025","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/kisunla-epar-public-assessment-report_en.pdf"},
    {"id":"70990","name":"Vgenfli : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2025-11-04T08:54:15Z","last_updated_date":"2025-11-20T16:06:00Z","reference_number":"EMA/CHMP/193207/2025","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/vgenfli-epar-public-assessment-report_en.pdf"},
    {"id":"71027","name":"Xoanacyl : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2025-11-06T09:19:15Z","last_updated_date":"2025-11-06T09:19:15Z","reference_number":"EMA/130313/2025","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/xoanacyl-epar-public-assessment-report_en.pdf"},
    {"id":"71068","name":"Rezdiffra : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2025-11-10T10:36:47Z","last_updated_date":"2025-11-10T10:36:47Z","reference_number":"EMA/194017/2025","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/rezdiffra-epar-public-assessment-report_en.pdf"},
    {"id":"71113","name":"Eyluxvi : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2025-11-12T16:24:04Z","last_updated_date":"2025-11-12T16:24:04Z","reference_number":"EMA/CHMP/272837/2025","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/eyluxvi-epar-public-assessment-report_en.pdf"},
    {"id":"71156","name":"Afiveg : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2025-11-13T16:56:11Z","last_updated_date":"2025-11-13T16:56:11Z","reference_number":"EMA/CHMP/203339/2025","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/afiveg-epar-public-assessment-report_en.pdf"},
    {"id":"71181","name":" Kizfizo : EPAR - Refusal public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2025-11-14T14:17:04Z","last_updated_date":"2025-11-14T14:17:04Z","reference_number":"EMA/96948/2025","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/kizfizo-epar-refusal-public-assessment-report_en.pdf"},
    {"id":"71195","name":"Imreplys : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2025-11-17T13:00:18Z","last_updated_date":"2025-11-17T13:00:18Z","reference_number":"EMA/233111/2025","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/imreplys-epar-public-assessment-report_en.pdf"},
    {"id":"71220","name":"Enwylma : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2025-11-18T13:10:48Z","last_updated_date":"2025-11-18T13:10:48Z","reference_number":"EMA/165176/2025","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/enwylma-epar-public-assessment-report_en.pdf"},
    {"id":"71263","name":"Gobivaz : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2025-11-20T14:12:19Z","last_updated_date":"2025-11-20T14:12:19Z","reference_number":"EMA/322353/2025","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/gobivaz-epar-public-assessment-report_en.pdf"},
    {"id":"71271","name":"Usgena : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2025-11-21T09:24:47Z","last_updated_date":"2025-11-21T09:24:47Z","reference_number":"EMA/323497/2025","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/usgena-epar-public-assessment-report_en.pdf"},
    {"id":"71282","name":"Eiyzey : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2025-11-21T11:26:39Z","last_updated_date":"2025-11-21T11:26:39Z","reference_number":"EMA/196426/2025","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/eiyzey-epar-public-assessment-report_en.pdf"},
    {"id":"71371","name":"Lynkuet : EPAR - Public assessment report","type":"assessment-report","status":"unknown","consultation_date":"","first_published_date":"2025-11-27T14:06:09Z","last_updated_date":"2025-11-27T14:06:09Z","reference_number":"EMA/CHMP/299122/2025","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/lynkuet-epar-public-assessment-report_en.pdf"},
    {"id":"71382","name":"Atropine sulfate FGK : EPAR - Refusal public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2025-11-28T09:49:16Z","last_updated_date":"2025-11-28T09:49:16Z","reference_number":"EMA/CHMP/239943/2025","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/atropine-sulfate-fgk-epar-refusal-public-assessment-report_en.pdf"},
    {"id":"71502","name":"Brinsupri : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2025-12-04T12:39:35Z","last_updated_date":"2025-12-04T12:39:35Z","reference_number":"EMA/345552/2025","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/brinsupri-epar-public-assessment-report_en.pdf"},
    {"id":"71507","name":"Denosumab Intas : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2025-12-04T14:07:46Z","last_updated_date":"2025-12-04T14:07:46Z","reference_number":"EMA/CHMP/311939/2025","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/denosumab-intas-epar-public-assessment-report_en.pdf"},
    {"id":"71732","name":"Imaavy : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2025-12-12T13:53:05Z","last_updated_date":"2025-12-12T13:53:05Z","reference_number":"EMA/CHMP/290491/2025","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/imaavy-epar-public-assessment-report_en.pdf"},
    {"id":"71793","name":"Rivaroxaban Koanaa : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2025-12-17T08:37:16Z","last_updated_date":"2025-12-17T08:37:16Z","reference_number":"EMA/335639/2025","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/rivaroxaban-koanaa-epar-public-assessment-report_en.pdf"},
    {"id":"71860","name":"Macitentan Accord : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2025-12-19T08:42:29Z","last_updated_date":"2025-12-19T08:42:29Z","reference_number":"EMA/CHMP/216790/2025","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/macitentan-accord-epar-public-assessment-report_en.pdf"},
    {"id":"71879","name":"Macitentan AccordPharma : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2025-12-19T13:13:14Z","last_updated_date":"2025-12-19T13:13:14Z","reference_number":"EMA/CHMP/216792/2025","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/macitentan-accordpharma-epar-public-assessment-report_en.pdf"},
    {"id":"71916","name":"Zvogra : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2026-01-05T13:06:39Z","last_updated_date":"2026-01-05T13:06:39Z","reference_number":"EMA/316739/2025","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/zvogra-epar-public-assessment-report_en.pdf"},
    {"id":"71924","name":"Kefdensis - EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2026-01-05T14:26:07Z","last_updated_date":"2026-01-05T14:26:07Z","reference_number":"EMA/CHMP/273902/2025","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/kefdensis-epar-public-assessment-report_en.pdf"},
    {"id":"71991","name":"Wayrilz : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2026-01-08T12:57:19Z","last_updated_date":"2026-01-08T12:57:19Z","reference_number":"EMA/348131/2025","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/wayrilz-epar-public-assessment-report_en.pdf"},
    {"id":"72030","name":"Winlevi : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2026-01-13T14:07:35Z","last_updated_date":"2026-01-13T14:07:35Z","reference_number":"EMA/292571/2025","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/winlevi-epar-public-assessment-report_en.pdf"},
    {"id":"72035","name":"GalenVita : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2026-01-13T14:43:14Z","last_updated_date":"2026-01-13T14:43:14Z","reference_number":"EMA/CHMP/200195/2025","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/galenvita-epar-public-assessment-report_en.pdf"},
    {"id":"72134","name":"Teduglutide Viatris : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2026-01-19T13:26:21Z","last_updated_date":"2026-01-19T13:26:21Z","reference_number":"EMA/382685/2025","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/teduglutide-viatris-epar-public-assessment-report_en.pdf"},
    {"id":"72158","name":"Ponlimsi : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2026-01-20T11:40:38Z","last_updated_date":"2026-01-20T11:40:38Z","reference_number":"EMA/323137/2025","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/ponlimsi-epar-public-assessment-report_en.pdf"},
    {"id":"72164","name":"Degevma : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2026-01-20T12:08:21Z","last_updated_date":"2026-01-20T12:08:21Z","reference_number":"EMA/323111/2025","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/degevma-epar-public-assessment-report_en.pdf"},
    {"id":"72192","name":"VacPertagen : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2026-01-21T14:54:36Z","last_updated_date":"2026-01-21T14:54:36Z","reference_number":"EMA/CHMP/252486/2025","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/vacpertagen-epar-public-assessment-report_en.pdf"},
    {"id":"72215","name":"Inluriyo : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2026-01-23T09:47:55Z","last_updated_date":"2026-01-23T09:47:55Z","reference_number":"EMA/CHMP/310589/2025","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/inluriyo-epar-public-assessment-report_en.pdf"},
    {"id":"72241","name":"Austedo : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2026-01-23T17:20:48Z","last_updated_date":"2026-01-23T17:20:48Z","reference_number":"EMA/CHMP/309212/2025","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/austedo-epar-public-assessment-report_en.pdf"},
    {"id":"72532","name":"Kyinsu : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2026-02-12T12:40:33Z","last_updated_date":"2026-02-12T12:40:33Z","reference_number":"EMA/CHMP/290792/2025","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/kyinsu-epar-public-assessment-report_en.pdf"},
    {"id":"72607","name":"Waskyra : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2026-02-19T14:25:24Z","last_updated_date":"2026-02-19T14:25:24Z","reference_number":"EMA/CHMP/364628/2025","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/waskyra-epar-public-assessment-report_en.pdf"},
    {"id":"72628","name":"Teizeild : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2026-02-20T15:10:59Z","last_updated_date":"2026-02-20T15:10:59Z","reference_number":"EMA/39938/2026","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/teizeild-epar-public-assessment-report_en.pdf"},
    {"id":"72634","name":"Osqay : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2026-02-20T15:58:25Z","last_updated_date":"2026-02-20T15:58:25Z","reference_number":"EMA/37498/2026","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/osqay-epar-public-assessment-report_en.pdf"},
    {"id":"72642","name":"Dawnzera : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2026-02-20T16:39:19Z","last_updated_date":"2026-02-20T16:39:19Z","reference_number":"EMA/CHMP/303940/2025","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/dawnzera-epar-public-assessment-report_en.pdf"},
    {"id":"72667","name":"Ranluspec : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2026-02-24T10:47:18Z","last_updated_date":"2026-02-24T10:47:18Z","reference_number":"EMADOC-1829012207-37824","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/ranluspec-epar-public-assessment-report_en.pdf"},
    {"id":"72673","name":"Acvybra : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2026-02-24T12:11:32Z","last_updated_date":"2026-02-24T12:11:32Z","reference_number":"EMA/CHMP/278073/2025","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/acvybra-epar-public-assessment-report_en.pdf"},
    {"id":"72677","name":"mNexspike : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2026-03-04T12:39:39Z","last_updated_date":"2026-03-04T12:39:39Z","reference_number":"EMA/6890/2026","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/mnexspike-epar-public-assessment-report_en.pdf"},
    {"id":"72692","name":"Gotenfia : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2026-02-25T12:31:35Z","last_updated_date":"2026-02-25T12:31:35Z","reference_number":"EMADOC-1829012207-39209","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/gotenfia-epar-public-assessment-report_en.pdf"},
    {"id":"72754","name":"Aumseqa : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2026-02-27T13:35:07Z","last_updated_date":"2026-02-27T13:35:07Z","reference_number":"EMA/1407/2026","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/aumseqa-epar-public-assessment-report_en.pdf"},
    {"id":"72766","name":"Xbonzy : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2026-03-02T10:05:05Z","last_updated_date":"2026-03-02T10:05:05Z","reference_number":"EMA/CHMP/278068/2025","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/xbonzy-epar-public-assessment-report_en.pdf"},
    {"id":"72795","name":"Aqneursa : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2026-03-03T11:22:12Z","last_updated_date":"2026-03-03T11:22:12Z","reference_number":"EMA/CHMP/113960/2025","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/aqneursa-epar-public-assessment-report_en.pdf"},
    {"id":"72804","name":"Myqorzo : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2026-03-03T14:15:52Z","last_updated_date":"2026-03-03T14:15:52Z","reference_number":"EMA/10052/2026","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/myqorzo-epar-public-assessment-report_en.pdf"},
    {"id":"72983","name":"Exdensur : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2026-03-12T15:31:46Z","last_updated_date":"2026-03-12T15:31:46Z","reference_number":"EMADOC-1829012207-16378","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/exdensur-epar-public-assessment-report_en.pdf"},
    {"id":"73011","name":"Anktiva : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2026-03-13T13:18:54Z","last_updated_date":"2026-03-20T16:36:00Z","reference_number":"EMA/9518/2026","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/anktiva-epar-public-assessment-report_en.pdf"},
    {"id":"73307","name":"Ilumira : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2026-04-01T16:40:01Z","last_updated_date":"2026-04-01T16:40:01Z","reference_number":"EMA/38034/2026","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/ilumira-epar-public-assessment-report_en.pdf"},
    {"id":"73362","name":"Supemtek : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2026-04-08T16:18:01Z","last_updated_date":"2026-04-08T16:18:01Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/supemtek-epar-public-assessment-report_en.pdf-0"},
    {"id":"73380","name":"Ondibta : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2026-04-09T12:32:53Z","last_updated_date":"2026-04-09T12:32:53Z","reference_number":"EMA/337757/2025","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/ondibta-epar-public-assessment-report_en.pdf"},
    {"id":"73391","name":"Fylrevy : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2026-04-09T15:34:53Z","last_updated_date":"2026-04-09T15:34:53Z","reference_number":"EMA/39397/2026","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/fylrevy-epar-public-assessment-report_en.pdf"},
    {"id":"73401","name":"Kayshild : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2026-04-09T16:40:27Z","last_updated_date":"2026-04-09T16:40:27Z","reference_number":"EMA/39428/2026","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/kayshild-epar-public-assessment-report_en.pdf"},
    {"id":"73458","name":"Kygevvi : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2026-04-15T15:22:05Z","last_updated_date":"2026-04-15T15:22:05Z","reference_number":"EMA/37828/2026","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/kygevvi-epar-public-assessment-report_en.pdf"},
    {"id":"73481","name":"Rezurock : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2026-04-17T08:21:56Z","last_updated_date":"2026-04-17T08:21:56Z","reference_number":"EMA/CHMP/3277/2026","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/rezurock-epar-public-assessment-report_en.pdf"},
    {"id":"73517","name":"Enflonsia : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2026-04-22T09:22:35Z","last_updated_date":"2026-04-22T09:22:35Z","reference_number":"EMA/CHMP/274515/2025","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/enflonsia-epar-public-assessment-report_en.pdf"},
    {"id":"73596","name":"mCombriax : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2026-04-30T15:44:47Z","last_updated_date":"2026-04-30T15:44:47Z","reference_number":"EMADOC-1829012207-46393","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/mcombriax-epar-public-assessment-report_en.pdf"},
    {"id":"73617","name":"Onerji : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2026-05-05T11:47:27Z","last_updated_date":"2026-05-05T11:47:27Z","reference_number":"EMA/CHMP/61327/2026","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/onerji-epar-public-assessment-report_en.pdf"},
    {"id":"73623","name":"Palsonify : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2026-05-05T12:01:10Z","last_updated_date":"2026-05-05T12:01:10Z","reference_number":"EMA/CHMP/61327/2026","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/palsonify-epar-public-assessment-report_en.pdf"},
    {"id":"73632","name":"Rhapsido : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2026-05-05T17:18:08Z","last_updated_date":"2026-05-05T17:18:08Z","reference_number":"EMADOC-1829012207-46485","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/rhapsido-epar-public-assessment-report_en.pdf"},
    {"id":"73698","name":"Ojemda : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2026-05-11T10:20:08Z","last_updated_date":"2026-05-11T10:20:08Z","reference_number":"EMA/67438/2026","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/ojemda-epar-public-assessment-report_en.pdf"},
    {"id":"73723","name":"Xolremdi : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2026-05-12T11:40:05Z","last_updated_date":"2026-05-12T11:40:05Z","reference_number":"EMADOC-1829012207-16377","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/xolremdi-epar-public-assessment-report_en.pdf"},
    {"id":"73767","name":"Tuyory : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2026-05-19T15:07:48Z","last_updated_date":"2026-05-19T15:07:48Z","reference_number":"EMADOC-1829012207-19045","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/tuyory-epar-public-assessment-report_en.pdf"},
    {"id":"73777","name":"Dazparda : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2026-05-20T09:25:21Z","last_updated_date":"2026-05-20T09:25:21Z","reference_number":"EMA/62379/2026","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/dazparda-epar-public-assessment-report_en.pdf"},
    {"id":"73848","name":"Poherdy : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2026-05-26T09:32:04Z","last_updated_date":"2026-05-26T09:32:04Z","reference_number":"EMA/69263/2026","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/poherdy-epar-public-assessment-report_en.pdf"},
    {"id":"73874","name":"Joenja : EPAR - Public assessement report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2026-05-28T12:51:15Z","last_updated_date":"2026-05-28T12:51:15Z","reference_number":"EMA/88598/2026","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/joenja-epar-public-assessement-report_en.pdf"},
    {"id":"73882","name":"Fubelv : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2026-05-28T13:53:18Z","last_updated_date":"2026-05-28T13:53:18Z","reference_number":"EMADOC-1829012207-29317","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/fubelv-epar-public-assessment-report_en.pdf"},
    {"id":"73927","name":"Zepzelca : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2026-06-01T16:18:55Z","last_updated_date":"2026-06-01T16:18:55Z","reference_number":"EMA/87579/2026","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/zepzelca-epar-public-assessment-report_en.pdf"},
    {"id":"73938","name":"Zandoriah : EPAR - Public assessment report","type":"assessment-report","status":"Adopted","consultation_date":"","first_published_date":"2026-06-02T14:34:20Z","last_updated_date":"2026-06-02T14:34:20Z","reference_number":"EMA/77774/2026","document_url":"https://www.ema.europa.eu/en/documents/assessment-report/zandoriah-epar-public-assessment-report_en.pdf"},
    {"id":"2507","name":"Incruse : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2014-05-22T02:00:00Z","last_updated_date":"2014-05-22T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/incruse-epar-risk-management-plan-summary_en.pdf"},
    {"id":"2652","name":"Actraphane : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2018-03-16T15:02:00Z","last_updated_date":"2018-03-16T15:02:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/actraphane-epar-risk-management-plan-summary_en.pdf"},
    {"id":"2766","name":"Kyprolis : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2015-12-01T01:00:00Z","last_updated_date":"2015-12-01T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/kyprolis-epar-risk-management-plan-summary_en.pdf"},
    {"id":"2894","name":"Eperzan : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2014-04-10T02:00:00Z","last_updated_date":"2014-05-13T02:00:00Z","reference_number":"EMA/79382/2014","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/eperzan-epar-risk-management-plan-summary_en.pdf"},
    {"id":"3133","name":"Vimizim : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2014-06-26T02:00:00Z","last_updated_date":"2014-06-26T02:00:00Z","reference_number":"EMA/127543/2014","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/vimizim-epar-risk-management-plan-summary_en.pdf"},
    {"id":"3562","name":"Ketoconazole HRA : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2015-01-30T01:00:00Z","last_updated_date":"2019-09-18T12:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/ketoconazole-hra-epar-risk-management-plan-summary_en.pdf"},
    {"id":"3581","name":"Neofordex : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2016-04-01T02:00:00Z","last_updated_date":"2019-04-16T02:00:00Z","reference_number":"EMA/934/2016","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/neofordex-epar-risk-management-plan-summary_en.pdf"},
    {"id":"4346","name":"Omidria : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2015-09-01T02:00:00Z","last_updated_date":"2020-08-13T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/omidria-epar-risk-management-plan-summary_en.pdf"},
    {"id":"4493","name":"Halimatoz : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2018-08-03T02:00:00Z","last_updated_date":"2021-01-29T12:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/halimatoz-epar-risk-management-plan-summary_en.pdf"},
    {"id":"4544","name":"Briviact : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2016-01-25T01:00:00Z","last_updated_date":"2024-04-17T09:27:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/briviact-epar-risk-management-plan-summary_en.pdf"},
    {"id":"4733","name":"Iblias : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2016-03-09T01:00:00Z","last_updated_date":"2016-03-09T01:00:00Z","reference_number":"EMA/1562/2016","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/iblias-epar-risk-management-plan-summary_en.pdf"},
    {"id":"4810","name":"Quinsair : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2015-06-12T02:00:00Z","last_updated_date":"2022-01-13T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/quinsair-epar-risk-management-plan-summary_en.pdf"},
    {"id":"4986","name":"Ulunar Breezhaler : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2014-05-16T02:00:00Z","last_updated_date":"2018-05-03T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/ulunar-breezhaler-epar-risk-management-plan-summary_en.pdf"},
    {"id":"5195","name":"Clopidogrel / Acetylsalicylic acid Teva : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2014-09-26T02:00:00Z","last_updated_date":"2017-04-28T02:00:00Z","reference_number":"EMA/411850/2014","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/clopidogrel-acetylsalicylic-acid-teva-epar-risk-management-plan-summary_en.pdf"},
    {"id":"5373","name":"Abasaglar (previously Abasria) : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2014-10-14T02:00:00Z","last_updated_date":"2015-01-20T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/abasaglar-previously-abasria-epar-risk-management-plan-summary_en.pdf"},
    {"id":"6290","name":"Dutrebis : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2015-04-21T02:00:00Z","last_updated_date":"2017-04-27T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/dutrebis-epar-risk-management-plan-summary_en.pdf"},
    {"id":"6399","name":"Zalviso : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2015-10-02T02:00:00Z","last_updated_date":"2022-09-27T11:25:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/zalviso-epar-risk-management-plan-summary_en.pdf"},
    {"id":"6737","name":"Vylaer Spiromax : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2014-12-05T01:00:00Z","last_updated_date":"2014-12-05T01:00:00Z","reference_number":"EMA/675937/2014","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/vylaer-spiromax-epar-risk-management-plan-summary_en.pdf"},
    {"id":"7530","name":"Lixiana : EPAR - Risk management plan","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2023-10-04T10:12:00Z","last_updated_date":"2026-04-20T11:50:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/lixiana-epar-risk-management-plan_en.pdf"},
    {"id":"7566","name":"Dzuveo : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2018-07-18T17:55:00Z","last_updated_date":"2024-05-29T14:27:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/dzuveo-epar-risk-management-plan-summary_en.pdf"},
    {"id":"7597","name":"Caspofungin Accord : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2016-03-21T01:00:00Z","last_updated_date":"2016-03-21T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/caspofungin-accord-epar-risk-management-plan-summary_en.pdf"},
    {"id":"8117","name":"Translarna : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2014-09-04T02:00:00Z","last_updated_date":"2025-04-16T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/translarna-epar-risk-management-plan-summary_en.pdf"},
    {"id":"8145","name":"Simbrinza : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2014-07-31T02:00:00Z","last_updated_date":"2020-06-11T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/simbrinza-epar-risk-management-plan-summary_en.pdf"},
    {"id":"8262","name":"Raxone : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2015-09-17T02:00:00Z","last_updated_date":"2022-10-27T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/raxone-epar-risk-management-plan-summary_en.pdf"},
    {"id":"8619","name":"Zoledronic acid Teva Generics : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2014-04-30T02:00:00Z","last_updated_date":"2016-08-08T02:00:00Z","reference_number":"EMA/77822/2014","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/zoledronic-acid-teva-generics-epar-risk-management-plan-summary_en.pdf"},
    {"id":"8755","name":"Insulatard : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2018-03-20T01:00:00Z","last_updated_date":"2020-06-16T11:25:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/insulatard-epar-risk-management-plan-summary_en.pdf"},
    {"id":"9144","name":"Sylvant : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2014-06-19T02:00:00Z","last_updated_date":"2014-06-19T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/sylvant-epar-risk-management-plan-summary_en.pdf"},
    {"id":"9389","name":"Respreeza : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2015-09-16T02:00:00Z","last_updated_date":"2015-09-16T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/respreeza-epar-risk-management-plan-summary_en.pdf"},
    {"id":"9601","name":"Zontivity : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2015-03-02T01:00:00Z","last_updated_date":"2017-09-20T02:00:00Z","reference_number":"EMA/739006/2014","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/zontivity-epar-risk-management-plan-summary_en.pdf"},
    {"id":"9901","name":"Rixubis : EPAR - Risk management plan","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2015-02-10T01:00:00Z","last_updated_date":"2024-11-27T01:00:00Z","reference_number":"EMA/677082/2014","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/rixubis-epar-risk-management-plan_en.pdf"},
    {"id":"9935","name":"Repatha : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2015-08-03T02:00:00Z","last_updated_date":"2024-09-06T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/repatha-epar-risk-management-plan-summary_en.pdf"},
    {"id":"9937","name":"Voriconazole Hospira : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2015-06-25T02:00:00Z","last_updated_date":"2015-06-25T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/voriconazole-hospira-epar-risk-management-plan-summary_en.pdf"},
    {"id":"10157","name":"Cablivi : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2018-09-10T11:27:00Z","last_updated_date":"2018-09-10T11:27:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/cablivi-epar-risk-management-plan-summary_en.pdf"},
    {"id":"10660","name":"Mirvaso : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2014-05-13T02:00:00Z","last_updated_date":"2014-05-13T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/mirvaso-epar-risk-management-plan-summary_en.pdf"},
    {"id":"10866","name":"Praluent : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2015-10-01T02:00:00Z","last_updated_date":"2024-01-04T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/praluent-epar-risk-management-plan-summary_en.pdf"},
    {"id":"11038","name":"Vantobra : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2015-03-19T01:00:00Z","last_updated_date":"2019-03-29T01:00:00Z","reference_number":"EMA/169513/2015","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/vantobra-epar-risk-management-plan-summary_en.pdf"},
    {"id":"11552","name":"Zerbaxa : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2015-10-01T02:00:00Z","last_updated_date":"2019-11-08T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/zerbaxa-epar-risk-management-plan-summary_en.pdf"},
    {"id":"12009","name":"Xadago : EPAR - Risk management plan","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2015-03-30T02:00:00Z","last_updated_date":"2024-10-11T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/xadago-epar-risk-management-plan_en.pdf"},
    {"id":"12751","name":"Lumark : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2015-07-16T02:00:00Z","last_updated_date":"2026-02-11T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/lumark-epar-risk-management-plan-summary_en.pdf"},
    {"id":"12997","name":"Hetlioz : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2015-07-22T02:00:00Z","last_updated_date":"2015-07-22T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/hetlioz-epar-risk-management-plan-summary_en.pdf"},
    {"id":"13229","name":"Xoterna Breezhaler : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2018-05-04T02:00:00Z","last_updated_date":"2019-08-02T11:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/xoterna-breezhaler-epar-risk-management-plan-summary_en.pdf"},
    {"id":"13312","name":"Obizur : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2015-11-23T01:00:00Z","last_updated_date":"2025-02-03T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/obizur-epar-risk-management-plan-summary_en.pdf"},
    {"id":"13376","name":"Evotaz : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2015-08-10T02:00:00Z","last_updated_date":"2015-08-10T02:00:00Z","reference_number":"EMA/391330/2015","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/evotaz-epar-risk-management-plan-summary_en.pdf"},
    {"id":"13407","name":"Zonisamide Mylan : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2016-04-06T01:00:00Z","last_updated_date":"2016-04-06T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/zonisamide-mylan-epar-risk-management-plan-summary_en.pdf"},
    {"id":"13519","name":"BiResp Spiromax : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2014-05-19T02:00:00Z","last_updated_date":"2021-06-09T16:14:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/biresp-spiromax-epar-risk-management-plan-summary_en.pdf"},
    {"id":"13530","name":"Mepsevii : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"Adopted","consultation_date":"","first_published_date":"2018-08-28T02:00:00Z","last_updated_date":"2018-08-28T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/mepsevii-epar-risk-management-plan-summary_en.pdf"},
    {"id":"13534","name":"Pregabalin Mylan : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2015-07-31T02:00:00Z","last_updated_date":"2015-09-03T02:00:00Z","reference_number":"EMA/285072/2015","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/pregabalin-mylan-epar-risk-management-plan-summary_en.pdf"},
    {"id":"13828","name":"Pemetrexed Accord : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2016-01-29T01:00:00Z","last_updated_date":"2021-03-05T10:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/pemetrexed-accord-epar-risk-management-plan-summary_en.pdf"},
    {"id":"14065","name":"Lopinavir/Ritonavir Mylan : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2016-02-09T01:00:00Z","last_updated_date":"2021-06-04T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/lopinavirritonavir-mylan-epar-risk-management-plan-summary_en.pdf"},
    {"id":"14190","name":"Ebilfumin : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2014-06-06T02:00:00Z","last_updated_date":"2021-12-08T02:00:00Z","reference_number":"EMA/186637/2014","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/ebilfumin-epar-risk-management-plan-summary_en.pdf"},
    {"id":"14276","name":"Duloxetine Mylan : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2015-06-24T02:00:00Z","last_updated_date":"2022-04-25T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/duloxetine-mylan-epar-risk-management-plan-summary_en.pdf"},
    {"id":"14707","name":"Unituxin : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2015-09-01T02:00:00Z","last_updated_date":"2017-04-28T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/unituxin-epar-risk-management-plan-summary_en.pdf"},
    {"id":"14819","name":"Actraphane : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2018-03-20T14:31:00Z","last_updated_date":"2020-06-16T14:31:00Z","reference_number":"EMA/169630/2018","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/actraphane-epar-risk-management-plan-summary_en.pdf-0"},
    {"id":"14943","name":"Kovaltry : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2016-03-07T01:00:00Z","last_updated_date":"2021-01-25T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/kovaltry-epar-risk-management-plan-summary_en.pdf"},
    {"id":"15095","name":"Raplixa : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2015-05-04T02:00:00Z","last_updated_date":"2018-10-10T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/raplixa-epar-risk-management-plan-summary_en.pdf"},
    {"id":"15101","name":"Bemfola : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2014-05-16T02:00:00Z","last_updated_date":"2014-05-16T02:00:00Z","reference_number":"EMA/83300/2014","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/bemfola-epar-risk-management-plan-summary_en.pdf"},
    {"id":"15446","name":"Fexeric : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2015-10-02T02:00:00Z","last_updated_date":"2015-10-02T02:00:00Z","reference_number":"EMA/576868/2015","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/fexeric-epar-risk-management-plan-summary_en.pdf"},
    {"id":"15883","name":"Prezista : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2018-07-19T13:44:00Z","last_updated_date":"2023-03-03T13:44:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/prezista-epar-risk-management-plan-summary_en.pdf"},
    {"id":"15964","name":"Accofil : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2014-10-28T01:00:00Z","last_updated_date":"2014-10-28T01:00:00Z","reference_number":"EMA/475472/2014","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/accofil-epar-risk-management-plan-summary_en.pdf"},
    {"id":"16466","name":"Duavive : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2015-01-30T01:00:00Z","last_updated_date":"2021-10-29T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/duavive-epar-risk-management-plan-summary_en.pdf"},
    {"id":"16617","name":"Orkambi : EPAR - Risk management plan","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2015-12-01T01:00:00Z","last_updated_date":"2026-06-02T11:09:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/orkambi-epar-risk-management-plan_en.pdf"},
    {"id":"16975","name":"Rasagiline Mylan : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2016-01-25T01:00:00Z","last_updated_date":"2021-07-23T10:22:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/rasagiline-mylan-epar-risk-management-plan-summary_en.pdf"},
    {"id":"17087","name":"Budesonide/Formoterol Teva Pharma B.V. : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2014-12-05T15:05:00Z","last_updated_date":"2017-01-30T15:05:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/budesonideformoterol-teva-pharma-bv-epar-risk-management-plan-summary_en.pdf"},
    {"id":"17121","name":"Protaphane : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2018-03-20T14:31:00Z","last_updated_date":"2020-06-16T11:28:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/protaphane-epar-risk-management-plan-summary_en.pdf"},
    {"id":"17285","name":"Ravicti : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2015-12-18T01:00:00Z","last_updated_date":"2023-04-26T13:36:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/ravicti-epar-risk-management-plan-summary_en.pdf"},
    {"id":"17825","name":"Eptifibatide Accord : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2016-01-18T01:00:00Z","last_updated_date":"2016-01-18T01:00:00Z","reference_number":"EMA/20134/2016","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/eptifibatide-accord-epar-risk-management-plan-summary_en.pdf"},
    {"id":"18109","name":"NovoEight : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2018-08-07T02:00:00Z","last_updated_date":"2021-05-19T09:38:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/novoeight-epar-risk-management-plan-summary_en.pdf"},
    {"id":"18261","name":"Hemlibra : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2018-03-01T16:30:00Z","last_updated_date":"2024-05-29T14:16:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/hemlibra-epar-risk-management-plan-summary_en.pdf"},
    {"id":"18554","name":"Lymphoseek : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2015-01-08T01:00:00Z","last_updated_date":"2024-08-14T14:04:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/lymphoseek-epar-risk-management-plan-summary_en.pdf"},
    {"id":"18798","name":"Zurampic : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2016-03-09T01:00:00Z","last_updated_date":"2016-03-09T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/zurampic-epar-risk-management-plan-summary_en.pdf"},
    {"id":"19040","name":"Viekirax : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2015-03-09T01:00:00Z","last_updated_date":"2024-10-02T16:45:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/viekirax-epar-risk-management-plan-summary_en.pdf"},
    {"id":"19228","name":"Velphoro : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2014-10-13T02:00:00Z","last_updated_date":"2020-11-26T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/velphoro-epar-risk-management-plan-summary_en.pdf"},
    {"id":"19407","name":"Tenkasi : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2015-05-04T02:00:00Z","last_updated_date":"2023-09-22T14:43:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/tenkasi-epar-risk-management-plan-summary_en.pdf"},
    {"id":"19456","name":"Tegsedi : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2018-08-06T02:00:00Z","last_updated_date":"2022-03-18T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/tegsedi-epar-risk-management-plan-summary_en.pdf"},
    {"id":"20381","name":"Duaklir Genuair : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2014-12-05T01:00:00Z","last_updated_date":"2020-11-26T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/duaklir-genuair-epar-risk-management-plan-summary_en.pdf"},
    {"id":"20775","name":"Tyverb : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2018-09-07T02:00:00Z","last_updated_date":"2022-11-30T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/tyverb-epar-risk-management-plan-summary_en.pdf"},
    {"id":"20819","name":"Tadalafil Mylan : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2014-12-19T01:00:00Z","last_updated_date":"2023-06-01T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/tadalafil-mylan-epar-risk-management-plan-summary_en.pdf"},
    {"id":"20955","name":"Ristempa : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2015-04-15T02:00:00Z","last_updated_date":"2018-03-07T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/ristempa-epar-risk-management-plan-summary_en.pdf"},
    {"id":"21001","name":"Cometriq : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2014-03-26T01:00:00Z","last_updated_date":"2021-10-06T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/cometriq-epar-risk-management-plan-summary_en.pdf"},
    {"id":"21237","name":"Hemangiol : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2014-05-19T02:00:00Z","last_updated_date":"2020-10-21T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/hemangiol-epar-risk-management-plan-summary_en.pdf"},
    {"id":"21462","name":"Sivextro : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2015-03-26T01:00:00Z","last_updated_date":"2015-03-26T01:00:00Z","reference_number":"EMA/169447/2015","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/sivextro-epar-risk-management-plan-summary_en.pdf"},
    {"id":"21623","name":"Prezista : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2018-07-16T18:17:00Z","last_updated_date":"2020-09-16T18:17:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/prezista-epar-risk-management-plan-summary_en.pdf-0"},
    {"id":"22059","name":"Rasagiline ratiopharm : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2015-03-02T01:00:00Z","last_updated_date":"2015-03-02T01:00:00Z","reference_number":"EMA/744222/2014","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/rasagiline-ratiopharm-epar-risk-management-plan-summary_en.pdf"},
    {"id":"22070","name":"Senshio : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2015-02-17T01:00:00Z","last_updated_date":"2015-02-17T01:00:00Z","reference_number":"EMA/736568/2014","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/senshio-epar-risk-management-plan-summary_en.pdf"},
    {"id":"22076","name":"Revinty Ellipta : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2014-06-17T02:00:00Z","last_updated_date":"2022-10-06T14:50:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/revinty-ellipta-epar-risk-management-plan-summary_en.pdf"},
    {"id":"22234","name":"DuoResp Spiromax : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2014-05-20T02:00:00Z","last_updated_date":"2021-06-09T17:38:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/duoresp-spiromax-epar-risk-management-plan-summary_en.pdf"},
    {"id":"22867","name":"Olysio : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2014-06-04T02:00:00Z","last_updated_date":"2018-05-23T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/olysio-epar-risk-management-plan-summary_en.pdf"},
    {"id":"23127","name":"Spherox : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2017-07-24T02:00:00Z","last_updated_date":"2022-08-22T11:52:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/spherox-epar-risk-management-plan-summary_en.pdf"},
    {"id":"24128","name":"Brimica Genuair : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2014-12-05T01:00:00Z","last_updated_date":"2014-12-05T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/brimica-genuair-epar-risk-management-plan-summary_en.pdf"},
    {"id":"24502","name":"Spectrila : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2016-01-28T01:00:00Z","last_updated_date":"2020-06-18T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/spectrila-epar-risk-management-plan-summary_en.pdf"},
    {"id":"24643","name":"Akynzeo : EPAR - Risk management plan","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2015-06-23T02:00:00Z","last_updated_date":"2026-03-18T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/akynzeo-epar-risk-management-plan_en.pdf"},
    {"id":"24794","name":"Budesonide/Formoterol Teva : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2014-12-04T14:21:00Z","last_updated_date":"2017-01-31T14:21:00Z","reference_number":"EMA/639304/2014","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/budesonideformoterol-teva-epar-risk-management-plan-summary_en.pdf"},
    {"id":"24878","name":"Aripiprazole Zentiva : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2015-07-30T02:00:00Z","last_updated_date":"2015-07-30T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/aripiprazole-zentiva-epar-risk-management-plan-summary_en.pdf"},
    {"id":"25697","name":"Cyramza : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2015-01-22T01:00:00Z","last_updated_date":"2020-02-25T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/cyramza-epar-risk-management-plan-summary_en.pdf"},
    {"id":"25859","name":"Ionsys : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2015-11-30T01:00:00Z","last_updated_date":"2018-11-06T15:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/ionsys-epar-risk-management-plan-summary_en.pdf"},
    {"id":"26062","name":"Kanuma : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2015-09-01T02:00:00Z","last_updated_date":"2020-12-10T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/kanuma-epar-risk-management-plan-summary_en.pdf"},
    {"id":"26394","name":"Episalvan : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2016-02-05T01:00:00Z","last_updated_date":"2022-07-15T13:39:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/episalvan-epar-risk-management-plan-summary_en.pdf"},
    {"id":"26528","name":"Relvar Ellipta : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2018-06-07T11:37:00Z","last_updated_date":"2022-10-06T12:14:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/relvar-ellipta-epar-risk-management-plan-summary_en.pdf"},
    {"id":"26549","name":"Duloxetine Lilly : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2015-01-26T01:00:00Z","last_updated_date":"2020-09-22T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/duloxetine-lilly-epar-risk-management-plan-summary_en.pdf"},
    {"id":"26657","name":"Wakix : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2016-04-13T02:00:00Z","last_updated_date":"2023-04-20T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/wakix-epar-risk-management-plan-summary_en.pdf"},
    {"id":"27046","name":"Portrazza : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2016-03-04T01:00:00Z","last_updated_date":"2021-07-27T12:31:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/portrazza-epar-risk-management-plan-summary_en.pdf"},
    {"id":"27385","name":"Vaxelis : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2016-02-26T01:00:00Z","last_updated_date":"2020-10-01T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/vaxelis-epar-risk-management-plan-summary_en.pdf"},
    {"id":"27435","name":"Exviera : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2015-02-12T01:00:00Z","last_updated_date":"2024-10-01T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/exviera-epar-risk-management-plan-summary_en.pdf"},
    {"id":"27615","name":"Pemetrexed Hospira : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2015-12-01T01:00:00Z","last_updated_date":"2015-12-01T01:00:00Z","reference_number":"EMA/790392/2015","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/pemetrexed-hospira-epar-risk-management-plan-summary_en.pdf"},
    {"id":"28152","name":"Armisarte : EPAR - Risk management plan","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2016-01-28T01:00:00Z","last_updated_date":"2025-07-25T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/armisarte-epar-risk-management-plan_en.pdf"},
    {"id":"28397","name":"Myalepta : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2018-08-06T02:00:00Z","last_updated_date":"2022-10-27T12:58:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/myalepta-epar-risk-management-plan-summary_en.pdf"},
    {"id":"29163","name":"Aripiprazole Sandoz : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2015-09-25T02:00:00Z","last_updated_date":"2015-09-25T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/aripiprazole-sandoz-epar-risk-management-plan-summary_en.pdf"},
    {"id":"29286","name":"Pemetrexed medac : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2015-12-09T01:00:00Z","last_updated_date":"2020-09-21T01:00:00Z","reference_number":"EMA/666615/2015","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/pemetrexed-medac-epar-risk-management-plan-summary_en.pdf"},
    {"id":"29391","name":"Imbruvica : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2014-11-25T01:00:00Z","last_updated_date":"2024-01-18T11:10:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/imbruvica-epar-risk-management-plan-summary_en.pdf"},
    {"id":"29766","name":"Empliciti : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2016-01-25T01:00:00Z","last_updated_date":"2019-09-18T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/empliciti-epar-risk-management-plan-summary_en.pdf"},
    {"id":"30251","name":"Pemetrexed Krka : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2018-06-08T12:19:00Z","last_updated_date":"2024-07-30T12:19:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/pemetrexed-krka-epar-risk-management-plan-summary_en.pdf"},
    {"id":"30525","name":"Taxespira (previously Docetaxel Hospira UK Limited) : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2015-09-17T02:00:00Z","last_updated_date":"2019-10-15T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/taxespira-previously-docetaxel-hospira-uk-limited-epar-risk-management-plan-summary_en.pdf"},
    {"id":"31004","name":"Ciambra : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2016-05-03T02:00:00Z","last_updated_date":"2024-10-17T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/ciambra-epar-risk-management-plan-summary_en.pdf"},
    {"id":"31376","name":"Zelboraf : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2018-08-23T12:06:00Z","last_updated_date":"2020-01-30T12:06:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/zelboraf-epar-risk-management-plan-summary_en.pdf"},
    {"id":"31424","name":"Envarsus : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2014-07-31T02:00:00Z","last_updated_date":"2014-07-31T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/envarsus-epar-risk-management-plan-summary_en.pdf"},
    {"id":"31580","name":"Feraccru : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2016-03-18T01:00:00Z","last_updated_date":"2016-03-18T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/feraccru-epar-risk-management-plan-summary_en.pdf"},
    {"id":"32292","name":"Eylea : EPAR - Risk management plan","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2018-10-16T12:29:00Z","last_updated_date":"2026-03-04T16:45:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/eylea-epar-risk-management-plan_en.pdf"},
    {"id":"32489","name":"Kengrexal : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2015-06-12T02:00:00Z","last_updated_date":"2022-01-12T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/kengrexal-epar-risk-management-plan-summary_en.pdf"},
    {"id":"32588","name":"Cotellic : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2015-12-10T01:00:00Z","last_updated_date":"2023-03-06T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/cotellic-epar-risk-management-plan-summary_en.pdf"},
    {"id":"32913","name":"Xultophy : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2014-11-21T01:00:00Z","last_updated_date":"2014-11-21T01:00:00Z","reference_number":"EMA/467911/2014","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/xultophy-epar-risk-management-plan-summary_en.pdf"},
    {"id":"32988","name":"Synjardy : EPAR - Risk management plan","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2015-06-12T02:00:00Z","last_updated_date":"2025-07-01T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/synjardy-epar-risk-management-plan_en.pdf"},
    {"id":"33054","name":"Nerlynx : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2018-09-12T02:00:00Z","last_updated_date":"2023-06-15T15:02:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/nerlynx-epar-risk-management-plan-summary_en.pdf"},
    {"id":"33131","name":"Trulicity : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2014-12-19T01:00:00Z","last_updated_date":"2023-03-16T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/trulicity-epar-risk-management-plan-summary_en.pdf"},
    {"id":"33184","name":"Alkindi : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2018-03-01T01:00:00Z","last_updated_date":"2018-03-01T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/alkindi-epar-risk-management-plan-summary_en.pdf"},
    {"id":"33516","name":"Aripiprazole Mylan Pharma : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2015-07-20T02:00:00Z","last_updated_date":"2023-01-12T02:00:00Z","reference_number":"EMA/303592/2015","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/aripiprazole-mylan-pharma-epar-risk-management-plan-summary_en.pdf"},
    {"id":"33534","name":"Nuwiq : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2014-12-19T01:00:00Z","last_updated_date":"2022-01-05T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/nuwiq-epar-risk-management-plan-summary_en.pdf"},
    {"id":"33872","name":"Pregabalin Zentiva : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2015-07-27T02:00:00Z","last_updated_date":"2015-07-27T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/pregabalin-zentiva-epar-risk-management-plan-summary_en.pdf"},
    {"id":"34000","name":"Bortezomib Accord : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2015-07-27T02:00:00Z","last_updated_date":"2015-07-27T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/bortezomib-accord-epar-risk-management-plan-summary_en.pdf"},
    {"id":"34417","name":"Mixtard : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2018-03-20T14:31:00Z","last_updated_date":"2020-06-16T11:26:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/mixtard-epar-risk-management-plan-summary_en.pdf"},
    {"id":"34601","name":"Duzallo : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2018-08-24T15:19:00Z","last_updated_date":"2020-08-06T15:19:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/duzallo-epar-risk-management-plan-summary_en.pdf"},
    {"id":"34644","name":"Pregabalin Sandoz GmbH : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2015-07-21T02:00:00Z","last_updated_date":"2023-10-12T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/pregabalin-sandoz-gmbh-epar-risk-management-plan-summary_en.pdf"},
    {"id":"34833","name":"Izba : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2014-05-13T02:00:00Z","last_updated_date":"2020-12-22T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/izba-epar-risk-management-plan-summary_en.pdf"},
    {"id":"35075","name":"Seebri Breezhaler : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2018-07-05T02:00:00Z","last_updated_date":"2018-07-05T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/seebri-breezhaler-epar-risk-management-plan-summary_en.pdf"},
    {"id":"35442","name":"Clopidogrel-ratiopharm : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2015-03-11T01:00:00Z","last_updated_date":"2024-03-26T10:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/clopidogrel-ratiopharm-epar-risk-management-plan-summary_en.pdf"},
    {"id":"35694","name":"Rivastigmine 3M Health Care Ltd : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2014-04-14T02:00:00Z","last_updated_date":"2014-09-18T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/rivastigmine-3m-health-care-ltd-epar-risk-management-plan-summary_en.pdf"},
    {"id":"36180","name":"Pregabalin Mylan Pharma : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2015-07-31T02:00:00Z","last_updated_date":"2022-04-26T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/pregabalin-mylan-pharma-epar-risk-management-plan-summary_en.pdf"},
    {"id":"36227","name":"Intrarosa : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2018-02-14T18:05:00Z","last_updated_date":"2018-02-14T18:05:00Z","reference_number":"EMA/70766/2018","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/intrarosa-epar-risk-management-plan-summary_en.pdf"},
    {"id":"36656","name":"Nivolumab BMS : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2015-07-27T02:00:00Z","last_updated_date":"2016-01-14T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/nivolumab-bms-epar-risk-management-plan-summary_en.pdf"},
    {"id":"36716","name":"Entresto : EPAR - Risk management plan","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2015-12-01T01:00:00Z","last_updated_date":"2025-10-14T10:09:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/entresto-epar-risk-management-plan_en.pdf"},
    {"id":"37753","name":"Zinforo : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2018-03-27T18:23:00Z","last_updated_date":"2019-10-17T18:23:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/zinforo-epar-risk-management-plan-summary_en.pdf"},
    {"id":"37865","name":"Pemetrexed Lilly : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2015-10-02T02:00:00Z","last_updated_date":"2021-11-26T02:00:00Z","reference_number":"EMA/512407/2015","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/pemetrexed-lilly-epar-risk-management-plan-summary_en.pdf"},
    {"id":"38124","name":"Ivabradine Anpharm : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2015-09-21T02:00:00Z","last_updated_date":"2023-12-21T16:29:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/ivabradine-anpharm-epar-risk-management-plan-summary_en.pdf"},
    {"id":"38539","name":"Aripiprazole Accord : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2015-11-27T01:00:00Z","last_updated_date":"2015-11-27T01:00:00Z","reference_number":"EMA/16634/2014","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/aripiprazole-accord-epar-risk-management-plan-summary_en.pdf"},
    {"id":"38688","name":"Zydelig : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2014-10-14T02:00:00Z","last_updated_date":"2021-05-20T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/zydelig-epar-risk-management-plan-summary_en.pdf"},
    {"id":"39515","name":"Numient : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2015-11-25T01:00:00Z","last_updated_date":"2015-11-25T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/numient-epar-risk-management-plan-summary_en.pdf"},
    {"id":"39541","name":"Actrapid : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2018-03-20T01:00:00Z","last_updated_date":"2020-06-16T14:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/actrapid-epar-risk-management-plan-summary_en.pdf"},
    {"id":"39562","name":"Kolbam  : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2015-12-09T01:00:00Z","last_updated_date":"2020-07-15T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/kolbam-epar-risk-management-plan-summary_en.pdf"},
    {"id":"39624","name":"Inovelon : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2018-08-23T02:00:00Z","last_updated_date":"2018-08-23T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/inovelon-epar-risk-management-plan-summary_en.pdf"},
    {"id":"39699","name":"Rapamune : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2018-08-08T15:48:00Z","last_updated_date":"2022-06-08T15:48:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/rapamune-epar-risk-management-plan-summary_en.pdf"},
    {"id":"40009","name":"Daklinza : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2014-09-15T02:00:00Z","last_updated_date":"2019-05-28T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/daklinza-epar-risk-management-plan-summary_en.pdf"},
    {"id":"40297","name":"Duloxetine Zentiva : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2015-08-27T02:00:00Z","last_updated_date":"2015-08-27T02:00:00Z","reference_number":"EMA/450483/2015","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/duloxetine-zentiva-epar-risk-management-plan-summary_en.pdf"},
    {"id":"40566","name":"Cinacalcet Mylan : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2015-11-27T01:00:00Z","last_updated_date":"2015-11-27T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/cinacalcet-mylan-epar-risk-management-plan-summary_en.pdf"},
    {"id":"40653","name":"Enurev Breezhaler : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2018-07-05T02:00:00Z","last_updated_date":"2018-07-05T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/enurev-breezhaler-epar-risk-management-plan-summary_en.pdf"},
    {"id":"40868","name":"Pemetrexed Sandoz : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2015-10-02T02:00:00Z","last_updated_date":"2024-11-06T02:00:00Z","reference_number":"EMA/520309/2015","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/pemetrexed-sandoz-epar-risk-management-plan-summary_en.pdf"},
    {"id":"41423","name":"Strensiq : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2015-09-28T02:00:00Z","last_updated_date":"2015-09-28T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/strensiq-epar-risk-management-plan-summary_en.pdf"},
    {"id":"41665","name":"Trazimera : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2018-08-16T02:00:00Z","last_updated_date":"2018-08-16T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/trazimera-epar-risk-management-plan-summary_en.pdf"},
    {"id":"41671","name":"Busulfan Fresenius Kabi : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2014-10-15T02:00:00Z","last_updated_date":"2019-10-09T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/busulfan-fresenius-kabi-epar-risk-management-plan-summary_en.pdf"},
    {"id":"41962","name":"Prasugrel Mylan : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2018-06-18T02:00:00Z","last_updated_date":"2025-06-02T11:00:00Z","reference_number":"EMA/164014/2018","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/prasugrel-mylan-epar-risk-management-plan-summary_en.pdf"},
    {"id":"42067","name":"Kymriah : EPAR - Risk-management-plan sumary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2018-09-19T02:00:00Z","last_updated_date":"2025-05-07T11:40:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/kymriah-epar-risk-management-plan-sumary_en.pdf"},
    {"id":"42109","name":"Hulio : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2018-09-21T02:00:00Z","last_updated_date":"2022-08-05T16:01:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/hulio-epar-risk-management-plan-summary_en.pdf"},
    {"id":"42183","name":"Abseamed : EPAR - Risk management plan","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2018-10-03T12:50:00Z","last_updated_date":"2024-07-24T11:45:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/abseamed-epar-risk-management-plan_en.pdf"},
    {"id":"42196","name":"Binocrit : EPAR - Risk management plan","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2018-10-04T17:11:00Z","last_updated_date":"2024-07-24T11:40:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/binocrit-epar-risk-management-plan_en.pdf"},
    {"id":"42210","name":"Deferiprone Lipomed : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2018-10-05T15:27:00Z","last_updated_date":"2023-07-14T09:10:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/deferiprone-lipomed-epar-risk-management-plan-summary_en.pdf"},
    {"id":"42248","name":"Ilumetri : EPAR - Risk management plan","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2018-10-09T17:06:00Z","last_updated_date":"2024-07-23T12:43:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/ilumetri-epar-risk-management-plan_en.pdf"},
    {"id":"42268","name":"Gefitinib Mylan : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2018-10-10T14:00:00Z","last_updated_date":"2024-10-17T11:11:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/gefitinib-mylan-epar-risk-management-plan-summary_en.pdf"},
    {"id":"42445","name":"Vyxeos : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2018-10-26T17:11:00Z","last_updated_date":"2018-10-26T17:11:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/vyxeos-epar-risk-management-plan-summary_en.pdf"},
    {"id":"42470","name":"Udenyca : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2018-10-29T16:08:00Z","last_updated_date":"2018-10-29T16:08:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/udenyca-epar-risk-management-plan-summary_en.pdf"},
    {"id":"42474","name":"Verzenios : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2018-10-29T18:22:00Z","last_updated_date":"2018-10-29T18:22:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/verzenios-epar-risk-management-plan-summary_en.pdf"},
    {"id":"42499","name":"Onpattro : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2018-10-30T15:17:00Z","last_updated_date":"2024-02-29T12:14:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/onpattro-epar-risk-management-plan-summary_en.pdf"},
    {"id":"42724","name":"Esmya : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2018-11-19T13:40:00Z","last_updated_date":"2021-02-03T15:53:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/esmya-epar-risk-management-plan-summary_en.pdf"},
    {"id":"42739","name":"Symkevi : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2018-11-22T10:07:00Z","last_updated_date":"2022-03-09T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/symkevi-epar-risk-management-plan-summary_en.pdf"},
    {"id":"42792","name":"Alunbrig : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2018-11-26T15:04:00Z","last_updated_date":"2025-04-25T11:30:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/alunbrig-epar-risk-management-plan-summary_en.pdf"},
    {"id":"42904","name":"Fulphila : EPAR Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2018-12-03T11:45:00Z","last_updated_date":"2023-11-20T11:26:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/fulphila-epar-risk-management-plan-summary_en.pdf"},
    {"id":"42909","name":"Pelmeg : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2018-12-03T12:43:00Z","last_updated_date":"2024-02-19T11:36:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/pelmeg-epar-risk-management-plan-summary_en.pdf"},
    {"id":"42921","name":"Apealea : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2018-12-05T16:13:00Z","last_updated_date":"2024-03-06T16:07:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/apealea-epar-risk-management-plan-summary_en.pdf"},
    {"id":"43110","name":"Pregabalin Pfizer : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2018-12-17T17:02:00Z","last_updated_date":"2024-07-01T14:40:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/pregabalin-pfizer-epar-risk-management-plan-summary_en.pdf"},
    {"id":"43120","name":"Buvidal : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2018-12-18T11:10:00Z","last_updated_date":"2023-08-16T09:15:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/buvidal-epar-risk-management-plan-summary_en.pdf"},
    {"id":"43134","name":"Vabomere : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2018-12-18T16:06:00Z","last_updated_date":"2018-12-18T16:06:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/vabomere-epar-risk-management-plan-summary_en.pdf"},
    {"id":"43151","name":"NovoSeven : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2018-12-18T19:01:00Z","last_updated_date":"2023-02-27T13:50:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/novoseven-epar-risk-management-plan-summary_en.pdf"},
    {"id":"43212","name":"Elebrato Ellipta : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2019-01-04T14:16:00Z","last_updated_date":"2019-01-04T14:16:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/elebrato-ellipta-epar-risk-management-plan-summary_en.pdf"},
    {"id":"43214","name":"Trelegy Ellipta : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2019-01-04T15:01:00Z","last_updated_date":"2019-01-04T15:01:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/trelegy-ellipta-epar-risk-management-plan-summary_en.pdf"},
    {"id":"43246","name":"Efavirenz/Emtricitabine/Tenofovir disoproxil Krka : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2019-01-08T11:57:00Z","last_updated_date":"2020-03-17T10:16:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/efavirenzemtricitabinetenofovir-disoproxil-krka-epar-risk-management-plan-summary_en.pdf"},
    {"id":"43254","name":"Ogivri : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2019-01-09T10:08:00Z","last_updated_date":"2019-01-09T10:08:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/ogivri-epar-risk-management-plan-summary_en.pdf"},
    {"id":"43269","name":"Pifeltro : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2019-01-10T12:14:00Z","last_updated_date":"2022-04-12T17:06:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/pifeltro-epar-risk-management-plan-summary_en.pdf"},
    {"id":"43301","name":"Delstrigo : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2019-01-10T15:57:00Z","last_updated_date":"2022-04-12T17:35:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/delstrigo-epar-risk-management-plan-summary_en.pdf"},
    {"id":"43425","name":"Dificlir : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2019-01-21T18:27:00Z","last_updated_date":"2020-03-11T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/dificlir-epar-risk-management-plan-summary_en.pdf"},
    {"id":"43437","name":"Silodosin Recordati : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2019-01-22T12:04:00Z","last_updated_date":"2019-01-22T12:04:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/silodosin-recordati-epar-risk-management-plan-summary_en.pdf"},
    {"id":"43641","name":"Bevespi Aerosphere :  EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2019-02-05T15:42:00Z","last_updated_date":"2019-02-05T15:42:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/bevespi-aerosphere-epar-risk-management-plan-summary_en.pdf"},
    {"id":"43663","name":"Tamiflu : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2019-02-07T13:21:00Z","last_updated_date":"2020-04-23T09:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/tamiflu-epar-risk-management-plan-summary_en.pdf"},
    {"id":"43687","name":"Cimzia : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2019-02-11T11:42:00Z","last_updated_date":"2021-07-08T14:13:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/cimzia-epar-risk-management-plan-summary_en.pdf"},
    {"id":"43690","name":"Volibris : EPAR - Risk-management-plan","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2019-02-11T14:06:00Z","last_updated_date":"2025-07-25T10:54:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/volibris-epar-risk-management-plan_en.pdf"},
    {"id":"43734","name":"Emgality : EPAR - Risk-management plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2019-02-14T17:35:00Z","last_updated_date":"2025-05-28T14:27:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/emgality-epar-risk-management-plan-summary_en.pdf"},
    {"id":"43805","name":"Thymanax : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2019-02-19T17:06:00Z","last_updated_date":"2023-08-08T16:58:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/thymanax-epar-risk-management-plan-summary_en.pdf"},
    {"id":"43810","name":"Dacogen : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2019-02-20T10:39:00Z","last_updated_date":"2024-06-03T15:12:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/dacogen-epar-risk-management-plan-summary_en.pdf"},
    {"id":"43870","name":"Epclusa : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2019-02-21T15:22:00Z","last_updated_date":"2023-02-09T13:36:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/epclusa-epar-risk-management-plan-summary_en.pdf"},
    {"id":"43905","name":"Ghryvelin (previously Macimorelin Aeterna Zentaris) : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2019-02-26T09:39:00Z","last_updated_date":"2019-02-26T09:39:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/ghryvelin-previously-macimorelin-aeterna-zentaris-epar-risk-management-plan-summary_en.pdf"},
    {"id":"43908","name":"Vosevi : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2019-02-26T10:36:00Z","last_updated_date":"2023-02-09T16:30:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/vosevi-epar-risk-management-plan-summary_en.pdf"},
    {"id":"43973","name":"Rizmoic : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2019-03-01T17:33:00Z","last_updated_date":"2019-03-01T17:33:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/rizmoic-epar-risk-management-plan-summary_en.pdf"},
    {"id":"44034","name":"Lusutrombopag Shionogi : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2019-03-14T15:40:00Z","last_updated_date":"2019-03-14T15:40:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/lusutrombopag-shionogi-epar-risk-management-plan-summary_en.pdf"},
    {"id":"44038","name":"Nulojix : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2019-03-14T17:11:00Z","last_updated_date":"2022-04-20T08:38:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/nulojix-epar-risk-management-plan-summary_en.pdf"},
    {"id":"44072","name":"Xolair : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2019-03-20T12:32:00Z","last_updated_date":"2023-11-20T11:26:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/xolair-epar-risk-management-plan-summary_en.pdf"},
    {"id":"44073","name":"Tenofovir disoproxil Zentiva : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2019-03-20T12:45:00Z","last_updated_date":"2019-10-29T11:27:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/tenofovir-disoproxil-zentiva-epar-risk-management-plan-summary_en.pdf"},
    {"id":"44075","name":"Trimbow : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2019-03-20T14:56:00Z","last_updated_date":"2021-04-09T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/trimbow-epar-risk-management-plan-summary_en.pdf"},
    {"id":"44084","name":"Axumin : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2019-03-21T10:51:00Z","last_updated_date":"2019-03-21T10:51:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/axumin-epar-risk-management-plan-summary_en.pdf"},
    {"id":"44105","name":"Truberzi : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2019-03-26T10:06:00Z","last_updated_date":"2021-02-25T14:25:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/truberzi-epar-risk-management-plan-summary_en.pdf"},
    {"id":"44140","name":"Sprycel : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2019-03-29T09:28:00Z","last_updated_date":"2019-03-29T09:28:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/sprycel-epar-risk-management-plan-summary_en.pdf"},
    {"id":"44156","name":"Febuxostat Krka : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2019-03-29T15:54:00Z","last_updated_date":"2019-03-29T15:54:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/febuxostat-krka-epar-risk-management-plan-summary_en.pdf"},
    {"id":"44206","name":"Alprolix : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2019-04-10T10:35:00Z","last_updated_date":"2020-11-04T09:51:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/alprolix-epar-risk-management-plan-summary_en.pdf"},
    {"id":"44282","name":"Zirabev : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2019-04-16T16:29:00Z","last_updated_date":"2019-04-16T16:29:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/zirabev-epar-risk-management-plan-summary_en.pdf"},
    {"id":"44305","name":"Vantobra (previously Tobramycin PARI) : EPAR - Risk-mangement-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2019-04-17T16:12:00Z","last_updated_date":"2019-04-17T16:12:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/vantobra-previously-tobramycin-pari-epar-risk-mangement-plan-summary_en.pdf"},
    {"id":"44333","name":"Maviret : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2019-04-24T11:55:00Z","last_updated_date":"2023-02-16T14:39:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/maviret-epar-risk-management-plan-summary_en.pdf"},
    {"id":"44375","name":"Kromeya : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2019-04-26T13:29:00Z","last_updated_date":"2019-04-26T13:29:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/kromeya-epar-risk-management-plan-summary_en.pdf"},
    {"id":"44408","name":"Gardasil : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2019-04-30T15:35:00Z","last_updated_date":"2025-07-24T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/gardasil-epar-risk-management-plan-summary_en.pdf"},
    {"id":"44482","name":"Thalidomide Celgene : EPAR - Risk management plan","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2024-03-19T09:30:00Z","last_updated_date":"2024-03-19T09:30:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/thalidomide-celgene-epar-risk-management-plan_en.pdf"},
    {"id":"44483","name":"Picato : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2019-05-13T10:47:00Z","last_updated_date":"2020-03-04T16:30:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/picato-epar-risk-management-plan-summary_en.pdf"},
    {"id":"44495","name":"Atripla : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2019-05-14T16:37:00Z","last_updated_date":"2022-01-21T10:56:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/atripla-epar-risk-management-plan-summary_en.pdf"},
    {"id":"44501","name":"Atazanavir Krka : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2019-05-15T10:44:00Z","last_updated_date":"2026-03-27T11:20:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/atazanavir-krka-epar-risk-management-plan-summary_en.pdf"},
    {"id":"44524","name":"Zynquista : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2019-05-16T16:09:00Z","last_updated_date":"2022-08-16T15:23:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/zynquista-epar-risk-management-plan-summary_en.pdf"},
    {"id":"44543","name":"Sifrol : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2019-05-20T16:41:00Z","last_updated_date":"2019-05-20T16:41:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/sifrol-epar-risk-management-plan-summary_en.pdf"},
    {"id":"44544","name":"Mirapexin : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2019-05-21T09:41:00Z","last_updated_date":"2019-05-21T09:41:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/mirapexin-epar-risk-management-plan-summary_en.pdf"},
    {"id":"44577","name":"Pazenir : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2019-05-23T11:05:00Z","last_updated_date":"2019-05-23T11:05:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/pazenir-epar-risk-management-plan-summary_en.pdf"},
    {"id":"44616","name":"Palynziq : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2019-05-29T13:09:00Z","last_updated_date":"2024-07-12T08:59:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/palynziq-epar-risk-management-plan-summary_en.pdf"},
    {"id":"44636","name":"Zynteglo : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2019-06-03T10:23:00Z","last_updated_date":"2021-10-04T11:54:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/zynteglo-epar-risk-management-plan-summary_en.pdf"},
    {"id":"44644","name":"Cayston : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2019-06-04T09:04:00Z","last_updated_date":"2019-06-04T09:04:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/cayston-epar-risk-management-plan-summary_en.pdf"},
    {"id":"44656","name":"Kyprolis : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2019-06-05T11:01:00Z","last_updated_date":"2019-06-05T11:01:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/kyprolis-epar-risk-management-plan-summary_en.pdf-0"},
    {"id":"44665","name":"Vizimpro : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2019-06-05T16:30:00Z","last_updated_date":"2021-02-22T11:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/vizimpro-epar-risk-management-plan-summary_en.pdf"},
    {"id":"44877","name":"Doptelet : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2019-06-25T12:34:00Z","last_updated_date":"2021-01-28T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/doptelet-epar-risk-management-plan-summary_en.pdf"},
    {"id":"44892","name":"Inlyta : EPAR - Risk-management-plan","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2019-06-26T12:53:00Z","last_updated_date":"2024-08-16T11:34:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/inlyta-epar-risk-management-plan_en.pdf"},
    {"id":"44902","name":"Levitra : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2019-06-27T10:21:00Z","last_updated_date":"2019-06-27T10:21:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/levitra-epar-risk-management-plan-summary_en.pdf"},
    {"id":"44935","name":"Grasustek : EPAR - Risk management plan","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2019-06-28T10:05:00Z","last_updated_date":"2024-07-04T11:50:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/grasustek-epar-risk-management-plan_en.pdf"},
    {"id":"44969","name":"Champix : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2019-07-02T10:29:00Z","last_updated_date":"2019-07-02T10:29:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/champix-epar-risk-management-plan-summary_en.pdf"},
    {"id":"44970","name":"Vivanza : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2019-07-02T11:07:00Z","last_updated_date":"2022-02-28T12:10:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/vivanza-epar-risk-management-plan-summary_en.pdf"},
    {"id":"44979","name":"Sixmo : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2019-07-02T15:23:00Z","last_updated_date":"2025-08-14T18:15:07Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/sixmo-epar-risk-management-plan-summary_en.pdf"},
    {"id":"45032","name":"Ultomiris : EPAR - Risk management plan","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2019-07-10T15:23:00Z","last_updated_date":"2025-06-19T14:39:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/ultomiris-epar-risk-management-plan_en.pdf"},
    {"id":"45046","name":"MabThera : EPAR - Risk-management-plan","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2019-07-12T11:04:00Z","last_updated_date":"2024-10-21T15:07:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/mabthera-epar-risk-management-plan_en.pdf"},
    {"id":"45057","name":"Ambrisentan Mylan : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2019-07-15T10:12:00Z","last_updated_date":"2019-07-15T10:12:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/ambrisentan-mylan-epar-risk-management-plan-summary_en.pdf"},
    {"id":"45095","name":"Abilify : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2019-07-19T12:23:00Z","last_updated_date":"2019-07-19T12:23:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/abilify-epar-risk-management-plan-summary_en.pdf"},
    {"id":"45109","name":"Trecondi : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2019-07-22T12:21:00Z","last_updated_date":"2023-08-08T16:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/trecondi-epar-risk-management-plan-summary_en.pdf"},
    {"id":"45114","name":"Instanyl : EPAR - Risk management plan","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2019-07-23T09:52:00Z","last_updated_date":"2024-04-05T09:43:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/instanyl-epar-risk-management-plan_en.pdf"},
    {"id":"45147","name":"Alofisel : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2019-07-29T12:05:00Z","last_updated_date":"2025-01-21T12:28:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/alofisel-epar-risk-management-plan-summary_en.pdf"},
    {"id":"45154","name":"Translarna : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2019-07-30T11:37:00Z","last_updated_date":"2025-04-16T11:11:11Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/translarna-epar-risk-management-plan-summary_en.pdf-0"},
    {"id":"45210","name":"Hepsera : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2019-08-08T10:28:00Z","last_updated_date":"2023-03-01T14:52:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/hepsera-epar-risk-management-plan-summary_en.pdf"},
    {"id":"45252","name":"Azacitidine Celgene : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2019-08-14T10:09:00Z","last_updated_date":"2021-08-04T16:55:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/azacitidine-celgene-epar-risk-management-plan-summary_en.pdf"},
    {"id":"45264","name":"NovoMix : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2019-08-16T16:51:00Z","last_updated_date":"2023-08-29T09:25:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/novomix-epar-risk-management-plan-summary_en.pdf"},
    {"id":"45299","name":"Mimpara : EPAR - Risk-management-plan","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2019-08-22T11:18:00Z","last_updated_date":"2026-05-20T13:54:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/mimpara-epar-risk-management-plan_en.pdf"},
    {"id":"45324","name":"Tracleer : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2019-08-26T09:34:00Z","last_updated_date":"2019-08-26T09:34:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/tracleer-epar-risk-management-plan-summary_en.pdf"},
    {"id":"45328","name":"Fiasp : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2019-08-26T13:32:00Z","last_updated_date":"2020-06-15T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/fiasp-epar-risk-management-plan-summary_en.pdf"},
    {"id":"45331","name":"Stayveer : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2019-08-27T15:02:00Z","last_updated_date":"2019-08-27T15:02:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/stayveer-epar-risk-management-plan-summary_en.pdf"},
    {"id":"45363","name":"Mozobil : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2019-09-02T10:24:00Z","last_updated_date":"2019-09-02T10:24:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/mozobil-epar-risk-management-plan-summary_en.pdf"},
    {"id":"45365","name":"Pixuvri : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2019-09-02T14:05:00Z","last_updated_date":"2019-09-02T14:05:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/pixuvri-epar-risk-management-plan-summary_en.pdf"},
    {"id":"45392","name":"Riarify : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2019-09-06T15:04:00Z","last_updated_date":"2025-03-18T17:55:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/riarify-epar-risk-management-plan-summary_en.pdf"},
    {"id":"45511","name":"Temybric Ellipta : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2019-09-23T15:42:00Z","last_updated_date":"2022-11-24T15:33:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/temybric-ellipta-epar-risk-management-plan-summary_en.pdf"},
    {"id":"45540","name":"Inbrija : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2019-09-30T15:18:00Z","last_updated_date":"2019-09-30T15:18:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/inbrija-epar-risk-management-plan-summary_en.pdf"},
    {"id":"45555","name":"Multaq : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2019-10-03T10:58:00Z","last_updated_date":"2019-10-03T10:58:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/multaq-epar-risk-management-plan-summary_en.pdf"},
    {"id":"45564","name":"Epidyolex : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2019-10-04T09:11:00Z","last_updated_date":"2024-08-20T11:11:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/epidyolex-epar-risk-management-plan-summary_en.pdf"},
    {"id":"45598","name":"Yentreve : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2019-10-08T16:21:00Z","last_updated_date":"2020-09-22T09:29:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/yentreve-epar-risk-management-plan-summary_en.pdf"},
    {"id":"45601","name":"Xeristar - EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2019-10-08T17:01:00Z","last_updated_date":"2021-06-22T15:01:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/xeristar-epar-risk-management-plan-summary_en.pdf"},
    {"id":"45634","name":"Trogarzo : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2019-10-10T10:22:00Z","last_updated_date":"2023-01-16T11:27:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/trogarzo-epar-risk-management-plan-summary_en.pdf"},
    {"id":"45645","name":"Giapreza : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2019-10-10T16:04:00Z","last_updated_date":"2019-10-10T16:04:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/giapreza-epar-risk-management-plan-summary_en.pdf"},
    {"id":"45651","name":"Deferasirox Mylan : EPAR - Risk management plan","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2019-10-10T17:48:00Z","last_updated_date":"2024-10-14T11:13:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/deferasirox-mylan-epar-risk-management-plan_en.pdf"},
    {"id":"45673","name":"Nuceiva : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2019-10-14T15:10:00Z","last_updated_date":"2021-02-19T10:07:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/nuceiva-epar-risk-management-plan-summary_en.pdf"},
    {"id":"45696","name":"Rebetol : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2019-10-14T17:08:00Z","last_updated_date":"2023-11-07T14:33:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/rebetol-epar-risk-management-plan-summary_en.pdf"},
    {"id":"45717","name":"Victoza : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2019-10-15T17:06:00Z","last_updated_date":"2019-10-15T17:06:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/victoza-epar-risk-management-plan-summary_en.pdf"},
    {"id":"45722","name":"Betaferon : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2019-10-16T11:37:00Z","last_updated_date":"2019-10-16T11:37:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/betaferon-epar-risk-management-plan-summary_en.pdf"},
    {"id":"45725","name":"Rebif : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2019-10-16T15:38:00Z","last_updated_date":"2020-02-25T12:13:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/rebif-epar-risk-management-plan-summary_en.pdf"},
    {"id":"45739","name":"Extavia : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2019-10-17T15:01:00Z","last_updated_date":"2025-04-30T16:18:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/extavia-epar-risk-management-plan-summary_en.pdf"},
    {"id":"45889","name":"Caprelsa : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2019-11-05T17:36:00Z","last_updated_date":"2020-12-07T10:44:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/caprelsa-epar-risk-management-plan-summary_en.pdf"},
    {"id":"45898","name":"Adjupanrix : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2019-11-06T15:52:00Z","last_updated_date":"2019-11-06T15:52:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/adjupanrix-epar-risk-management-plan-summary_en.pdf"},
    {"id":"45939","name":"Xospata : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2019-11-08T11:02:00Z","last_updated_date":"2023-11-07T15:13:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/xospata-epar-risk-management-plan-summary_en.pdf"},
    {"id":"45960","name":"Sutent : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2019-11-11T16:57:00Z","last_updated_date":"2019-11-11T16:57:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/sutent-epar-risk-management-plan-summary_en.pdf"},
    {"id":"46031","name":"Tysabri : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2019-11-14T16:25:00Z","last_updated_date":"2022-09-13T14:42:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/tysabri-epar-risk-management-plan-summary_en.pdf"},
    {"id":"46057","name":"Defitelio : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2019-11-19T10:52:00Z","last_updated_date":"2023-06-15T11:06:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/defitelio-epar-risk-management-plan-summary_en.pdf"},
    {"id":"46109","name":"Trevicta : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2015-07-30T02:00:00Z","last_updated_date":"2020-08-26T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/trevicta-epar-risk-management-plan-summary_en.pdf"},
    {"id":"46119","name":"Ivozall : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2019-11-22T15:29:00Z","last_updated_date":"2023-12-07T16:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/ivozall-epar-risk-management-plan-summary_en.pdf"},
    {"id":"46127","name":"Bortezomib Fresenius Kabi : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2019-11-25T15:29:00Z","last_updated_date":"2019-11-25T15:29:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/bortezomib-fresenius-kabi-epar-risk-management-plan-summary_en.pdf"},
    {"id":"46170","name":"Arsenic trioxide Accord : EPAR - Risk -management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2019-11-26T15:19:00Z","last_updated_date":"2019-11-26T15:19:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/arsenic-trioxide-accord-epar-risk-management-plan-summary_en.pdf"},
    {"id":"46189","name":"Senstend : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2019-11-29T16:16:00Z","last_updated_date":"2022-07-05T12:17:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/senstend-epar-risk-management-plan-summary_en.pdf"},
    {"id":"46191","name":"Atriance : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2019-11-27T16:31:00Z","last_updated_date":"2019-11-27T16:31:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/atriance-epar-risk-management-plan-summary_en.pdf"},
    {"id":"46288","name":"M-M-RVaxPro : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2019-12-10T17:21:00Z","last_updated_date":"2019-12-10T17:21:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/m-m-rvaxpro-epar-risk-management-plan-summary_en.pdf"},
    {"id":"46296","name":"Taxotere : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2019-12-11T17:00:00Z","last_updated_date":"2020-06-11T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/taxotere-epar-risk-management-plan-summary_en.pdf"},
    {"id":"46309","name":"Ervebo : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2019-12-12T16:39:00Z","last_updated_date":"2026-01-16T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/ervebo-epar-risk-management-plan-summary_en.pdf"},
    {"id":"46346","name":"Spravato : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2019-12-19T15:34:00Z","last_updated_date":"2021-07-06T11:24:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/spravato-epar-risk-management-plan-summary_en.pdf"},
    {"id":"46362","name":"Pegfilgrastim Mundipharma : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2019-12-20T10:08:00Z","last_updated_date":"2019-12-20T10:08:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/pegfilgrastim-mundipharma-epar-risk-management-plan-summary_en.pdf"},
    {"id":"46374","name":"Mircera : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2019-12-20T14:49:00Z","last_updated_date":"2019-12-20T14:49:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/mircera-epar-risk-management-plan-summary_en.pdf"},
    {"id":"46375","name":"Docetaxel Zentiva : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2019-12-20T15:06:00Z","last_updated_date":"2022-05-20T12:02:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/docetaxel-zentiva-epar-risk-management-plan-summary_en.pdf"},
    {"id":"46382","name":"Qtrilmet : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2019-12-10T14:19:00Z","last_updated_date":"2020-10-09T02:28:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/qtrilmet-epar-risk-management-plan-summary_en.pdf"},
    {"id":"46578","name":"Polivy : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2020-01-27T13:58:00Z","last_updated_date":"2022-06-08T16:45:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/polivy-epar-risk-management-plan-summary_en.pdf"},
    {"id":"46709","name":"Zoely : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2020-02-11T15:43:00Z","last_updated_date":"2023-02-16T10:16:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/zoely-epar-risk-management-plan-summary_en.pdf"},
    {"id":"46714","name":"Tavlesse : EPAR - Risk management plan","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2020-02-11T16:07:00Z","last_updated_date":"2024-12-02T17:19:12Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/tavlesse-epar-risk-management-plan_en.pdf"},
    {"id":"46746","name":"Emtricitabine/Tenofovir disoproxil Krka : EPAR - Risk-management plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2020-02-13T12:11:00Z","last_updated_date":"2020-02-13T12:11:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/emtricitabinetenofovir-disoproxil-krka-epar-risk-management-plan-summary_en.pdf"},
    {"id":"46787","name":"Dexmedetomidine Accord : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2020-02-19T13:10:00Z","last_updated_date":"2022-12-02T13:43:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/dexmedetomidine-accord-epar-risk-management-plan-summary_en.pdf"},
    {"id":"46872","name":"Afinitor : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2020-02-25T15:38:00Z","last_updated_date":"2021-12-07T11:49:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/afinitor-epar-risk-management-plan-summary_en.pdf"},
    {"id":"46884","name":"Recarbrio : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2020-02-26T15:36:00Z","last_updated_date":"2026-01-26T11:31:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/recarbrio-epar-risk-management-plan-summary_en.pdf"},
    {"id":"46940","name":"Deferasirox Accord : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2020-03-04T14:27:00Z","last_updated_date":"2025-01-06T14:36:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/deferasirox-accord-epar-risk-management-plan-summary_en.pdf"},
    {"id":"46977","name":"Givlaari : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2020-03-09T14:11:00Z","last_updated_date":"2024-12-18T14:16:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/givlaari-epar-risk-management-plan-summary_en.pdf"},
    {"id":"47037","name":"Descovy : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2020-03-17T16:03:00Z","last_updated_date":"2022-11-14T15:18:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/descovy-epar-risk-management-plan-summary_en.pdf"},
    {"id":"47041","name":"Edarbi : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2020-03-18T11:12:00Z","last_updated_date":"2020-03-18T11:12:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/edarbi-epar-risk-management-plan-summary_en.pdf"},
    {"id":"47044","name":"Colobreathe : EPAR - Risk management plan","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2020-03-18T15:05:00Z","last_updated_date":"2024-09-30T10:47:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/colobreathe-epar-risk-management-plan_en.pdf"},
    {"id":"47266","name":"Azacitidine betapharm : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2020-04-01T14:06:00Z","last_updated_date":"2020-04-01T14:06:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/azacitidine-betapharm-epar-risk-management-plan-summary_en.pdf"},
    {"id":"47271","name":"Synflorix : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2020-04-01T14:24:00Z","last_updated_date":"2020-04-01T14:24:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/synflorix-epar-risk-management-plan-summary_en.pdf"},
    {"id":"47310","name":"Incresync : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2020-04-02T17:37:00Z","last_updated_date":"2020-04-02T17:37:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/incresync-epar-risk-management-plan-summary_en.pdf"},
    {"id":"47346","name":"Azacitidine Mylan : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2020-04-06T09:35:00Z","last_updated_date":"2020-04-06T09:35:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/azacitidine-mylan-epar-risk-management-plan-summary_en.pdf"},
    {"id":"47382","name":"Vaxchora : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2020-04-08T14:44:00Z","last_updated_date":"2022-05-31T14:21:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/vaxchora-epar-risk-management-plan-summary_en.pdf"},
    {"id":"47383","name":"Velcade : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2020-04-08T14:24:00Z","last_updated_date":"2020-04-08T14:24:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/velcade-epar-risk-management-plan-summary_en.pdf"},
    {"id":"47420","name":"Liumjev : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2020-04-16T16:44:00Z","last_updated_date":"2020-04-16T16:44:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/liumjev-epar-risk-management-plan-summary_en.pdf"},
    {"id":"47428","name":"Arsenic trioxide Mylan : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2020-04-17T10:49:00Z","last_updated_date":"2025-05-06T11:22:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/arsenic-trioxide-mylan-epar-risk-management-plan-summary_en.pdf"},
    {"id":"47434","name":"Increlex : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2020-04-20T10:43:00Z","last_updated_date":"2022-01-11T16:09:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/increlex-epar-risk-management-plan-summary_en.pdf"},
    {"id":"47452","name":"Staquis : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2020-04-22T11:42:00Z","last_updated_date":"2022-02-08T14:13:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/staquis-epar-risk-management-plan-summary_en.pdf"},
    {"id":"47480","name":"Tigecycline Accord : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2020-04-24T11:23:00Z","last_updated_date":"2020-04-24T11:23:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/tigecycline-accord-epar-risk-management-plan-summary_en.pdf"},
    {"id":"47515","name":"Fetcroja : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2020-04-29T15:18:00Z","last_updated_date":"2020-04-29T15:18:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/fetcroja-epar-risk-management-plan-summary_en.pdf"},
    {"id":"47572","name":"Ozurdex : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2020-05-06T16:01:00Z","last_updated_date":"2023-11-24T15:07:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/ozurdex-epar-risk-management-plan-summary_en.pdf"},
    {"id":"47657","name":"ReFacto AF : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2020-05-13T12:30:00Z","last_updated_date":"2020-05-13T12:30:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/refacto-af-epar-risk-management-plan-summary_en.pdf"},
    {"id":"47669","name":"BeneFIX : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2020-05-14T15:59:00Z","last_updated_date":"2020-05-14T15:59:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/benefix-epar-risk-management-plan-summary_en.pdf"},
    {"id":"47671","name":"Intelence : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2020-05-15T10:26:00Z","last_updated_date":"2022-09-16T14:52:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/intelence-epar-risk-management-plan-summary_en.pdf"},
    {"id":"47686","name":"Flixabi : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2020-05-18T09:59:00Z","last_updated_date":"2024-05-13T09:32:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/flixabi-epar-risk-management-plan-summary_en.pdf"},
    {"id":"47768","name":"Rybelsus : EPAR - Risk management plan","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2020-05-27T11:31:00Z","last_updated_date":"2024-11-28T17:20:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/rybelsus-epar-risk-management-plan_en.pdf"},
    {"id":"47777","name":"Zolgensma : EPAR - Risk-management-plan","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2020-05-27T14:52:00Z","last_updated_date":"2024-07-11T16:11:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/zolgensma-epar-risk-management-plan_en.pdf"},
    {"id":"47793","name":"Baraclude : EPAR - Risk-management-plan","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2020-05-28T12:58:00Z","last_updated_date":"2024-08-16T11:26:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/baraclude-epar-risk-management-plan_en.pdf"},
    {"id":"47827","name":"Fabrazyme : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2020-05-29T15:47:00Z","last_updated_date":"2020-05-29T15:47:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/fabrazyme-epar-risk-management-plan-summary_en.pdf"},
    {"id":"47839","name":"Sialanar : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2020-06-02T12:21:00Z","last_updated_date":"2023-06-19T15:27:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/sialanar-epar-risk-management-plan-summary_en.pdf"},
    {"id":"47847","name":"Nepexto : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2020-06-04T09:05:00Z","last_updated_date":"2021-02-22T15:45:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/nepexto-epar-risk-management-plan-summary_en.pdf"},
    {"id":"47954","name":"Strimvelis : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2020-06-11T12:48:00Z","last_updated_date":"2026-05-08T11:18:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/strimvelis-epar-risk-management-plan-summary_en.pdf"},
    {"id":"47968","name":"Evicel : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2020-06-12T09:29:00Z","last_updated_date":"2024-08-02T15:04:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/evicel-epar-risk-management-plan-summary_en.pdf"},
    {"id":"48018","name":"Sancuso : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2020-06-16T10:47:00Z","last_updated_date":"2023-03-29T14:45:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/sancuso-epar-risk-management-plan-summary_en.pdf"},
    {"id":"48068","name":"Carmustine Obvius : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2020-06-23T11:00:00Z","last_updated_date":"2020-06-23T11:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/carmustine-obvius-epar-risk-management-plan-summary_en.pdf"},
    {"id":"48073","name":"Atectura Breezhaler : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2020-06-23T11:24:00Z","last_updated_date":"2020-06-23T11:24:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/atectura-breezhaler-epar-risk-management-plan-summary_en.pdf"},
    {"id":"48110","name":"Bemrist Breezhaler : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2020-06-24T16:07:00Z","last_updated_date":"2020-06-24T16:07:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/bemrist-breezhaler-epar-risk-management-plan-summary_en.pdf"},
    {"id":"48168","name":"ProQuad : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2020-06-26T13:50:00Z","last_updated_date":"2020-06-26T13:50:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/proquad-epar-risk-management-plan-summary_en.pdf"},
    {"id":"48177","name":"Grastofil : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2020-06-29T09:03:00Z","last_updated_date":"2020-06-29T09:03:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/grastofil-epar-risk-management-plan-summary_en.pdf"},
    {"id":"48178","name":"Xermelo : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2020-06-29T09:28:00Z","last_updated_date":"2020-06-29T09:28:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/xermelo-epar-risk-management-plan-summary_en.pdf"},
    {"id":"48238","name":"Nevanac : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2020-07-06T17:10:00Z","last_updated_date":"2020-07-06T17:10:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/nevanac-epar-risk-management-plan-summary_en.pdf"},
    {"id":"48247","name":"Byannli (previously Paliperidone Janssen-Cilag International) : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2020-07-07T15:01:00Z","last_updated_date":"2022-02-18T09:04:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/byannli-previously-paliperidone-janssen-cilag-international-epar-risk-management-plan-summary_en.pdf"},
    {"id":"48252","name":"Insulin aspart Sanofi : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2020-07-07T16:29:00Z","last_updated_date":"2020-07-07T16:29:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/insulin-aspart-sanofi-epar-risk-management-plan-summary_en.pdf"},
    {"id":"48280","name":"Daurismo : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2020-07-10T11:00:00Z","last_updated_date":"2020-07-10T11:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/daurismo-epar-risk-management-plan-summary_en.pdf"},
    {"id":"48332","name":"Glidipion : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2020-07-20T11:39:00Z","last_updated_date":"2022-10-17T11:28:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/glidipion-epar-risk-management-plan-summary_en.pdf"},
    {"id":"48342","name":"Voncento - EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2020-07-21T11:42:00Z","last_updated_date":"2020-07-21T11:42:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/voncento-epar-risk-management-plan-summary_en.pdf"},
    {"id":"48343","name":"Pioglitazone Teva Pharma : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2020-07-21T12:05:00Z","last_updated_date":"2022-08-30T16:59:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/pioglitazone-teva-pharma-epar-risk-management-plan-summary_en.pdf"},
    {"id":"48349","name":"Enerzair Breezhaler : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2020-07-21T14:57:00Z","last_updated_date":"2020-07-21T14:57:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/enerzair-breezhaler-epar-risk-management-plan-summary_en.pdf"},
    {"id":"48418","name":"Firmagon - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2020-07-24T16:00:00Z","last_updated_date":"2020-07-24T16:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/firmagon-risk-management-plan-summary_en.pdf"},
    {"id":"48448","name":"Pioglitazone Teva : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2020-07-28T11:28:00Z","last_updated_date":"2023-05-04T12:11:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/pioglitazone-teva-epar-risk-management-plan-summary_en.pdf"},
    {"id":"48483","name":"Tybost : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2020-07-29T16:05:00Z","last_updated_date":"2020-07-29T16:05:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/tybost-epar-risk-management-plan-summary_en.pdf"},
    {"id":"48567","name":"Xenleta : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2020-08-06T17:18:00Z","last_updated_date":"2020-08-06T17:18:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/xenleta-epar-risk-management-plan-summary_en.pdf"},
    {"id":"48577","name":"Pretomanid FGK : EPAR - Risk management plan","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2020-08-11T09:43:00Z","last_updated_date":"2024-07-05T12:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/pretomanid-fgk-epar-risk-management-plan_en.pdf"},
    {"id":"48609","name":"Invega : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2020-08-13T17:15:00Z","last_updated_date":"2020-08-13T17:15:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/invega-epar-risk-management-plan-summary_en.pdf"},
    {"id":"48686","name":"Lamzede : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2020-08-24T16:24:00Z","last_updated_date":"2020-08-24T16:24:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/lamzede-epar-risk-management-plan-summary_en.pdf"},
    {"id":"48693","name":"Methylthioninium chloride Cosmo : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2020-08-26T10:30:00Z","last_updated_date":"2020-08-26T10:30:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/methylthioninium-chloride-cosmo-epar-risk-management-plan-summary_en.pdf"},
    {"id":"48695","name":"Afstyla : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2020-08-26T11:14:00Z","last_updated_date":"2020-08-26T11:14:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/afstyla-epar-risk-management-plan-summary_en.pdf"},
    {"id":"48704","name":"Gencebok : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2020-08-27T11:37:00Z","last_updated_date":"2020-08-27T11:37:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/gencebok-epar-risk-management-plan-summary_en.pdf"},
    {"id":"48737","name":"Zimbus Breezhaler : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2020-09-02T16:16:00Z","last_updated_date":"2020-09-02T16:16:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/zimbus-breezhaler-epar-risk-management-plan-summary_en.pdf"},
    {"id":"48741","name":"Aybintio : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2020-09-02T17:24:00Z","last_updated_date":"2021-09-10T13:44:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/aybintio-epar-risk-management-plan-summary_en.pdf"},
    {"id":"48749","name":"Elocta : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2020-09-03T12:44:00Z","last_updated_date":"2020-09-03T12:44:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/elocta-epar-risk-management-plan-summary_en.pdf"},
    {"id":"48762","name":"Protopic : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2020-09-07T12:56:00Z","last_updated_date":"2020-09-07T12:56:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/protopic-epar-risk-management-plan-summary_en.pdf"},
    {"id":"48801","name":"Rozlytrek: EPAR - Risk management plan","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2023-05-15T15:14:00Z","last_updated_date":"2025-06-10T15:24:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/rozlytrek-epar-risk-management-plan_en.pdf"},
    {"id":"48816","name":"Pioglitazone Actavis : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2020-09-16T09:07:00Z","last_updated_date":"2020-09-16T09:07:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/pioglitazone-actavis-epar-risk-management-plan-summary_en.pdf"},
    {"id":"48889","name":"Cymbalta : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2020-09-25T09:25:00Z","last_updated_date":"2020-09-25T09:25:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/cymbalta-epar-risk-management-plan-summary_en.pdf"},
    {"id":"48925","name":"Siklos : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2020-10-01T10:59:00Z","last_updated_date":"2020-10-01T10:59:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/siklos-epar-risk-management-plan-summary_en.pdf"},
    {"id":"48935","name":"Fampridine Accord : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2020-10-02T11:23:00Z","last_updated_date":"2020-10-02T11:23:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/fampridine-accord-epar-risk-management-plan-summary_en.pdf"},
    {"id":"48960","name":"Zynrelef : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2020-10-06T18:00:00Z","last_updated_date":"2023-11-22T12:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/zynrelef-epar-risk-management-plan-summary_en.pdf"},
    {"id":"48989","name":"Equidacent : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2020-10-12T10:07:00Z","last_updated_date":"2021-11-25T16:49:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/equidacent-epar-risk-management-plan-summary_en.pdf"},
    {"id":"49001","name":"Rydapt - EPAR - Risk-management plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2020-10-12T16:04:00Z","last_updated_date":"2022-04-01T11:43:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/rydapt-epar-risk-management-plan-summary_en.pdf"},
    {"id":"49043","name":"Bortezomib Hospira : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2020-10-19T10:28:00Z","last_updated_date":"2026-04-15T11:40:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/bortezomib-hospira-epar-risk-management-plan-summary_en.pdf"},
    {"id":"49045","name":"Fortacin : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2020-10-19T01:00:00Z","last_updated_date":"2020-10-19T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/fortacin-epar-risk-management-plan-summary_en.pdf"},
    {"id":"49058","name":"Ratiograstim : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2020-10-19T17:08:00Z","last_updated_date":"2020-10-19T17:08:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/ratiograstim-epar-risk-management-plan-summary_en.pdf"},
    {"id":"49060","name":"Naglazyme : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2020-10-20T10:00:00Z","last_updated_date":"2022-04-26T10:16:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/naglazyme-epar-risk-management-plan-summary_en.pdf"},
    {"id":"49146","name":"Cabazitaxel Accord : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2020-10-28T15:09:00Z","last_updated_date":"2023-01-16T13:47:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/cabazitaxel-accord-epar-risk-management-plan-summary_en.pdf"},
    {"id":"49151","name":"Terrosa : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2020-10-28T02:00:00Z","last_updated_date":"2021-11-03T10:58:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/terrosa-epar-risk-management-plan-summary_en.pdf"},
    {"id":"49154","name":"Imraldi : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2020-10-29T10:36:00Z","last_updated_date":"2022-06-01T16:23:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/imraldi-epar-risk-management-plan-summary_en.pdf"},
    {"id":"49156","name":"Movymia : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2020-10-29T11:37:00Z","last_updated_date":"2021-11-03T16:14:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/movymia-epar-risk-management-plan-summary_en.pdf"},
    {"id":"49167","name":"NexoBrid : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2020-11-03T10:06:00Z","last_updated_date":"2024-01-09T16:52:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/nexobrid-epar-risk-management-plan-summary_en.pdf"},
    {"id":"49168","name":"Orfadin : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2020-11-03T10:48:00Z","last_updated_date":"2021-03-01T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/orfadin-epar-risk-management-plan-summary_en.pdf"},
    {"id":"49177","name":"Crysvita : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2020-11-04T16:22:00Z","last_updated_date":"2022-11-08T11:55:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/crysvita-epar-risk-management-plan-summary_en.pdf"},
    {"id":"49323","name":"Nyvepria : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2020-11-23T17:10:00Z","last_updated_date":"2020-11-23T17:10:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/nyvepria-epar-risk-management-plan-summary_en.pdf"},
    {"id":"49330","name":"Adakveo : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2020-11-24T11:26:00Z","last_updated_date":"2023-08-21T13:59:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/adakveo-epar-risk-management-plan-summary_en.pdf"},
    {"id":"49335","name":"Rivaroxaban Accord : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2020-11-24T12:07:00Z","last_updated_date":"2020-11-24T12:07:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/rivaroxaban-accord-epar-risk-management-plan-summary_en.pdf"},
    {"id":"49356","name":"Oxlumo : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2020-11-25T14:14:00Z","last_updated_date":"2022-10-13T09:37:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/oxlumo-epar-risk-management-plan-summary_en.pdf"},
    {"id":"49371","name":"Phelinun : EPAR - Risk-assessment-report summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2020-11-25T16:26:00Z","last_updated_date":"2020-11-25T16:26:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/phelinun-epar-risk-assessment-report-summary_en.pdf"},
    {"id":"49380","name":"NovoThirteen : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2020-11-26T17:31:00Z","last_updated_date":"2022-03-21T10:47:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/novothirteen-epar-risk-management-plan-summary_en.pdf"},
    {"id":"49394","name":"Obiltoxaximab SFL : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2020-11-27T11:55:00Z","last_updated_date":"2024-09-09T12:09:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/obiltoxaximab-sfl-epar-risk-management-plan-summary_en.pdf"},
    {"id":"49409","name":"Eklira Genuair : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2020-12-01T10:18:00Z","last_updated_date":"2020-12-01T10:18:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/eklira-genuair-epar-risk-management-plan-summary_en.pdf"},
    {"id":"49453","name":"Desloratadine ratiopharm : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2020-12-03T17:08:00Z","last_updated_date":"2020-12-03T17:08:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/desloratadine-ratiopharm-epar-risk-management-plan-summary_en.pdf"},
    {"id":"49528","name":"Exparel liposomal : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2020-12-10T17:17:00Z","last_updated_date":"2020-12-10T17:17:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/exparel-liposomal-epar-risk-management-plan-summary_en.pdf"},
    {"id":"49547","name":"Travatan : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2020-12-14T14:59:00Z","last_updated_date":"2020-12-14T14:59:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/travatan-epar-risk-management-plan-summary_en.pdf"},
    {"id":"49614","name":"Jevtana : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2020-12-17T16:30:00Z","last_updated_date":"2020-12-17T16:30:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/jevtana-epar-risk-management-plan-summary_en.pdf"},
    {"id":"49705","name":"Ontruzant : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2021-01-04T15:01:00Z","last_updated_date":"2022-07-26T15:40:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/ontruzant-epar-risk-management-plan-summary_en.pdf"},
    {"id":"49739","name":"Leqvio : EPAR - Risk management plan","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2021-01-06T15:20:00Z","last_updated_date":"2024-07-04T12:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/leqvio-epar-risk-management-plan_en.pdf"},
    {"id":"49749","name":"Lenalidomide Mylan : EPAR - Risk-management-plan","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2021-01-07T16:03:00Z","last_updated_date":"2026-05-11T14:25:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/lenalidomide-mylan-epar-risk-management-plan_en.pdf"},
    {"id":"49755","name":"Fintepla : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2021-01-08T10:51:00Z","last_updated_date":"2021-01-08T10:51:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/fintepla-epar-risk-management-plan-summary_en.pdf"},
    {"id":"49757","name":"Xyrem : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2021-01-08T10:54:00Z","last_updated_date":"2023-07-05T12:44:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/xyrem-epar-risk-management-plan-summary_en.pdf"},
    {"id":"49800","name":"Phesgo : EPAR - Risk-management-plan","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2021-01-13T15:36:00Z","last_updated_date":"2024-08-22T11:52:00Z","reference_number":"EMA/CHMP/646782/2020","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/phesgo-epar-risk-management-plan_en.pdf"},
    {"id":"49818","name":"Lyxumia : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2021-01-18T13:02:00Z","last_updated_date":"2026-02-05T12:42:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/lyxumia-epar-risk-management-plan-summary_en.pdf"},
    {"id":"49824","name":"Qutavina : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2021-01-18T15:00:00Z","last_updated_date":"2021-01-18T15:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/qutavina-epar-risk-management-plan-summary_en.pdf"},
    {"id":"49876","name":"Odefsey : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2021-01-21T12:52:00Z","last_updated_date":"2021-01-21T12:52:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/odefsey-epar-risk-management-plan-summary_en.pdf"},
    {"id":"49926","name":"Elzonris : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2021-01-25T10:25:00Z","last_updated_date":"2022-07-29T16:18:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/elzonris-epar-risk-management-plan-summary_en.pdf"},
    {"id":"49938","name":"Tecartus : EPAR - Risk management plan","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2021-01-25T16:02:00Z","last_updated_date":"2026-05-19T16:25:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/tecartus-epar-risk-management-plan_en.pdf"},
    {"id":"50018","name":"Tookad : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2021-02-01T11:46:00Z","last_updated_date":"2022-03-02T12:15:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/tookad-epar-risk-management-plan-summary_en.pdf"},
    {"id":"50026","name":"Nordimet : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2021-02-02T12:04:00Z","last_updated_date":"2023-10-27T13:34:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/nordimet-epar-risk-management-plan-summary_en.pdf"},
    {"id":"50042","name":"Ulipristal Acetate Gedeon Richter : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2021-02-03T11:27:00Z","last_updated_date":"2021-07-02T12:07:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/ulipristal-acetate-gedeon-richter-epar-risk-management-plan-summary_en.pdf"},
    {"id":"50070","name":"Idelvion : EPAR - Risk-mangement-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2021-02-04T17:49:00Z","last_updated_date":"2021-02-04T17:49:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/idelvion-epar-risk-mangement-plan-summary_en.pdf"},
    {"id":"50193","name":"Darunavir Mylan : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2021-02-16T16:14:00Z","last_updated_date":"2021-02-16T16:14:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/darunavir-mylan-epar-risk-management-plan-summary_en.pdf"},
    {"id":"50219","name":"Lenalidomide Krka d.d. : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2021-02-18T12:22:00Z","last_updated_date":"2023-07-10T15:16:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/lenalidomide-krka-dd-epar-risk-management-plan-summary_en.pdf"},
    {"id":"50224","name":"Lenalidomide Krka : EPAR - Risk management plan","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2021-02-18T13:06:00Z","last_updated_date":"2026-03-12T13:32:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/lenalidomide-krka-epar-risk-management-plan_en.pdf"},
    {"id":"50229","name":"Lenalidomide Krka d.d. Novo mesto : EPAR - Risk-management plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2021-02-18T14:27:00Z","last_updated_date":"2021-02-18T14:27:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/lenalidomide-krka-dd-novo-mesto-epar-risk-management-plan-summary_en.pdf"},
    {"id":"50263","name":"Rolufta Ellipta : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2021-02-24T15:31:00Z","last_updated_date":"2025-03-28T14:05:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/rolufta-ellipta-epar-risk-management-plan-summary_en.pdf"},
    {"id":"50300","name":"Pioglitazone Accord : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2021-02-26T16:32:00Z","last_updated_date":"2021-02-26T16:32:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/pioglitazone-accord-epar-risk-management-plan-summary_en.pdf"},
    {"id":"50366","name":"Glustin : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2021-03-02T16:08:00Z","last_updated_date":"2022-10-17T10:34:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/glustin-epar-risk-management-plan-summary_en.pdf"},
    {"id":"50368","name":"Tandemact : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2021-03-02T16:12:00Z","last_updated_date":"2021-03-02T16:12:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/tandemact-epar-risk-management-plan-summary_en.pdf"},
    {"id":"50386","name":"Actos : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2021-03-04T09:56:00Z","last_updated_date":"2021-03-04T09:56:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/actos-epar-risk-management-plan-summary_en.pdf"},
    {"id":"50387","name":"Competact : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2021-03-04T10:01:00Z","last_updated_date":"2021-03-04T10:01:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/competact-epar-risk-management-plan-summary_en.pdf"},
    {"id":"50388","name":"Glubrava : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2021-03-04T10:12:00Z","last_updated_date":"2022-10-18T15:54:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/glubrava-epar-risk-management-plan-summary_en.pdf"},
    {"id":"50472","name":"Onbevzi : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2021-03-05T16:48:00Z","last_updated_date":"2024-10-24T14:33:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/onbevzi-epar-risk-management-plan-summary_en.pdf"},
    {"id":"50494","name":"Lumoxiti : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2021-03-09T09:17:00Z","last_updated_date":"2021-08-11T16:39:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/lumoxiti-epar-risk-management-plan-summary_en.pdf"},
    {"id":"50582","name":"Kixelle : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2021-03-16T14:19:00Z","last_updated_date":"2021-03-16T14:19:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/kixelle-epar-risk-management-plan-summary_en.pdf"},
    {"id":"50635","name":"Keppra : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2021-03-18T09:23:00Z","last_updated_date":"2025-01-06T12:55:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/keppra-epar-risk-management-plan-summary_en.pdf"},
    {"id":"50638","name":"Forsteo : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2021-03-18T12:13:00Z","last_updated_date":"2021-03-18T12:13:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/forsteo-epar-risk-management-plan-summary_en.pdf"},
    {"id":"50663","name":"Komboglyze : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2021-03-22T11:37:00Z","last_updated_date":"2022-09-22T11:12:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/komboglyze-epar-risk-management-plan-summary_en.pdf"},
    {"id":"50752","name":"Alli : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2021-03-31T15:27:00Z","last_updated_date":"2021-03-31T15:27:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/alli-epar-risk-management-plan-summary_en.pdf"},
    {"id":"50768","name":"Sunitinib Accord : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2021-04-06T17:37:00Z","last_updated_date":"2021-04-06T17:37:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/sunitinib-accord-epar-risk-management-plan-summary_en.pdf"},
    {"id":"50783","name":"Coagadex : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2021-04-09T11:26:00Z","last_updated_date":"2021-04-09T11:26:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/coagadex-epar-risk-management-plan-summary_en.pdf"},
    {"id":"50811","name":"Seffalair Spiromax : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2021-04-13T16:35:00Z","last_updated_date":"2021-04-13T16:35:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/seffalair-spiromax-epar-risk-management-plan-summary_en.pdf"},
    {"id":"50821","name":"BroPair Spiromax : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2021-04-14T11:19:00Z","last_updated_date":"2025-06-30T16:08:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/bropair-spiromax-epar-risk-management-plan-summary_en.pdf"},
    {"id":"50840","name":"Vazkepa : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2021-04-14T17:13:00Z","last_updated_date":"2021-04-14T17:13:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/vazkepa-epar-risk-management-plan-summary_en.pdf"},
    {"id":"50862","name":"Sogroya : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2021-04-15T14:16:00Z","last_updated_date":"2023-07-31T10:59:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/sogroya-epar-risk-management-plan-summary_en.pdf"},
    {"id":"50868","name":"Oyavas : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2021-04-15T15:09:00Z","last_updated_date":"2021-04-15T15:09:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/oyavas-epar-risk-management-plan-summary_en.pdf"},
    {"id":"50897","name":"Onglyza : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2021-04-16T17:51:00Z","last_updated_date":"2022-09-22T11:49:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/onglyza-epar-risk-management-plan-summary_en.pdf"},
    {"id":"50909","name":"Lonquex : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2021-04-19T17:00:00Z","last_updated_date":"2022-08-02T14:07:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/lonquex-epar-risk-management-plan-summary_en.pdf"},
    {"id":"50922","name":"Byfavo : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2021-04-20T17:31:00Z","last_updated_date":"2023-04-18T09:34:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/byfavo-epar-risk-management-plan-summary_en.pdf"},
    {"id":"50984","name":"Alymsys : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2021-04-26T10:21:00Z","last_updated_date":"2021-04-26T10:21:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/alymsys-epar-risk-management-plan-summary_en.pdf"},
    {"id":"50990","name":"Bronchitol : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2021-04-26T15:36:00Z","last_updated_date":"2021-04-26T15:36:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/bronchitol-epar-risk-management-plan-summary_en.pdf"},
    {"id":"51023","name":"Thiotepa Riemser : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2021-04-30T11:30:00Z","last_updated_date":"2021-04-30T11:30:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/thiotepa-riemser-epar-risk-management-plan-summary_en.pdf"},
    {"id":"51035","name":"Sibnayal : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2021-05-03T09:31:00Z","last_updated_date":"2021-05-03T09:31:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/sibnayal-epar-risk-management-plan-summary_en.pdf"},
    {"id":"51052","name":"Pemazyre : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2021-05-04T09:11:00Z","last_updated_date":"2021-05-04T09:11:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/pemazyre-epar-risk-management-plan-summary_en.pdf"},
    {"id":"51251","name":"Mvasi : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2021-05-21T17:15:00Z","last_updated_date":"2021-05-21T17:15:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/mvasi-epar-risk-management-plan-summary_en.pdf"},
    {"id":"51282","name":"Nexpovio : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2021-05-27T14:37:00Z","last_updated_date":"2022-08-09T15:40:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/nexpovio-epar-risk-management-plan-summary_en.pdf"},
    {"id":"51300","name":"Orladeyo : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2021-06-01T10:42:00Z","last_updated_date":"2024-08-01T17:24:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/orladeyo-epar-risk-management-plan-summary_en.pdf"},
    {"id":"51309","name":"Copiktra : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2021-05-31T14:11:00Z","last_updated_date":"2026-04-09T11:12:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/copiktra-epar-risk-management-plan-summary_en.pdf"},
    {"id":"51311","name":"Adasuve : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2021-05-31T17:36:00Z","last_updated_date":"2021-05-31T17:36:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/adasuve-epar-risk-management-plan-summary_en.pdf"},
    {"id":"51333","name":"Lydisilka : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2021-06-02T11:00:00Z","last_updated_date":"2021-06-02T11:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/lydisilka-epar-risk-management-plan-summary_en.pdf"},
    {"id":"51338","name":"Drovelis : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2021-06-02T11:00:00Z","last_updated_date":"2023-03-14T08:50:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/drovelis-epar-risk-management-plan-summary_en.pdf"},
    {"id":"51341","name":"Lenalidomide Accord : EPAR - Risk management plan","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2021-06-02T13:33:00Z","last_updated_date":"2026-02-24T14:30:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/lenalidomide-accord-epar-risk-management-plan_en.pdf"},
    {"id":"51358","name":"RotaTeq : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2021-06-04T09:00:00Z","last_updated_date":"2021-06-04T09:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/rotateq-epar-risk-management-plan-summary_en.pdf"},
    {"id":"51431","name":"Efmody : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2021-06-14T13:52:00Z","last_updated_date":"2021-06-14T13:52:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/efmody-epar-risk-management-plan-summary_en.pdf"},
    {"id":"51441","name":"Diacomit : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2021-06-15T16:30:00Z","last_updated_date":"2021-06-15T16:30:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/diacomit-epar-risk-management-plan-summary_en.pdf"},
    {"id":"51446","name":"Vimizim : EPAR - EMEA/H/C/002779 - Risk management plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2021-06-16T08:44:00Z","last_updated_date":"2021-06-16T08:44:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/vimizim-epar-emeahc002779-risk-management-plan-summary_en.pdf"},
    {"id":"51522","name":"Aerius : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2021-06-21T18:01:00Z","last_updated_date":"2021-06-21T18:01:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/aerius-epar-risk-management-plan-summary_en.pdf"},
    {"id":"51543","name":"Neoclarityn : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2021-06-22T13:45:00Z","last_updated_date":"2021-06-22T13:45:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/neoclarityn-epar-risk-management-plan-summary_en.pdf"},
    {"id":"51547","name":"Azomyr : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2021-06-22T16:41:00Z","last_updated_date":"2021-06-22T16:41:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/azomyr-epar-risk-management-plan-summary_en.pdf"},
    {"id":"51553","name":"Jayempi : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2021-06-23T10:47:00Z","last_updated_date":"2024-02-12T17:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/jayempi-epar-risk-management-plan-summary_en.pdf"},
    {"id":"51650","name":"Onureg : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2021-06-28T14:23:00Z","last_updated_date":"2021-06-28T14:23:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/onureg-epar-risk-management-plan-summary_en.pdf"},
    {"id":"51668","name":"Zevalin : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2021-06-29T17:06:00Z","last_updated_date":"2021-06-29T17:06:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/zevalin-epar-risk-management-plan-summary_en.pdf"},
    {"id":"51671","name":"Enspryng : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2021-06-30T10:00:00Z","last_updated_date":"2021-06-30T10:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/enspryng-epar-risk-management-plan-summary_en.pdf"},
    {"id":"51733","name":"Bretaris Genuair : EPAR - Risk management plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2021-07-02T08:19:00Z","last_updated_date":"2021-07-02T08:21:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/bretaris-genuair-epar-risk-management-plan-summary_en.pdf"},
    {"id":"51734","name":"Celsunax : EPAR - Risk management plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2021-07-02T09:29:00Z","last_updated_date":"2021-07-02T09:29:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/celsunax-epar-risk-management-plan-summary_en.pdf"},
    {"id":"51986","name":"Klisyri  : EPAR - Risk management plan","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2021-07-21T11:20:00Z","last_updated_date":"2025-08-26T16:02:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/klisyri-epar-risk-management-plan_en.pdf"},
    {"id":"52094","name":"Verquvo : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2021-07-27T10:45:00Z","last_updated_date":"2021-07-27T10:45:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/verquvo-epar-risk-management-plan-summary_en.pdf"},
    {"id":"52104","name":"Skysona : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2021-07-27T15:42:00Z","last_updated_date":"2022-04-04T12:50:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/skysona-epar-risk-management-plan-summary_en.pdf"},
    {"id":"52108","name":"Herceptin : EPAR - Risk management plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2021-07-28T09:11:00Z","last_updated_date":"2021-09-10T11:37:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/herceptin-epar-risk-management-plan-summary_en.pdf"},
    {"id":"52121","name":"Orphacol : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2021-07-28T11:23:00Z","last_updated_date":"2021-07-28T11:23:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/orphacol-epar-risk-management-plan-summary_en.pdf"},
    {"id":"52139","name":"Ryeqo : EPAR - Risk management plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2021-07-29T09:23:00Z","last_updated_date":"2021-07-29T09:23:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/ryeqo-epar-risk-management-plan-summary_en.pdf"},
    {"id":"52193","name":"Lemtrada : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2021-08-04T13:12:00Z","last_updated_date":"2022-07-19T09:52:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/lemtrada-epar-risk-management-plan-summary_en.pdf"},
    {"id":"52228","name":"Isentress : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2021-08-17T09:17:00Z","last_updated_date":"2021-08-17T09:17:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/isentress-epar-risk-management-plan-summary_en.pdf"},
    {"id":"52235","name":"Vemlidy : EPAR - Risk management plan","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2021-08-18T16:32:00Z","last_updated_date":"2024-09-17T16:40:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/vemlidy-epar-risk-management-plan_en.pdf"},
    {"id":"52266","name":"Evrenzo : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2021-08-24T17:03:00Z","last_updated_date":"2021-08-24T17:03:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/evrenzo-epar-risk-management-plan-summary_en.pdf"},
    {"id":"52280","name":"Abiraterone Mylan : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2021-08-26T09:15:00Z","last_updated_date":"2021-08-26T09:15:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/abiraterone-mylan-epar-risk-management-plan-summary_en.pdf"},
    {"id":"52289","name":"Abevmy : EPAR - Risk management plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2021-08-27T10:29:00Z","last_updated_date":"2021-08-27T10:29:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/abevmy-epar-risk-management-plan-summary_en.pdf"},
    {"id":"52349","name":"Icatibant Accord : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2021-09-06T15:45:00Z","last_updated_date":"2026-03-20T10:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/icatibant-accord-epar-risk-management-plan-summary_en.pdf"},
    {"id":"52403","name":"Voxzogo : EPAR - Risk management plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2021-09-09T15:44:00Z","last_updated_date":"2025-03-20T09:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/voxzogo-epar-risk-management-plan-summary_en.pdf"},
    {"id":"52439","name":"Peyona : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2021-09-14T12:35:00Z","last_updated_date":"2021-09-14T12:35:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/peyona-epar-risk-management-plan-summary_en.pdf"},
    {"id":"52450","name":"Revatio : EPAR - Risk management plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2021-09-15T12:31:00Z","last_updated_date":"2021-09-15T12:31:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/revatio-epar-risk-management-plan-summary_en.pdf"},
    {"id":"52580","name":"Cystadene : EPAR - Risk management plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2021-09-23T12:43:00Z","last_updated_date":"2021-09-23T12:43:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/cystadene-epar-risk-management-plan-summary_en.pdf"},
    {"id":"52651","name":"Ranexa : EPAR - Risk management plan","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2021-09-28T11:28:00Z","last_updated_date":"2024-04-10T13:28:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/ranexa-epar-risk-management-plan_en.pdf"},
    {"id":"52704","name":"Imatinib Koanaa : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2021-10-01T15:42:00Z","last_updated_date":"2023-10-19T10:41:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/imatinib-koanaa-epar-risk-management-plan-summary_en.pdf"},
    {"id":"52826","name":"Koselugo : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2021-10-13T10:51:00Z","last_updated_date":"2021-10-13T10:51:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/koselugo-epar-risk-management-plan-summary_en.pdf"},
    {"id":"52846","name":"Ozawade : EPAR - Risk management plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2021-10-14T13:34:00Z","last_updated_date":"2021-10-14T13:34:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/ozawade-epar-risk-management-plan-summary_en.pdf"},
    {"id":"52878","name":"Inductos : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2021-10-18T12:48:00Z","last_updated_date":"2021-10-18T12:48:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/inductos-epar-risk-management-plan-summary_en.pdf"},
    {"id":"52879","name":"Inductos : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2021-10-18T12:48:00Z","last_updated_date":"2021-10-18T12:48:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/inductos-epar-risk-management-plan-summary_en.pdf-0"},
    {"id":"52880","name":"Inductos : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2021-10-18T12:48:00Z","last_updated_date":"2021-10-18T12:48:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/inductos-epar-risk-management-plan-summary_en.pdf-1"},
    {"id":"52894","name":"GONAL-f : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2021-10-25T10:03:00Z","last_updated_date":"2021-10-25T10:03:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/gonal-f-epar-risk-management-plan-summary_en.pdf"},
    {"id":"52913","name":"Fotivda : EPAR - Risk management plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2021-10-27T10:29:00Z","last_updated_date":"2021-10-27T10:29:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/fotivda-epar-risk-management-plan-summary_en.pdf"},
    {"id":"53047","name":"Bexsero : EPAR - Risk management plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2021-11-10T10:30:00Z","last_updated_date":"2021-11-10T10:30:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/bexsero-epar-risk-management-plan-summary_en.pdf"},
    {"id":"53141","name":"Azarga : EPAR - Risk management plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2021-11-17T10:18:00Z","last_updated_date":"2021-11-17T10:18:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/azarga-epar-risk-management-plan-summary_en.pdf"},
    {"id":"53142","name":"Ocaliva : EPAR - Risk management plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2021-11-17T13:19:00Z","last_updated_date":"2025-01-20T17:13:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/ocaliva-epar-risk-management-plan-summary_en.pdf"},
    {"id":"53200","name":"Sugammadex Mylan : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2021-11-22T15:20:00Z","last_updated_date":"2021-11-22T15:20:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/sugammadex-mylan-epar-risk-management-plan-summary_en.pdf"},
    {"id":"53226","name":"Qinlock : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2021-11-23T10:08:00Z","last_updated_date":"2023-08-30T11:49:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/qinlock-epar-risk-management-plan-summary_en.pdf"},
    {"id":"53244","name":"Abiraterone Krka : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2021-11-23T13:44:00Z","last_updated_date":"2021-11-23T13:44:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/abiraterone-krka-epar-risk-management-plan-summary_en.pdf"},
    {"id":"53265","name":"Hycamtin : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2021-11-24T15:48:00Z","last_updated_date":"2021-11-24T15:48:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/hycamtin-epar-risk-management-plan-summary_en.pdf"},
    {"id":"53285","name":"Steglujan : EPAR - Risk management plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2021-11-26T08:42:00Z","last_updated_date":"2021-11-26T08:42:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/steglujan-epar-risk-management-plan-summary_en.pdf"},
    {"id":"53339","name":"Lojuxta : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2021-11-30T14:27:00Z","last_updated_date":"2022-03-22T15:27:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/lojuxta-epar-risk-management-plan-summary_en.pdf"},
    {"id":"53598","name":"Procoralan : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2021-12-17T01:00:00Z","last_updated_date":"2023-12-21T16:13:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/procoralan-epar-risk-management-plan-summary_en.pdf"},
    {"id":"53599","name":"Corlentor : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2021-12-17T01:00:00Z","last_updated_date":"2023-12-21T15:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/corlentor-epar-risk-management-plan-summary_en.pdf"},
    {"id":"53622","name":"Artesunate Amivas : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2022-01-04T09:17:00Z","last_updated_date":"2022-01-04T09:17:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/artesunate-amivas-epar-risk-management-plan-summary_en.pdf"},
    {"id":"53629","name":"Inhixa : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2022-01-04T10:54:00Z","last_updated_date":"2022-01-04T10:54:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/inhixa-epar-risk-management-plan-summary_en.pdf"},
    {"id":"53634","name":"Vihuma : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2022-01-05T10:59:00Z","last_updated_date":"2022-01-05T10:59:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/vihuma-epar-risk-management-plan-summary_en.pdf"},
    {"id":"53709","name":"Hizentra : EPAR - Risk management plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2022-01-13T13:57:00Z","last_updated_date":"2022-01-13T13:57:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/hizentra-epar-risk-management-plan-summary_en.pdf"},
    {"id":"53744","name":"Sitagliptin SUN : EPAR - Risk management plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2022-01-17T09:47:00Z","last_updated_date":"2022-01-17T09:47:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/sitagliptin-sun-epar-risk-management-plan-summary_en.pdf"},
    {"id":"53774","name":"Vaxneuvance : EPAR - Risk management plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2022-01-17T17:34:00Z","last_updated_date":"2023-05-12T08:06:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/vaxneuvance-epar-risk-management-plan-summary_en.pdf"},
    {"id":"53794","name":"Libmyris : EPAR - Risk management plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2022-01-18T09:47:00Z","last_updated_date":"2022-01-18T09:47:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/libmyris-epar-risk-management-plan-summary_en.pdf"},
    {"id":"53804","name":"Trydonis : EPAR - Risk management plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2022-01-18T11:30:00Z","last_updated_date":"2024-01-25T18:15:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/trydonis-epar-risk-management-plan-summary_en.pdf"},
    {"id":"53842","name":"Voraxaze : EPAR - Risk management plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2022-01-20T09:33:00Z","last_updated_date":"2022-01-20T09:33:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/voraxaze-epar-risk-management-plan-summary_en.pdf"},
    {"id":"53900","name":"Ledaga : EPAR - Risk management plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2022-01-24T16:59:00Z","last_updated_date":"2022-01-24T16:59:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/ledaga-epar-risk-management-plan-summary_en.pdf"},
    {"id":"53921","name":"Dengvaxia : EPAR - Risk management plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2022-01-26T15:14:00Z","last_updated_date":"2025-12-04T15:01:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/dengvaxia-epar-risk-management-plan-summary_en.pdf"},
    {"id":"54045","name":"Rybrevant : EPAR - Risk management plan","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2022-02-01T16:03:00Z","last_updated_date":"2025-06-12T12:02:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/rybrevant-epar-risk-management-plan_en.pdf"},
    {"id":"54066","name":"Riltrava Aerosphere : EPAR - Risk management plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2022-02-04T09:07:00Z","last_updated_date":"2022-02-04T09:07:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/riltrava-aerosphere-epar-risk-management-plan-summary_en.pdf"},
    {"id":"54071","name":"Lonapegsomatropin Ascendis Pharma : EPAR - Risk management plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2022-02-04T12:29:00Z","last_updated_date":"2022-02-04T12:29:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/lonapegsomatropin-ascendis-pharma-epar-risk-management-plan-summary_en.pdf"},
    {"id":"54118","name":"Zepatier : EPAR - Risk management plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2022-02-09T11:47:00Z","last_updated_date":"2022-02-09T11:47:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/zepatier-epar-risk-management-plan-summary_en.pdf"},
    {"id":"54168","name":"Vyepti : EPAR - Risk management plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2022-02-15T11:18:00Z","last_updated_date":"2022-02-15T11:18:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/vyepti-epar-risk-management-plan-summary_en.pdf"},
    {"id":"54197","name":"Segluromet : EPAR - Risk management plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2022-02-16T16:46:00Z","last_updated_date":"2022-02-16T16:46:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/segluromet-epar-risk-management-plan-summary_en.pdf"},
    {"id":"54201","name":"Steglatro : EPAR - Risk management plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2022-02-16T17:22:00Z","last_updated_date":"2022-02-16T17:22:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/steglatro-epar-risk-management-plan-summary_en.pdf"},
    {"id":"54315","name":"Okedi : EPAR - Risk management plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2022-03-01T15:10:00Z","last_updated_date":"2022-03-01T15:10:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/okedi-epar-risk-management-plan-summary_en.pdf"},
    {"id":"54327","name":"Yargesa : EPAR - Risk management plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2022-03-02T15:10:00Z","last_updated_date":"2022-03-02T15:10:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/yargesa-epar-risk-management-plan-summary_en.pdf"},
    {"id":"54339","name":"Ngenla : EPAR - Risk management plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2022-03-02T17:18:00Z","last_updated_date":"2022-03-02T17:18:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/ngenla-epar-risk-management-plan-summary_en.pdf"},
    {"id":"54359","name":"Ontilyv : EPAR - Risk management plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2022-03-07T10:28:00Z","last_updated_date":"2025-03-28T15:45:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/ontilyv-epar-risk-management-plan-summary_en.pdf"},
    {"id":"54393","name":"Sitagliptin / Metformin hydrochloride Mylan : EPAR - Risk management plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2022-03-08T12:39:00Z","last_updated_date":"2022-03-08T12:39:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/sitagliptin-metformin-hydrochloride-mylan-epar-risk-management-plan-summary_en.pdf"},
    {"id":"54397","name":"Skilarence : EPAR - Risk management plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2022-03-08T16:01:00Z","last_updated_date":"2022-03-08T16:01:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/skilarence-epar-risk-management-plan-summary_en.pdf"},
    {"id":"54414","name":"Wegovy : EPAR - Risk management plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2022-03-10T17:17:00Z","last_updated_date":"2023-06-09T14:47:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/wegovy-epar-risk-management-plan-summary_en.pdf"},
    {"id":"54416","name":"Ninlaro : EPAR - Risk management plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2022-03-11T09:14:00Z","last_updated_date":"2023-11-21T10:34:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/ninlaro-epar-risk-management-plan-summary_en.pdf"},
    {"id":"54504","name":"Oxbryta : EPAR - Risk management plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2022-03-17T13:43:00Z","last_updated_date":"2022-03-17T13:43:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/oxbryta-epar-risk-management-plan-summary_en.pdf"},
    {"id":"54544","name":"Reagila : EPAR - Risk management plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2022-03-22T15:18:00Z","last_updated_date":"2022-04-26T13:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/reagila-epar-risk-management-plan-summary_en.pdf"},
    {"id":"54549","name":"Nitisinone MDK : EPAR - Risk management plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2022-03-24T10:11:00Z","last_updated_date":"2023-06-14T14:57:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/nitisinone-mdk-epar-risk-management-plan-summary_en.pdf"},
    {"id":"54603","name":"Symtuza : EPAR - Risk management plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2022-03-28T17:26:00Z","last_updated_date":"2022-09-14T17:16:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/symtuza-epar-risk-management-plan-summary_en.pdf"},
    {"id":"54616","name":"Dasatinib Accordpharma : EPAR - Risk management plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2022-03-30T10:02:00Z","last_updated_date":"2023-03-30T11:52:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/dasatinib-accordpharma-epar-risk-management-plan-summary_en.pdf"},
    {"id":"54621","name":"Dasatinib Accord : EPAR - Risk management plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2022-03-30T10:29:00Z","last_updated_date":"2023-03-30T11:17:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/dasatinib-accord-epar-risk-management-plan-summary_en.pdf"},
    {"id":"54657","name":"Stimufend : EPAR - Risk management plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2022-04-04T10:03:00Z","last_updated_date":"2022-04-04T10:03:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/stimufend-epar-risk-management-plan-summary_en.pdf"},
    {"id":"54662","name":"Oxervate : EPAR - Risk management plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2022-04-04T11:20:00Z","last_updated_date":"2022-04-04T11:20:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/oxervate-epar-risk-management-plan-summary_en.pdf"},
    {"id":"54677","name":"Tresiba : EPAR - Risk management plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2022-04-05T11:34:00Z","last_updated_date":"2022-04-05T11:34:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/tresiba-epar-risk-management-plan-summary_en.pdf"},
    {"id":"54691","name":"Insulin lispro Sanofi : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2022-04-07T15:18:00Z","last_updated_date":"2022-04-07T15:18:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/insulin-lispro-sanofi-epar-risk-management-plan-summary_en.pdf"},
    {"id":"54803","name":"Kimmtrak : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2022-04-22T17:06:00Z","last_updated_date":"2022-04-22T17:06:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/kimmtrak-epar-risk-management-plan-summary_en.pdf"},
    {"id":"54834","name":"Cervarix : EPAR - Risk management plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2022-04-26T16:01:00Z","last_updated_date":"2023-05-23T12:06:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/cervarix-epar-risk-management-plan-summary_en.pdf"},
    {"id":"54887","name":"Quviviq : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2022-05-03T16:51:00Z","last_updated_date":"2022-05-03T16:51:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/quviviq-epar-risk-management-plan-summary_en.pdf"},
    {"id":"54898","name":"Tepmetko : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2022-05-05T09:15:00Z","last_updated_date":"2022-05-05T09:15:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/tepmetko-epar-risk-management-plan-summary_en.pdf"},
    {"id":"54900","name":"Pregabalin Zentiva k.s. : EPAR - Risk management plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2022-05-05T10:00:00Z","last_updated_date":"2023-03-20T12:18:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/pregabalin-zentiva-ks-epar-risk-management-plan-summary_en.pdf"},
    {"id":"54916","name":"Advagraf : EPAR - Risk-management-plan","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2022-05-06T15:21:00Z","last_updated_date":"2024-11-05T10:34:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/advagraf-epar-risk-management-plan_en.pdf"},
    {"id":"54924","name":"Orgovyx : EPAR - Risk management plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2022-05-10T11:48:00Z","last_updated_date":"2022-06-10T12:28:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/orgovyx-epar-risk-management-plan-summary_en.pdf"},
    {"id":"54929","name":"Kyntheum : EPAR - Risk management plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2022-05-10T15:50:00Z","last_updated_date":"2022-05-10T15:50:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/kyntheum-epar-risk-management-plan-summary_en.pdf"},
    {"id":"54948","name":"Vydura : EPAR - Risk management plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2022-05-11T16:10:00Z","last_updated_date":"2022-05-11T16:10:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/vydura-epar-risk-management-plan-summary_en.pdf"},
    {"id":"54990","name":"PreHevbri : EPAR - Risk management plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2022-05-18T15:34:00Z","last_updated_date":"2025-01-10T17:14:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/prehevbri-epar-risk-management-plan-summary_en.pdf"},
    {"id":"55068","name":"Dimethyl fumarate Mylan : EPAR - Risk management plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2023-12-22T10:44:00Z","last_updated_date":"2023-12-22T10:44:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/dimethyl-fumarate-mylan-epar-risk-management-plan-summary_en.pdf"},
    {"id":"55073","name":"Dimethyl fumarate Neuraxpharm  : EPAR - Risk management plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2022-05-24T11:21:00Z","last_updated_date":"2023-12-22T14:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/dimethyl-fumarate-neuraxpharm-epar-risk-management-plan-summary_en.pdf"},
    {"id":"55078","name":"Dimethyl fumarate Polpharma : EPAR - Risk management plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2023-12-22T11:56:00Z","last_updated_date":"2023-12-22T11:56:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/dimethyl-fumarate-polpharma-epar-risk-management-plan-summary_en.pdf"},
    {"id":"55085","name":"Amifampridine Serb : EPAR - Risk management plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2022-05-24T15:19:00Z","last_updated_date":"2022-05-24T15:19:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/amifampridine-serb-epar-risk-management-plan-summary_en.pdf"},
    {"id":"55120","name":"Efficib : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2022-05-31T14:05:00Z","last_updated_date":"2022-05-31T14:05:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/efficib-epar-risk-management-plan-summary_en.pdf"},
    {"id":"55245","name":"Truvelog Mix 30 : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2022-06-15T09:33:00Z","last_updated_date":"2026-05-07T12:42:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/truvelog-mix-30-epar-risk-management-plan-summary_en.pdf"},
    {"id":"55263","name":"Sondelbay : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2022-06-16T14:41:00Z","last_updated_date":"2022-06-16T14:41:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/sondelbay-epar-risk-management-plan-summary_en.pdf"},
    {"id":"55278","name":"Vildagliptin / Metformin hydrochloride Accord : EPAR - Risk management plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2022-06-17T12:17:00Z","last_updated_date":"2022-06-17T12:17:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/vildagliptin-metformin-hydrochloride-accord-epar-risk-management-plan-summary_en.pdf"},
    {"id":"55305","name":"Zolsketil pegylated liposomal : EPAR - Risk management plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2022-06-20T16:22:00Z","last_updated_date":"2022-06-20T16:22:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/zolsketil-pegylated-liposomal-epar-risk-management-plan-summary_en.pdf"},
    {"id":"55331","name":"Lunsumio : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2022-06-23T13:50:00Z","last_updated_date":"2022-06-23T13:50:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/lunsumio-epar-risk-management-plan-summary_en.pdf"},
    {"id":"55400","name":"Pirfenidone AET : EPAR - Risk management plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2022-06-28T16:46:00Z","last_updated_date":"2022-06-28T16:46:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/pirfenidone-aet-epar-risk-management-plan-summary_en.pdf"},
    {"id":"55418","name":"Inpremzia : EPAR - Risk management plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2022-06-30T12:27:00Z","last_updated_date":"2023-04-20T12:16:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/inpremzia-epar-risk-management-plan-summary_en.pdf"},
    {"id":"55419","name":"Tesavel : EPAR - Risk management plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2022-06-30T13:41:00Z","last_updated_date":"2022-06-30T13:41:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/tesavel-epar-risk-management-plan-summary_en.pdf"},
    {"id":"55420","name":"Velmetia : EPAR - Risk management plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2022-06-30T13:51:00Z","last_updated_date":"2022-06-30T13:51:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/velmetia-epar-risk-management-plan-summary_en.pdf"},
    {"id":"55425","name":"Januvia : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2022-06-30T15:52:00Z","last_updated_date":"2022-06-30T15:52:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/januvia-epar-risk-management-plan-summary_en.pdf"},
    {"id":"55426","name":"Xelevia : EPAR - Risk management plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2022-06-30T17:12:00Z","last_updated_date":"2022-06-30T17:12:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/xelevia-epar-risk-management-plan-summary_en.pdf"},
    {"id":"55427","name":"Ristaben : EPAR - Risk management plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2022-07-01T10:27:00Z","last_updated_date":"2022-07-01T10:27:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/ristaben-epar-risk-management-plan-summary_en.pdf"},
    {"id":"55433","name":"Ristfor : EPAR - Risk management plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2022-07-01T12:10:00Z","last_updated_date":"2022-07-01T12:10:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/ristfor-epar-risk-management-plan-summary_en.pdf"},
    {"id":"55460","name":"Elonva : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2022-07-05T13:58:00Z","last_updated_date":"2022-07-05T13:58:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/elonva-epar-risk-management-plan-summary_en.pdf"},
    {"id":"55466","name":"Sitagliptin Accord : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2022-07-05T16:27:00Z","last_updated_date":"2022-07-05T16:27:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/sitagliptin-accord-epar-risk-management-plan-summary_en.pdf"},
    {"id":"55569","name":"Kinpeygo : EPAR - Risk management plan","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2022-07-18T10:11:00Z","last_updated_date":"2024-11-06T11:10:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/kinpeygo-epar-risk-management-plan_en.pdf"},
    {"id":"55603","name":"Ganirelix Gedeon Richter : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2022-07-20T11:08:00Z","last_updated_date":"2022-07-20T11:08:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/ganirelix-gedeon-richter-epar-risk-management-plan-summary_en.pdf"},
    {"id":"55628","name":"Mylotarg : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2022-07-21T16:11:00Z","last_updated_date":"2022-07-21T16:11:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/mylotarg-epar-risk-management-plan-summary_en.pdf"},
    {"id":"55727","name":"Amversio : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2022-07-28T15:47:00Z","last_updated_date":"2022-07-28T15:48:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/amversio-epar-risk-management-plan-summary_en.pdf"},
    {"id":"55735","name":"Entecavir Mylan : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2022-07-29T15:27:00Z","last_updated_date":"2022-07-29T15:27:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/entecavir-mylan-epar-risk-management-plan-summary_en.pdf"},
    {"id":"55742","name":"Bydureon : EPAR - Risk management plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2022-08-01T11:00:00Z","last_updated_date":"2023-05-22T16:46:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/bydureon-epar-risk-management-plan-summary_en.pdf"},
    {"id":"55753","name":"Zokinvy : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2022-08-01T16:14:00Z","last_updated_date":"2022-08-01T16:14:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/zokinvy-epar-risk-management-plan-summary_en.pdf"},
    {"id":"55777","name":"Sitagliptin / Metformin hydrochloride Accord : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2022-08-03T16:14:00Z","last_updated_date":"2025-11-13T09:44:44Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/sitagliptin-metformin-hydrochloride-accord-epar-risk-management-plan-summary_en.pdf"},
    {"id":"55803","name":"Upstaza : EPAR - Risk management plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2022-08-09T11:10:00Z","last_updated_date":"2022-08-09T11:10:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/upstaza-epar-risk-management-plan-summary_en.pdf"},
    {"id":"55845","name":"Posaconazole AHCL : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2022-08-19T13:44:00Z","last_updated_date":"2022-08-19T13:44:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/posaconazole-ahcl-epar-risk-management-plan-summary_en.pdf"},
    {"id":"55847","name":"Tacforius : EPAR - Risk management plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2022-08-19T14:11:00Z","last_updated_date":"2022-08-19T14:11:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/tacforius-epar-risk-management-plan-summary_en.pdf"},
    {"id":"55852","name":"Palforzia : EPAR - Risk management plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2022-08-22T11:37:00Z","last_updated_date":"2022-08-22T11:37:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/palforzia-epar-risk-management-plan-summary_en.pdf-0"},
    {"id":"56017","name":"Vegzelma : EPAR - Risk Management Plan Summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2022-09-07T15:41:00Z","last_updated_date":"2022-09-07T15:41:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/vegzelma-epar-risk-management-plan-summary_en.pdf"},
    {"id":"56019","name":"Tepadina : EPAR - Risk management plan","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2022-09-07T15:52:00Z","last_updated_date":"2024-04-09T13:09:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/tepadina-epar-risk-management-plan_en.pdf"},
    {"id":"56136","name":"Tenofovir disoproxil Mylan : EPAR - Risk management plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2022-09-20T08:24:00Z","last_updated_date":"2022-09-20T08:24:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/tenofovir-disoproxil-mylan-epar-risk-management-plan-summary_en.pdf"},
    {"id":"56151","name":"Tabrecta : EPAR - Risk management plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2022-09-21T10:34:00Z","last_updated_date":"2022-09-21T10:34:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/tabrecta-epar-risk-management-plan-summary_en.pdf"},
    {"id":"56274","name":"Ertapenem SUN : EPAR - Risk Management Plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2022-09-30T16:58:00Z","last_updated_date":"2022-09-30T16:58:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/ertapenem-sun-epar-risk-management-plan-summary_en.pdf"},
    {"id":"56289","name":"Rayvow : EPAR - Risk management plan","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2022-10-03T14:48:00Z","last_updated_date":"2024-10-28T16:24:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/rayvow-epar-risk-management-plan_en.pdf"},
    {"id":"56374","name":"Cancidas : EPAR - Risk Management Plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2022-10-12T15:50:00Z","last_updated_date":"2022-10-12T15:50:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/cancidas-epar-risk-management-plan-summary_en.pdf"},
    {"id":"56544","name":"PecFent : EPAR - Risk management plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2022-11-08T09:33:00Z","last_updated_date":"2022-11-08T09:33:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/pecfent-epar-risk-management-plan-summary_en.pdf"},
    {"id":"56596","name":"Effentora : EPAR - Risk management plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2022-11-11T11:03:00Z","last_updated_date":"2022-11-11T11:03:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/effentora-epar-risk-management-plan-summary_en.pdf"},
    {"id":"56738","name":"Teriflunomide Mylan : EPAR - Risk management plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2022-11-22T10:58:00Z","last_updated_date":"2022-11-22T10:58:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/teriflunomide-mylan-epar-risk-management-plan-summary_en.pdf"},
    {"id":"56758","name":"Melatonin Neurim : EPAR - Risk management plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2022-11-23T13:04:00Z","last_updated_date":"2022-11-23T13:04:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/melatonin-neurim-epar-risk-management-plan-summary_en.pdf"},
    {"id":"56763","name":"Javlor : EPAR - Risk management plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2022-11-23T15:28:00Z","last_updated_date":"2022-11-23T15:28:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/javlor-epar-risk-management-plan-summary_en.pdf"},
    {"id":"56810","name":"Ximluci : EPAR - Risk Management Plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2022-11-28T10:47:00Z","last_updated_date":"2022-11-28T10:47:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/ximluci-epar-risk-management-plan-summary_en.pdf"},
    {"id":"56827","name":"Cevenfacta : EPAR - Risk managment plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2022-11-29T10:49:00Z","last_updated_date":"2022-11-29T10:49:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/cevenfacta-epar-risk-managment-plan-summary_en.pdf"},
    {"id":"56943","name":"Teriparatide Sun : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2022-12-12T17:12:00Z","last_updated_date":"2022-12-12T17:12:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/teriparatide-sun-epar-risk-management-plan-summary_en.pdf"},
    {"id":"57027","name":"Nityr : EPAR - Risk management plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2022-12-15T09:56:00Z","last_updated_date":"2022-12-15T09:56:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/nityr-epar-risk-management-plan-summary_en.pdf"},
    {"id":"57116","name":"Dimethyl fumarate Teva: EPAR - Risk management plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2022-12-21T16:50:00Z","last_updated_date":"2023-12-22T14:57:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/dimethyl-fumarate-teva-epar-risk-management-plan-summary_en.pdf"},
    {"id":"57134","name":"Vipidia : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2022-12-22T11:02:00Z","last_updated_date":"2023-07-21T17:15:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/vipidia-epar-risk-management-plan-summary_en.pdf"},
    {"id":"57333","name":"Pemetrexed Baxter : EPAR - Risk management plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2023-01-19T12:59:00Z","last_updated_date":"2023-01-19T12:59:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/pemetrexed-baxter-epar-risk-management-plan-summary_en.pdf"},
    {"id":"57352","name":"Omnitrope : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2023-01-23T10:05:00Z","last_updated_date":"2023-01-23T10:05:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/omnitrope-epar-risk-management-plan-summary_en.pdf"},
    {"id":"57441","name":"Zarzio : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2023-01-30T09:18:00Z","last_updated_date":"2023-01-30T09:18:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/zarzio-epar-risk-management-plan-summary_en.pdf"},
    {"id":"57444","name":"Filgrastim Hexal : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2023-01-30T10:25:00Z","last_updated_date":"2023-01-30T10:25:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/filgrastim-hexal-epar-risk-management-plan-summary_en.pdf"},
    {"id":"57480","name":"Celdoxome pegylated liposomal : EPAR - Risk management plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2023-01-31T13:19:00Z","last_updated_date":"2025-11-27T09:34:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/celdoxome-pegylated-liposomal-epar-risk-management-plan-summary_en.pdf"},
    {"id":"57532","name":"Plerixafor Accord : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2023-02-06T13:56:00Z","last_updated_date":"2023-02-06T13:56:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/plerixafor-accord-epar-risk-management-plan-summary_en.pdf"},
    {"id":"57656","name":"Vfend : EPAR - Risk Management Plan","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2023-02-13T16:38:00Z","last_updated_date":"2023-11-09T12:49:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/vfend-epar-risk-management-plan_en.pdf"},
    {"id":"57689","name":"DuoPlavin : EPAR - Risk management plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2023-02-16T09:26:00Z","last_updated_date":"2023-02-16T09:26:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/duoplavin-epar-risk-management-plan-summary_en.pdf"},
    {"id":"57788","name":"Dimethyl fumarate Accord : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2023-02-22T12:37:00Z","last_updated_date":"2023-12-22T13:22:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/dimethyl-fumarate-accord-epar-risk-management-plan-summary_en.pdf"},
    {"id":"57852","name":"Brintellix : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2023-03-01T17:03:00Z","last_updated_date":"2023-03-01T17:03:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/brintellix-epar-risk-management-plan-summary_en.pdf"},
    {"id":"57880","name":"Viagra : EPAR - Risk-management plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2023-03-03T15:08:00Z","last_updated_date":"2023-03-03T15:08:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/viagra-epar-risk-management-plan-summary_en.pdf"},
    {"id":"57901","name":"SomaKit TOC : EPAR - Risk management plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2023-03-07T11:37:00Z","last_updated_date":"2023-03-07T11:37:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/somakit-toc-epar-risk-management-plan-summary_en.pdf"},
    {"id":"57941","name":"Kauliv : EPAR - Risk management plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2023-03-07T15:50:00Z","last_updated_date":"2023-03-07T15:50:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/kauliv-epar-risk-management-plan-summary_en.pdf"},
    {"id":"57962","name":"Arava : EPAR - Risk Management Plan","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2023-03-09T10:11:00Z","last_updated_date":"2026-05-08T12:54:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/arava-epar-risk-management-plan_en.pdf"},
    {"id":"58109","name":"Synagis : EPAR - Risk Management Plan","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2023-03-22T10:06:00Z","last_updated_date":"2025-12-12T11:22:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/synagis-epar-risk-management-plan_en.pdf"},
    {"id":"58114","name":"Herzuma : EPAR - Risk management plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2023-03-22T10:59:00Z","last_updated_date":"2023-03-22T10:59:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/herzuma-epar-risk-management-plan-summary_en.pdf"},
    {"id":"58156","name":"Azopt : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2023-03-24T14:21:00Z","last_updated_date":"2023-03-24T14:21:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/azopt-epar-risk-management-plan-summary_en.pdf"},
    {"id":"58195","name":"Eucreas : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2023-03-29T10:29:00Z","last_updated_date":"2023-03-29T10:29:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/eucreas-epar-risk-management-plan-summary_en.pdf"},
    {"id":"58251","name":"Cholib : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2023-03-31T14:05:00Z","last_updated_date":"2023-03-31T14:05:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/cholib-epar-risk-management-plan-summary_en.pdf"},
    {"id":"58280","name":"Dapagliflozin Viatris : EPAR - Risk management plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2023-04-04T16:40:00Z","last_updated_date":"2023-04-04T16:40:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/dapagliflozin-viatris-epar-risk-management-plan-summary_en.pdf"},
    {"id":"58522","name":"Stocrin : EPAR - Risk management plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2023-04-25T14:17:00Z","last_updated_date":"2023-04-25T14:17:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/stocrin-epar-risk-management-plan-summary_en.pdf"},
    {"id":"58629","name":"Anagrelide Mylan : EPAR - Risk management plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2023-05-11T12:07:00Z","last_updated_date":"2023-05-11T12:07:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/anagrelide-mylan-epar-risk-management-plan-summary_en.pdf"},
    {"id":"58641","name":"Adcirca : EPAR - Risk management plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2023-05-12T09:33:00Z","last_updated_date":"2023-05-12T09:33:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/adcirca-epar-risk-management-plan-summary_en.pdf"},
    {"id":"58689","name":"Bekemv : EPAR - Risk management plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2023-05-15T15:40:00Z","last_updated_date":"2025-10-22T16:08:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/bekemv-epar-risk-management-plan-summary_en.pdf"},
    {"id":"58704","name":"Pombiliti : EPAR - Risk management plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2023-05-16T15:40:00Z","last_updated_date":"2023-05-16T15:40:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/pombiliti-epar-risk-management-plan-summary_en.pdf"},
    {"id":"58772","name":"Byetta : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2023-05-24T16:41:00Z","last_updated_date":"2023-05-24T16:41:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/byetta-epar-risk-management-plan-summary_en.pdf"},
    {"id":"58849","name":"Pedmarqsi : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2023-06-02T09:02:00Z","last_updated_date":"2023-06-02T09:02:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/pedmarqsi-epar-risk-management-plan-summary_en.pdf"},
    {"id":"58868","name":"Lacosamide Adroiq : EPAR - Risk management plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2023-06-05T10:28:00Z","last_updated_date":"2023-06-05T10:28:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/lacosamide-adroiq-epar-risk-management-plan-summary_en.pdf"},
    {"id":"58952","name":"Emtricitabine/Tenofovir disoproxil Mylan : EPAR - Risk Management Plan","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2023-06-15T10:41:00Z","last_updated_date":"2023-06-15T10:41:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/emtricitabinetenofovir-disoproxil-mylan-epar-risk-management-plan_en.pdf"},
    {"id":"58973","name":"Sugammadex Adroiq : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2023-06-16T10:19:00Z","last_updated_date":"2023-06-16T10:19:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/sugammadex-adroiq-epar-risk-management-plan-summary_en.pdf"},
    {"id":"59007","name":"Lantus : EPAR - Risk Management Plan","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2023-06-20T15:07:00Z","last_updated_date":"2023-08-09T15:03:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/lantus-epar-risk-management-plan_en.pdf"},
    {"id":"59298","name":"Opfolda : EPAR - Risk management plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2023-07-07T12:54:00Z","last_updated_date":"2023-07-07T12:54:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/opfolda-epar-risk-management-plan-summary_en.pdf"},
    {"id":"59313","name":"Ceprotin : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2023-07-10T16:26:00Z","last_updated_date":"2023-07-18T16:20:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/ceprotin-epar-risk-management-plan-summary_en.pdf"},
    {"id":"59319","name":"Efient : EPAR - Risk Management Plan","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2023-07-11T12:20:00Z","last_updated_date":"2024-09-04T14:14:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/efient-epar-risk-management-plan_en.pdf"},
    {"id":"59395","name":"Sugammadex Piramal : EPAR - Risk management plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2023-07-18T17:28:00Z","last_updated_date":"2023-07-18T17:28:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/sugammadex-piramal-epar-risk-management-plan-summary_en.pdf"},
    {"id":"59404","name":"Carbaglu : EPAR - Risk management plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2023-07-19T15:20:00Z","last_updated_date":"2023-07-19T15:20:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/carbaglu-epar-risk-management-plan-summary_en.pdf"},
    {"id":"59477","name":"Camzyos : EPAR - Risk management plan","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2023-07-24T15:50:00Z","last_updated_date":"2025-10-23T14:25:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/camzyos-epar-risk-management-plan_en.pdf"},
    {"id":"59482","name":"Qaialdo : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2023-07-25T11:57:00Z","last_updated_date":"2023-07-25T11:57:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/qaialdo-epar-risk-management-plan-summary_en.pdf"},
    {"id":"59518","name":"Pylclari : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2023-07-28T11:54:00Z","last_updated_date":"2023-07-28T11:54:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/pylclari-epar-risk-management-plan-summary_en.pdf"},
    {"id":"59525","name":"Ztalmy : EPAR - Risk management plan","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2023-07-31T12:02:00Z","last_updated_date":"2026-02-27T09:53:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/ztalmy-epar-risk-management-plan_en.pdf"},
    {"id":"59562","name":"Fluenz Tetra : EPAR - Risk-management-plan","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2023-08-07T16:02:00Z","last_updated_date":"2025-08-14T18:43:57Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/fluenz-tetra-epar-risk-management-plan_en.pdf"},
    {"id":"59574","name":"Toujeo : EPAR - Risk Management Plan Summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2023-08-09T10:34:00Z","last_updated_date":"2023-08-09T10:34:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/toujeo-epar-risk-management-plan-summary_en.pdf"},
    {"id":"59600","name":"Tolvaptan Accord : EPAR - Risk Management Plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2023-08-14T15:12:00Z","last_updated_date":"2023-08-14T15:12:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/tolvaptan-accord-epar-risk-management-plan-summary_en.pdf"},
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    {"id":"59860","name":"Xeplion : EPAR - Risk management plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2023-06-22T17:55:00Z","last_updated_date":"2023-06-22T17:55:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/xeplion-epar-risk-management-plan-summary_en.pdf"},
    {"id":"59966","name":"Jardiance : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2023-09-14T09:29:00Z","last_updated_date":"2024-02-07T16:20:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/jardiance-epar-risk-management-plan-summary_en.pdf"},
    {"id":"60109","name":"Semglee : EPAR - Risk management plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2023-09-22T10:43:00Z","last_updated_date":"2023-09-22T10:43:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/semglee-epar-risk-management-plan-summary_en.pdf"},
    {"id":"60222","name":"Tyenne : EPAR - Risk management plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2023-10-02T13:13:00Z","last_updated_date":"2024-02-28T15:40:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/tyenne-epar-risk-management-plan-summary_en.pdf"},
    {"id":"60236","name":"Foclivia : EPAR - Risk management plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2023-10-03T12:42:00Z","last_updated_date":"2023-10-03T12:42:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/foclivia-epar-risk-management-plan-summary_en.pdf"},
    {"id":"60245","name":"Roteas : EPAR - Risk management plan","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2023-10-04T10:26:00Z","last_updated_date":"2026-04-20T12:02:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/roteas-epar-risk-management-plan_en.pdf"},
    {"id":"60258","name":"Enrylaze : EPAR - Risk management plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2023-10-05T08:56:00Z","last_updated_date":"2023-10-05T08:56:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/enrylaze-epar-risk-management-plan-summary_en.pdf"},
    {"id":"60362","name":"Plenadren : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2023-10-11T10:42:00Z","last_updated_date":"2023-10-13T09:12:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/plenadren-epar-risk-management-plan-summary_en.pdf"},
    {"id":"60445","name":"Xeplion : EPAR - Risk management plan","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2023-10-17T11:14:00Z","last_updated_date":"2023-10-17T11:14:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/xeplion-epar-risk-management-plan_en.pdf"},
    {"id":"60537","name":"Gardasil 9 : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2015-07-03T02:00:00Z","last_updated_date":"2023-07-25T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/gardasil-9-epar-risk-management-plan-summary_en.pdf"},
    {"id":"60562","name":"Benepali : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2016-01-28T01:00:00Z","last_updated_date":"2023-06-01T11:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/benepali-epar-risk-management-plan-summary_en.pdf"},
    {"id":"60584","name":"Epoetin Alfa Hexal : EPAR Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2018-10-02T11:46:00Z","last_updated_date":"2018-10-02T11:46:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/epoetin-alfa-hexal-epar-risk-management-plan-summary_en.pdf"},
    {"id":"60588","name":"KIgabeq : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2018-10-12T14:55:00Z","last_updated_date":"2023-07-07T09:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/kigabeq-epar-risk-management-plan-summary_en.pdf"},
    {"id":"60589","name":"Pelgraz : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2018-10-26T15:09:00Z","last_updated_date":"2023-07-13T18:05:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/pelgraz-epar-risk-management-plan-summary_en.pdf"},
    {"id":"60599","name":"Ondexxya : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2019-06-27T15:55:00Z","last_updated_date":"2021-06-23T13:05:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/ondexxya-epar-risk-management-plan-summary_en.pdf"},
    {"id":"60618","name":"Jyseleca : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2020-09-28T10:44:00Z","last_updated_date":"2023-07-27T12:44:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/jyseleca-epar-risk-management-plan-summary_en.pdf"},
    {"id":"60619","name":"Tevagrastim : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2020-10-19T17:08:00Z","last_updated_date":"2023-06-13T12:06:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/tevagrastim-epar-risk-management-plan-summary_en.pdf"},
    {"id":"60623","name":"Prometax : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2021-01-14T14:03:00Z","last_updated_date":"2023-02-02T10:22:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/prometax-epar-risk-management-plan-summary_en.pdf"},
    {"id":"60624","name":"Exelon : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2021-01-14T15:01:00Z","last_updated_date":"2023-02-02T09:08:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/exelon-epar-risk-management-plan-summary_en.pdf"},
    {"id":"60625","name":"Galafold : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2021-02-23T16:19:00Z","last_updated_date":"2022-02-25T01:34:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/galafold-epar-risk-management-plan-summary_en.pdf"},
    {"id":"60628","name":"Kesimpta : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2021-04-16T15:25:00Z","last_updated_date":"2023-03-29T11:40:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/kesimpta-epar-risk-management-plan-summary_en.pdf"},
    {"id":"60653","name":"Bylvay : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2021-07-28T16:59:00Z","last_updated_date":"2023-07-05T12:58:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/bylvay-epar-risk-management-plan-summary_en.pdf"},
    {"id":"60654","name":"Kadcyla : EPAR - Risk management plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2021-08-27T15:19:00Z","last_updated_date":"2023-03-22T10:51:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/kadcyla-epar-risk-management-plan-summary_en.pdf"},
    {"id":"60657","name":"Alecensa : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2021-10-11T16:09:00Z","last_updated_date":"2023-01-23T15:57:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/alecensa-epar-risk-management-plan-summary_en.pdf"},
    {"id":"60667","name":"Apexxnar : EPAR - Risk management plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2022-03-02T17:38:00Z","last_updated_date":"2023-01-16T15:57:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/apexxnar-epar-risk-management-plan-summary_en.pdf"},
    {"id":"60688","name":"Rasilez : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2023-01-23T17:42:00Z","last_updated_date":"2023-01-23T17:42:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/rasilez-epar-risk-management-plan-summary_en.pdf"},
    {"id":"60702","name":"Akeega : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2023-06-02T10:18:00Z","last_updated_date":"2023-06-02T10:18:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/akeega-epar-risk-management-plan-summary_en.pdf"},
    {"id":"60708","name":"Hyftor : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2023-06-08T17:20:00Z","last_updated_date":"2023-06-08T17:20:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/hyftor-epar-risk-management-plan-summary_en.pdf"},
    {"id":"60721","name":"Ceprotin:  EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2023-07-10T08:27:00Z","last_updated_date":"2023-07-10T08:27:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/ceprotin-epar-risk-management-plan-summary_en.pdf-0"},
    {"id":"60722","name":"Cereprotin: EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2023-07-10T08:44:00Z","last_updated_date":"2023-07-10T08:44:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/cereprotin-epar-risk-management-plan-summary_en.pdf"},
    {"id":"60726","name":"Sitagliptin/Metformin hydrochloride Sun : EPAR - Risk-management-plan-summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2023-07-17T12:05:00Z","last_updated_date":"2023-07-17T12:05:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/sitagliptin-metformin-hydrochloride-sun-epar-risk-management-plan-summary_en.pdf"},
    {"id":"60734","name":"Emtricitabine/Tenofovir disoproxil Mylan : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2023-07-27T09:58:00Z","last_updated_date":"2023-07-27T09:58:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/emtricitabine-tenofovir-disoproxil-mylan-epar-risk-management-plan-summary_en.pdf"},
    {"id":"60772","name":"Norvir : EPAR - Summary of risk management plan","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2023-10-25T08:17:00Z","last_updated_date":"2023-10-25T08:17:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/norvir-epar-summary-risk-management-plan_en.pdf"},
    {"id":"60778","name":"Flebogamma DIF : EPAR - Risk management plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2023-11-06T14:15:00Z","last_updated_date":"2023-11-06T14:15:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/flebogamma-dif-epar-risk-management-plan-summary_en.pdf"},
    {"id":"60786","name":"Opsumit : EPAR - Risk Management Plan","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2023-11-07T13:10:00Z","last_updated_date":"2023-11-07T13:10:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/opsumit-epar-risk-management-plan_en.pdf"},
    {"id":"60957","name":"Aqumeldi : EPAR - Risk management plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2023-11-22T14:31:35Z","last_updated_date":"2023-11-22T14:31:35Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/aqumeldi-epar-risk-management-plan-summary_en.pdf"},
    {"id":"60972","name":"Herwenda : EPAR - Risk management plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2023-11-23T10:51:25Z","last_updated_date":"2023-11-23T10:51:25Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/herwenda-epar-risk-management-plan-summary_en.pdf"},
    {"id":"61243","name":"Finlee : EPAR - Risk management plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2023-12-05T13:57:55Z","last_updated_date":"2023-12-05T13:57:55Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/finlee-epar-risk-management-plan-summary_en.pdf"},
    {"id":"61246","name":"Finlee : EPAR - Risk management plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2023-12-05T14:05:13Z","last_updated_date":"2023-12-05T14:05:13Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/finlee-epar-risk-management-plan-summary_en.pdf-0"},
    {"id":"61364","name":"Catiolanze : EPAR - Risk-Management-Plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2023-12-11T16:34:52Z","last_updated_date":"2023-12-11T16:34:52Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/catiolanze-epar-risk-management-plan-summary_en.pdf"},
    {"id":"61679","name":"Humalog : EPAR - Risk management plan","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2024-01-10T08:48:17Z","last_updated_date":"2024-01-10T08:48:17Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/humalog-epar-risk-management-plan_en.pdf"},
    {"id":"61867","name":"Rezzayo : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2024-01-24T13:08:27Z","last_updated_date":"2024-01-24T13:08:27Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/rezzayo-epar-risk-management-plan-summary_en.pdf"},
    {"id":"61951","name":"Prevenar 13 : EPAR - Risk management plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2024-01-30T12:27:32Z","last_updated_date":"2024-01-30T12:27:32Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/prevenar-13-epar-risk-management-plan-summary_en.pdf"},
    {"id":"61953","name":"Caelyx pegylated liposomal : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2024-01-30T16:25:00Z","last_updated_date":"2024-01-30T16:25:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/caelyx-pegylated-liposomal-epar-risk-management-plan-summary_en.pdf"},
    {"id":"61993","name":"Quofenix : EPAR - Risk management plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2021-06-10T11:22:43Z","last_updated_date":"2021-06-10T11:22:43Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/quofenix-epar-risk-management-plan-summary_en.pdf"},
    {"id":"62011","name":"Voriconazole Accord : EPAR - Risk management plan","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2024-02-06T14:39:21Z","last_updated_date":"2024-02-06T14:39:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/voriconazole-accord-epar-risk-management-plan_en.pdf"},
    {"id":"62170","name":"Myozyme : EPAR - Risk Management Plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2024-02-15T10:25:05Z","last_updated_date":"2024-02-15T10:25:05Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/myozyme-epar-risk-management-plan-summary_en.pdf"},
    {"id":"62208","name":"DaTSCAN : EPAR - Risk-management-plan","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2024-02-19T12:09:05Z","last_updated_date":"2024-02-19T12:09:05Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/datscan-epar-risk-management-plan_en.pdf"},
    {"id":"62233","name":"Velsipity : EPAR - Risk Management Plan","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2024-02-21T10:30:57Z","last_updated_date":"2024-02-21T10:30:57Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/velsipity-epar-risk-management-plan_en.pdf"},
    {"id":"62312","name":"Naveruclif : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2024-02-27T12:55:15Z","last_updated_date":"2024-02-27T12:55:15Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/naveruclif-epar-risk-management-plan-summary_en.pdf"},
    {"id":"62316","name":"Aldurazyme : EPAR - Risk-management-plan","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2024-02-28T09:28:39Z","last_updated_date":"2024-02-28T09:28:39Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/aldurazyme-epar-risk-management-plan_en.pdf"},
    {"id":"62399","name":"Toviaz : EPAR - Risk management plan","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2024-03-01T13:42:56Z","last_updated_date":"2024-03-01T13:42:56Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/toviaz-epar-risk-management-plan_en.pdf"},
    {"id":"63055","name":"Nivestim : EPAR - Risk-management-plan","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2024-04-24T16:18:47Z","last_updated_date":"2024-04-24T16:18:47Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/nivestim-epar-risk-management-plan_en.pdf"},
    {"id":"63202","name":"Ryzneuta : EPAR - Risk management plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2024-05-13T15:49:13Z","last_updated_date":"2024-05-13T15:49:13Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/ryzneuta-epar-risk-management-plan-summary_en.pdf"},
    {"id":"63403","name":"Avamys : EPAR - Risk Management Plan Summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2024-05-30T14:53:00Z","last_updated_date":"2024-05-30T14:53:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/avamys-epar-risk-management-plan-summary_en.pdf"},
    {"id":"63934","name":"Obgemsa : EPAR - Risk management plan","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2024-07-05T15:52:00Z","last_updated_date":"2024-07-05T15:52:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/obgemsa-epar-risk-management-plan_en.pdf"},
    {"id":"63965","name":"Eribulin Baxter : EPAR - Risk management plan","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2024-07-09T14:10:00Z","last_updated_date":"2024-07-09T14:10:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/eribulin-baxter-epar-risk-management-plan_en.pdf"},
    {"id":"64004","name":"Fruzaqla : EPAR - Risk-management-plan","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2024-07-10T11:11:01Z","last_updated_date":"2024-07-10T11:11:01Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/fruzaqla-epar-risk-management-plan_en.pdf"},
    {"id":"64009","name":"Tofidence : EPAR - Risk-management-plan","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2024-07-10T11:11:01Z","last_updated_date":"2024-07-10T11:11:01Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/tofidence-epar-risk-management-plan_en.pdf"},
    {"id":"64016","name":"Dimethyl fumarate Neuraxpharm : EPAR - Risk-management-plan","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2024-07-11T11:11:01Z","last_updated_date":"2024-07-11T11:11:01Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/dimethyl-fumarate-neuraxpharm-epar-risk-management-plan_en.pdf"},
    {"id":"64040","name":"Dimethyl fumarate Accord : EPAR - Risk-management-plan","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2024-07-11T11:11:01Z","last_updated_date":"2025-03-14T14:45:52Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/dimethyl-fumarate-accord-epar-risk-management-plan_en.pdf"},
    {"id":"64048","name":"Dimethyl fumarate Mylan : EPAR - Risk-management-plan","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2024-07-11T11:11:01Z","last_updated_date":"2024-07-11T11:11:01Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/dimethyl-fumarate-mylan-epar-risk-management-plan_en.pdf"},
    {"id":"64072","name":"Altuvoct : EPAR - Risk-management-plan","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2024-07-12T00:00:00Z","last_updated_date":"2024-07-12T00:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/altuvoct-epar-risk-management-plan_en.pdf"},
    {"id":"64174","name":"Jeraygo : EPAR - Risk management plan","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2024-07-24T15:01:08Z","last_updated_date":"2025-08-29T12:18:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/jeraygo-epar-risk-management-plan_en.pdf"},
    {"id":"64193","name":"Wezenla : EPAR - Risk management plan (archive)","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2024-07-18T10:50:00Z","last_updated_date":"2025-04-24T11:55:43Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/wezenla-epar-risk-management-plan-archive_en.pdf"},
    {"id":"64228","name":"Gliolan : EPAR - Risk management plan","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2024-07-19T13:42:00Z","last_updated_date":"2024-07-19T13:42:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/gliolan-epar-risk-management-plan_en.pdf"},
    {"id":"64269","name":"NeoRecormon : EPAR - Risk management plan","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2024-07-22T13:55:00Z","last_updated_date":"2024-07-22T13:55:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/neorecormon-epar-risk-management-plan_en.pdf"},
    {"id":"64276","name":"Evoltra : EPAR - Risk management plan","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2024-07-22T16:56:00Z","last_updated_date":"2024-07-22T16:56:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/evoltra-epar-risk-management-plan_en.pdf"},
    {"id":"64289","name":"Epoetin alfa Hexal : EPAR - Risk management plan","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2024-07-24T11:49:00Z","last_updated_date":"2024-07-24T11:49:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/epoetin-alfa-hexal-epar-risk-management-plan_en.pdf"},
    {"id":"64526","name":"Adzynma : EPAR - Risk management plan","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2024-08-07T12:48:32Z","last_updated_date":"2026-02-19T14:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/adzynma-epar-risk-management-plan_en.pdf"},
    {"id":"64543","name":"Avzivi : EPAR - Risk management plan","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2024-08-08T14:31:42Z","last_updated_date":"2024-08-08T14:31:42Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/avzivi-epar-risk-management-plan_en.pdf"},
    {"id":"64595","name":"Akeega : EPAR - Risk management plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2024-08-19T15:34:22Z","last_updated_date":"2026-03-17T12:49:59Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/akeega-epar-risk-management-plan-summary_en.pdf-0"},
    {"id":"65915","name":"Lumykras : EPAR - Risk management plan","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2024-12-03T11:34:56Z","last_updated_date":"2024-12-03T11:34:56Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/lumykras-epar-risk-management-plan_en.pdf"},
    {"id":"66324","name":"Mysildecard : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2025-01-15T16:40:26Z","last_updated_date":"2025-01-15T16:40:26Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/mysildecard-epar-risk-management-plan-summary_en.pdf"},
    {"id":"66424","name":"Kigabeq : EPAR - Risk management plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2023-07-07T09:48:10Z","last_updated_date":"2023-07-07T09:48:10Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/kigabeq-epar-risk-management-plan-summary_en.pdf-0"},
    {"id":"68536","name":"Nyxoid : EPAR - Risk-management-plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2025-06-12T17:08:14Z","last_updated_date":"2025-06-12T17:08:14Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/nyxoid-epar-risk-management-plan-summary_en.pdf"},
    {"id":"69489","name":"Ondexxya : EPAR - Risk-management plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2025-07-25T11:17:13Z","last_updated_date":"2025-07-25T11:17:13Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/ondexxya-epar-risk-management-plan-summary_en.pdf-0"},
    {"id":"69842","name":"Oczyesa : EPAR - Risk management plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2025-08-22T10:37:52Z","last_updated_date":"2025-08-22T10:37:52Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/oczyesa-epar-risk-management-plan-summary_en.pdf"},
    {"id":"72311","name":"Vpriv : EPAR - Risk management plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2026-01-28T12:31:20Z","last_updated_date":"2026-01-28T12:31:20Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/vpriv-epar-risk-management-plan-summary_en.pdf"},
    {"id":"73514","name":"Enflonsia : EPAR - Risk management plan summary","type":"rmp-summary","status":"unknown","consultation_date":"","first_published_date":"2026-04-22T09:19:16Z","last_updated_date":"2026-04-22T09:19:16Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp-summary/enflonsia-epar-risk-management-plan-summary_en.pdf"},
    {"id":"2663","name":"Faslodex : EPAR - Scientific Discussion","type":"scientific-discussion","status":"unknown","consultation_date":"","first_published_date":"2006-01-09T00:09:21Z","last_updated_date":"2006-01-09T00:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/scientific-discussion/faslodex-epar-scientific-discussion_en.pdf"},
    {"id":"2704","name":"Enviage : EPAR - Scientific Discussion","type":"scientific-discussion","status":"unknown","consultation_date":"","first_published_date":"2008-10-15T02:00:00Z","last_updated_date":"2011-05-19T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/scientific-discussion/enviage-epar-scientific-discussion_en.pdf"},
    {"id":"2712","name":"Bondenza : EPAR - Scientific Discussion","type":"scientific-discussion","status":"unknown","consultation_date":"","first_published_date":"2006-10-16T02:09:21Z","last_updated_date":"2013-05-13T19:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/scientific-discussion/bondenza-epar-scientific-discussion_en.pdf"},
    {"id":"2804","name":"Targretin : EPAR - Scientific Discussion","type":"scientific-discussion","status":"unknown","consultation_date":"","first_published_date":"2006-08-08T02:09:21Z","last_updated_date":"2006-08-08T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/scientific-discussion/targretin-epar-scientific-discussion_en.pdf"},
    {"id":"2811","name":"Insulatard : EPAR - Scientific Discussion","type":"scientific-discussion","status":"unknown","consultation_date":"","first_published_date":"2006-09-06T02:00:00Z","last_updated_date":"2006-09-06T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/scientific-discussion/insulatard-epar-scientific-discussion_en.pdf"},
    {"id":"2859","name":"Naxcel : EPAR - Scientific Discussion","type":"scientific-discussion","status":"unknown","consultation_date":"","first_published_date":"2009-10-20T02:00:00Z","last_updated_date":"2024-06-28T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/scientific-discussion/naxcel-epar-scientific-discussion_en.pdf"},
    {"id":"2865","name":"Zerit : EPAR - Scientific Discussion","type":"scientific-discussion","status":"unknown","consultation_date":"","first_published_date":"2006-08-11T02:00:00Z","last_updated_date":"2006-08-11T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/scientific-discussion/zerit-epar-scientific-discussion_en.pdf"},
    {"id":"2932","name":"Prezista : EPAR - Scientific Discussion","type":"scientific-discussion","status":"unknown","consultation_date":"","first_published_date":"2008-11-25T01:00:00Z","last_updated_date":"2008-11-25T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/scientific-discussion/prezista-epar-scientific-discussion_en.pdf"},
    {"id":"2986","name":"SonoVue : EPAR - Scientific Discussion","type":"scientific-discussion","status":"unknown","consultation_date":"","first_published_date":"2005-10-21T02:00:00Z","last_updated_date":"2005-10-21T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/scientific-discussion/sonovue-epar-scientific-discussion_en.pdf"},
    {"id":"3181","name":"Beromun : EPAR - Scientific Discussion","type":"scientific-discussion","status":"unknown","consultation_date":"","first_published_date":"2005-10-21T02:09:21Z","last_updated_date":"2005-10-21T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/scientific-discussion/beromun-epar-scientific-discussion_en.pdf"},
    {"id":"3198","name":"NeoRecormon : EPAR - Scientific Discussion","type":"scientific-discussion","status":"unknown","consultation_date":"","first_published_date":"2005-10-21T02:09:21Z","last_updated_date":"2005-10-21T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/scientific-discussion/neorecormon-epar-scientific-discussion_en.pdf"},
    {"id":"3338","name":"Luveris : EPAR - Scientific Discussion","type":"scientific-discussion","status":"unknown","consultation_date":"","first_published_date":"2006-11-10T01:00:00Z","last_updated_date":"2006-11-10T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/scientific-discussion/luveris-epar-scientific-discussion_en.pdf"},
    {"id":"3382","name":"Exforge : EPAR - Scientific Discussion","type":"scientific-discussion","status":"unknown","consultation_date":"","first_published_date":"2007-02-21T01:00:00Z","last_updated_date":"2007-02-21T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/scientific-discussion/exforge-epar-scientific-discussion_en.pdf"},
    {"id":"3590","name":"Cyanokit : EPAR - Scientific Discussion","type":"scientific-discussion","status":"unknown","consultation_date":"","first_published_date":"2007-12-18T01:00:00Z","last_updated_date":"2007-12-18T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/scientific-discussion/cyanokit-epar-scientific-discussion_en.pdf"},
    {"id":"3656","name":"Isentress : EPAR - Scientific Discussion","type":"scientific-discussion","status":"unknown","consultation_date":"","first_published_date":"2008-01-14T01:00:00Z","last_updated_date":"2008-01-14T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/scientific-discussion/isentress-epar-scientific-discussion_en.pdf"},
    {"id":"3686","name":"Mircera : EPAR - Scientific Discussion","type":"scientific-discussion","status":"unknown","consultation_date":"","first_published_date":"2007-08-02T02:00:00Z","last_updated_date":"2007-08-02T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/scientific-discussion/mircera-epar-scientific-discussion_en.pdf"},
    {"id":"3693","name":"Optison : EPAR - Scientific Discussion","type":"scientific-discussion","status":"unknown","consultation_date":"","first_published_date":"2008-08-01T02:00:00Z","last_updated_date":"2008-08-01T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/scientific-discussion/optison-epar-scientific-discussion_en.pdf"},
    {"id":"3791","name":"Ovitrelle : EPAR - Scientific Discussion","type":"scientific-discussion","status":"unknown","consultation_date":"","first_published_date":"2006-11-10T00:09:21Z","last_updated_date":"2006-11-10T00:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/scientific-discussion/ovitrelle-epar-scientific-discussion_en.pdf"},
    {"id":"3817","name":"Alli : EPAR - Scientific Discussion","type":"scientific-discussion","status":"unknown","consultation_date":"","first_published_date":"2007-07-27T02:00:00Z","last_updated_date":"2007-07-27T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/scientific-discussion/alli-epar-scientific-discussion_en.pdf"},
    {"id":"3864","name":"Velcade : EPAR - Scientific Discussion","type":"scientific-discussion","status":"unknown","consultation_date":"","first_published_date":"2006-08-15T02:00:00Z","last_updated_date":"2006-08-15T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/scientific-discussion/velcade-epar-scientific-discussion_en.pdf"},
    {"id":"3894","name":"Zevalin : EPAR - Scientific Discussion","type":"scientific-discussion","status":"unknown","consultation_date":"","first_published_date":"2006-11-13T01:00:00Z","last_updated_date":"2006-11-13T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/scientific-discussion/zevalin-epar-scientific-discussion_en.pdf"},
    {"id":"3900","name":"Orencia : EPAR - Scientific Discussion","type":"scientific-discussion","status":"unknown","consultation_date":"","first_published_date":"2007-06-05T02:09:21Z","last_updated_date":"2007-06-05T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/scientific-discussion/orencia-epar-scientific-discussion_en.pdf"},
    {"id":"4006","name":"Helicobacter Test INFAI : EPAR - Scientific Discussion","type":"scientific-discussion","status":"unknown","consultation_date":"","first_published_date":"2005-10-21T02:09:21Z","last_updated_date":"2005-10-21T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/scientific-discussion/helicobacter-test-infai-epar-scientific-discussion_en.pdf"},
    {"id":"4063","name":"Karvezide : EPAR - Scientific Discussion","type":"scientific-discussion","status":"unknown","consultation_date":"","first_published_date":"2006-10-16T02:00:00Z","last_updated_date":"2006-10-16T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/scientific-discussion/karvezide-epar-scientific-discussion_en.pdf"},
    {"id":"4120","name":"NeoSpect : EPAR - Scientific Discussion","type":"scientific-discussion","status":"unknown","consultation_date":"","first_published_date":"2006-05-12T02:09:21Z","last_updated_date":"2010-11-18T01:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/scientific-discussion/neospect-epar-scientific-discussion_en.pdf"},
    {"id":"4138","name":"Norvir : EPAR - Scientific discussion","type":"scientific-discussion","status":"unknown","consultation_date":"","first_published_date":"2005-10-21T02:09:21Z","last_updated_date":"2005-10-21T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/scientific-discussion/norvir-epar-scientific-discussion_en.pdf"},
    {"id":"4221","name":"Advocate : EPAR - Scientific Discussion","type":"scientific-discussion","status":"unknown","consultation_date":"","first_published_date":"2009-07-28T01:09:21Z","last_updated_date":"2024-01-29T15:33:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/scientific-discussion/advocate-epar-scientific-discussion_en.pdf"},
    {"id":"4282","name":"Twinrix Paediatric : EPAR - Scientific Discussion","type":"scientific-discussion","status":"unknown","consultation_date":"","first_published_date":"2005-10-21T02:09:21Z","last_updated_date":"2005-10-21T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/scientific-discussion/twinrix-paediatric-epar-scientific-discussion_en.pdf"},
    {"id":"4283","name":"Procox : EPAR - Scientific Discussion","type":"scientific-discussion","status":"unknown","consultation_date":"","first_published_date":"2011-05-05T02:00:00Z","last_updated_date":"2025-10-14T02:00:00Z","reference_number":"EMA/CVMP/236066/2011","document_url":"https://www.ema.europa.eu/en/documents/scientific-discussion/procox-epar-scientific-discussion_en.pdf"},
    {"id":"4500","name":"Novem : EPAR - Scientific Discussion","type":"scientific-discussion","status":"unknown","consultation_date":"","first_published_date":"2006-10-05T02:00:00Z","last_updated_date":"2025-10-09T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/scientific-discussion/novem-epar-scientific-discussion_en.pdf"},
    {"id":"4647","name":"Forcaltonin : EPAR - Scientific Discussion","type":"scientific-discussion","status":"unknown","consultation_date":"","first_published_date":"2008-11-21T00:09:21Z","last_updated_date":"2008-11-21T00:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/scientific-discussion/forcaltonin-epar-scientific-discussion_en.pdf"},
    {"id":"4653","name":"Draxxin : EPAR - Scientific Discussion","type":"scientific-discussion","status":"unknown","consultation_date":"","first_published_date":"2008-09-02T02:09:21Z","last_updated_date":"2010-04-09T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/scientific-discussion/draxxin-epar-scientific-discussion_en.pdf"},
    {"id":"4677","name":"Parareg : EPAR - Scientific Discussion","type":"scientific-discussion","status":"unknown","consultation_date":"","first_published_date":"2009-05-14T02:00:00Z","last_updated_date":"2009-05-14T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/scientific-discussion/parareg-epar-scientific-discussion_en.pdf"},
    {"id":"4742","name":"Orfadin : EPAR - Scientific Discussion","type":"scientific-discussion","status":"unknown","consultation_date":"","first_published_date":"2007-04-04T02:00:00Z","last_updated_date":"2007-04-04T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/scientific-discussion/orfadin-epar-scientific-discussion_en.pdf"},
    {"id":"4776","name":"Infanrix Hexa : EPAR - Scientific Discussion","type":"scientific-discussion","status":"unknown","consultation_date":"","first_published_date":"2005-10-21T02:00:00Z","last_updated_date":"2005-10-21T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/scientific-discussion/infanrix-hexa-epar-scientific-discussion_en.pdf"},
    {"id":"4791","name":"Atriance : EPAR - Scientific Discussion","type":"scientific-discussion","status":"unknown","consultation_date":"","first_published_date":"2007-09-20T02:00:00Z","last_updated_date":"2007-09-20T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/scientific-discussion/atriance-epar-scientific-discussion_en.pdf"},
    {"id":"4801","name":"Aclasta : EPAR - Scientific Discussion","type":"scientific-discussion","status":"unknown","consultation_date":"","first_published_date":"2006-04-03T02:00:00Z","last_updated_date":"2006-04-03T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/scientific-discussion/aclasta-epar-scientific-discussion_en.pdf"},
    {"id":"4852","name":"Zolvix : EPAR - Scientific Discussion","type":"scientific-discussion","status":"unknown","consultation_date":"","first_published_date":"2009-11-26T00:09:21Z","last_updated_date":"2024-06-25T00:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/scientific-discussion/zolvix-epar-scientific-discussion_en.pdf"},
    {"id":"5211","name":"Irbesartan Winthrop : EPAR - Scientific Discussion","type":"scientific-discussion","status":"unknown","consultation_date":"","first_published_date":"2007-02-05T01:00:00Z","last_updated_date":"2007-02-05T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/scientific-discussion/irbesartan-winthrop-epar-scientific-discussion_en.pdf"},
    {"id":"5217","name":"Increlex : EPAR - Scientific Discussion","type":"scientific-discussion","status":"unknown","consultation_date":"","first_published_date":"2007-08-13T02:00:00Z","last_updated_date":"2007-08-13T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/scientific-discussion/increlex-epar-scientific-discussion_en.pdf"},
    {"id":"5310","name":"BTVPUR AlSap 2-4 : EPAR - Scientific Discussion","type":"scientific-discussion","status":"unknown","consultation_date":"","first_published_date":"2010-11-09T01:00:00Z","last_updated_date":"2018-11-13T01:00:00Z","reference_number":"EMA/CVMP/343595/2010","document_url":"https://www.ema.europa.eu/en/documents/scientific-discussion/btvpur-alsap-2-4-epar-scientific-discussion_en.pdf"},
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    {"id":"13970","name":"Irbesartan BMS : EPAR - Scientific Discussion","type":"scientific-discussion","status":"unknown","consultation_date":"","first_published_date":"2009-11-26T01:00:00Z","last_updated_date":"2009-11-26T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/scientific-discussion/irbesartan-bms-epar-scientific-discussion_en.pdf"},
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    {"id":"14109","name":"Equilis Prequenza Te : EPAR - Scientific Discussion","type":"scientific-discussion","status":"unknown","consultation_date":"","first_published_date":"2008-07-22T02:09:21Z","last_updated_date":"2025-03-07T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/scientific-discussion/equilis-prequenza-te-epar-scientific-discussion_en.pdf"},
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    {"id":"14168","name":"Helixate NexGen : EPAR - Scientific Discussion","type":"scientific-discussion","status":"unknown","consultation_date":"","first_published_date":"2006-11-06T00:09:00Z","last_updated_date":"2020-06-02T00:09:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/scientific-discussion/helixate-nexgen-epar-scientific-discussion_en.pdf"},
    {"id":"14318","name":"DuoTrav : EPAR - Scientific Discussion","type":"scientific-discussion","status":"unknown","consultation_date":"","first_published_date":"2007-05-31T02:00:00Z","last_updated_date":"2007-05-31T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/scientific-discussion/duotrav-epar-scientific-discussion_en.pdf"},
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    {"id":"18160","name":"Preotact : EPAR - Scientific Discussion","type":"scientific-discussion","status":"unknown","consultation_date":"","first_published_date":"2007-05-31T02:00:00Z","last_updated_date":"2014-07-02T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/scientific-discussion/preotact-epar-scientific-discussion_en.pdf"},
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    {"id":"18966","name":"Hiprabovis IBR Marker Live : EPAR - Scientific Discussion","type":"scientific-discussion","status":"unknown","consultation_date":"","first_published_date":"2011-02-07T01:00:00Z","last_updated_date":"2024-11-05T15:34:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/scientific-discussion/hiprabovis-ibr-marker-live-epar-scientific-discussion_en.pdf"},
    {"id":"18969","name":"Actraphane : EPAR - Scientific Discussion","type":"scientific-discussion","status":"unknown","consultation_date":"","first_published_date":"2006-04-03T02:00:00Z","last_updated_date":"2006-04-03T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/scientific-discussion/actraphane-epar-scientific-discussion_en.pdf"},
    {"id":"18971","name":"Cerenia : EPAR - Scientific Discussion","type":"scientific-discussion","status":"unknown","consultation_date":"","first_published_date":"2006-10-05T01:09:21Z","last_updated_date":"2024-06-28T17:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/scientific-discussion/cerenia-epar-scientific-discussion_en.pdf"},
    {"id":"18978","name":"Flexicam : EPAR - Scientific Discussion","type":"scientific-discussion","status":"unknown","consultation_date":"","first_published_date":"2008-12-22T01:00:00Z","last_updated_date":"2014-05-20T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/scientific-discussion/flexicam-epar-scientific-discussion_en.pdf"},
    {"id":"19002","name":"Synagis : EPAR - Scientific Discussion","type":"scientific-discussion","status":"unknown","consultation_date":"","first_published_date":"2005-10-21T02:00:00Z","last_updated_date":"2005-10-21T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/scientific-discussion/synagis-epar-scientific-discussion_en.pdf"},
    {"id":"19023","name":"Effentora : EPAR - Scientific Discussion","type":"scientific-discussion","status":"unknown","consultation_date":"","first_published_date":"2008-04-23T02:00:00Z","last_updated_date":"2008-04-23T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/scientific-discussion/effentora-epar-scientific-discussion_en.pdf"},
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    {"id":"23107","name":"Ambirix : EPAR - Scientific Discussion","type":"scientific-discussion","status":"unknown","consultation_date":"","first_published_date":"2005-11-23T01:00:00Z","last_updated_date":"2005-11-23T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/scientific-discussion/ambirix-epar-scientific-discussion_en.pdf"},
    {"id":"23147","name":"Panretin : EPAR - Scientific Discussion","type":"scientific-discussion","status":"unknown","consultation_date":"","first_published_date":"2006-01-26T01:00:00Z","last_updated_date":"2006-01-26T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/scientific-discussion/panretin-epar-scientific-discussion_en.pdf"},
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    {"id":"23230","name":"PhotoBarr : EPAR - Scientific Discussion","type":"scientific-discussion","status":"unknown","consultation_date":"","first_published_date":"2008-11-25T01:00:00Z","last_updated_date":"2012-05-07T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/scientific-discussion/photobarr-epar-scientific-discussion_en.pdf"},
    {"id":"23247","name":"Nonafact : EPAR - Scientific Discussion","type":"scientific-discussion","status":"unknown","consultation_date":"","first_published_date":"2005-11-15T00:09:00Z","last_updated_date":"2020-02-18T00:09:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/scientific-discussion/nonafact-epar-scientific-discussion_en.pdf"},
    {"id":"23263","name":"Acticam : EPAR - Scientific discussion","type":"scientific-discussion","status":"Adopted","consultation_date":"","first_published_date":"2009-01-05T01:00:00Z","last_updated_date":"2021-03-24T12:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/scientific-discussion/acticam-epar-scientific-discussion_en.pdf"},
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    {"id":"23529","name":"Zulvac 1 Ovis : EPAR - Scientific discussion","type":"scientific-discussion","status":"unknown","consultation_date":"","first_published_date":"2011-10-10T02:00:00Z","last_updated_date":"2020-04-01T02:00:00Z","reference_number":"EMA/457946/2011","document_url":"https://www.ema.europa.eu/en/documents/scientific-discussion/zulvac-1-ovis-epar-scientific-discussion_en.pdf"},
    {"id":"23701","name":"Pedea : EPAR - Scientific Discussion","type":"scientific-discussion","status":"unknown","consultation_date":"","first_published_date":"2005-10-21T02:00:00Z","last_updated_date":"2005-10-21T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/scientific-discussion/pedea-epar-scientific-discussion_en.pdf"},
    {"id":"23997","name":"Nobivac Piro : EPAR - Scientific Discussion","type":"scientific-discussion","status":"unknown","consultation_date":"","first_published_date":"2006-07-31T02:00:00Z","last_updated_date":"2006-07-31T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/scientific-discussion/nobivac-piro-epar-scientific-discussion_en.pdf"},
    {"id":"24056","name":"Quintanrix : EPAR - Scientific Discussion","type":"scientific-discussion","status":"unknown","consultation_date":"","first_published_date":"2008-09-10T02:00:00Z","last_updated_date":"2008-09-10T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/scientific-discussion/quintanrix-epar-scientific-discussion_en.pdf"},
    {"id":"24073","name":"Xeristar : EPAR - Scientific Discussion","type":"scientific-discussion","status":"unknown","consultation_date":"","first_published_date":"2006-02-07T01:00:00Z","last_updated_date":"2021-06-22T14:45:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/scientific-discussion/xeristar-epar-scientific-discussion_en.pdf"},
    {"id":"24103","name":"Yondelis : EPAR - Scientific Discussion","type":"scientific-discussion","status":"unknown","consultation_date":"","first_published_date":"2007-10-12T02:09:21Z","last_updated_date":"2007-10-12T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/scientific-discussion/yondelis-epar-scientific-discussion_en.pdf"},
    {"id":"24142","name":"Cerezyme : EPAR - Scientific Discussion","type":"scientific-discussion","status":"unknown","consultation_date":"","first_published_date":"2005-10-21T02:09:21Z","last_updated_date":"2005-10-21T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/scientific-discussion/cerezyme-epar-scientific-discussion_en.pdf"},
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    {"id":"24557","name":"Emend : EPAR - Scientific Discussion","type":"scientific-discussion","status":"unknown","consultation_date":"","first_published_date":"2006-09-05T02:00:00Z","last_updated_date":"2006-09-05T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/scientific-discussion/emend-epar-scientific-discussion_en.pdf"},
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    {"id":"27770","name":"NovoNorm : EPAR - Scientific Discussion","type":"scientific-discussion","status":"unknown","consultation_date":"","first_published_date":"2005-10-21T02:00:00Z","last_updated_date":"2005-10-21T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/scientific-discussion/novonorm-epar-scientific-discussion_en.pdf"},
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    {"id":"27854","name":"Erbitux : EPAR - Scientific Discussion","type":"scientific-discussion","status":"unknown","consultation_date":"","first_published_date":"2006-10-30T01:00:00Z","last_updated_date":"2006-10-30T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/scientific-discussion/erbitux-epar-scientific-discussion_en.pdf"},
    {"id":"27856","name":"Atripla : EPAR - Scientific Discussion","type":"scientific-discussion","status":"unknown","consultation_date":"","first_published_date":"2007-12-18T01:00:00Z","last_updated_date":"2022-01-21T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/scientific-discussion/atripla-epar-scientific-discussion_en.pdf"},
    {"id":"27882","name":"ProteqFlu-Te : EPAR - Scientific Discussion","type":"scientific-discussion","status":"unknown","consultation_date":"","first_published_date":"2008-06-03T02:00:00Z","last_updated_date":"2024-10-24T10:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/scientific-discussion/proteqflu-te-epar-scientific-discussion_en.pdf"},
    {"id":"27896","name":"Valtropin : EPAR - Scientific Discussion","type":"scientific-discussion","status":"unknown","consultation_date":"","first_published_date":"2007-05-31T02:00:00Z","last_updated_date":"2012-08-14T18:50:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/scientific-discussion/valtropin-epar-scientific-discussion_en.pdf"},
    {"id":"28010","name":"Optisulin : EPAR - Scientific Discussion","type":"scientific-discussion","status":"unknown","consultation_date":"","first_published_date":"2005-10-21T02:09:21Z","last_updated_date":"2005-10-21T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/scientific-discussion/optisulin-epar-scientific-discussion_en.pdf"},
    {"id":"28167","name":"Hycamtin : EPAR - Scientific Discussion","type":"scientific-discussion","status":"unknown","consultation_date":"","first_published_date":"2006-02-20T00:09:21Z","last_updated_date":"2006-02-20T00:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/scientific-discussion/hycamtin-epar-scientific-discussion_en.pdf"},
    {"id":"28408","name":"Porcilis Porcoli : EPAR - Scientific Discussion","type":"scientific-discussion","status":"unknown","consultation_date":"","first_published_date":"2008-10-01T02:09:21Z","last_updated_date":"2025-10-09T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/scientific-discussion/porcilis-porcoli-epar-scientific-discussion_en.pdf"},
    {"id":"28524","name":"Elaprase : EPAR - Scientific Discussion","type":"scientific-discussion","status":"unknown","consultation_date":"","first_published_date":"2007-01-18T01:00:00Z","last_updated_date":"2007-01-18T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/scientific-discussion/elaprase-epar-scientific-discussion_en.pdf"},
    {"id":"28615","name":"Yarvitan : EPAR - Scientific Discussion","type":"scientific-discussion","status":"unknown","consultation_date":"","first_published_date":"2007-09-04T02:00:00Z","last_updated_date":"2007-09-04T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/scientific-discussion/yarvitan-epar-scientific-discussion_en.pdf"},
    {"id":"28711","name":"Epoetin Alfa Hexal : EPAR - Scientific Discussion","type":"scientific-discussion","status":"unknown","consultation_date":"","first_published_date":"2007-09-13T02:00:00Z","last_updated_date":"2007-09-13T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/scientific-discussion/epoetin-alfa-hexal-epar-scientific-discussion_en.pdf"},
    {"id":"28727","name":"Azomyr : EPAR - Scientific Discussion","type":"scientific-discussion","status":"unknown","consultation_date":"","first_published_date":"2005-10-21T02:00:00Z","last_updated_date":"2005-10-21T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/scientific-discussion/azomyr-epar-scientific-discussion_en.pdf"},
    {"id":"28811","name":"Arixtra : EPAR - Scientific Discussion","type":"scientific-discussion","status":"unknown","consultation_date":"","first_published_date":"2005-11-04T01:00:00Z","last_updated_date":"2005-11-04T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/scientific-discussion/arixtra-epar-scientific-discussion_en.pdf"},
    {"id":"28848","name":"Insuman : EPAR - Scientific Discussion","type":"scientific-discussion","status":"unknown","consultation_date":"","first_published_date":"2006-08-09T02:00:00Z","last_updated_date":"2006-08-09T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/scientific-discussion/insuman-epar-scientific-discussion_en.pdf"},
    {"id":"28914","name":"Levviax : EPAR - Scientific Discussion","type":"scientific-discussion","status":"unknown","consultation_date":"","first_published_date":"2008-02-15T00:09:21Z","last_updated_date":"2008-02-15T00:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/scientific-discussion/levviax-epar-scientific-discussion_en.pdf"},
    {"id":"28938","name":"Rebetol : EPAR - Scientific Discussion","type":"scientific-discussion","status":"unknown","consultation_date":"","first_published_date":"2006-08-11T02:00:00Z","last_updated_date":"2023-11-07T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/scientific-discussion/rebetol-epar-scientific-discussion_en.pdf"},
    {"id":"28994","name":"Prialt : EPAR - Scientific Discussion","type":"scientific-discussion","status":"unknown","consultation_date":"","first_published_date":"2006-08-31T02:00:00Z","last_updated_date":"2006-08-31T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/scientific-discussion/prialt-epar-scientific-discussion_en.pdf"},
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    {"id":"33604","name":"Puregon : EPAR - Scientific Discussion","type":"scientific-discussion","status":"unknown","consultation_date":"","first_published_date":"2008-08-31T02:00:00Z","last_updated_date":"2008-08-31T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/scientific-discussion/puregon-epar-scientific-discussion_en.pdf"},
    {"id":"33713","name":"Porcilis PCV : EPAR - Scientific Discussion","type":"scientific-discussion","status":"unknown","consultation_date":"","first_published_date":"2009-01-27T00:09:21Z","last_updated_date":"2025-03-14T00:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/scientific-discussion/porcilis-pcv-epar-scientific-discussion_en.pdf"},
    {"id":"33803","name":"Zulvac 8 Bovis : EPAR - Scientific Discussion","type":"scientific-discussion","status":"unknown","consultation_date":"","first_published_date":"2010-01-21T01:00:00Z","last_updated_date":"2010-01-21T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/scientific-discussion/zulvac-8-bovis-epar-scientific-discussion_en.pdf"},
    {"id":"33881","name":"Nespo : EPAR - Scientific Discussion","type":"scientific-discussion","status":"unknown","consultation_date":"","first_published_date":"2009-01-29T00:09:21Z","last_updated_date":"2009-01-29T00:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/scientific-discussion/nespo-epar-scientific-discussion_en.pdf"},
    {"id":"33919","name":"Viread : EPAR - Scientific Discussion","type":"scientific-discussion","status":"unknown","consultation_date":"","first_published_date":"2006-04-06T02:00:00Z","last_updated_date":"2006-04-06T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/scientific-discussion/viread-epar-scientific-discussion_en.pdf"},
    {"id":"33937","name":"ViraferonPeg : EPAR - Scientific Discussion","type":"scientific-discussion","status":"unknown","consultation_date":"","first_published_date":"2006-08-11T02:00:00Z","last_updated_date":"2021-01-22T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/scientific-discussion/viraferonpeg-epar-scientific-discussion_en.pdf"},
    {"id":"34173","name":"Gonazon : EPAR - Scientific Discussion","type":"scientific-discussion","status":"unknown","consultation_date":"","first_published_date":"2007-01-15T01:00:00Z","last_updated_date":"2012-08-15T12:20:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/scientific-discussion/gonazon-epar-scientific-discussion_en.pdf"},
    {"id":"34258","name":"Torisel : EPAR - Scientific Discussion","type":"scientific-discussion","status":"unknown","consultation_date":"","first_published_date":"2007-12-05T01:00:00Z","last_updated_date":"2007-12-05T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/scientific-discussion/torisel-epar-scientific-discussion_en.pdf"},
    {"id":"34372","name":"Soliris : EPAR - Scientific Discussion","type":"scientific-discussion","status":"unknown","consultation_date":"","first_published_date":"2007-06-29T02:00:00Z","last_updated_date":"2007-06-29T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/scientific-discussion/soliris-epar-scientific-discussion_en.pdf"},
    {"id":"34419","name":"Pylobactell : EPAR - Scientific Discussion","type":"scientific-discussion","status":"unknown","consultation_date":"","first_published_date":"2005-12-07T01:00:00Z","last_updated_date":"2005-12-07T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/scientific-discussion/pylobactell-epar-scientific-discussion_en.pdf"},
    {"id":"34674","name":"Nobilis IB 4-91 : EPAR - Scientific Discussion","type":"scientific-discussion","status":"unknown","consultation_date":"","first_published_date":"2006-08-29T02:00:00Z","last_updated_date":"2024-10-17T09:33:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/scientific-discussion/nobilis-ib-4-91-epar-scientific-discussion_en.pdf"},
    {"id":"34728","name":"Aprovel : EPAR - Scientific Discussion","type":"scientific-discussion","status":"unknown","consultation_date":"","first_published_date":"2006-10-16T02:00:00Z","last_updated_date":"2006-10-16T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/scientific-discussion/aprovel-epar-scientific-discussion_en.pdf"},
    {"id":"34776","name":"Equilis Te : EPAR - Scientific Discussion","type":"scientific-discussion","status":"unknown","consultation_date":"","first_published_date":"2008-07-23T02:09:21Z","last_updated_date":"2025-03-07T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/scientific-discussion/equilis-te-epar-scientific-discussion_en.pdf"},
    {"id":"34912","name":"Poulvac Flufend H5N3 RG : EPAR - Scientific Discussion","type":"scientific-discussion","status":"unknown","consultation_date":"","first_published_date":"2006-09-13T02:00:00Z","last_updated_date":"2012-05-07T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/scientific-discussion/poulvac-flufend-h5n3-rg-epar-scientific-discussion_en.pdf"},
    {"id":"35023","name":"Prilactone : EPAR - Scientific Discussion","type":"scientific-discussion","status":"unknown","consultation_date":"","first_published_date":"2007-07-18T02:09:00Z","last_updated_date":"2007-07-18T02:09:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/scientific-discussion/prilactone-epar-scientific-discussion_en.pdf"},
    {"id":"35078","name":"Actrapid : EPAR - Scientific Discussion","type":"scientific-discussion","status":"unknown","consultation_date":"","first_published_date":"2006-04-03T02:00:00Z","last_updated_date":"2006-04-03T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/scientific-discussion/actrapid-epar-scientific-discussion_en.pdf"},
    {"id":"35134","name":"Ceprotin : EPAR - Scientific discussion","type":"scientific-discussion","status":"unknown","consultation_date":"","first_published_date":"2005-10-21T02:09:21Z","last_updated_date":"2005-10-21T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/scientific-discussion/ceprotin-epar-scientific-discussion_en.pdf"},
    {"id":"35138","name":"Ultratard : EPAR - Scientific Discussion","type":"scientific-discussion","status":"unknown","consultation_date":"","first_published_date":"2008-02-15T00:09:21Z","last_updated_date":"2008-02-15T00:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/scientific-discussion/ultratard-epar-scientific-discussion_en.pdf"},
    {"id":"35186","name":"Fevaxyn Pentofel : EPAR - Scientific Discussion","type":"scientific-discussion","status":"unknown","consultation_date":"","first_published_date":"2007-03-08T01:00:00Z","last_updated_date":"2024-11-21T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/scientific-discussion/fevaxyn-pentofel-epar-scientific-discussion_en.pdf"},
    {"id":"35428","name":"Oxyglobin : EPAR - Scientific Discussion","type":"scientific-discussion","status":"unknown","consultation_date":"","first_published_date":"2005-11-26T01:00:00Z","last_updated_date":"2025-10-09T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/scientific-discussion/oxyglobin-epar-scientific-discussion_en.pdf"},
    {"id":"35534","name":"Nobilis Influenza H7N1 : EPAR - Scientific Discussion","type":"scientific-discussion","status":"unknown","consultation_date":"","first_published_date":"2007-06-01T02:00:00Z","last_updated_date":"2010-07-26T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/scientific-discussion/nobilis-influenza-h7n1-epar-scientific-discussion_en.pdf"},
    {"id":"35562","name":"Twinrix Adult : EPAR - Scientific Discussion","type":"scientific-discussion","status":"unknown","consultation_date":"","first_published_date":"2005-12-01T00:09:21Z","last_updated_date":"2005-12-01T00:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/scientific-discussion/twinrix-adult-epar-scientific-discussion_en.pdf"},
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    {"id":"37592","name":"Irbesartan Hydrochlorothiazide Winthrop : EPAR - Scientific Discussion","type":"scientific-discussion","status":"unknown","consultation_date":"","first_published_date":"2007-02-05T01:00:00Z","last_updated_date":"2007-02-05T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/scientific-discussion/irbesartan-hydrochlorothiazide-winthrop-epar-scientific-discussion_en.pdf"},
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    {"id":"38460","name":"Keppra : EPAR - Scientific Discussion","type":"scientific-discussion","status":"unknown","consultation_date":"","first_published_date":"2005-10-21T02:00:00Z","last_updated_date":"2005-10-21T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/scientific-discussion/keppra-epar-scientific-discussion_en.pdf"},
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    {"id":"38552","name":"Celsentri : EPAR - Scientific Discussion","type":"scientific-discussion","status":"unknown","consultation_date":"","first_published_date":"2007-12-19T00:09:21Z","last_updated_date":"2007-12-19T00:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/scientific-discussion/celsentri-epar-scientific-discussion_en.pdf"},
    {"id":"38586","name":"Nobilis Influenza H5N6 : EPAR - Scientific Discussion","type":"scientific-discussion","status":"unknown","consultation_date":"","first_published_date":"2008-02-13T01:00:00Z","last_updated_date":"2010-07-26T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/scientific-discussion/nobilis-influenza-h5n6-epar-scientific-discussion_en.pdf"},
    {"id":"38634","name":"Ionsys : EPAR - Scientific Discussion","type":"scientific-discussion","status":"unknown","consultation_date":"","first_published_date":"2006-02-02T01:00:00Z","last_updated_date":"2011-01-28T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/scientific-discussion/ionsys-epar-scientific-discussion_en.pdf"},
    {"id":"38659","name":"Azilect : EPAR - Scientific Discussion","type":"scientific-discussion","status":"unknown","consultation_date":"","first_published_date":"2006-08-11T02:00:00Z","last_updated_date":"2006-08-11T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/scientific-discussion/azilect-epar-scientific-discussion_en.pdf"},
    {"id":"38758","name":"Xeloda : EPAR - Scientific Discussion","type":"scientific-discussion","status":"unknown","consultation_date":"","first_published_date":"2005-12-07T01:00:00Z","last_updated_date":"2005-12-07T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/scientific-discussion/xeloda-epar-scientific-discussion_en.pdf"},
    {"id":"38891","name":"Cubicin : EPAR - Scientific Discussion","type":"scientific-discussion","status":"unknown","consultation_date":"","first_published_date":"2006-08-11T02:00:00Z","last_updated_date":"2006-08-11T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/scientific-discussion/cubicin-epar-scientific-discussion_en.pdf"},
    {"id":"38974","name":"Cortavance : EPAR - Scientific Discussion","type":"scientific-discussion","status":"unknown","consultation_date":"","first_published_date":"2007-01-31T00:09:21Z","last_updated_date":"2007-01-31T00:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/scientific-discussion/cortavance-epar-scientific-discussion_en.pdf"},
    {"id":"39009","name":"Pirsue : EPAR - Scientific Discussion","type":"scientific-discussion","status":"unknown","consultation_date":"","first_published_date":"2006-11-23T00:09:21Z","last_updated_date":"2025-05-12T00:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/scientific-discussion/pirsue-epar-scientific-discussion_en.pdf"},
    {"id":"39201","name":"Combivir : EPAR - Scientific Discussion","type":"scientific-discussion","status":"unknown","consultation_date":"","first_published_date":"2005-11-17T00:09:21Z","last_updated_date":"2005-11-17T00:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/scientific-discussion/combivir-epar-scientific-discussion_en.pdf"},
    {"id":"39248","name":"Equilis Prequenza : EPAR - Scientific Discussion","type":"scientific-discussion","status":"unknown","consultation_date":"","first_published_date":"2005-10-21T02:09:21Z","last_updated_date":"2025-03-07T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/scientific-discussion/equilis-prequenza-epar-scientific-discussion_en.pdf"},
    {"id":"39428","name":"Raptiva : EPAR - Scientific Discussion","type":"scientific-discussion","status":"unknown","consultation_date":"","first_published_date":"2009-08-04T02:00:00Z","last_updated_date":"2009-08-04T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/scientific-discussion/raptiva-epar-scientific-discussion_en.pdf"},
    {"id":"39464","name":"Intrinsa : EPAR - Scientific Discussion","type":"scientific-discussion","status":"unknown","consultation_date":"","first_published_date":"2006-09-05T02:00:00Z","last_updated_date":"2012-06-18T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/scientific-discussion/intrinsa-epar-scientific-discussion_en.pdf"},
    {"id":"39481","name":"Luminity : EPAR - Scientific Discussion","type":"scientific-discussion","status":"unknown","consultation_date":"","first_published_date":"2006-10-19T02:00:00Z","last_updated_date":"2014-06-17T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/scientific-discussion/luminity-epar-scientific-discussion_en.pdf"},
    {"id":"39487","name":"Revatio : EPAR - Scientific Discussion","type":"scientific-discussion","status":"unknown","consultation_date":"","first_published_date":"2006-10-11T02:00:00Z","last_updated_date":"2006-10-11T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/scientific-discussion/revatio-epar-scientific-discussion_en.pdf"},
    {"id":"39494","name":"Gliolan : EPAR - Scientific Discussion","type":"scientific-discussion","status":"unknown","consultation_date":"","first_published_date":"2007-09-24T02:09:21Z","last_updated_date":"2007-09-24T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/scientific-discussion/gliolan-epar-scientific-discussion_en.pdf"},
    {"id":"39583","name":"Previcox : EPAR - Scientific Discussion","type":"scientific-discussion","status":"unknown","consultation_date":"","first_published_date":"2007-03-16T00:09:21Z","last_updated_date":"2025-01-10T00:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/scientific-discussion/previcox-epar-scientific-discussion_en.pdf"},
    {"id":"39660","name":"Aldurazyme : EPAR - Scientific Discussion","type":"scientific-discussion","status":"unknown","consultation_date":"","first_published_date":"2005-10-21T02:00:00Z","last_updated_date":"2005-10-21T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/scientific-discussion/aldurazyme-epar-scientific-discussion_en.pdf"},
    {"id":"39715","name":"Opatanol : EPAR - Scientific Discussion","type":"scientific-discussion","status":"unknown","consultation_date":"","first_published_date":"2005-10-21T02:00:00Z","last_updated_date":"2005-10-21T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/scientific-discussion/opatanol-epar-scientific-discussion_en.pdf"},
    {"id":"39919","name":"Procoralan : EPAR - Scientific Discussion","type":"scientific-discussion","status":"unknown","consultation_date":"","first_published_date":"2005-11-04T01:00:00Z","last_updated_date":"2005-11-04T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/scientific-discussion/procoralan-epar-scientific-discussion_en.pdf"},
    {"id":"40080","name":"Macugen : EPAR - Scientific Discussion","type":"scientific-discussion","status":"unknown","consultation_date":"","first_published_date":"2007-05-31T02:00:00Z","last_updated_date":"2019-06-27T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/scientific-discussion/macugen-epar-scientific-discussion_en.pdf"},
    {"id":"40132","name":"Zulvac 8 Ovis : EPAR - Scientific Discussion","type":"scientific-discussion","status":"unknown","consultation_date":"","first_published_date":"2010-01-21T01:00:00Z","last_updated_date":"2025-10-15T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/scientific-discussion/zulvac-8-ovis-epar-scientific-discussion_en.pdf"},
    {"id":"40236","name":"BTVPUR AlSap 1 : EPAR - Scientific Discussion","type":"scientific-discussion","status":"unknown","consultation_date":"","first_published_date":"2011-01-03T01:00:00Z","last_updated_date":"2018-05-17T02:00:00Z","reference_number":"EMA/CVMP/622300/2010","document_url":"https://www.ema.europa.eu/en/documents/scientific-discussion/btvpur-alsap-1-epar-scientific-discussion_en.pdf"},
    {"id":"40253","name":"Temodal : EPAR - Scientific Discussion","type":"scientific-discussion","status":"unknown","consultation_date":"","first_published_date":"2005-12-13T00:09:21Z","last_updated_date":"2005-12-13T00:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/scientific-discussion/temodal-epar-scientific-discussion_en.pdf"},
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    {"id":"45772","name":"Tecentriq-H-C-PSUSA-00010644-201811 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2019-10-23T12:31:00Z","last_updated_date":"2019-10-23T12:31:00Z","reference_number":"EMA/577018/2019","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/tecentriq-h-c-psusa-00010644-201811-epar-scientific-conclusions-and-grounds-variation-terms-marketing-authorisation_en.pdf"},
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    {"id":"46052","name":"Abraxane-H-C-PSUSA-00010123-201901 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2019-11-18T16:11:00Z","last_updated_date":"2019-11-18T16:11:00Z","reference_number":"EMA/564160/2019","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/abraxane-h-c-psusa-00010123-201901-epar-scientific-conclusions-and-grounds-variation-terms-marketing-authorisation_en.pdf"},
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    {"id":"46096","name":"Fulphila-H-C-PSUSA-00002326-201901 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"Adopted","consultation_date":"","first_published_date":"2019-11-21T14:50:00Z","last_updated_date":"2019-11-21T14:50:00Z","reference_number":"EMA/562284/2019","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/fulphila-h-c-psusa-00002326-201901-epar-scientific-conclusions-and-grounds-variation-terms-marketing-authorisation_en.pdf"},
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    {"id":"53700","name":"Zoely-H-C-001213-SW-0058 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2022-01-12T13:01:00Z","last_updated_date":"2022-01-12T13:01:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/zoely-h-c-001213-sw-0058-epar-scientific-conclusions-and-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"53701","name":"Zoely-H-C-001213-PSUSA-2182-202101 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2022-01-12T13:06:00Z","last_updated_date":"2022-01-12T13:06:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/zoely-h-c-001213-psusa-2182-202101-epar-scientific-conclusions-and-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"53703","name":"Selincro-H-C-PSUSA-00010120-202102 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2022-01-13T09:59:00Z","last_updated_date":"2022-01-13T09:59:00Z","reference_number":"EMA/17065/2022","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/selincro-h-c-psusa-00010120-202102-epar-scientific-conclusions-and-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"53733","name":"Tecfidera-H-C-PSUSA-00010143-202103 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2022-01-14T15:47:00Z","last_updated_date":"2022-01-14T15:47:00Z","reference_number":"EMA/730120/2021","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/tecfidera-h-c-psusa-00010143-202103-epar-scientific-conclusions-and-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"53737","name":"Rinvoq-H-C-PSUSA-00010823-202102 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"Adopted","consultation_date":"","first_published_date":"2022-01-10T16:34:00Z","last_updated_date":"2022-01-10T16:34:00Z","reference_number":"EMA/773886/2021","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/rinvoq-h-c-psusa-00010823-202102-epar-scientific-conclusions-and-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"53814","name":"Vfend-H-C-PSUSA-00003127-202102 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2022-01-18T13:00:00Z","last_updated_date":"2022-01-18T13:00:00Z","reference_number":"EMA/616868/2021","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/vfend-h-c-psusa-00003127-202102-epar-scientific-conclusions-and-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"53837","name":"Inhixa-H-C-PSUSA-00010833-202104 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2022-01-19T15:01:00Z","last_updated_date":"2022-01-19T15:01:00Z","reference_number":"EMA/617395/2021","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/inhixa-h-c-psusa-00010833-202104-epar-scientific-conclusions-and-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"53877","name":"Bavencio-H-C-PSUSA-00010635-202103 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2022-01-21T14:43:00Z","last_updated_date":"2022-01-21T14:43:00Z","reference_number":"EMA/760025/2021","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/bavencio-h-c-psusa-00010635-202103-epar-scientific-conclusions-and-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"53889","name":"Yervoy-H-C-PSUSA-00009200-202103 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2022-01-24T11:48:00Z","last_updated_date":"2022-01-24T11:48:00Z","reference_number":"EMA/760060/2021","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/yervoy-h-c-psusa-00009200-202103-epar-scientific-conclusions-and-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"53905","name":"Lumigan-H-C-PSUSA-00000413-202103 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2022-01-25T16:25:00Z","last_updated_date":"2022-01-25T16:25:00Z","reference_number":"EMA/49623/2022","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/lumigan-h-c-psusa-00000413-202103-epar-scientific-conclusions-and-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"53937","name":"Vocabria-H-C-PSUSA-00010900-202109 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2022-01-27T09:27:00Z","last_updated_date":"2022-01-27T09:27:00Z","reference_number":"EMA/10440/2022","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/vocabria-h-c-psusa-00010900-202109-epar-scientific-conclusions-and-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"53955","name":"Dupixent-H-C-PSUSA-00010645-202103 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2022-01-27T14:31:00Z","last_updated_date":"2022-01-27T14:31:00Z","reference_number":"EMA/53041/2022","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/dupixent-h-c-psusa-00010645-202103-epar-scientific-conclusions-and-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"54000","name":"Libtayo-H-C-PSUSA-00010780-202103 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2022-01-28T11:43:00Z","last_updated_date":"2022-01-28T11:43:00Z","reference_number":"EMA/33062/2022","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/libtayo-h-c-psusa-00010780-202103-epar-scientific-conclusions-and-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"54006","name":"Caprelsa-H-C-PSUSA-00009327-202104 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2022-01-28T12:47:00Z","last_updated_date":"2022-01-28T12:47:00Z","reference_number":"EMA/49355/2022","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/caprelsa-h-c-psusa-00009327-202104-epar-scientific-conclusions-and-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"54079","name":"Sarclisa-H-C-PSUSA-00010851-202103 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2022-02-04T13:47:00Z","last_updated_date":"2022-02-04T13:47:00Z","reference_number":"EMA/73528/2022","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/sarclisa-h-c-psusa-00010851-202103-epar-scientific-conclusions-and-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"54190","name":"Spikevax (previously COVID-19 Vaccine Moderna)-H-C-PSUSA-00010897-202106: EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2022-02-16T13:30:00Z","last_updated_date":"2022-02-16T13:30:00Z","reference_number":"EMA/104540/2022","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/spikevax-previously-covid-19-vaccine-moderna-h-c-psusa-00010897-202106-epar-scientific-conclusions-and-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"54247","name":"Deltyba-H-C-PSUSA-00010213-202104 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2022-02-22T16:06:00Z","last_updated_date":"2022-02-22T16:06:00Z","reference_number":"EMA/723817/2021","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/deltyba-h-c-psusa-00010213-202104-epar-scientific-conclusions-and-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"54321","name":"Advagraf-H-C-PSUSA-00002839-202103 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2022-03-01T16:14:00Z","last_updated_date":"2022-03-01T16:14:00Z","reference_number":"EMA/59278/2022","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/advagraf-h-c-psusa-00002839-202103-epar-scientific-conclusions-and-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"54322","name":"Modigraf-H-C-PSUSA-00002839- 202103 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2022-03-01T16:35:00Z","last_updated_date":"2022-03-01T16:35:00Z","reference_number":"EMA/59278/2022","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/modigraf-h-c-psusa-00002839-202103-epar-scientific-conclusions-and-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"54323","name":"Envarsus-H-C-PSUSA-00002839-202103 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2022-03-01T16:49:00Z","last_updated_date":"2022-03-01T16:49:00Z","reference_number":"EMA/59278/2022","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/envarsus-h-c-psusa-00002839-202103-epar-scientific-conclusions-and-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"54328","name":"Mycophenolate mofetil Teva-H-C-PSUSA-00010550-202105 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2022-03-02T16:02:00Z","last_updated_date":"2022-03-02T16:02:00Z","reference_number":"EMA/45415/2022","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/mycophenolate-mofetil-teva-h-c-psusa-00010550-202105-epar-scientific-conclusions-and-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"54329","name":"Myfenax-H-C-PSUSA-00010550-202105 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2022-03-02T16:12:00Z","last_updated_date":"2022-03-02T16:12:00Z","reference_number":"EMA/45415/2022","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/myfenax-h-c-psusa-00010550-202105-epar-scientific-conclusions-and-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"54331","name":"Myclausen-H-C-PSUSA-00010550-202105 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2022-03-02T16:29:00Z","last_updated_date":"2022-03-02T16:29:00Z","reference_number":"EMA/45415/2022","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/myclausen-h-c-psusa-00010550-202105-epar-scientific-conclusions-and-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"54332","name":"CellCept-H-C-PSUSA-00010550-202105 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2022-03-02T16:44:00Z","last_updated_date":"2022-03-02T16:44:00Z","reference_number":"EMA/45415/2022","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/cellcept-h-c-psusa-00010550-202105-epar-scientific-conclusions-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"54346","name":"Myclausen-H-C-PSUSA-00010550-202005 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2022-03-03T08:25:00Z","last_updated_date":"2022-03-03T08:25:00Z","reference_number":"EMA/45315/2022","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/myclausen-h-c-psusa-00010550-202005-epar-scientific-conclusions-and-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"54439","name":"Retsevmo-H-C-PSUSA-00010917-202105 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2022-03-14T11:48:00Z","last_updated_date":"2022-03-14T11:48:00Z","reference_number":"EMA/34538/2022","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/retsevmo-h-c-psusa-00010917-202105-epar-scientific-conclusions-and-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"54440","name":"Tecentriq-H-C-PSUSA-00010644-202105 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2022-03-14T13:15:00Z","last_updated_date":"2022-03-14T13:15:00Z","reference_number":"EMA/31563/2022","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/tecentriq-h-c-psusa-00010644-202105-epar-scientific-conclusions-and-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"54527","name":"ellaOne-H-C-PSUSA-00003074-202105 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2022-03-21T12:27:00Z","last_updated_date":"2022-03-21T12:27:00Z","reference_number":"EMA/28536/2022","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/ellaone-h-c-psusa-00003074-202105-epar-scientific-conclusions-and-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"54604","name":"Ajovy-H-C-PSUSA-00010758-202103 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2022-03-29T09:47:00Z","last_updated_date":"2022-03-29T09:47:00Z","reference_number":"EMA/186908/2022","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/ajovy-h-c-psusa-00010758-202103-epar-scientific-conclusions-and-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"54608","name":"Intuniv-H-C-PSUSA-00010413-202103 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2022-03-29T12:05:00Z","last_updated_date":"2022-03-29T12:05:00Z","reference_number":"EMA/189856/2022","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/intuniv-h-c-psusa-00010413-202103-epar-scientific-conclusions-and-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"54625","name":"Jardiance-H-C-PSUSA-00010388-202104 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2022-03-30T13:54:00Z","last_updated_date":"2022-03-30T13:54:00Z","reference_number":"EMA/193077/2022","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/jardiance-h-c-psusa-00010388-202104-epar-scientific-conclusions-and-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"54628","name":"Synjardy-H-C-PSUSA-00010388-202104 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2022-03-30T16:04:00Z","last_updated_date":"2022-03-30T16:04:00Z","reference_number":"EMA/189983/2022","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/synjardy-h-c-psusa-00010388-202104-epar-scientific-conclusions-and-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"54633","name":"Lenalidomide Mylan-H-C-PSUSA-00001838-202012 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2022-03-31T10:42:00Z","last_updated_date":"2022-03-31T10:42:00Z","reference_number":"EMA/618753/2021","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/lenalidomide-mylan-h-c-psusa-00001838-202012-epar-scientific-conclusions-and-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"54664","name":"Imfinzi-H-C-PSUSA-00010723-202104 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2022-04-04T12:28:00Z","last_updated_date":"2022-04-04T12:28:00Z","reference_number":"EMA/759829/2021","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/imfinzi-h-c-psusa-00010723-202104-epar-scientific-conclusions-and-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"54665","name":"Eliquis-H-C-PSUSA-00000226-202105 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2022-04-04T13:09:00Z","last_updated_date":"2022-04-04T13:09:00Z","reference_number":"EMA/201095/2022","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/eliquis-h-c-psusa-00000226-202105-epar-scientific-conclusions-and-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"54667","name":"Palynziq-H-C-PSUSA-00010761-202011 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2022-04-04T16:45:00Z","last_updated_date":"2022-04-04T16:45:00Z","reference_number":"EMA/201624/2022","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/palynziq-h-c-psusa-00010761-202011-epar-scientific-conclusions-and-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"54676","name":"Glivec-H-C-PSUSA-00001725-202105 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2022-04-05T11:27:00Z","last_updated_date":"2022-04-05T11:27:00Z","reference_number":"EMA/176831/2022","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/glivec-h-c-psusa-00001725-202105-epar-scientific-conclusions-and-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"54782","name":"Sprycel-PSUSA-00000935-202106 : EPAR - Scientific conclusions and grounds recommending the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"Adopted","consultation_date":"","first_published_date":"2022-04-21T14:05:00Z","last_updated_date":"2022-04-21T14:05:00Z","reference_number":"EMA/176825/2022","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/sprycel-psusa-00000935-202106-epar-scientific-conclusions-and-grounds-recommending-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"54854","name":"Revatio-H-C-PSUSA-00002700-202105 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"Adopted","consultation_date":"","first_published_date":"2022-04-28T13:45:00Z","last_updated_date":"2022-04-28T13:45:00Z","reference_number":"EMA/233858/2022","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/revatio-h-c-psusa-00002700-202105-epar-scientific-conclusions-and-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"54860","name":"Byfavo-H-C-PSUSA-00010924-202107 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2022-04-28T15:38:00Z","last_updated_date":"2022-04-28T15:38:00Z","reference_number":"EMA/CHMP/236426/2022","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/byfavo-h-c-psusa-00010924-202107-epar-scientific-conclusions-and-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"54867","name":"Ultomiris-H-C-PSUSA-00010787-202106 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2022-04-29T15:13:00Z","last_updated_date":"2022-04-29T15:13:00Z","reference_number":"EMA/208358/2022","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/ultomiris-h-c-psusa-00010787-202106-epar-scientific-conclusions-and-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"54877","name":"Vazkepa-H-C-PSUSA-00010922-202107 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2022-05-02T17:33:00Z","last_updated_date":"2022-05-02T17:33:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/vazkepa-h-c-psusa-00010922-202107-epar-scientific-conclusions-and-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"54878","name":"Vidaza-H-C-PSUSA-00000274-202105 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2022-05-03T09:02:00Z","last_updated_date":"2022-05-03T09:02:00Z","reference_number":"EMA/244434/2022","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/vidaza-h-c-psusa-00000274-202105-epar-scientific-conclusions-and-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"54915","name":"Nerlynx-H-C-PSUSA-00010712-202107 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2022-05-06T09:02:00Z","last_updated_date":"2022-05-06T09:02:00Z","reference_number":"EMA/253595/2022","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/nerlynx-h-c-psusa-00010712-202107-epar-scientific-conclusions-and-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"54919","name":"Opdivo-H-C-PSUSA-00010379-202107 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2022-05-10T14:28:00Z","last_updated_date":"2022-05-10T14:28:00Z","reference_number":"EMA/178011/2022","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/opdivo-h-c-psusa-00010379-202107-epar-scientific-conclusions-and-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"54931","name":"Lenalidomide Mylan-H-C-PSUSA-00001838-202012 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2022-05-11T10:22:00Z","last_updated_date":"2022-05-31T11:55:00Z","reference_number":"EMA/618753/2021","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/lenalidomide-mylan-h-c-psusa-00001838-202012-epar-scientific-conclusions-and-grounds-variation-terms-marketing-authorisation_en.pdf-0"},
    {"id":"55135","name":"Symkevi-H-C-PSUSA-00010730-202108 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2022-06-07T10:21:00Z","last_updated_date":"2022-06-07T10:21:00Z","reference_number":"EMA/214293/2022","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/symkevi-h-c-psusa-00010730-202108-epar-scientific-conclusions-and-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"55149","name":"Tysabri-H-C-PSUSA-00002127-202108 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2022-06-08T11:35:00Z","last_updated_date":"2022-06-08T11:35:00Z","reference_number":"EMA/561269/2022","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/tysabri-h-c-psusa-00002127-202108-epar-scientific-conclusions-and-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"55150","name":"Rinvoq-H-C-PSUSA-00010823-202108 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2022-06-08T11:44:00Z","last_updated_date":"2022-06-08T11:44:00Z","reference_number":"EMA/567578/2022","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/rinvoq-h-c-psusa-00010823-202108-epar-scientific-conclusions-and-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"55159","name":"Aerinaze-H-C-PSUSA-00000963-202107 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2022-06-09T09:49:00Z","last_updated_date":"2022-06-09T09:49:00Z","reference_number":"EMA/567613/2022","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/aerinaze-h-c-psusa-00000963-202107-epar-scientific-conclusions-and-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"55160","name":"Aerius-H-C-PSUSA-00000962-202107 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2022-06-09T10:27:00Z","last_updated_date":"2022-06-09T10:27:00Z","reference_number":"EMA/567651/2022","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/aerius-h-c-psusa-00000962-202107-epar-scientific-conclusions-and-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"55161","name":"Azomyr-H-C-PSUSA-00000962-202107 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"Adopted","consultation_date":"","first_published_date":"2022-06-09T10:43:00Z","last_updated_date":"2022-06-09T10:43:00Z","reference_number":"EMA/567651/2022","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/azomyr-h-c-psusa-00000962-202107-epar-scientific-conclusions-and-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"55162","name":"Neoclarityn-H-C-PSUSA-00000962-202107 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2022-06-09T10:52:00Z","last_updated_date":"2022-06-09T10:52:00Z","reference_number":"EMA/567651/2022","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/neoclarityn-h-c-psusa-00000962-202107-epar-scientific-conclusions-and-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"55163","name":"Dasselta-H-C-PSUSA-00000962-202107 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2022-06-09T11:21:00Z","last_updated_date":"2022-06-09T11:21:00Z","reference_number":"EMA/567651/2022","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/dasselta-h-c-psusa-00000962-202107-epar-scientific-conclusions-and-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"55164","name":"Desloratadine Actavis-H-C-PSUSA-00000962-202107: EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2022-06-09T11:37:00Z","last_updated_date":"2022-06-09T11:37:00Z","reference_number":"EMA/567651/2022","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/desloratadine-actavis-h-c-psusa-00000962-202107-epar-scientific-conclusions-and-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"55165","name":"Desloratadine ratiopharm-H-C-PSUSA-00000962-202107 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2022-06-09T11:46:00Z","last_updated_date":"2022-06-09T11:46:00Z","reference_number":"EMA/567651/2022","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/desloratadine-ratiopharm-h-c-psusa-00000962-202107-epar-scientific-conclusions-and-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"55166","name":"Desloratadine Teva-H-C-PSUSA-00000962-202107 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2022-06-09T11:55:00Z","last_updated_date":"2022-06-09T11:55:00Z","reference_number":"EMA/567651/2022","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/desloratadine-teva-h-c-psusa-00000962-202107-epar-scientific-conclusions-and-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"55383","name":"Xalkori-PSUSA-00010042-202108 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2022-06-27T11:14:00Z","last_updated_date":"2022-06-27T11:14:00Z","reference_number":"EMA/246133/2022","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/xalkori-psusa-00010042-202108-epar-scientific-conclusions-and-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"55407","name":"Keytruda-H-C-PSUSA-00010403-202109 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2022-06-29T13:47:00Z","last_updated_date":"2022-06-29T13:47:00Z","reference_number":"EMA/245000/2022","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/keytruda-h-c-psusa-00010403-202109-epar-scientific-conclusions-and-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"55452","name":"Mysimba-H-C-PSUSA-00010366-202109: EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2022-07-05T09:48:00Z","last_updated_date":"2022-07-05T09:48:00Z","reference_number":"EMA/621881/2022","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/mysimba-h-c-psusa-00010366-202109-epar-scientific-conclusions-and-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"55455","name":"Fycompa-H-C-PSUSA-00009255-202107: EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2022-07-05T10:28:00Z","last_updated_date":"2022-07-05T10:28:00Z","reference_number":"EMA/248596/2022","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/fycompa-h-c-psusa-00009255-202107-epar-scientific-conclusions-and-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"55470","name":"Epclusa : EPAR - Scientific conclusions - Annex IV","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2022-07-06T13:51:00Z","last_updated_date":"2022-07-06T13:51:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/epclusa-epar-scientific-conclusions-annex-iv_en.pdf"},
    {"id":"55471","name":"Sovaldi : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation(s)","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2022-07-06T14:29:00Z","last_updated_date":"2022-07-06T14:29:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/sovaldi-epar-scientific-conclusions-and-grounds-variation-terms-marketing-authorisations_en.pdf"},
    {"id":"55475","name":"Harvoni : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation(s)","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2022-07-06T14:43:00Z","last_updated_date":"2022-07-06T14:43:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/harvoni-epar-scientific-conclusions-and-grounds-variation-terms-marketing-authorisations_en.pdf"},
    {"id":"55489","name":"Viekirax-H-C-PSUV/SA/Art 20/Art 107i/Art 3 : Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2022-07-07T14:32:00Z","last_updated_date":"2024-10-02T09:42:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/viekirax-h-c-psuv-sa-art-20-art-107i-art-3-scientific-conclusions-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"55490","name":"Zepatier : EPAR - Scientific conclusions - Annex IV","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2022-07-07T14:37:00Z","last_updated_date":"2022-07-07T14:37:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/zepatier-epar-scientific-conclusions-annex-iv_en.pdf"},
    {"id":"55492","name":"Exviera : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation(s)","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2022-07-07T15:25:00Z","last_updated_date":"2024-10-01T16:12:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/exviera-epar-scientific-conclusions-grounds-variation-terms-marketing-authorisations_en.pdf"},
    {"id":"55494","name":"Vosevi-H-C-PSUV/SA/Art 20/Art 107i/Art 31 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2022-07-07T16:33:00Z","last_updated_date":"2022-07-07T16:33:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/vosevi-h-c-psuvsaart-20art-107iart-31-epar-scientific-conclusions-and-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"55495","name":"Xofigo : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation(s)","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2022-07-07T17:03:00Z","last_updated_date":"2022-07-07T17:03:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/xofigo-epar-scientific-conclusions-and-grounds-variation-terms-marketing-authorisations_en.pdf"},
    {"id":"55509","name":"Azopt-H-C-PSUSA-00000432-202108 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation(s)","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2022-07-11T11:25:00Z","last_updated_date":"2022-07-11T11:25:00Z","reference_number":"EMA/288085/2022","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/azopt-h-c-psusa-00000432-202108-epar-scientific-conclusions-and-grounds-variation-terms-marketing-authorisations_en.pdf"},
    {"id":"55665","name":"Emgality-H-C-PSUSA-00010733-202109 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2022-07-22T14:54:00Z","last_updated_date":"2022-07-22T14:54:00Z","reference_number":"EMA/260516/2022","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/emgality-h-c-psusa-00010733-202109-epar-scientific-conclusions-and-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"55678","name":"Mayzent-PSUSA-00010818-202109: EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2022-07-25T11:45:00Z","last_updated_date":"2022-07-25T11:45:00Z","reference_number":"EMA/260476/2022","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/mayzent-psusa-00010818-202109-epar-scientific-conclusions-and-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"55728","name":"Veklury-H-C-PSUSA-00010840-202111: EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"Adopted","consultation_date":"","first_published_date":"2022-07-28T17:13:00Z","last_updated_date":"2022-07-28T17:13:00Z","reference_number":"EMA/666352/2022","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/veklury-h-c-psusa-00010840-202111-epar-scientific-conclusions-and-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"55729","name":"Sarclisa-H-C-PSUSA-00010851-202103 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2022-07-28T17:49:00Z","last_updated_date":"2022-10-03T15:53:00Z","reference_number":"EMA/798010/2022","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/sarclisa-h-c-psusa-00010851-202103-epar-scientific-conclusions-and-grounds-variation-terms-marketing-authorisation_en.pdf-0"},
    {"id":"55759","name":"Bonviva-H-C-PSUSA-00001702-202106 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation(s)","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2022-08-02T10:55:00Z","last_updated_date":"2022-08-02T10:55:00Z","reference_number":"EMA/674875/2022","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/bonviva-h-c-psusa-00001702-202106-epar-scientific-conclusions-and-grounds-variation-terms-marketing-authorisations_en.pdf"},
    {"id":"55819","name":"Vaxzevria (previously COVID-19 Vaccine AstraZeneca)-H-C-PSUSA-00010912-202112 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation(s)","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2022-08-12T12:47:00Z","last_updated_date":"2024-05-07T11:00:00Z","reference_number":"EMA/666408/2022","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/vaxzevria-previously-covid-19-vaccine-astrazeneca-h-c-psusa-00010912-202112-epar-scientific-conclusions-grounds-variation-terms-marketing-authorisations_en.pdf"},
    {"id":"55863","name":"Maviret : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation(s)","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2022-08-23T10:24:00Z","last_updated_date":"2022-08-23T10:24:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/maviret-epar-scientific-conclusions-and-grounds-variation-terms-marketing-authorisations_en.pdf"},
    {"id":"55870","name":"Spikevax (previously COVID-19 Vaccine Moderna)-H-C-PSUSA-00010897-202112: EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2022-08-25T09:05:00Z","last_updated_date":"2022-08-25T09:05:00Z","reference_number":"EMA/708151/2022","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/spikevax-previously-covid-19-vaccine-moderna-h-c-psusa-00010897-202112-epar-scientific-conclusions-and-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"55904","name":"MabThera-H-C-PSUSA-00002652-202111 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2022-08-31T14:45:00Z","last_updated_date":"2022-08-31T14:45:00Z","reference_number":"EMA/592634/2022","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/mabthera-h-c-psusa-00002652-202111-epar-scientific-conclusions-and-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"55961","name":"Genvoya-H-C-PSUSA-00010449-202111 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2022-09-02T12:54:00Z","last_updated_date":"2022-09-02T12:54:00Z","reference_number":"EMA/723246/2022","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/genvoya-h-c-psusa-00010449-202111-epar-scientific-conclusions-and-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"55973","name":"Truxima : EPAR-H-C-PSUSA-00002652-202111 - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation(s)","type":"scientific-conclusion","status":"Adopted","consultation_date":"","first_published_date":"2022-09-05T12:13:00Z","last_updated_date":"2022-09-05T12:13:00Z","reference_number":"EMA/592634/2022","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/truxima-epar-h-c-psusa-00002652-202111-scientific-conclusions-and-grounds-variation-terms-marketing-authorisations_en.pdf"},
    {"id":"55978","name":"Myozyme-H-C-PSUSA-00000086-02109 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2022-09-05T14:48:00Z","last_updated_date":"2022-09-05T14:48:00Z","reference_number":"EMA/723723/2022 ","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/myozyme-h-c-psusa-00000086-02109-epar-scientific-conclusions-and-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"55983","name":"Suliqua-H-C-PSUSA-00010577-202111 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2022-09-05T15:54:00Z","last_updated_date":"2022-09-05T15:54:00Z","reference_number":"EMA/725796/2022","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/suliqua-h-c-psusa-00010577-202111-epar-scientific-conclusions-and-grounds-variation-terms-marketing-authorisation_en.pdf"},
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    {"id":"55992","name":"Fetcroja-H-C-PSUSA-00010849-202111 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2022-09-06T08:57:00Z","last_updated_date":"2022-09-06T08:57:00Z","reference_number":"EMA/711450/2022","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/fetcroja-h-c-psusa-00010849-202111-epar-scientific-conclusions-and-grounds-variation-terms-marketing-authorisation_en.pdf"},
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    {"id":"56236","name":"Xeljanz-H-C-PSUSA-00010588-202111 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2022-09-28T15:15:00Z","last_updated_date":"2022-09-28T15:15:00Z","reference_number":"EMA/780791/2022","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/xeljanz-h-c-psusa-00010588-202111-epar-scientific-conclusions-and-grounds-variation-terms-marketing-authorisation_en.pdf"},
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    {"id":"56467","name":"SomaKit TOC-H-C-PSUSA-00010552-202112 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2022-10-25T11:34:00Z","last_updated_date":"2022-10-25T11:34:00Z","reference_number":"EMA/846899/2022","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/somakit-toc-h-c-psusa-00010552-202112-epar-scientific-conclusions-and-grounds-variation-terms-marketing-authorisation_en.pdf"},
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    {"id":"56566","name":"Rubraca : EPAR - Scientific conclusions Annex IV","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2022-11-09T16:34:00Z","last_updated_date":"2022-11-09T16:34:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/rubraca-epar-scientific-conclusions-annex-iv_en.pdf","translations":{"bg":"https://www.ema.europa.eu/bg/documents/scientific-conclusion/rubraca-epar-scientific-conclusions-annex-iv_bg.pdf","es":"https://www.ema.europa.eu/es/documents/scientific-conclusion/rubraca-epar-scientific-conclusions-annex-iv_es.pdf","cs":"https://www.ema.europa.eu/cs/documents/scientific-conclusion/rubraca-epar-scientific-conclusions-annex-iv_cs.pdf","da":"https://www.ema.europa.eu/da/documents/scientific-conclusion/rubraca-epar-scientific-conclusions-annex-iv_da.pdf","de":"https://www.ema.europa.eu/de/documents/scientific-conclusion/rubraca-epar-scientific-conclusions-annex-iv_de.pdf","et":"https://www.ema.europa.eu/et/documents/scientific-conclusion/rubraca-epar-scientific-conclusions-annex-iv_et.pdf","el":"https://www.ema.europa.eu/el/documents/scientific-conclusion/rubraca-epar-scientific-conclusions-annex-iv_el.pdf","fr":"https://www.ema.europa.eu/fr/documents/scientific-conclusion/rubraca-epar-scientific-conclusions-annex-iv_fr.pdf","hr":"https://www.ema.europa.eu/hr/documents/scientific-conclusion/rubraca-epar-scientific-conclusions-annex-iv_hr.pdf","it":"https://www.ema.europa.eu/it/documents/scientific-conclusion/rubraca-epar-scientific-conclusions-annex-iv_it.pdf","lv":"https://www.ema.europa.eu/lv/documents/scientific-conclusion/rubraca-epar-scientific-conclusions-annex-iv_lv.pdf","lt":"https://www.ema.europa.eu/lt/documents/scientific-conclusion/rubraca-epar-scientific-conclusions-annex-iv_lt.pdf","hu":"https://www.ema.europa.eu/hu/documents/scientific-conclusion/rubraca-epar-scientific-conclusions-annex-iv_hu.pdf","mt":"https://www.ema.europa.eu/mt/documents/scientific-conclusion/rubraca-epar-scientific-conclusions-annex-iv_mt.pdf","nl":"https://www.ema.europa.eu/nl/documents/scientific-conclusion/rubraca-epar-scientific-conclusions-annex-iv_nl.pdf","pl":"https://www.ema.europa.eu/pl/documents/scientific-conclusion/rubraca-epar-scientific-conclusions-annex-iv_pl.pdf","pt":"https://www.ema.europa.eu/pt/documents/scientific-conclusion/rubraca-epar-scientific-conclusions-annex-iv_pt.pdf","ro":"https://www.ema.europa.eu/ro/documents/scientific-conclusion/rubraca-epar-scientific-conclusions-annex-iv_ro.pdf","sk":"https://www.ema.europa.eu/sk/documents/scientific-conclusion/rubraca-epar-scientific-conclusions-annex-iv_sk.pdf","sl":"https://www.ema.europa.eu/sl/documents/scientific-conclusion/rubraca-epar-scientific-conclusions-annex-iv_sl.pdf","fi":"https://www.ema.europa.eu/fi/documents/scientific-conclusion/rubraca-epar-scientific-conclusions-annex-iv_fi.pdf","sv":"https://www.ema.europa.eu/sv/documents/scientific-conclusion/rubraca-epar-scientific-conclusions-annex-iv_sv.pdf"}},
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    {"id":"56734","name":"Rilutek-H-C-PSUSA-00002645-202112 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation(s)","type":"scientific-conclusion","status":"Adopted","consultation_date":"","first_published_date":"2022-11-22T10:52:00Z","last_updated_date":"2022-11-22T10:52:00Z","reference_number":"EMA/732027/2022","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/rilutek-h-c-psusa-00002645-202112-epar-scientific-conclusions-and-grounds-variation-terms-marketing-authorisations_en.pdf"},
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    {"id":"56948","name":"Onivyde pegylated liposomal-H-C-PSUSA-00010534-202110 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2022-12-13T09:49:00Z","last_updated_date":"2022-12-13T09:49:00Z","reference_number":"EMA/915538/2022","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/onivyde-pegylated-liposomal-h-c-psusa-00010534-202110-epar-scientific-conclusions-and-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"56992","name":"Xarelto-H-C-PSR-S-0027 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"Adopted","consultation_date":"","first_published_date":"2022-12-14T09:24:00Z","last_updated_date":"2022-12-14T09:24:00Z","reference_number":"EMA/940159/2022","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/xarelto-h-c-psr-s-0027-epar-scientific-conclusions-and-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"57029","name":"Xaluprine-H-C-PSUSA-00001988-202109 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2022-12-15T11:14:00Z","last_updated_date":"2022-12-15T11:14:00Z","reference_number":"EMA/943492/2022","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/xaluprine-h-c-psusa-00001988-202109-epar-scientific-conclusions-and-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"57030","name":"Abevmy-H-C-PSUSA-00000403-202202 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2022-12-15T11:57:00Z","last_updated_date":"2022-12-15T11:57:00Z","reference_number":"EMA/921971/2022","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/abevmy-h-c-psusa-00000403-202202-epar-scientific-conclusions-and-grounds-variation-terms-marketing-authorisation_en.pdf"},
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    {"id":"57041","name":"Alymsys-H-C-PSUSA-00000403-202202 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2022-12-15T14:21:00Z","last_updated_date":"2022-12-15T14:21:00Z","reference_number":"EMA/921971/2022","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/alymsys-h-c-psusa-00000403-202202-epar-scientific-conclusions-and-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"57070","name":"Zoely-H-A-31-1510-C-1213-60 : EPAR - Divergent positions to CHMP opinion","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2022-12-16T10:32:00Z","last_updated_date":"2022-12-16T10:32:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/zoely-h-31-1510-c-1213-60-epar-divergent-positions-chmp-opinion_en.pdf"},
    {"id":"57155","name":"Kisqali-H-C-PSUSA-00010633-202203 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"Adopted","consultation_date":"","first_published_date":"2023-01-04T11:31:00Z","last_updated_date":"2023-01-04T11:31:00Z","reference_number":"EMA/942004/2022","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/kisqali-h-c-psusa-00010633-202203-epar-scientific-conclusions-and-grounds-variation-terms-marketing-authorisation_en.pdf"},
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    {"id":"57167","name":"Onbevzi-H-C-PSUSA-00000403-202202 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"Adopted","consultation_date":"","first_published_date":"2023-01-05T11:53:00Z","last_updated_date":"2024-10-24T14:40:00Z","reference_number":"EMA/921971/2022","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/onbevzi-h-c-psusa-00000403-202202-epar-scientific-conclusions-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"57168","name":"Mvasi-H-C-PSUSA-00000403-202202 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"Adopted","consultation_date":"","first_published_date":"2023-01-05T12:21:00Z","last_updated_date":"2023-01-05T12:21:00Z","reference_number":"EMA/921971/2022","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/mvasi-h-c-psusa-00000403-202202-epar-scientific-conclusions-and-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"57173","name":"Byfavo-H-C-PSUSA-00010924-202201 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"Adopted","consultation_date":"","first_published_date":"2023-01-06T16:34:00Z","last_updated_date":"2023-01-06T16:34:00Z","reference_number":"EMA/902653/2022","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/byfavo-h-c-psusa-00010924-202201-epar-scientific-conclusions-and-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"57259","name":"Lokelma-H-C-PSUSA-00010675-202203 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"Adopted","consultation_date":"","first_published_date":"2023-01-12T13:54:00Z","last_updated_date":"2023-01-12T13:54:00Z","reference_number":"EMA/18088/2023","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/lokelma-h-c-psusa-00010675-202203-epar-scientific-conclusions-and-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"57269","name":"Vocabria-H-C-PSUSA-00010900-202203 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"Adopted","consultation_date":"","first_published_date":"2023-01-12T16:27:00Z","last_updated_date":"2023-01-12T16:27:00Z","reference_number":"EMA/859633/2022","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/vocabria-h-c-psusa-00010900-202203-epar-scientific-conclusions-and-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"57307","name":"Skyrizi-H-C-PSUSA-00010765-202203 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation(s)","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2023-01-17T11:27:00Z","last_updated_date":"2023-01-17T11:27:00Z","reference_number":"EMA/15506/2023","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/skyrizi-h-c-psusa-00010765-202203-epar-scientific-conclusions-and-grounds-variation-terms-marketing-authorisations_en.pdf"},
    {"id":"57320","name":"Sarclisa-H-C-PSUSA-00010851-202203 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2023-01-18T14:00:00Z","last_updated_date":"2023-01-18T14:00:00Z","reference_number":"EMA/29807/2023","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/sarclisa-h-c-psusa-00010851-202203-epar-scientific-conclusions-and-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"57483","name":"Skytrofa-H-C-PSUSA-00010969-202202 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2023-01-31T14:28:00Z","last_updated_date":"2023-01-31T14:28:00Z","reference_number":"EMA/50448/2023","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/skytrofa-h-c-psusa-00010969-202202-epar-scientific-conclusions-and-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"57486","name":"Mayzent-PSUSA-00010818-202203 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2023-01-31T14:57:00Z","last_updated_date":"2023-01-31T14:57:00Z","reference_number":"EMA/856981/2022","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/mayzent-psusa-00010818-202203-epar-scientific-conclusions-and-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"57492","name":"Caprelsa-H-C-PSUSA-00009327-202204 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2023-02-01T13:52:00Z","last_updated_date":"2023-02-01T13:52:00Z","reference_number":"EMA/48093/2023","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/caprelsa-h-c-psusa-00009327-202204-epar-scientific-conclusions-and-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"57794","name":"Zonegran-H-C-PSUSA-00003152-202203 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation(s)","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2023-02-23T10:21:00Z","last_updated_date":"2023-02-23T10:21:00Z","reference_number":"EMA/CHMP/78061/2023","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/zonegran-h-c-psusa-00003152-202203-epar-scientific-conclusions-and-grounds-variation-terms-marketing-authorisations_en.pdf"},
    {"id":"57825","name":"Vyndaqel-H-C-PSUSA-00002842-202205: EPAR - Scientific conclusions and grounds recommending the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2023-02-24T14:15:00Z","last_updated_date":"2023-02-24T14:15:00Z","reference_number":"EMA/918324/2022","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/vyndaqel-h-c-psusa-00002842-202205-epar-scientific-conclusions-and-grounds-recommending-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"57829","name":"Tukysa-H-C-PSUSA-00010918-202204 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2023-02-27T15:04:00Z","last_updated_date":"2023-02-27T15:04:00Z","reference_number":"EMA/93554/2023","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/tukysa-h-c-psusa-00010918-202204-epar-scientific-conclusions-and-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"57847","name":"Edistride-H-C-PSUSA-00010029-202110 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation(s)","type":"scientific-conclusion","status":"Adopted","consultation_date":"","first_published_date":"2023-03-01T13:28:00Z","last_updated_date":"2023-03-01T13:28:00Z","reference_number":"EMA/700831/2022","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/edistride-h-c-psusa-00010029-202110-epar-scientific-conclusions-and-grounds-variation-terms-marketing-authorisations_en.pdf"},
    {"id":"57851","name":"Spravato-H-C-PSUSA-00010825-202203 : EPAR - Scientific Conclusion","type":"scientific-conclusion","status":"Adopted","consultation_date":"","first_published_date":"2023-03-01T16:33:00Z","last_updated_date":"2023-03-01T16:33:00Z","reference_number":"EMA/97281/2023","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/spravato-h-c-psusa-00010825-202203-epar-scientific-conclusion_en.pdf"},
    {"id":"57867","name":"Pemazyre-H-C-PSUSA-00010923-202204 : EPAR - Scientific conclusions and grounds recommending the variation to the terms of the marketing authorisation  new","type":"scientific-conclusion","status":"Adopted","consultation_date":"","first_published_date":"2023-03-02T16:40:00Z","last_updated_date":"2023-03-02T16:40:00Z","reference_number":"EMA/93779/2023","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/pemazyre-h-c-psusa-00010923-202204-epar-scientific-conclusions-and-grounds-recommending-variation-terms-marketing-authorisation-new_en.pdf"},
    {"id":"57945","name":"Tecentriq-H-C-PSUSA-00010644-202205 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2023-03-07T16:40:00Z","last_updated_date":"2023-03-07T16:40:00Z","reference_number":"EMA/108897/2023","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/tecentriq-h-c-psusa-00010644-202205-epar-scientific-conclusions-and-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"58064","name":"Jevtana-PSUSA-00000476-202106 : EPAR - Scientific conclusions and grounds recommending the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2023-03-17T16:52:00Z","last_updated_date":"2023-03-17T16:52:00Z","reference_number":"EMA/128719/2023","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/jevtana-psusa-00000476-202106-epar-scientific-conclusions-and-grounds-recommending-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"58066","name":"Erleada-H-C-PSUSA-00010745-202202 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"Adopted","consultation_date":"","first_published_date":"2023-03-20T11:24:00Z","last_updated_date":"2023-03-20T11:24:00Z","reference_number":"EMA/129416/2023","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/erleada-h-c-psusa-00010745-202202-epar-scientific-conclusions-and-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"58067","name":"Vaxzevria (previously COVID-19 Vaccine AstraZeneca)-H-C-PSUSA-00010912-202206: EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation(s)","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2023-03-20T12:47:00Z","last_updated_date":"2024-05-07T11:00:00Z","reference_number":"EMA/38839/2023","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/vaxzevria-previously-covid-19-vaccine-astrazeneca-h-c-psusa-00010912-202206-epar-scientific-conclusions-grounds-variation-terms-marketing-authorisations_en.pdf"},
    {"id":"58073","name":"Isturisa-H-C-PSUSA-00010820-202201 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2023-03-20T15:12:00Z","last_updated_date":"2023-03-20T15:12:00Z","reference_number":"EMA/129314/2023","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/isturisa-h-c-psusa-00010820-202201-epar-scientific-conclusions-and-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"58152","name":"Brukinsa-H-C-PSUSA-00010960-202205 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2023-03-24T11:28:00Z","last_updated_date":"2023-03-24T11:28:00Z","reference_number":"EMA/140012/2023","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/brukinsa-h-c-psusa-00010960-202205-epar-scientific-conclusions-and-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"58202","name":"Kineret-H-C-PSUSA-00000209-202205 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2023-03-29T13:32:00Z","last_updated_date":"2023-03-29T13:32:00Z","reference_number":"EMA/144773/2023","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/kineret-h-c-psusa-00000209-202205-epar-scientific-conclusions-and-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"58250","name":"Brintellix-H-C-PSUSA-00010052-202009 : Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2023-03-31T13:48:00Z","last_updated_date":"2023-03-31T13:48:00Z","reference_number":"EMA/152944/2023","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/brintellix-h-c-psusa-00010052-202009-scientific-conclusions-and-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"58381","name":"Tarceva-H-C-PSUSA-1255-202111 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation(s)","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2023-04-17T14:28:00Z","last_updated_date":"2023-04-17T14:28:00Z","reference_number":"EMA/173328/2023","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/tarceva-h-c-psusa-1255-202111-epar-scientific-conclusions-and-grounds-variation-terms-marketing-authorisations_en.pdf"},
    {"id":"58489","name":"Gardasil 9-H-C-PSUSA-00010389-202206 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2023-04-21T13:10:00Z","last_updated_date":"2023-04-21T13:10:00Z","reference_number":"EMA/183707/2023","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/gardasil-9-h-c-psusa-00010389-202206-epar-scientific-conclusions-and-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"58573","name":"Ozempic-H-C-PSUSA-00010671-202205 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2023-05-03T14:19:00Z","last_updated_date":"2023-05-03T14:19:00Z","reference_number":"EMA/193347/2023","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/ozempic-h-c-psusa-00010671-202205-epar-scientific-conclusions-and-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"58575","name":"Rybelsus-EMEA-H-C-PSUSA-00010671-202205 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2023-05-03T15:23:00Z","last_updated_date":"2023-05-03T15:23:00Z","reference_number":"EMA/193544/2023","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/rybelsus-emea-h-c-psusa-00010671-202205-epar-scientific-conclusions-and-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"58582","name":"Luxturna-H-C-PSUSA-00010742-202207 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2023-05-04T11:48:00Z","last_updated_date":"2023-05-04T11:48:00Z","reference_number":"EMA/152946/2023","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/luxturna-h-c-psusa-00010742-202207-epar-scientific-conclusions-and-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"58601","name":"Fycompa-H-C-PSUSA-00009255-202207 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2023-05-10T09:39:00Z","last_updated_date":"2023-05-10T09:39:00Z","reference_number":"EMA/151418/2023","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/fycompa-h-c-psusa-00009255-202207-epar-scientific-conclusions-and-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"58809","name":"Qinlock-H-C-PSUSA-00010962-202205 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2023-05-30T11:29:00Z","last_updated_date":"2023-05-30T11:29:00Z","reference_number":"EMA/242978/2023","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/qinlock-h-c-psusa-00010962-202205-epar-scientific-conclusions-and-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"58845","name":"Kentera-H-C-PSUSA-00002253-202207 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2023-06-01T16:02:00Z","last_updated_date":"2023-06-01T16:02:00Z","reference_number":"EMA/811281/2023","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/kentera-h-c-psusa-00002253-202207-epar-scientific-conclusions-and-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"58858","name":"Oxervate-H-C-PSUSA-00010624-202207 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2023-06-02T12:08:00Z","last_updated_date":"2023-06-02T12:08:00Z","reference_number":"EMA/146953/2023","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/oxervate-h-c-psusa-00010624-202207-epar-scientific-conclusions-and-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"58861","name":"Onpattro-H-C-PSUSA-00010715-202208 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2023-06-02T12:38:00Z","last_updated_date":"2023-06-02T12:38:00Z","reference_number":"EMA/187790/2023","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/onpattro-h-c-psusa-00010715-202208-epar-scientific-conclusions-and-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"58893","name":"Ryeqo-H-C-PSUSA-00010942-202205 : EPAR - Scientific conclusions and grounds recommending the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2023-06-08T15:13:00Z","last_updated_date":"2023-06-08T15:13:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/ryeqo-h-c-psusa-00010942-202205-epar-scientific-conclusions-and-grounds-recommending-variation-terms-marketing-authorisation_en.pdf"},
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    {"id":"61050","name":"Trixuma-H-C-PSUSA-00002652-202211 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation(s)","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2023-11-29T16:12:41Z","last_updated_date":"2023-11-29T16:12:41Z","reference_number":"EMA/540498/2023","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/trixuma-h-c-psusa-00002652-202211-epar-scientific-conclusions-and-grounds-variation-terms-marketing-authorisations_en.pdf"},
    {"id":"61051","name":"Orgovyx-H-C-PSUSA-00010994-202301 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation(s)","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2023-11-29T12:00:00Z","last_updated_date":"2023-11-29T12:00:00Z","reference_number":"EMA/531133/2023","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/orgovyx-h-c-psusa-00010994-202301-epar-scientific-conclusions-and-grounds-variation-terms-marketing-authorisations_en.pdf"},
    {"id":"61053","name":"Trizivir-H-C-PSUSA-00003144-202212 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation(s)","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2023-11-29T17:22:06Z","last_updated_date":"2023-11-29T17:22:06Z","reference_number":"EMA/395778/2023","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/trizivir-h-c-psusa-00003144-202212-epar-scientific-conclusions-and-grounds-variation-terms-marketing-authorisations_en.pdf"},
    {"id":"61071","name":"Kivexa-H-C-PSUSA-00000011-202212 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2023-11-27T12:00:00Z","last_updated_date":"2023-11-27T12:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/kivexa-h-c-psusa-00000011-202212-epar-scientific-conclusions-and-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"61259","name":"Paxlovid-H-C-PSUSA-00010984-202212 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2023-12-05T16:41:38Z","last_updated_date":"2023-12-05T16:41:38Z","reference_number":"EMA/533949/2023","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/paxlovid-h-c-psusa-00010984-202212-epar-scientific-conclusions-and-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"61347","name":"Daxas-H-C-PSR-S-0041 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2023-12-11T12:52:20Z","last_updated_date":"2023-12-11T12:52:20Z","reference_number":"EMA/566491/2023","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/daxas-h-c-psr-s-0041-epar-scientific-conclusions-and-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"61391","name":"Carvykti-H-C-PSUSA-00011000-202302 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2023-12-12T16:39:55Z","last_updated_date":"2023-12-12T16:39:55Z","reference_number":"EMA/442501/2023","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/carvykti-h-c-psusa-00011000-202302-epar-scientific-conclusions-and-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"61434","name":"Ziagen-H-C-PSUSA-00000010-202212 - EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2023-12-15T11:28:46Z","last_updated_date":"2023-12-15T11:28:46Z","reference_number":"EMA/395754/2023","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/ziagen-h-c-psusa-00000010-202212-epar-scientific-conclusions-and-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"61435","name":"Lyrica-H-C-PSUSA-00002511-202301 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2023-12-15T11:47:18Z","last_updated_date":"2023-12-15T11:47:18Z","reference_number":"EMA/440258/2023","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/lyrica-h-c-psusa-00002511-202301-epar-scientific-conclusions-and-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"61444","name":"Pregabalin Pfizer-H-C-PSUSA-00002511-202301 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2023-12-15T15:13:37Z","last_updated_date":"2023-12-15T15:13:37Z","reference_number":"EMA/440258/2023","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/pregabalin-pfizer-h-c-psusa-00002511-202301-epar-scientific-conclusions-and-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"61552","name":"Rinvoq-H-C-PSUSA-00010823-202302: EPAR - Scientific conclusions and grounds recommending the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2023-12-20T17:11:34Z","last_updated_date":"2023-12-20T17:11:34Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/rinvoq-h-c-psusa-00010823-202302-epar-scientific-conclusions-and-grounds-recommending-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"61613","name":"Symkevi-H-C-PSUSA-00010730-202302 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation(s)","type":"scientific-conclusion","status":"Adopted","consultation_date":"","first_published_date":"2023-12-22T16:56:15Z","last_updated_date":"2023-12-22T16:56:15Z","reference_number":"EMA/580796/2023","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/symkevi-h-c-psusa-00010730-202302-epar-scientific-conclusions-and-grounds-variation-terms-marketing-authorisations_en.pdf"},
    {"id":"61657","name":"Mayzent-PSUSA-00010818-202303 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2024-01-08T13:26:36Z","last_updated_date":"2024-01-08T13:26:36Z","reference_number":"EMA/484731/2023","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/mayzent-psusa-00010818-202303-epar-scientific-conclusions-and-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"61675","name":"Erleada-H-C-PSUSA-00010745-202302 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2024-01-09T16:06:08Z","last_updated_date":"2024-01-09T16:06:08Z","reference_number":"EMA/CHMP/10331/2024","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/erleada-h-c-psusa-00010745-202302-epar-scientific-conclusions-and-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"61701","name":"Bavencio-H-C-PSUSA-00010635-202303 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"Adopted","consultation_date":"","first_published_date":"2024-01-10T15:35:30Z","last_updated_date":"2024-01-10T15:35:30Z","reference_number":"EMA/12383/2024","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/bavencio-h-c-psusa-00010635-202303-epar-scientific-conclusions-and-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"61745","name":"Lorviqua-H-C-PSUSA-00010760-202303 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2024-01-12T10:20:31Z","last_updated_date":"2024-01-12T10:20:31Z","reference_number":"EMA/16421/2024","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/lorviqua-h-c-psusa-00010760-202303-epar-scientific-conclusions-and-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"61756","name":"Intrarosa-H-C-PSR-S-0044 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2024-01-15T12:00:25Z","last_updated_date":"2024-01-15T12:00:25Z","reference_number":"EMA/578551/2023","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/intrarosa-h-c-psr-s-0044-epar-scientific-conclusions-and-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"61803","name":"Ontozry-H-C-PSUSA-00010921-202303 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2024-01-18T08:44:37Z","last_updated_date":"2024-01-18T08:44:37Z","reference_number":"EMA/505768/2023","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/ontozry-h-c-psusa-00010921-202303-epar-scientific-conclusions-and-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"61855","name":"Sifrol-H-C-PSUSA-00002491-202304 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2024-01-24T09:18:39Z","last_updated_date":"2024-01-24T09:18:39Z","reference_number":"EMA/37077/2024","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/sifrol-h-c-psusa-00002491-202304-epar-scientific-conclusions-and-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"61856","name":"Mirapexin-H-C-PSUSA-00002491-202304 : EPAR - Scientific conclusions and grounds recommending the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2024-01-24T09:27:01Z","last_updated_date":"2024-01-24T09:27:01Z","reference_number":"EMA/37077/2024","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/mirapexin-h-c-psusa-00002491-202304-epar-scientific-conclusions-and-grounds-recommending-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"62099","name":"Protopic-H-C-PSUSA-00002840-202303 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation(s)","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2024-02-13T12:20:00Z","last_updated_date":"2024-02-13T12:20:00Z","reference_number":"EMA/65864/2024","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/protopic-h-c-psusa-00002840-202303-epar-scientific-conclusions-grounds-variation-terms-marketing-authorisations_en.pdf"},
    {"id":"62111","name":"VidPrevtyn Beta-H-C-PSUSA-00011035-202305 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation(s)","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2024-02-13T15:00:00Z","last_updated_date":"2024-03-20T13:20:00Z","reference_number":"EMA/67397/2024","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/vidprevtyn-beta-h-c-psusa-00011035-202305-epar-scientific-conclusions-grounds-variation-terms-marketing-authorisations_en.pdf"},
    {"id":"62206","name":"Dynastat-H-C-PSUSA-00002314-202303 : EPAR - Scientific conclusions and grounds recommending the variation to the terms of the marketing authorisation ","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2024-02-19T09:39:24Z","last_updated_date":"2024-02-19T09:39:24Z","reference_number":"EMA/532577/2023","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/dynastat-h-c-psusa-00002314-202303-epar-scientific-conclusions-grounds-recommending-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"62228","name":"Mounjaro-H-C-PSUSA-00011019-202211 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation ","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2024-02-21T10:20:16Z","last_updated_date":"2024-02-21T10:20:16Z","reference_number":"EMA/342202/2023","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/mounjaro-h-c-psusa-00011019-202211-epar-scientific-conclusions-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"62344","name":"Tecvayli-H-C-PSUSA-00011010-202302 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2024-02-28T15:18:18Z","last_updated_date":"2024-02-28T15:18:18Z","reference_number":"EMA/79368/2024","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/tecvayli-h-c-psusa-00011010-202302-epar-scientific-conclusions-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"62358","name":"Truvada-H-C-PSUSA-00001210-202304 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2024-02-29T13:52:39Z","last_updated_date":"2024-02-29T13:52:39Z","reference_number":"EMA/91628/2024","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/truvada-h-c-psusa-00001210-202304-epar-scientific-conclusions-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"62360","name":"Deltyba-H-C-PSUSA-00010213-202304: EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2024-02-29T15:04:24Z","last_updated_date":"2024-02-29T15:04:24Z","reference_number":"EMA/540391/2023","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/deltyba-h-c-psusa-00010213-202304-epar-scientific-conclusions-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"62361","name":"Viread-H-C-PSUSA-00002892-202303 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2024-02-29T15:22:30Z","last_updated_date":"2024-02-29T15:22:30Z","reference_number":"EMA/75726/2024","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/viread-h-c-psusa-00002892-202303-epar-scientific-conclusions-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"62438","name":"Kalydeco-H-C-PSUSA-00009204-202301 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2024-03-05T15:05:13Z","last_updated_date":"2024-03-05T15:05:13Z","reference_number":"EMA/97030/2024","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/kalydeco-h-c-psusa-00009204-202301-epar-scientific-conclusions-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"62441","name":"Kaftrio-H-C-PSUSA-00010868-202304 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation(s)","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2024-03-05T16:19:49Z","last_updated_date":"2024-03-05T16:19:49Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/kaftrio-h-c-psusa-00010868-202304-epar-scientific-conclusions-grounds-variation-terms-marketing-authorisations_en.pdf"},
    {"id":"62603","name":"Imjudo-H-C-PSUSA/00011038/202304 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2024-03-13T15:40:45Z","last_updated_date":"2024-03-13T15:40:45Z","reference_number":"EMA/CHMP/PRAC/108547/2024","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/imjudo-h-c-psusa-00011038-202304-epar-scientific-conclusions-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"62681","name":"Mekinist-H-C-PSUSA-00010262-202305 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2024-03-21T15:23:09Z","last_updated_date":"2024-03-21T15:23:09Z","reference_number":"EMA/121187/2024","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/mekinist-h-c-psusa-00010262-202305-epar-scientific-conclusions-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"62709","name":"Mektovi-PSUSA-00010717-202306 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2024-03-22T13:33:05Z","last_updated_date":"2024-03-22T13:33:05Z","reference_number":"EMA/20913/2024","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/mektovi-psusa-00010717-202306-epar-scientific-conclusions-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"62722","name":"Tecentriq-H-C-PSUSA-00010644-202305: EPAR - Scientific conclusions and grounds recommending the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2024-03-25T14:07:21Z","last_updated_date":"2024-03-25T14:07:21Z","reference_number":"EMA/130056/2024","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/tecentriq-h-c-psusa-00010644-202305-epar-scientific-conclusions-grounds-recommending-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"62749","name":"Pravafenix-H-C-PSUSA-00001363-202304 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"Adopted","consultation_date":"","first_published_date":"2024-03-26T15:07:27Z","last_updated_date":"2024-03-26T15:07:27Z","reference_number":"EMA/CHMP/564966/2023","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/pravafenix-h-c-psusa-00001363-202304-epar-scientific-conclusions-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"62753","name":"Zolgensma-H-C-PSUSA-00010848-202305 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation(s)","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2024-03-26T16:40:00Z","last_updated_date":"2024-03-26T16:40:00Z","reference_number":"EMA/86623/2024","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/zolgensma-h-c-psusa-00010848-202305-epar-scientific-conclusions-grounds-variation-terms-marketing-authorisations_en.pdf"},
    {"id":"62762","name":"Fintepla-H-C-PSUSA-00010907-202306 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2024-03-27T16:57:45Z","last_updated_date":"2024-03-27T16:57:45Z","reference_number":"EMA/57721/2024","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/fintepla-h-c-psusa-00010907-202306-epar-scientific-conclusions-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"62781","name":"Sutent-H-C-PSUSA-00002833-202304 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2024-04-02T16:38:09Z","last_updated_date":"2024-04-02T16:38:09Z","reference_number":"EMA/84642/2024","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/sutent-h-c-psusa-00002833-202304-epar-scientific-conclusions-grounds-variation-terms-marketing-authorisation_en.pdf"},
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    {"id":"64098","name":"Kesimpta-H-C-PSUSA-00010927-202309 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2024-07-12T15:09:00Z","last_updated_date":"2025-02-07T16:34:00Z","reference_number":"EMA/328965/2024","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/kesimpta-h-c-psusa-00010927-202309-epar-scientific-conclusions-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"64178","name":"Nucala-H-C-PSUSA-00010456-202309: EPAR - Scientific conclusions and grounds recommending the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2024-07-16T16:03:36Z","last_updated_date":"2024-07-16T16:03:36Z","reference_number":"EMA/331057/2024","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/nucala-h-c-psusa-00010456-202309-epar-scientific-conclusions-grounds-recommending-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"64187","name":"Voxzogo-H-C-PSUSA-00010952-202308: EPAR - Scientific conclusions and grounds recommending the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2024-07-17T16:46:22Z","last_updated_date":"2024-07-17T16:46:22Z","reference_number":"EMA/335501/2024","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/voxzogo-h-c-psusa-00010952-202308-epar-scientific-conclusions-grounds-recommending-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"64280","name":"Stribild-H-C-PSUSA-00010082-202308 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2024-07-23T13:33:00Z","last_updated_date":"2024-07-23T13:33:00Z","reference_number":"EMA/340999/2024","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/stribild-h-c-psusa-00010082-202308-epar-scientific-conclusions-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"64291","name":"Teriflunomide Mylan-H-C-PSUSA-00010135-202309 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2024-07-24T12:51:00Z","last_updated_date":"2024-07-24T12:51:00Z","reference_number":"EMA/240603/2024","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/teriflunomide-mylan-h-c-psusa-00010135-202309-epar-scientific-conclusions-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"64360","name":"Aubagio-H-C-PSUSA-00010135-202309 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2024-07-29T12:25:00Z","last_updated_date":"2024-07-29T12:25:00Z","reference_number":"EMA/240603/2024","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/aubagio-h-c-psusa-00010135-202309-epar-scientific-conclusions-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"64361","name":"Teriflunomide Accord-H-C-PSUSA-00010135-202309 : Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2024-07-29T12:36:00Z","last_updated_date":"2024-07-29T12:36:00Z","reference_number":"EMA/240603/2024","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/teriflunomide-accord-h-c-psusa-00010135-202309-scientific-conclusions-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"64391","name":"Fareston-H-C-PSUSA-00002999-202309 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2024-07-30T09:16:39Z","last_updated_date":"2024-07-30T09:16:39Z","reference_number":"EMA/354722/2024","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/fareston-h-c-psusa-00002999-202309-epar-scientific-conclusions-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"64398","name":"Leflunomide medac-H-C-PSUSA-00001837-202309 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2024-07-30T11:23:18Z","last_updated_date":"2024-07-30T11:23:18Z","reference_number":"EMA/352161/2024","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/leflunomide-medac-h-c-psusa-00001837-202309-epar-scientific-conclusions-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"64408","name":"Zubsolv-H-C-PSUSA-00002113-202309 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2024-07-31T09:25:16Z","last_updated_date":"2024-07-31T09:25:16Z","reference_number":"EMA/243985/2024","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/zubsolv-h-c-psusa-00002113-202309-epar-scientific-conclusions-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"64544","name":"Scemblix-H-C-PSUSA-00011008-202310 : EPAR - Scientific conclusions and grounds recommending the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2024-08-08T17:33:54Z","last_updated_date":"2024-08-08T17:33:54Z","reference_number":"EMA/236201/2024","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/scemblix-h-c-psusa-00011008-202310-epar-scientific-conclusions-grounds-recommending-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"64545","name":"Buvidal-H-C-PSUSA-00000459-202309 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2024-08-08T17:43:31Z","last_updated_date":"2024-08-08T17:43:31Z","reference_number":"EMA/245621/2024","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/buvidal-h-c-psusa-00000459-202309-epar-scientific-conclusions-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"64582","name":"Leflunomide-H-C-PSUSA-00001837-202309 : Scientific conclusions and grounds for the variation to the terms of the marketing authorisation(s)","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2024-08-14T17:40:00Z","last_updated_date":"2024-08-14T17:40:00Z","reference_number":"EMA/352982/2024","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/leflunomide-h-c-psusa-00001837-202309-scientific-conclusions-grounds-variation-terms-marketing-authorisations_en.pdf"},
    {"id":"64626","name":"Verzenios-H-C-PSUSA-00010724-202309 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2024-08-23T15:31:00Z","last_updated_date":"2024-08-23T15:31:00Z","reference_number":"EMA/169761/2024","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/verzenios-h-c-psusa-00010724-202309-epar-scientific-conclusions-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"64680","name":"Jylamvo-H-C-PSUSA-00002014-202310 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2024-09-02T14:46:42Z","last_updated_date":"2024-09-02T14:46:42Z","reference_number":"EMA/407130/2024","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/jylamvo-h-c-psusa-00002014-202310-epar-scientific-conclusions-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"64705","name":"Arava-H-C-PSUSA-00001837-202309 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2024-09-05T09:44:18Z","last_updated_date":"2024-09-05T09:44:18Z","reference_number":"EMA/356172/2024","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/arava-h-c-psusa-00001837-202309-epar-scientific-conclusions-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"64706","name":"Abrysvo-H-C-PSUSA-00000102-202311 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2024-09-05T09:52:00Z","last_updated_date":"2024-09-05T09:52:00Z","reference_number":"EMA/394691/2024","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/abrysvo-h-c-psusa-00000102-202311-epar-scientific-conclusions-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"64710","name":"Nordimet-H-C-PSUSA-00002014-202310 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2024-09-05T10:27:52Z","last_updated_date":"2024-09-05T10:27:52Z","reference_number":"EMA/410704/2024","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/nordimet-h-c-psusa-00002014-202310-epar-scientific-conclusions-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"64712","name":"Aspaveli-H-C-PSUSA-00010974-202311 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2024-09-05T10:50:51Z","last_updated_date":"2024-09-05T10:50:51Z","reference_number":"EMA/411706/2024","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/aspaveli-h-c-psusa-00010974-202311-epar-scientific-conclusions-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"64741","name":"Noxafil-H-C-610-PSUSA-00002480-202310 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"Adopted","consultation_date":"","first_published_date":"2024-09-06T13:37:19Z","last_updated_date":"2024-09-06T13:37:19Z","reference_number":"EMA/375776/2024","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/noxafil-h-c-610-psusa-00002480-202310-epar-scientific-conclusions-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"64955","name":"Imbruvica-H-C-PSUSA-00010301-202311 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2024-09-20T09:40:00Z","last_updated_date":"2024-09-20T09:40:00Z","reference_number":"EMA/437838/2024","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/imbruvica-h-c-psusa-00010301-202311-epar-scientific-conclusions-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"64958","name":"Ninlaro-H-C-PSUSA-00010535-202311 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2024-09-20T09:52:00Z","last_updated_date":"2024-09-20T09:52:00Z","reference_number":"EMA/437612/2024","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/ninlaro-h-c-psusa-00010535-202311-epar-scientific-conclusions-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"65002","name":"Orladeyo-H-C-PSUSA-00010930-202312 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2024-09-23T16:13:00Z","last_updated_date":"2024-09-23T16:13:00Z","reference_number":"EMA/332675/2024","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/orladeyo-h-c-psusa-00010930-202312-epar-scientific-conclusions-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"65052","name":"Kinpeygo-H-C-PSUSA-00011007-202312 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2024-09-27T14:13:00Z","last_updated_date":"2024-09-27T14:13:00Z","reference_number":"EMA/452285/2024","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/kinpeygo-h-c-psusa-00011007-202312-epar-scientific-conclusions-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"65362","name":"Lunsumio-H-C-PSUSA-00010999-202312 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2024-10-22T14:49:00Z","last_updated_date":"2024-10-22T14:49:00Z","reference_number":"EMA/493647/2024","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/lunsumio-h-c-psusa-00010999-202312-epar-scientific-conclusions-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"65370","name":"Gazyvaro-H-C-PSUSA-00010279-202310 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2024-10-23T10:52:56Z","last_updated_date":"2024-10-23T10:52:56Z","reference_number":"EMA/449468/2024","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/gazyvaro-h-c-psusa-00010279-202310-epar-scientific-conclusions-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"65380","name":"Mounjaro-H-C-PSUSA-00011019-202311 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2024-10-23T16:20:00Z","last_updated_date":"2024-10-23T16:20:00Z","reference_number":"EMA/495656/2024","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/mounjaro-h-c-psusa-00011019-202311-epar-scientific-conclusions-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"65499","name":"Edistride-H-C-PSUSA-00010029-202310 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2024-10-31T09:11:50Z","last_updated_date":"2024-10-31T09:11:50Z","reference_number":"EMA/504919/2024","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/edistride-h-c-psusa-00010029-202310-epar-scientific-conclusions-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"65500","name":"Forxiga-H-C-PSUSA-00010029-202310 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2024-10-31T09:14:18Z","last_updated_date":"2024-10-31T09:14:18Z","reference_number":"EMA/505062/2024","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/forxiga-h-c-psusa-00010029-202310-epar-scientific-conclusions-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"65773","name":"Tecovirimat SIGA-H-C-PSUSA-00010971-202401 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2024-11-22T13:39:12Z","last_updated_date":"2024-11-22T13:39:12Z","reference_number":"EMA/539162/2024","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/tecovirimat-siga-h-c-psusa-00010971-202401-epar-scientific-conclusions-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"65785","name":"Cosentyx-H-C-PSUSA-00010341-202312 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"Adopted","consultation_date":"","first_published_date":"2024-11-25T11:50:58Z","last_updated_date":"2024-11-25T11:50:58Z","reference_number":"EMA/443964/2024","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/cosentyx-h-c-psusa-00010341-202312-epar-scientific-conclusions-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"65824","name":"Lupkynis-H-C-PSUSA-00011020-202401 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2024-11-27T08:41:30Z","last_updated_date":"2024-11-27T08:41:30Z","reference_number":"EMA/552100/2024","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/lupkynis-h-c-psusa-00011020-202401-epar-scientific-conclusions-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"65857","name":"Puregon-H-C-PSUSA-00001465-202305 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"Adopted","consultation_date":"","first_published_date":"2024-11-28T10:32:09Z","last_updated_date":"2024-11-28T10:32:09Z","reference_number":"EMA/554310/2024","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/puregon-h-c-psusa-00001465-202305-epar-scientific-conclusions-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"65923","name":"Kimmtrak-H-C-PSUSA-00010991-202401 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"Adopted","consultation_date":"","first_published_date":"2024-12-03T13:50:06Z","last_updated_date":"2024-12-03T13:50:06Z","reference_number":"EMA/430997/2024","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/kimmtrak-h-c-psusa-00010991-202401-epar-scientific-conclusions-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"65932","name":"Briviact-H-C-PSUSA-00010447-202401 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"Adopted","consultation_date":"","first_published_date":"2024-12-03T15:02:58Z","last_updated_date":"2024-12-03T15:02:58Z","reference_number":"EMA/CHMP/560256/2024","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/briviact-h-c-psusa-00010447-202401-epar-scientific-conclusions-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"65938","name":"Scintimun-H-C-PSUSA-00000385-202401 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"Adopted","consultation_date":"","first_published_date":"2024-12-04T11:08:45Z","last_updated_date":"2024-12-04T11:08:45Z","reference_number":"EMA/560220/2024","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/scintimun-h-c-psusa-00000385-202401-epar-scientific-conclusions-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"65951","name":"Erleada-H-C-PSUSA-00010745-202402 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"Adopted","consultation_date":"","first_published_date":"2024-12-04T16:15:30Z","last_updated_date":"2024-12-04T16:15:30Z","reference_number":"EMA/563609/2024","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/erleada-h-c-psusa-00010745-202402-epar-scientific-conclusions-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"66072","name":"Isturisa-H-C-PSUSA-00010820-202401 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"Adopted","consultation_date":"","first_published_date":"2024-12-12T10:24:24Z","last_updated_date":"2024-12-12T10:24:24Z","reference_number":"EMA/484743/2024","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/isturisa-h-c-psusa-00010820-202401-epar-scientific-conclusions-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"66089","name":"Anoro Ellipta-H-C-PSR-S-0048: EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"Adopted","consultation_date":"","first_published_date":"2024-12-12T14:12:50Z","last_updated_date":"2024-12-12T14:12:50Z","reference_number":"EMA/565768/2024","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/anoro-ellipta-h-c-psr-s-0048-epar-scientific-conclusions-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"66090","name":"Laventair Ellipta-H-C-PSR-S-0048: EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"Adopted","consultation_date":"","first_published_date":"2024-12-12T14:54:05Z","last_updated_date":"2024-12-12T14:54:05Z","reference_number":"EMA/565819/2024","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/laventair-ellipta-h-c-psr-s-0048-epar-scientific-conclusions-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"66092","name":"Incruse Ellipta-H-C-PSR-S-0048 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation(s)","type":"scientific-conclusion","status":"Adopted","consultation_date":"","first_published_date":"2024-12-12T15:03:21Z","last_updated_date":"2024-12-12T15:03:21Z","reference_number":"EMA/565794/2024","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/incruse-ellipta-h-c-psr-s-0048-epar-scientific-conclusions-grounds-variation-terms-marketing-authorisations_en.pdf"},
    {"id":"66096","name":"Rolufta Ellipta-H-C-PSR-S-0048 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation(s)","type":"scientific-conclusion","status":"Adopted","consultation_date":"","first_published_date":"2024-12-12T16:05:48Z","last_updated_date":"2024-12-12T16:05:48Z","reference_number":"EMA/565832/2024","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/rolufta-ellipta-h-c-psr-s-0048-epar-scientific-conclusions-grounds-variation-terms-marketing-authorisations_en.pdf"},
    {"id":"66129","name":"Evrenzo-H-C-PSUSA-00010955-202312 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2024-12-16T10:39:31Z","last_updated_date":"2024-12-16T10:39:31Z","reference_number":"EMA/329501/2024","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/evrenzo-h-c-psusa-00010955-202312-epar-scientific-conclusions-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"66181","name":"Bridion-H-C-PSUSA-00002799-202401 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2024-12-17T18:53:00Z","last_updated_date":"2024-12-17T18:53:00Z","reference_number":"EMA/530994/2024","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/bridion-h-c-psusa-00002799-202401-epar-scientific-conclusions-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"66223","name":"Vocabria-H-C-PSUSA-00010900-202403 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2024-12-19T11:41:52Z","last_updated_date":"2024-12-19T11:41:52Z","reference_number":"EMA/596127/2024","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/vocabria-h-c-psusa-00010900-202403-epar-scientific-conclusions-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"66235","name":"Quinsair-H-C-PSR-S-0046 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"Adopted","consultation_date":"","first_published_date":"2025-01-06T11:57:54Z","last_updated_date":"2025-01-06T11:57:54Z","reference_number":"EMA/594722/2024","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/quinsair-h-c-psr-s-0046-epar-scientific-conclusions-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"66238","name":"Valdoxan-H-C-PSUSA-00000071-202402 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2025-01-06T14:11:25Z","last_updated_date":"2025-01-06T14:11:25Z","reference_number":"EMA/551566/2024","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/valdoxan-h-c-psusa-00000071-202402-epar-scientific-conclusions-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"66244","name":"Opdualag-H-C-PSUSA-00011018-202403: EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"Adopted","consultation_date":"","first_published_date":"2025-01-06T15:24:41Z","last_updated_date":"2025-01-06T15:24:41Z","reference_number":"EMA/531182/2024","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/opdualag-h-c-psusa-00011018-202403-epar-scientific-conclusions-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"66312","name":"Ocrevus-H-C-PSUSA-00010662-202403 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"Adopted","consultation_date":"","first_published_date":"2025-01-15T08:55:42Z","last_updated_date":"2025-01-15T08:55:42Z","reference_number":"EMA/514030/2024","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/ocrevus-h-c-psusa-00010662-202403-epar-scientific-conclusions-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"66347","name":"Mayzent-H-C-PSUSA-00010818-202403 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2025-01-17T11:54:34Z","last_updated_date":"2025-01-17T11:54:34Z","reference_number":"EMA/512741/2024","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/mayzent-h-c-psusa-00010818-202403-epar-scientific-conclusions-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"66369","name":"Skyrizi-H-C-PSUSA-00010765-202403 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation(s)","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2025-01-20T11:23:51Z","last_updated_date":"2025-01-20T11:23:51Z","reference_number":"EMA/19434/2025","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/skyrizi-h-c-psusa-00010765-202403-epar-scientific-conclusions-grounds-variation-terms-marketing-authorisations_en.pdf"},
    {"id":"66382","name":"Benlysta-H-C-2015-PSUSA-00009075-202403 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation(s)","type":"scientific-conclusion","status":"Adopted","consultation_date":"","first_published_date":"2025-01-20T17:03:07Z","last_updated_date":"2025-01-20T17:03:07Z","reference_number":"EMA/18607/2025","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/benlysta-h-c-2015-psusa-00009075-202403-epar-scientific-conclusions-grounds-variation-terms-marketing-authorisations_en.pdf"},
    {"id":"66383","name":"Levitra-H-C-PSUSA-00003098-202403 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"Adopted","consultation_date":"","first_published_date":"2025-01-20T17:12:29Z","last_updated_date":"2025-01-20T17:12:29Z","reference_number":"EMA/19518/2025","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/levitra-h-c-psusa-00003098-202403-epar-scientific-conclusions-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"66433","name":"Spravato-H-C-PSUSA-00010825-202403 : EPAR - Scientific Conclusion","type":"scientific-conclusion","status":"Adopted","consultation_date":"","first_published_date":"2025-01-23T13:11:46Z","last_updated_date":"2025-01-23T13:11:46Z","reference_number":"EMA/552364/2024","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/spravato-h-c-psusa-00010825-202403-epar-scientific-conclusion_en.pdf"},
    {"id":"66494","name":"Exelon-H-C-PSUSA-00002654-202401 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2025-01-28T17:06:46Z","last_updated_date":"2025-01-28T17:06:46Z","reference_number":"EMA/594840/2024","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/exelon-h-c-psusa-00002654-202401-epar-scientific-conclusions-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"66503","name":"Prometax-H-C-PSUSA-00002654-202401 : EPAR - Scientific conclusions and grounds recommending the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2025-01-29T11:51:54Z","last_updated_date":"2025-01-29T11:51:54Z","reference_number":"EMA/594840/2024","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/prometax-h-c-psusa-00002654-202401-epar-scientific-conclusions-grounds-recommending-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"66505","name":"Rivastigmine 1 A Pharma-H-C-PSUSA-00002654-202401 : EPAR - Scientific conclusions and grounds recommending the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2025-01-29T13:56:45Z","last_updated_date":"2025-01-29T13:56:45Z","reference_number":"EMA/594840/2024","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/rivastigmine-1-pharma-h-c-psusa-00002654-202401-epar-scientific-conclusions-grounds-recommending-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"66507","name":"Rivastigmine Hexal-H-C-PSUSA-00002654-202401: EPAR - Scientific conclusions and grounds recommending the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2025-01-29T14:11:13Z","last_updated_date":"2025-01-29T14:11:13Z","reference_number":"EMA/594840/2024","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/rivastigmine-hexal-h-c-psusa-00002654-202401-epar-scientific-conclusions-grounds-recommending-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"66520","name":"Nexium Control-H-C-PSUSA-00001269-202403 - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2025-01-30T09:36:02Z","last_updated_date":"2025-01-30T09:36:02Z","reference_number":"EMA/40344/2025","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/nexium-control-h-c-psusa-00001269-202403-scientific-conclusions-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"66560","name":"Tavneos-H-C-PSUSA-00010967/202403 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation(s)","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2025-01-31T14:12:59Z","last_updated_date":"2025-01-31T14:12:59Z","reference_number":"EMA/517000/2024","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/tavneos-h-c-psusa-00010967-202403-epar-scientific-conclusions-grounds-variation-terms-marketing-authorisations_en.pdf"},
    {"id":"66589","name":"Elucirem-H-C-PSUSA-00000232-202403 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2025-02-04T12:19:42Z","last_updated_date":"2025-02-04T12:19:42Z","reference_number":"EMA/42286/2025","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/elucirem-h-c-psusa-00000232-202403-epar-scientific-conclusions-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"66590","name":"Vueway-H-C-PSUSA-00000232-202403 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2025-02-04T12:26:25Z","last_updated_date":"2025-02-04T12:26:25Z","reference_number":"EMA/42286/2025","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/vueway-h-c-psusa-00000232-202403-epar-scientific-conclusions-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"66622","name":"Quviviq-H-C-PSUSA-00010993-202401: EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2025-02-06T12:33:15Z","last_updated_date":"2025-02-06T12:33:15Z","reference_number":"EMA/49924/2025","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/quviviq-h-c-psusa-00010993-202401-epar-scientific-conclusions-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"66683","name":"Armisarte-PSUSA-00002330-202402 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2025-02-11T16:06:09Z","last_updated_date":"2025-02-11T16:06:09Z","reference_number":"EMA/42489/2025","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/armisarte-psusa-00002330-202402-epar-scientific-conclusions-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"66692","name":"Pemetrexed Accord-PSUSA-00002330-202402 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2025-02-12T09:58:44Z","last_updated_date":"2025-02-12T09:58:44Z","reference_number":"EMA/42489/2025","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/pemetrexed-accord-psusa-00002330-202402-epar-scientific-conclusions-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"66693","name":"Pemetrexed Fresenius Kabi-PSUSA-00002330-202402 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2025-02-12T10:21:18Z","last_updated_date":"2025-02-12T10:21:18Z","reference_number":"EMA/42489/2025","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/pemetrexed-fresenius-kabi-psusa-00002330-202402-epar-scientific-conclusions-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"66711","name":"Skytrofa-H-C-PSUSA-00010969-202402 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"Adopted","consultation_date":"","first_published_date":"2025-02-12T16:39:38Z","last_updated_date":"2025-02-12T16:39:38Z","reference_number":"EMA/53391/2025","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/skytrofa-h-c-psusa-00010969-202402-epar-scientific-conclusions-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"66767","name":"Veoza : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation(s)","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2025-02-14T11:10:52Z","last_updated_date":"2025-02-14T11:10:52Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/veoza-epar-scientific-conclusions-grounds-variation-terms-marketing-authorisations_en.pdf"},
    {"id":"66842","name":"Imjudo-H-C-PSUSA-00011038-202404 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2025-02-18T12:59:29Z","last_updated_date":"2025-02-18T12:59:29Z","reference_number":"EMA/62297/2025","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/imjudo-h-c-psusa-00011038-202404-epar-scientific-conclusions-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"66844","name":"Avamys-H-C-PSUSA-00009154-202404 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2025-02-18T13:17:07Z","last_updated_date":"2025-02-18T13:17:07Z","reference_number":"EMA/62367/2025","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/avamys-h-c-psusa-00009154-202404-epar-scientific-conclusions-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"66874","name":"Apretude-H-C-PSUSA-00000116-202403 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2025-02-19T13:48:40Z","last_updated_date":"2025-02-19T13:48:40Z","reference_number":"EMA/43280/2025","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/apretude-h-c-psusa-00000116-202403-epar-scientific-conclusions-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"66877","name":"Zoely-H-C-PSUSA-00002182-202401 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"Adopted","consultation_date":"","first_published_date":"2025-02-19T15:11:31Z","last_updated_date":"2025-02-19T15:11:31Z","reference_number":"EMA/64142/2025","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/zoely-h-c-psusa-00002182-202401-epar-scientific-conclusions-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"66890","name":"Qaialdo-H-C-PSUSA-00002780-202403 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2025-02-20T08:53:51Z","last_updated_date":"2025-02-20T08:53:51Z","reference_number":"EMA/64675/2025","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/qaialdo-h-c-psusa-00002780-202403-epar-scientific-conclusions-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"66904","name":"Imfinzi-H-C-PSUSA-00010723-202404 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2025-02-20T12:50:17Z","last_updated_date":"2025-02-20T12:50:17Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/imfinzi-h-c-psusa-00010723-202404-epar-scientific-conclusions-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"66953","name":"Bretaris Genuair-H-C-PSR-0047 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation(s)","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2025-02-25T14:29:16Z","last_updated_date":"2025-02-25T14:29:16Z","reference_number":"EMA/335/2025","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/bretaris-genuair-h-c-psr-0047-epar-scientific-conclusions-grounds-variation-terms-marketing-authorisations_en.pdf"},
    {"id":"66955","name":"Brimica Genuair-H-C-PSR-0047 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation(s)","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2025-02-25T15:06:16Z","last_updated_date":"2025-02-25T15:06:16Z","reference_number":"EMA/338/2025","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/brimica-genuair-h-c-psr-0047-epar-scientific-conclusions-grounds-variation-terms-marketing-authorisations_en.pdf"},
    {"id":"66982","name":"Duaklir Genuair-PSR-0047 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation(s)","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2025-02-26T11:32:46Z","last_updated_date":"2025-02-26T11:32:46Z","reference_number":"EMA/341/2025","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/duaklir-genuair-psr-0047-epar-scientific-conclusions-grounds-variation-terms-marketing-authorisations_en.pdf"},
    {"id":"66983","name":"Eklira Genuair-PSR-0047 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation(s)","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2025-02-26T11:43:02Z","last_updated_date":"2025-02-26T11:43:02Z","reference_number":"EMA/342/2025","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/eklira-genuair-psr-0047-epar-scientific-conclusions-grounds-variation-terms-marketing-authorisations_en.pdf"},
    {"id":"67017","name":"Advagraf-H-C-PSUSA-00002839-202403 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2025-02-27T14:16:47Z","last_updated_date":"2025-02-27T14:16:47Z","reference_number":"EMA/73854/2025","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/advagraf-h-c-psusa-00002839-202403-epar-scientific-conclusions-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"67064","name":"Envarsus-H-C-PSUSA-00002839-202403 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2025-02-28T16:00:29Z","last_updated_date":"2025-02-28T16:00:29Z","reference_number":"EMA/73854/2025","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/envarsus-h-c-psusa-00002839-202403-epar-scientific-conclusions-grounds-variation-terms-marketing-authorisation_en.pdf"},
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    {"id":"73605","name":"Leqembi-PSUSA-00011132-202507 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"Adopted","consultation_date":"","first_published_date":"2026-05-04T16:13:40Z","last_updated_date":"2026-05-04T16:13:40Z","reference_number":"EMADOC-1700519818-3028190","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/leqembi-psusa-00011132-202507-epar-scientific-conclusions-grounds-variation-terms-marketing-authorisation_en.pdf"},
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    {"id":"73752","name":"Zoledronic acid Medac-H-C-PSUSA-00003149-202308 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2026-05-18T17:04:17Z","last_updated_date":"2026-05-19T10:16:00Z","reference_number":"EMA/113943/2026","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/zoledronic-acid-medac-h-c-psusa-00003149-202308-epar-scientific-conclusions-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"73757","name":"Tecartus-PSUSA-00010903-202507 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2026-05-19T12:34:47Z","last_updated_date":"2026-05-19T12:34:47Z","reference_number":"EMADOC-1700519818-3026217","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/tecartus-psusa-00010903-202507-epar-scientific-conclusions-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"73851","name":"Fycompa-PSUSA-00009255-202507 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2026-05-26T11:19:36Z","last_updated_date":"2026-05-26T11:19:36Z","reference_number":"EMADOC-1700519818-3024888","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/fycompa-psusa-00009255-202507-epar-scientific-conclusions-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"73859","name":"Polivy-PSUSA-00010817-202506 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2026-05-27T11:47:04Z","last_updated_date":"2026-05-27T11:47:04Z","reference_number":"EMADOC-1700519818-3190711","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/polivy-psusa-00010817-202506-epar-scientific-conclusions-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"73911","name":"Kapruvia-PSUSA-00010995-202508 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2026-06-01T09:32:43Z","last_updated_date":"2026-06-01T09:32:43Z","reference_number":"EMADOC-1700519818-2995672","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/kapruvia-psusa-00010995-202508-epar-scientific-conclusions-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"73912","name":"Carvykti-PSUSA-00011000-202508 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2026-06-01T09:51:42Z","last_updated_date":"2026-06-01T09:51:42Z","reference_number":"EMADOC-1700519818-3128519","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/carvykti-psusa-00011000-202508-epar-scientific-conclusions-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"73941","name":"Orkambi-PSUSA-00010455-202505 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation","type":"scientific-conclusion","status":"unknown","consultation_date":"","first_published_date":"2026-06-02T16:35:49Z","last_updated_date":"2026-06-02T16:35:49Z","reference_number":"EMADOC-1700519818-3213132","document_url":"https://www.ema.europa.eu/en/documents/scientific-conclusion/orkambi-psusa-00010455-202505-epar-scientific-conclusions-grounds-variation-terms-marketing-authorisation_en.pdf"},
    {"id":"2671","name":"Quixidar : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2008-05-16T02:00:00Z","last_updated_date":"2008-05-16T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/quixidar-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
    {"id":"2757","name":"Cetrotide : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2005-10-21T02:00:00Z","last_updated_date":"2005-10-21T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/cetrotide-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
    {"id":"3425","name":"Aprovel : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2006-10-16T02:00:00Z","last_updated_date":"2006-10-16T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/aprovel-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
    {"id":"3615","name":"Combivir : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2005-11-17T00:09:21Z","last_updated_date":"2005-11-17T00:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/combivir-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
    {"id":"3773","name":"Integrilin : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2006-07-10T02:00:00Z","last_updated_date":"2006-07-10T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/integrilin-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
    {"id":"4335","name":"Travatan : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2006-10-26T02:09:21Z","last_updated_date":"2006-10-26T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/travatan-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
    {"id":"4423","name":"Simulect : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2005-11-28T01:00:00Z","last_updated_date":"2005-11-28T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/simulect-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
    {"id":"4554","name":"Helixate NexGen : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2006-11-06T00:09:00Z","last_updated_date":"2020-06-02T00:09:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/helixate-nexgen-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
    {"id":"4840","name":"Trazec : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2009-08-24T02:00:00Z","last_updated_date":"2009-08-24T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/trazec-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
    {"id":"4917","name":"Zeffix : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2006-08-07T02:09:21Z","last_updated_date":"2006-08-07T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/zeffix-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
    {"id":"5057","name":"Twinrix Adult : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2005-12-01T00:09:21Z","last_updated_date":"2005-12-01T00:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/twinrix-adult-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
    {"id":"5304","name":"Xeloda : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2005-12-07T01:00:00Z","last_updated_date":"2005-12-07T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/xeloda-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
    {"id":"5662","name":"Epivir : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2005-11-25T01:00:00Z","last_updated_date":"2005-11-25T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/epivir-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
    {"id":"5806","name":"Kogenate Bayer : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2006-09-08T02:00:00Z","last_updated_date":"2006-09-08T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/kogenate-bayer-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
    {"id":"6080","name":"Ferriprox : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2006-07-10T02:09:21Z","last_updated_date":"2006-07-10T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/ferriprox-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
    {"id":"6205","name":"Regranex : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2005-10-21T02:00:00Z","last_updated_date":"2012-08-15T16:50:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/regranex-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
    {"id":"6752","name":"Forcaltonin : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2008-11-21T00:09:21Z","last_updated_date":"2008-11-21T00:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/forcaltonin-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
    {"id":"6991","name":"Rapamune : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2006-08-08T02:00:00Z","last_updated_date":"2006-08-08T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/rapamune-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
    {"id":"7175","name":"Aerius : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2006-04-03T02:00:00Z","last_updated_date":"2006-04-03T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/aerius-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
    {"id":"7250","name":"Osigraft : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2005-10-21T02:09:21Z","last_updated_date":"2016-07-27T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/osigraft-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
    {"id":"7331","name":"Visudyne : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2006-01-23T01:00:00Z","last_updated_date":"2006-01-23T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/visudyne-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
    {"id":"8572","name":"NeoRecormon : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2005-10-21T02:09:21Z","last_updated_date":"2005-10-21T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/neorecormon-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
    {"id":"8907","name":"Zometa : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2005-10-21T02:00:00Z","last_updated_date":"2005-10-21T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/zometa-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
    {"id":"9022","name":"Agenerase : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2005-10-21T02:00:00Z","last_updated_date":"2011-06-21T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/agenerase-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
    {"id":"9195","name":"Orgalutran : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2005-10-21T02:00:00Z","last_updated_date":"2005-10-21T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/orgalutran-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
    {"id":"9230","name":"Zenapax : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2008-04-08T03:09:21Z","last_updated_date":"2008-04-08T03:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/zenapax-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
    {"id":"9274","name":"MabThera : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2006-09-29T02:00:00Z","last_updated_date":"2024-03-01T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/mabthera-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
    {"id":"9317","name":"MabCampath : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2005-10-21T02:09:21Z","last_updated_date":"2012-08-15T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/mabcampath-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
    {"id":"9355","name":"Puregon : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2008-08-31T02:00:00Z","last_updated_date":"2008-08-31T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/puregon-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
    {"id":"9480","name":"Tracleer : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2005-10-21T02:09:21Z","last_updated_date":"2005-10-21T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/tracleer-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
    {"id":"9625","name":"Prevenar : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2005-10-21T02:00:00Z","last_updated_date":"2017-11-24T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/prevenar-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
    {"id":"9840","name":"Teslascan : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2006-10-30T00:09:21Z","last_updated_date":"2012-08-02T16:15:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/teslascan-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
    {"id":"9852","name":"Prometax : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2006-01-19T01:00:00Z","last_updated_date":"2006-01-19T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/prometax-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
    {"id":"9912","name":"Karvezide : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2006-10-16T02:00:00Z","last_updated_date":"2006-10-16T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/karvezide-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
    {"id":"10000","name":"Betaferon : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2006-08-09T02:09:21Z","last_updated_date":"2006-08-09T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/betaferon-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
    {"id":"10153","name":"Tritanrix HepB : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2005-10-21T02:09:21Z","last_updated_date":"2014-01-07T01:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/tritanrix-hepb-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
    {"id":"10477","name":"Plavix : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2006-10-24T02:00:00Z","last_updated_date":"2006-10-24T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/plavix-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
    {"id":"10523","name":"Emadine : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2005-10-21T02:00:00Z","last_updated_date":"2005-10-21T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/emadine-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
    {"id":"10847","name":"Ammonaps : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2006-11-10T01:00:00Z","last_updated_date":"2006-11-10T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/ammonaps-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
    {"id":"11053","name":"HBVaxPro : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2006-09-05T02:09:21Z","last_updated_date":"2006-09-05T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/hbvaxpro-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
    {"id":"11179","name":"Zyprexa Velotab : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2005-10-21T02:00:00Z","last_updated_date":"2005-10-21T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/zyprexa-velotab-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
    {"id":"11561","name":"Paxene : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2005-12-15T01:00:00Z","last_updated_date":"2010-03-22T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/paxene-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
    {"id":"11726","name":"Sonata : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2005-10-21T02:00:00Z","last_updated_date":"2015-10-21T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/sonata-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
    {"id":"11822","name":"Rebif : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2006-08-09T02:00:00Z","last_updated_date":"2006-08-09T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/rebif-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
    {"id":"11907","name":"Xenical : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2005-12-19T01:00:00Z","last_updated_date":"2005-12-19T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/xenical-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
    {"id":"12236","name":"Glivec : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2005-10-28T02:09:21Z","last_updated_date":"2005-10-28T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/glivec-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
    {"id":"12245","name":"Procomvax : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2009-07-29T02:00:00Z","last_updated_date":"2009-07-29T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/procomvax-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
    {"id":"12470","name":"Zerene : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2005-10-21T02:09:21Z","last_updated_date":"2012-10-15T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/zerene-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
    {"id":"12598","name":"Infanrix Hexa : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2005-10-21T02:00:00Z","last_updated_date":"2005-10-21T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/infanrix-hexa-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
    {"id":"12934","name":"Arava : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2005-11-23T01:00:00Z","last_updated_date":"2005-11-23T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/arava-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
    {"id":"12942","name":"Viread : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2006-04-06T02:00:00Z","last_updated_date":"2006-04-06T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/viread-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
    {"id":"12995","name":"Viraferon : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2008-05-27T03:09:21Z","last_updated_date":"2008-05-27T03:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/viraferon-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
    {"id":"13162","name":"SonoVue : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2005-10-21T02:00:00Z","last_updated_date":"2005-10-21T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/sonovue-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
    {"id":"13256","name":"Pritor : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2006-07-11T02:00:00Z","last_updated_date":"2006-07-11T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/pritor-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
    {"id":"13330","name":"Zyprexa : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2005-10-21T02:00:00Z","last_updated_date":"2005-10-21T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/zyprexa-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
    {"id":"13402","name":"LeukoScan : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2005-10-21T02:00:00Z","last_updated_date":"2018-02-09T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/leukoscan-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
    {"id":"13438","name":"Helicobacter Test INFAI : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2005-10-21T02:09:21Z","last_updated_date":"2005-10-21T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/helicobacter-test-infai-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
    {"id":"13443","name":"Foscan : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2006-01-10T00:09:21Z","last_updated_date":"2006-01-10T00:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/foscan-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
    {"id":"13682","name":"Mirapexin : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2005-10-26T02:09:21Z","last_updated_date":"2005-10-26T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/mirapexin-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
    {"id":"13844","name":"Viracept : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2006-11-20T01:00:00Z","last_updated_date":"2014-06-10T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/viracept-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
    {"id":"14121","name":"Pylobactell : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2005-12-07T01:00:00Z","last_updated_date":"2005-12-07T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/pylobactell-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
    {"id":"14292","name":"Aldara : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2006-07-21T02:00:00Z","last_updated_date":"2006-07-21T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/aldara-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
    {"id":"14700","name":"Azomyr : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2005-10-21T02:00:00Z","last_updated_date":"2005-10-21T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/azomyr-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
    {"id":"15069","name":"Thyrogen : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2006-01-24T00:09:21Z","last_updated_date":"2006-01-24T00:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/thyrogen-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
    {"id":"15157","name":"Caelyx : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2005-10-21T02:09:21Z","last_updated_date":"2005-10-21T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/caelyx-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
    {"id":"15507","name":"Remicade : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2005-12-07T01:00:00Z","last_updated_date":"2005-12-07T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/remicade-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
    {"id":"15604","name":"Refludan : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2006-07-10T02:00:00Z","last_updated_date":"2012-07-27T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/refludan-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
    {"id":"16070","name":"Neoclarityn : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2006-07-21T02:09:21Z","last_updated_date":"2006-07-21T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/neoclarityn-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
    {"id":"16244","name":"Zerit : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2006-08-11T02:00:00Z","last_updated_date":"2006-08-11T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/zerit-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
    {"id":"17040","name":"NovoRapid : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2009-06-19T02:00:00Z","last_updated_date":"2009-06-19T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/novorapid-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
    {"id":"17220","name":"Starlix : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2006-08-09T02:00:00Z","last_updated_date":"2022-06-28T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/starlix-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
    {"id":"17410","name":"Rebetol : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2006-08-11T02:00:00Z","last_updated_date":"2023-11-07T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/rebetol-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
    {"id":"17416","name":"Karvea : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2006-07-11T02:00:00Z","last_updated_date":"2006-07-11T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/karvea-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
    {"id":"17933","name":"Viagra : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2006-09-22T02:00:00Z","last_updated_date":"2006-09-22T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/viagra-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
    {"id":"18066","name":"Onsenal : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2005-11-15T01:00:00Z","last_updated_date":"2011-04-06T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/onsenal-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
    {"id":"18087","name":"BeneFIX : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2005-12-06T01:00:00Z","last_updated_date":"2005-12-06T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/benefix-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
    {"id":"18166","name":"ViraferonPeg : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2006-08-11T02:00:00Z","last_updated_date":"2021-01-22T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/viraferonpeg-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
    {"id":"18271","name":"Sustiva : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2006-11-20T01:00:00Z","last_updated_date":"2024-03-14T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/sustiva-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
    {"id":"18544","name":"Sifrol : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2005-10-26T02:00:00Z","last_updated_date":"2005-10-26T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/sifrol-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
    {"id":"18565","name":"Enbrel : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2006-10-18T02:00:00Z","last_updated_date":"2010-01-20T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/enbrel-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
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    {"id":"19188","name":"Kinzalmono : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2006-07-10T02:00:00Z","last_updated_date":"2006-07-10T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/kinzalmono-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
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    {"id":"19895","name":"NovoNorm : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2005-10-21T02:00:00Z","last_updated_date":"2005-10-21T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/novonorm-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
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    {"id":"20912","name":"Reyataz : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2006-08-08T02:00:00Z","last_updated_date":"2006-08-08T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/reyataz-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
    {"id":"21126","name":"Xigris : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2005-11-17T01:00:00Z","last_updated_date":"2012-02-21T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/xigris-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
    {"id":"21146","name":"Actos : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2006-04-03T02:00:00Z","last_updated_date":"2006-04-03T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/actos-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
    {"id":"21489","name":"Evra : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2005-10-21T02:00:00Z","last_updated_date":"2022-06-14T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/evra-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
    {"id":"21821","name":"Viramune : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2005-10-21T02:00:00Z","last_updated_date":"2005-10-21T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/viramune-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
    {"id":"21869","name":"Pegasys : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2006-08-08T02:00:00Z","last_updated_date":"2006-08-08T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/pegasys-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
    {"id":"22602","name":"Ovitrelle : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2006-11-10T00:09:21Z","last_updated_date":"2006-11-10T00:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/ovitrelle-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
    {"id":"22694","name":"Avandia : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2006-08-15T02:00:00Z","last_updated_date":"2016-06-08T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/avandia-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
    {"id":"22768","name":"Bondronat : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2005-10-21T02:09:21Z","last_updated_date":"2005-10-21T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/bondronat-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
    {"id":"22821","name":"Trizivir : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2006-08-07T02:09:21Z","last_updated_date":"2006-08-07T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/trizivir-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
    {"id":"22935","name":"Infanrix Penta : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2005-10-21T02:00:00Z","last_updated_date":"2013-07-10T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/infanrix-penta-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
    {"id":"23118","name":"Arixtra : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2005-11-04T01:00:00Z","last_updated_date":"2005-11-04T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/arixtra-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
    {"id":"23194","name":"Rapilysin : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2006-07-11T02:00:00Z","last_updated_date":"2006-07-11T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/rapilysin-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
    {"id":"23218","name":"MicardisPlus : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2006-07-20T02:09:21Z","last_updated_date":"2006-07-20T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/micardisplus-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
    {"id":"23327","name":"Evista : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2005-10-21T02:00:00Z","last_updated_date":"2005-10-21T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/evista-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
    {"id":"24321","name":"Revasc : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2006-07-11T02:00:00Z","last_updated_date":"2014-07-29T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/revasc-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
    {"id":"24407","name":"Dynastat : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2005-11-15T01:00:00Z","last_updated_date":"2005-11-15T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/dynastat-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
    {"id":"24548","name":"Lumigan : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2005-12-08T01:00:00Z","last_updated_date":"2005-12-08T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/lumigan-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
    {"id":"24560","name":"Temodal : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2005-12-13T00:09:21Z","last_updated_date":"2005-12-13T00:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/temodal-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
    {"id":"25022","name":"Ambirix : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2005-11-23T01:00:00Z","last_updated_date":"2005-11-23T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/ambirix-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
    {"id":"25025","name":"Synagis : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2005-10-21T02:00:00Z","last_updated_date":"2005-10-21T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/synagis-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
    {"id":"25200","name":"Renagel : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2005-10-21T02:00:00Z","last_updated_date":"2005-10-21T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/renagel-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
    {"id":"25705","name":"Zavesca : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2005-10-21T02:09:21Z","last_updated_date":"2005-10-21T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/zavesca-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
    {"id":"25748","name":"Micardis : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2006-07-10T02:09:21Z","last_updated_date":"2006-07-10T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/micardis-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
    {"id":"26641","name":"Hycamtin : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2006-02-20T00:09:21Z","last_updated_date":"2006-02-20T00:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/hycamtin-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
    {"id":"26761","name":"CoAprovel : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2006-10-17T02:09:21Z","last_updated_date":"2006-10-17T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/coaprovel-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
    {"id":"27394","name":"CellCept : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2006-04-06T02:09:21Z","last_updated_date":"2006-04-06T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/cellcept-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
    {"id":"27595","name":"Stocrin : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2005-11-03T01:00:00Z","last_updated_date":"2005-11-03T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/stocrin-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
    {"id":"28337","name":"Inductos : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2005-10-21T02:00:00Z","last_updated_date":"2017-06-15T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/inductos-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
    {"id":"28599","name":"Fabrazyme : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2005-12-21T00:09:21Z","last_updated_date":"2005-12-21T00:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/fabrazyme-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
    {"id":"28659","name":"Nonafact : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2005-11-15T00:09:00Z","last_updated_date":"2020-04-29T00:09:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/nonafact-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
    {"id":"28954","name":"Fuzeon : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2006-08-11T02:09:21Z","last_updated_date":"2006-08-11T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/fuzeon-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
    {"id":"28979","name":"Trisenox : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2005-10-28T02:09:21Z","last_updated_date":"2005-10-28T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/trisenox-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
    {"id":"29195","name":"Avonex : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2006-08-16T02:00:00Z","last_updated_date":"2006-08-16T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/avonex-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
    {"id":"29258","name":"Vistide : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2005-11-17T01:00:00Z","last_updated_date":"2015-01-19T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/vistide-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
    {"id":"29709","name":"Neupopeg : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2009-01-26T00:09:21Z","last_updated_date":"2009-01-26T00:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/neupopeg-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
    {"id":"29714","name":"Invirase : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2006-10-31T01:00:00Z","last_updated_date":"2023-09-25T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/invirase-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
    {"id":"29739","name":"Aranesp : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2006-06-14T02:00:00Z","last_updated_date":"2006-06-14T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/aranesp-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
    {"id":"29796","name":"Keppra : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2005-10-21T02:00:00Z","last_updated_date":"2005-10-21T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/keppra-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
    {"id":"30660","name":"PegIntron : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2006-08-11T02:00:00Z","last_updated_date":"2021-06-03T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/pegintron-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
    {"id":"31152","name":"Twinrix Paediatric : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2005-10-21T02:09:21Z","last_updated_date":"2005-10-21T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/twinrix-paediatric-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
    {"id":"31456","name":"NovoMix : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2005-10-21T02:00:00Z","last_updated_date":"2005-10-21T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/novomix-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
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    {"id":"31721","name":"Cystagon : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2005-10-21T02:09:21Z","last_updated_date":"2005-10-21T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/cystagon-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
    {"id":"31794","name":"Beromun : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2005-10-21T02:09:21Z","last_updated_date":"2005-10-21T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/beromun-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
    {"id":"31813","name":"Kinzalkomb : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2005-10-21T02:00:00Z","last_updated_date":"2005-10-21T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/kinzalkomb-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
    {"id":"31990","name":"Optisulin : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2005-10-21T02:09:21Z","last_updated_date":"2005-10-21T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/optisulin-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
    {"id":"32316","name":"NovoSeven : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2005-10-21T02:00:00Z","last_updated_date":"2005-10-21T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/novoseven-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
    {"id":"34724","name":"Tasmar : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2006-01-25T00:09:21Z","last_updated_date":"2006-01-25T00:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/tasmar-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
    {"id":"34853","name":"NeuroBloc : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2008-06-01T02:09:00Z","last_updated_date":"2023-05-04T02:09:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/neurobloc-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
    {"id":"35146","name":"GONAL-f : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2007-05-29T02:09:21Z","last_updated_date":"2007-05-29T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/gonal-f-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
    {"id":"35774","name":"Protopy : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2008-10-29T01:00:00Z","last_updated_date":"2008-10-29T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/protopy-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
    {"id":"35975","name":"Neulasta : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2009-06-19T02:00:00Z","last_updated_date":"2009-06-19T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/neulasta-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
    {"id":"36062","name":"Comtan : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2005-10-21T02:00:00Z","last_updated_date":"2005-10-21T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/comtan-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
    {"id":"36357","name":"Herceptin : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2005-10-21T02:09:21Z","last_updated_date":"2005-10-21T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/herceptin-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
    {"id":"36767","name":"Glustin : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2006-09-06T02:09:00Z","last_updated_date":"2022-10-17T02:09:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/glustin-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
    {"id":"36807","name":"Optruma : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2005-10-21T02:09:21Z","last_updated_date":"2005-10-21T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/optruma-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
    {"id":"37203","name":"Kineret : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2006-07-21T02:00:00Z","last_updated_date":"2006-07-21T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/kineret-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
    {"id":"37219","name":"Norvir : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2005-10-21T02:09:21Z","last_updated_date":"2005-10-21T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/norvir-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
    {"id":"37270","name":"Azopt : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2005-10-21T02:00:00Z","last_updated_date":"2005-10-21T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/azopt-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
    {"id":"38174","name":"Humalog : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2006-01-09T00:09:21Z","last_updated_date":"2006-01-09T00:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/humalog-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
    {"id":"38302","name":"Nespo : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2009-01-29T00:09:21Z","last_updated_date":"2009-01-29T00:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/nespo-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
    {"id":"38382","name":"Metalyse : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2006-07-10T02:00:00Z","last_updated_date":"2006-07-10T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/metalyse-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
    {"id":"38592","name":"Exelon : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2006-01-12T01:00:00Z","last_updated_date":"2006-01-12T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/exelon-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
    {"id":"38719","name":"Myocet : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2006-08-16T02:00:00Z","last_updated_date":"2006-08-16T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/myocet-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
    {"id":"38790","name":"DaTSCAN : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2006-09-05T02:00:00Z","last_updated_date":"2006-09-05T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/datscan-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
    {"id":"38886","name":"Taxotere : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2005-12-22T00:09:21Z","last_updated_date":"2005-12-22T00:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/taxotere-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
    {"id":"38915","name":"ReFacto AF : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2006-09-08T02:00:00Z","last_updated_date":"2006-09-08T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/refacto-af-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
    {"id":"39476","name":"Comtess : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2005-10-21T02:00:00Z","last_updated_date":"2005-10-21T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/comtess-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
    {"id":"39721","name":"Crixivan : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2005-10-21T02:00:00Z","last_updated_date":"2022-07-07T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/crixivan-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
    {"id":"40145","name":"Luveris : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2006-11-10T01:00:00Z","last_updated_date":"2006-11-10T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/luveris-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
    {"id":"40295","name":"Insuman : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2006-08-09T02:00:00Z","last_updated_date":"2006-08-09T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/insuman-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
    {"id":"40515","name":"Rilutek : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2005-10-21T02:09:21Z","last_updated_date":"2005-10-21T02:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/rilutek-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
    {"id":"40805","name":"IntronA : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2006-08-11T02:00:00Z","last_updated_date":"2022-12-14T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/introna-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
    {"id":"40971","name":"Fareston : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2005-11-29T00:09:21Z","last_updated_date":"2005-11-29T00:09:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/fareston-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
    {"id":"40985","name":"Iscover : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2006-10-24T02:00:00Z","last_updated_date":"2006-10-24T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/iscover-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
    {"id":"41071","name":"Optison : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2008-08-01T02:00:00Z","last_updated_date":"2008-08-01T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/optison-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
    {"id":"41514","name":"Panretin : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2006-01-26T01:00:00Z","last_updated_date":"2006-01-26T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/panretin-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
    {"id":"41706","name":"Kaletra : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2006-08-09T02:00:00Z","last_updated_date":"2006-08-09T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/kaletra-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
    {"id":"55311","name":"Sitagliptin / Metformin hydrochloride Mylan : EPAR - Procedural steps taken and scientific information after authorisation (archive)","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2022-06-21T14:41:00Z","last_updated_date":"2025-04-04T15:01:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/sitagliptin-metformin-hydrochloride-mylan-epar-procedural-steps-taken-scientific-information-after-authorisation-archive_en.pdf"},
    {"id":"60555","name":"Ceprotin : EPAR - Steps taken after authorisation when a cutoff date has been used","type":"steps-after-cutoff","status":"unknown","consultation_date":"","first_published_date":"2005-10-21T02:09:00Z","last_updated_date":"2005-10-21T02:09:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/steps-after-cutoff/ceprotin-epar-steps-taken-after-authorisation-when-cutoff-date-has-been-used_en.pdf"},
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    {"id":"35208","name":"Fexeric : EPAR - Summary for the public","type":"overview","status":"unknown","consultation_date":"","first_published_date":"2015-10-02T02:00:00Z","last_updated_date":"2015-10-02T02:00:00Z","reference_number":"EMA/510659/2015 ","document_url":"https://www.ema.europa.eu/en/documents/overview/fexeric-epar-summary-public_en.pdf","translations":{"bg":"https://www.ema.europa.eu/bg/documents/overview/fexeric-epar-summary-public_bg.pdf","es":"https://www.ema.europa.eu/es/documents/overview/fexeric-epar-summary-public_es.pdf","cs":"https://www.ema.europa.eu/cs/documents/overview/fexeric-epar-summary-public_cs.pdf","da":"https://www.ema.europa.eu/da/documents/overview/fexeric-epar-summary-public_da.pdf","de":"https://www.ema.europa.eu/de/documents/overview/fexeric-epar-summary-public_de.pdf","et":"https://www.ema.europa.eu/et/documents/overview/fexeric-epar-summary-public_et.pdf","el":"https://www.ema.europa.eu/el/documents/overview/fexeric-epar-summary-public_el.pdf","fr":"https://www.ema.europa.eu/fr/documents/overview/fexeric-epar-summary-public_fr.pdf","hr":"https://www.ema.europa.eu/hr/documents/overview/fexeric-epar-summary-public_hr.pdf","it":"https://www.ema.europa.eu/it/documents/overview/fexeric-epar-summary-public_it.pdf","lv":"https://www.ema.europa.eu/lv/documents/overview/fexeric-epar-summary-public_lv.pdf","lt":"https://www.ema.europa.eu/lt/documents/overview/fexeric-epar-summary-public_lt.pdf","hu":"https://www.ema.europa.eu/hu/documents/overview/fexeric-epar-summary-public_hu.pdf","mt":"https://www.ema.europa.eu/mt/documents/overview/fexeric-epar-summary-public_mt.pdf","nl":"https://www.ema.europa.eu/nl/documents/overview/fexeric-epar-summary-public_nl.pdf","pl":"https://www.ema.europa.eu/pl/documents/overview/fexeric-epar-summary-public_pl.pdf","pt":"https://www.ema.europa.eu/pt/documents/overview/fexeric-epar-summary-public_pt.pdf","ro":"https://www.ema.europa.eu/ro/documents/overview/fexeric-epar-summary-public_ro.pdf","sk":"https://www.ema.europa.eu/sk/documents/overview/fexeric-epar-summary-public_sk.pdf","sl":"https://www.ema.europa.eu/sl/documents/overview/fexeric-epar-summary-public_sl.pdf","fi":"https://www.ema.europa.eu/fi/documents/overview/fexeric-epar-summary-public_fi.pdf","sv":"https://www.ema.europa.eu/sv/documents/overview/fexeric-epar-summary-public_sv.pdf"}},
    {"id":"35216","name":"Fevaxyn Pentofel : EPAR - Summary for the public","type":"overview","status":"unknown","consultation_date":"","first_published_date":"2007-03-08T01:00:00Z","last_updated_date":"2024-11-21T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/overview/fevaxyn-pentofel-epar-summary-public_en.pdf","translations":{"bg":"https://www.ema.europa.eu/bg/documents/overview/fevaxyn-pentofel-epar-summary-public_bg.pdf","es":"https://www.ema.europa.eu/es/documents/overview/fevaxyn-pentofel-epar-summary-public_es.pdf","cs":"https://www.ema.europa.eu/cs/documents/overview/fevaxyn-pentofel-epar-summary-public_cs.pdf","da":"https://www.ema.europa.eu/da/documents/overview/fevaxyn-pentofel-epar-summary-public_da.pdf","de":"https://www.ema.europa.eu/de/documents/overview/fevaxyn-pentofel-epar-summary-public_de.pdf","et":"https://www.ema.europa.eu/et/documents/overview/fevaxyn-pentofel-epar-summary-public_et.pdf","el":"https://www.ema.europa.eu/el/documents/overview/fevaxyn-pentofel-epar-summary-public_el.pdf","fr":"https://www.ema.europa.eu/fr/documents/overview/fevaxyn-pentofel-epar-summary-public_fr.pdf","ga":"https://www.ema.europa.eu/ga/documents/overview/fevaxyn-pentofel-epar-summary-public_ga.pdf","hr":"https://www.ema.europa.eu/hr/documents/overview/fevaxyn-pentofel-epar-summary-public_hr.pdf","it":"https://www.ema.europa.eu/it/documents/overview/fevaxyn-pentofel-epar-summary-public_it.pdf","lv":"https://www.ema.europa.eu/lv/documents/overview/fevaxyn-pentofel-epar-summary-public_lv.pdf","lt":"https://www.ema.europa.eu/lt/documents/overview/fevaxyn-pentofel-epar-summary-public_lt.pdf","hu":"https://www.ema.europa.eu/hu/documents/overview/fevaxyn-pentofel-epar-summary-public_hu.pdf","mt":"https://www.ema.europa.eu/mt/documents/overview/fevaxyn-pentofel-epar-summary-public_mt.pdf","nl":"https://www.ema.europa.eu/nl/documents/overview/fevaxyn-pentofel-epar-summary-public_nl.pdf","pl":"https://www.ema.europa.eu/pl/documents/overview/fevaxyn-pentofel-epar-summary-public_pl.pdf","pt":"https://www.ema.europa.eu/pt/documents/overview/fevaxyn-pentofel-epar-summary-public_pt.pdf","ro":"https://www.ema.europa.eu/ro/documents/overview/fevaxyn-pentofel-epar-summary-public_ro.pdf","sk":"https://www.ema.europa.eu/sk/documents/overview/fevaxyn-pentofel-epar-summary-public_sk.pdf","sl":"https://www.ema.europa.eu/sl/documents/overview/fevaxyn-pentofel-epar-summary-public_sl.pdf","fi":"https://www.ema.europa.eu/fi/documents/overview/fevaxyn-pentofel-epar-summary-public_fi.pdf","sv":"https://www.ema.europa.eu/sv/documents/overview/fevaxyn-pentofel-epar-summary-public_sv.pdf","is":"https://www.ema.europa.eu/is/documents/overview/fevaxyn-pentofel-epar-summary-public_is.pdf","no":"https://www.ema.europa.eu/no/documents/overview/fevaxyn-pentofel-epar-summary-public_no.pdf"}},
    {"id":"35229","name":"Lynparza : EPAR - Medicine overview","type":"overview","status":"unknown","consultation_date":"","first_published_date":"2015-01-09T01:00:00Z","last_updated_date":"2024-09-02T14:13:00Z","reference_number":"EMA/889990/2022","document_url":"https://www.ema.europa.eu/en/documents/overview/lynparza-epar-medicine-overview_en.pdf","translations":{"bg":"https://www.ema.europa.eu/bg/documents/overview/lynparza-epar-medicine-overview_bg.pdf","es":"https://www.ema.europa.eu/es/documents/overview/lynparza-epar-medicine-overview_es.pdf","cs":"https://www.ema.europa.eu/cs/documents/overview/lynparza-epar-medicine-overview_cs.pdf","da":"https://www.ema.europa.eu/da/documents/overview/lynparza-epar-medicine-overview_da.pdf","de":"https://www.ema.europa.eu/de/documents/overview/lynparza-epar-medicine-overview_de.pdf","et":"https://www.ema.europa.eu/et/documents/overview/lynparza-epar-medicine-overview_et.pdf","el":"https://www.ema.europa.eu/el/documents/overview/lynparza-epar-medicine-overview_el.pdf","fr":"https://www.ema.europa.eu/fr/documents/overview/lynparza-epar-medicine-overview_fr.pdf","hr":"https://www.ema.europa.eu/hr/documents/overview/lynparza-epar-medicine-overview_hr.pdf","it":"https://www.ema.europa.eu/it/documents/overview/lynparza-epar-medicine-overview_it.pdf","lv":"https://www.ema.europa.eu/lv/documents/overview/lynparza-epar-medicine-overview_lv.pdf","lt":"https://www.ema.europa.eu/lt/documents/overview/lynparza-epar-medicine-overview_lt.pdf","hu":"https://www.ema.europa.eu/hu/documents/overview/lynparza-epar-medicine-overview_hu.pdf","mt":"https://www.ema.europa.eu/mt/documents/overview/lynparza-epar-medicine-overview_mt.pdf","nl":"https://www.ema.europa.eu/nl/documents/overview/lynparza-epar-medicine-overview_nl.pdf","pl":"https://www.ema.europa.eu/pl/documents/overview/lynparza-epar-medicine-overview_pl.pdf","pt":"https://www.ema.europa.eu/pt/documents/overview/lynparza-epar-medicine-overview_pt.pdf","ro":"https://www.ema.europa.eu/ro/documents/overview/lynparza-epar-medicine-overview_ro.pdf","sk":"https://www.ema.europa.eu/sk/documents/overview/lynparza-epar-medicine-overview_sk.pdf","sl":"https://www.ema.europa.eu/sl/documents/overview/lynparza-epar-medicine-overview_sl.pdf","fi":"https://www.ema.europa.eu/fi/documents/overview/lynparza-epar-medicine-overview_fi.pdf","sv":"https://www.ema.europa.eu/sv/documents/overview/lynparza-epar-medicine-overview_sv.pdf"}},
    {"id":"35258","name":"Naxcel : EPAR - Summary for the public","type":"overview","status":"unknown","consultation_date":"","first_published_date":"2009-10-20T02:00:00Z","last_updated_date":"2024-06-28T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/overview/naxcel-epar-summary-public_en.pdf","translations":{"bg":"https://www.ema.europa.eu/bg/documents/overview/naxcel-epar-summary-public_bg.pdf","es":"https://www.ema.europa.eu/es/documents/overview/naxcel-epar-summary-public_es.pdf","cs":"https://www.ema.europa.eu/cs/documents/overview/naxcel-epar-summary-public_cs.pdf","da":"https://www.ema.europa.eu/da/documents/overview/naxcel-epar-summary-public_da.pdf","de":"https://www.ema.europa.eu/de/documents/overview/naxcel-epar-summary-public_de.pdf","et":"https://www.ema.europa.eu/et/documents/overview/naxcel-epar-summary-public_et.pdf","el":"https://www.ema.europa.eu/el/documents/overview/naxcel-epar-summary-public_el.pdf","fr":"https://www.ema.europa.eu/fr/documents/overview/naxcel-epar-summary-public_fr.pdf","ga":"https://www.ema.europa.eu/ga/documents/overview/naxcel-epar-summary-public_ga.pdf","hr":"https://www.ema.europa.eu/hr/documents/overview/naxcel-epar-summary-public_hr.pdf","it":"https://www.ema.europa.eu/it/documents/overview/naxcel-epar-summary-public_it.pdf","lv":"https://www.ema.europa.eu/lv/documents/overview/naxcel-epar-summary-public_lv.pdf","lt":"https://www.ema.europa.eu/lt/documents/overview/naxcel-epar-summary-public_lt.pdf","hu":"https://www.ema.europa.eu/hu/documents/overview/naxcel-epar-summary-public_hu.pdf","mt":"https://www.ema.europa.eu/mt/documents/overview/naxcel-epar-summary-public_mt.pdf","nl":"https://www.ema.europa.eu/nl/documents/overview/naxcel-epar-summary-public_nl.pdf","pl":"https://www.ema.europa.eu/pl/documents/overview/naxcel-epar-summary-public_pl.pdf","pt":"https://www.ema.europa.eu/pt/documents/overview/naxcel-epar-summary-public_pt.pdf","ro":"https://www.ema.europa.eu/ro/documents/overview/naxcel-epar-summary-public_ro.pdf","sk":"https://www.ema.europa.eu/sk/documents/overview/naxcel-epar-summary-public_sk.pdf","sl":"https://www.ema.europa.eu/sl/documents/overview/naxcel-epar-summary-public_sl.pdf","fi":"https://www.ema.europa.eu/fi/documents/overview/naxcel-epar-summary-public_fi.pdf","sv":"https://www.ema.europa.eu/sv/documents/overview/naxcel-epar-summary-public_sv.pdf","is":"https://www.ema.europa.eu/is/documents/overview/naxcel-epar-summary-public_is.pdf","no":"https://www.ema.europa.eu/no/documents/overview/naxcel-epar-summary-public_no.pdf"}},
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    {"id":"36351","name":"Intelence : EPAR - Summary for the public","type":"overview","status":"unknown","consultation_date":"","first_published_date":"2009-08-07T02:00:00Z","last_updated_date":"2020-05-15T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/overview/intelence-epar-summary-public_en.pdf","translations":{"bg":"https://www.ema.europa.eu/bg/documents/overview/intelence-epar-summary-public_bg.pdf","es":"https://www.ema.europa.eu/es/documents/overview/intelence-epar-summary-public_es.pdf","cs":"https://www.ema.europa.eu/cs/documents/overview/intelence-epar-summary-public_cs.pdf","da":"https://www.ema.europa.eu/da/documents/overview/intelence-epar-summary-public_da.pdf","de":"https://www.ema.europa.eu/de/documents/overview/intelence-epar-summary-public_de.pdf","et":"https://www.ema.europa.eu/et/documents/overview/intelence-epar-summary-public_et.pdf","el":"https://www.ema.europa.eu/el/documents/overview/intelence-epar-summary-public_el.pdf","fr":"https://www.ema.europa.eu/fr/documents/overview/intelence-epar-summary-public_fr.pdf","hr":"https://www.ema.europa.eu/hr/documents/overview/intelence-epar-summary-public_hr.pdf","it":"https://www.ema.europa.eu/it/documents/overview/intelence-epar-summary-public_it.pdf","lv":"https://www.ema.europa.eu/lv/documents/overview/intelence-epar-summary-public_lv.pdf","lt":"https://www.ema.europa.eu/lt/documents/overview/intelence-epar-summary-public_lt.pdf","hu":"https://www.ema.europa.eu/hu/documents/overview/intelence-epar-summary-public_hu.pdf","mt":"https://www.ema.europa.eu/mt/documents/overview/intelence-epar-summary-public_mt.pdf","nl":"https://www.ema.europa.eu/nl/documents/overview/intelence-epar-summary-public_nl.pdf","pl":"https://www.ema.europa.eu/pl/documents/overview/intelence-epar-summary-public_pl.pdf","pt":"https://www.ema.europa.eu/pt/documents/overview/intelence-epar-summary-public_pt.pdf","ro":"https://www.ema.europa.eu/ro/documents/overview/intelence-epar-summary-public_ro.pdf","sk":"https://www.ema.europa.eu/sk/documents/overview/intelence-epar-summary-public_sk.pdf","sl":"https://www.ema.europa.eu/sl/documents/overview/intelence-epar-summary-public_sl.pdf","fi":"https://www.ema.europa.eu/fi/documents/overview/intelence-epar-summary-public_fi.pdf","sv":"https://www.ema.europa.eu/sv/documents/overview/intelence-epar-summary-public_sv.pdf"}},
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    {"id":"42905","name":"Pelmeg : EPAR - Medicine overview","type":"overview","status":"unknown","consultation_date":"","first_published_date":"2018-12-03T12:34:00Z","last_updated_date":"2018-12-03T12:34:00Z","reference_number":"EMA/653835/2018 ","document_url":"https://www.ema.europa.eu/en/documents/overview/pelmeg-epar-medicine-overview_en.pdf","translations":{"bg":"https://www.ema.europa.eu/bg/documents/overview/pelmeg-epar-medicine-overview_bg.pdf","es":"https://www.ema.europa.eu/es/documents/overview/pelmeg-epar-medicine-overview_es.pdf","cs":"https://www.ema.europa.eu/cs/documents/overview/pelmeg-epar-medicine-overview_cs.pdf","da":"https://www.ema.europa.eu/da/documents/overview/pelmeg-epar-medicine-overview_da.pdf","de":"https://www.ema.europa.eu/de/documents/overview/pelmeg-epar-medicine-overview_de.pdf","et":"https://www.ema.europa.eu/et/documents/overview/pelmeg-epar-medicine-overview_et.pdf","el":"https://www.ema.europa.eu/el/documents/overview/pelmeg-epar-medicine-overview_el.pdf","fr":"https://www.ema.europa.eu/fr/documents/overview/pelmeg-epar-medicine-overview_fr.pdf","hr":"https://www.ema.europa.eu/hr/documents/overview/pelmeg-epar-medicine-overview_hr.pdf","it":"https://www.ema.europa.eu/it/documents/overview/pelmeg-epar-medicine-overview_it.pdf","lv":"https://www.ema.europa.eu/lv/documents/overview/pelmeg-epar-medicine-overview_lv.pdf","lt":"https://www.ema.europa.eu/lt/documents/overview/pelmeg-epar-medicine-overview_lt.pdf","hu":"https://www.ema.europa.eu/hu/documents/overview/pelmeg-epar-medicine-overview_hu.pdf","mt":"https://www.ema.europa.eu/mt/documents/overview/pelmeg-epar-medicine-overview_mt.pdf","nl":"https://www.ema.europa.eu/nl/documents/overview/pelmeg-epar-medicine-overview_nl.pdf","pl":"https://www.ema.europa.eu/pl/documents/overview/pelmeg-epar-medicine-overview_pl.pdf","pt":"https://www.ema.europa.eu/pt/documents/overview/pelmeg-epar-medicine-overview_pt.pdf","ro":"https://www.ema.europa.eu/ro/documents/overview/pelmeg-epar-medicine-overview_ro.pdf","sk":"https://www.ema.europa.eu/sk/documents/overview/pelmeg-epar-medicine-overview_sk.pdf","sl":"https://www.ema.europa.eu/sl/documents/overview/pelmeg-epar-medicine-overview_sl.pdf","fi":"https://www.ema.europa.eu/fi/documents/overview/pelmeg-epar-medicine-overview_fi.pdf","sv":"https://www.ema.europa.eu/sv/documents/overview/pelmeg-epar-medicine-overview_sv.pdf"}},
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    {"id":"44974","name":"Sixmo : EPAR - Overview","type":"overview","status":"unknown","consultation_date":"","first_published_date":"2019-07-02T15:18:00Z","last_updated_date":"2025-08-14T18:14:27Z","reference_number":"EMA/251834/2019","document_url":"https://www.ema.europa.eu/en/documents/overview/sixmo-epar-overview_en.pdf","translations":{"bg":"https://www.ema.europa.eu/bg/documents/overview/sixmo-epar-overview_bg.pdf","es":"https://www.ema.europa.eu/es/documents/overview/sixmo-epar-overview_es.pdf","cs":"https://www.ema.europa.eu/cs/documents/overview/sixmo-epar-overview_cs.pdf","da":"https://www.ema.europa.eu/da/documents/overview/sixmo-epar-overview_da.pdf","de":"https://www.ema.europa.eu/de/documents/overview/sixmo-epar-overview_de.pdf","et":"https://www.ema.europa.eu/et/documents/overview/sixmo-epar-overview_et.pdf","el":"https://www.ema.europa.eu/el/documents/overview/sixmo-epar-overview_el.pdf","fr":"https://www.ema.europa.eu/fr/documents/overview/sixmo-epar-overview_fr.pdf","hr":"https://www.ema.europa.eu/hr/documents/overview/sixmo-epar-overview_hr.pdf","it":"https://www.ema.europa.eu/it/documents/overview/sixmo-epar-overview_it.pdf","lv":"https://www.ema.europa.eu/lv/documents/overview/sixmo-epar-overview_lv.pdf","lt":"https://www.ema.europa.eu/lt/documents/overview/sixmo-epar-overview_lt.pdf","hu":"https://www.ema.europa.eu/hu/documents/overview/sixmo-epar-overview_hu.pdf","mt":"https://www.ema.europa.eu/mt/documents/overview/sixmo-epar-overview_mt.pdf","nl":"https://www.ema.europa.eu/nl/documents/overview/sixmo-epar-overview_nl.pdf","pl":"https://www.ema.europa.eu/pl/documents/overview/sixmo-epar-overview_pl.pdf","pt":"https://www.ema.europa.eu/pt/documents/overview/sixmo-epar-overview_pt.pdf","ro":"https://www.ema.europa.eu/ro/documents/overview/sixmo-epar-overview_ro.pdf","sk":"https://www.ema.europa.eu/sk/documents/overview/sixmo-epar-overview_sk.pdf","sl":"https://www.ema.europa.eu/sl/documents/overview/sixmo-epar-overview_sl.pdf","fi":"https://www.ema.europa.eu/fi/documents/overview/sixmo-epar-overview_fi.pdf","sv":"https://www.ema.europa.eu/sv/documents/overview/sixmo-epar-overview_sv.pdf"}},
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    {"id":"45143","name":"Cufence : EPAR - Medicine overview","type":"overview","status":"unknown","consultation_date":"","first_published_date":"2019-07-29T11:49:00Z","last_updated_date":"2022-10-28T13:29:00Z","reference_number":"EMA/775669/2022","document_url":"https://www.ema.europa.eu/en/documents/overview/cufence-epar-medicine-overview_en.pdf","translations":{"bg":"https://www.ema.europa.eu/bg/documents/overview/cufence-epar-medicine-overview_bg.pdf","es":"https://www.ema.europa.eu/es/documents/overview/cufence-epar-medicine-overview_es.pdf","cs":"https://www.ema.europa.eu/cs/documents/overview/cufence-epar-medicine-overview_cs.pdf","da":"https://www.ema.europa.eu/da/documents/overview/cufence-epar-medicine-overview_da.pdf","de":"https://www.ema.europa.eu/de/documents/overview/cufence-epar-medicine-overview_de.pdf","et":"https://www.ema.europa.eu/et/documents/overview/cufence-epar-medicine-overview_et.pdf","el":"https://www.ema.europa.eu/el/documents/overview/cufence-epar-medicine-overview_el.pdf","fr":"https://www.ema.europa.eu/fr/documents/overview/cufence-epar-medicine-overview_fr.pdf","hr":"https://www.ema.europa.eu/hr/documents/overview/cufence-epar-medicine-overview_hr.pdf","it":"https://www.ema.europa.eu/it/documents/overview/cufence-epar-medicine-overview_it.pdf","lv":"https://www.ema.europa.eu/lv/documents/overview/cufence-epar-medicine-overview_lv.pdf","lt":"https://www.ema.europa.eu/lt/documents/overview/cufence-epar-medicine-overview_lt.pdf","hu":"https://www.ema.europa.eu/hu/documents/overview/cufence-epar-medicine-overview_hu.pdf","mt":"https://www.ema.europa.eu/mt/documents/overview/cufence-epar-medicine-overview_mt.pdf","nl":"https://www.ema.europa.eu/nl/documents/overview/cufence-epar-medicine-overview_nl.pdf","pl":"https://www.ema.europa.eu/pl/documents/overview/cufence-epar-medicine-overview_pl.pdf","pt":"https://www.ema.europa.eu/pt/documents/overview/cufence-epar-medicine-overview_pt.pdf","ro":"https://www.ema.europa.eu/ro/documents/overview/cufence-epar-medicine-overview_ro.pdf","sk":"https://www.ema.europa.eu/sk/documents/overview/cufence-epar-medicine-overview_sk.pdf","sl":"https://www.ema.europa.eu/sl/documents/overview/cufence-epar-medicine-overview_sl.pdf","fi":"https://www.ema.europa.eu/fi/documents/overview/cufence-epar-medicine-overview_fi.pdf","sv":"https://www.ema.europa.eu/sv/documents/overview/cufence-epar-medicine-overview_sv.pdf"}},
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    {"id":"48251","name":"Insulin aspart Sanofi : EPAR - Medicine overview","type":"overview","status":"unknown","consultation_date":"","first_published_date":"2020-07-07T16:26:00Z","last_updated_date":"2020-07-07T16:26:00Z","reference_number":"EMA/242544/2020","document_url":"https://www.ema.europa.eu/en/documents/overview/insulin-aspart-sanofi-epar-medicine-overview_en.pdf","translations":{"bg":"https://www.ema.europa.eu/bg/documents/overview/insulin-aspart-sanofi-epar-medicine-overview_bg.pdf","es":"https://www.ema.europa.eu/es/documents/overview/insulin-aspart-sanofi-epar-medicine-overview_es.pdf","cs":"https://www.ema.europa.eu/cs/documents/overview/insulin-aspart-sanofi-epar-medicine-overview_cs.pdf","da":"https://www.ema.europa.eu/da/documents/overview/insulin-aspart-sanofi-epar-medicine-overview_da.pdf","de":"https://www.ema.europa.eu/de/documents/overview/insulin-aspart-sanofi-epar-medicine-overview_de.pdf","et":"https://www.ema.europa.eu/et/documents/overview/insulin-aspart-sanofi-epar-medicine-overview_et.pdf","el":"https://www.ema.europa.eu/el/documents/overview/insulin-aspart-sanofi-epar-medicine-overview_el.pdf","fr":"https://www.ema.europa.eu/fr/documents/overview/insulin-aspart-sanofi-epar-medicine-overview_fr.pdf","hr":"https://www.ema.europa.eu/hr/documents/overview/insulin-aspart-sanofi-epar-medicine-overview_hr.pdf","it":"https://www.ema.europa.eu/it/documents/overview/insulin-aspart-sanofi-epar-medicine-overview_it.pdf","lv":"https://www.ema.europa.eu/lv/documents/overview/insulin-aspart-sanofi-epar-medicine-overview_lv.pdf","lt":"https://www.ema.europa.eu/lt/documents/overview/insulin-aspart-sanofi-epar-medicine-overview_lt.pdf","hu":"https://www.ema.europa.eu/hu/documents/overview/insulin-aspart-sanofi-epar-medicine-overview_hu.pdf","mt":"https://www.ema.europa.eu/mt/documents/overview/insulin-aspart-sanofi-epar-medicine-overview_mt.pdf","nl":"https://www.ema.europa.eu/nl/documents/overview/insulin-aspart-sanofi-epar-medicine-overview_nl.pdf","pl":"https://www.ema.europa.eu/pl/documents/overview/insulin-aspart-sanofi-epar-medicine-overview_pl.pdf","pt":"https://www.ema.europa.eu/pt/documents/overview/insulin-aspart-sanofi-epar-medicine-overview_pt.pdf","ro":"https://www.ema.europa.eu/ro/documents/overview/insulin-aspart-sanofi-epar-medicine-overview_ro.pdf","sk":"https://www.ema.europa.eu/sk/documents/overview/insulin-aspart-sanofi-epar-medicine-overview_sk.pdf","sl":"https://www.ema.europa.eu/sl/documents/overview/insulin-aspart-sanofi-epar-medicine-overview_sl.pdf","fi":"https://www.ema.europa.eu/fi/documents/overview/insulin-aspart-sanofi-epar-medicine-overview_fi.pdf","sv":"https://www.ema.europa.eu/sv/documents/overview/insulin-aspart-sanofi-epar-medicine-overview_sv.pdf"}},
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    {"id":"49796","name":"Phesgo : EPAR - Medicine overview","type":"overview","status":"unknown","consultation_date":"","first_published_date":"2021-01-13T15:29:00Z","last_updated_date":"2021-01-13T15:29:00Z","reference_number":"EMA/620936/2020","document_url":"https://www.ema.europa.eu/en/documents/overview/phesgo-epar-medicine-overview_en.pdf","translations":{"bg":"https://www.ema.europa.eu/bg/documents/overview/phesgo-epar-medicine-overview_bg.pdf","es":"https://www.ema.europa.eu/es/documents/overview/phesgo-epar-medicine-overview_es.pdf","cs":"https://www.ema.europa.eu/cs/documents/overview/phesgo-epar-medicine-overview_cs.pdf","da":"https://www.ema.europa.eu/da/documents/overview/phesgo-epar-medicine-overview_da.pdf","de":"https://www.ema.europa.eu/de/documents/overview/phesgo-epar-medicine-overview_de.pdf","et":"https://www.ema.europa.eu/et/documents/overview/phesgo-epar-medicine-overview_et.pdf","el":"https://www.ema.europa.eu/el/documents/overview/phesgo-epar-medicine-overview_el.pdf","fr":"https://www.ema.europa.eu/fr/documents/overview/phesgo-epar-medicine-overview_fr.pdf","hr":"https://www.ema.europa.eu/hr/documents/overview/phesgo-epar-medicine-overview_hr.pdf","it":"https://www.ema.europa.eu/it/documents/overview/phesgo-epar-medicine-overview_it.pdf","lv":"https://www.ema.europa.eu/lv/documents/overview/phesgo-epar-medicine-overview_lv.pdf","lt":"https://www.ema.europa.eu/lt/documents/overview/phesgo-epar-medicine-overview_lt.pdf","hu":"https://www.ema.europa.eu/hu/documents/overview/phesgo-epar-medicine-overview_hu.pdf","mt":"https://www.ema.europa.eu/mt/documents/overview/phesgo-epar-medicine-overview_mt.pdf","nl":"https://www.ema.europa.eu/nl/documents/overview/phesgo-epar-medicine-overview_nl.pdf","pl":"https://www.ema.europa.eu/pl/documents/overview/phesgo-epar-medicine-overview_pl.pdf","pt":"https://www.ema.europa.eu/pt/documents/overview/phesgo-epar-medicine-overview_pt.pdf","ro":"https://www.ema.europa.eu/ro/documents/overview/phesgo-epar-medicine-overview_ro.pdf","sk":"https://www.ema.europa.eu/sk/documents/overview/phesgo-epar-medicine-overview_sk.pdf","sl":"https://www.ema.europa.eu/sl/documents/overview/phesgo-epar-medicine-overview_sl.pdf","fi":"https://www.ema.europa.eu/fi/documents/overview/phesgo-epar-medicine-overview_fi.pdf","sv":"https://www.ema.europa.eu/sv/documents/overview/phesgo-epar-medicine-overview_sv.pdf"}},
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    {"id":"50473","name":"Onbevzi : EPAR - Medicine overview","type":"overview","status":"unknown","consultation_date":"","first_published_date":"2021-03-05T16:50:00Z","last_updated_date":"2024-10-24T14:32:00Z","reference_number":"EMA/617109/2020","document_url":"https://www.ema.europa.eu/en/documents/overview/onbevzi-epar-medicine-overview_en.pdf","translations":{"bg":"https://www.ema.europa.eu/bg/documents/overview/onbevzi-epar-medicine-overview_bg.pdf","es":"https://www.ema.europa.eu/es/documents/overview/onbevzi-epar-medicine-overview_es.pdf","cs":"https://www.ema.europa.eu/cs/documents/overview/onbevzi-epar-medicine-overview_cs.pdf","da":"https://www.ema.europa.eu/da/documents/overview/onbevzi-epar-medicine-overview_da.pdf","de":"https://www.ema.europa.eu/de/documents/overview/onbevzi-epar-medicine-overview_de.pdf","et":"https://www.ema.europa.eu/et/documents/overview/onbevzi-epar-medicine-overview_et.pdf","el":"https://www.ema.europa.eu/el/documents/overview/onbevzi-epar-medicine-overview_el.pdf","fr":"https://www.ema.europa.eu/fr/documents/overview/onbevzi-epar-medicine-overview_fr.pdf","hr":"https://www.ema.europa.eu/hr/documents/overview/onbevzi-epar-medicine-overview_hr.pdf","it":"https://www.ema.europa.eu/it/documents/overview/onbevzi-epar-medicine-overview_it.pdf","lv":"https://www.ema.europa.eu/lv/documents/overview/onbevzi-epar-medicine-overview_lv.pdf","lt":"https://www.ema.europa.eu/lt/documents/overview/onbevzi-epar-medicine-overview_lt.pdf","hu":"https://www.ema.europa.eu/hu/documents/overview/onbevzi-epar-medicine-overview_hu.pdf","mt":"https://www.ema.europa.eu/mt/documents/overview/onbevzi-epar-medicine-overview_mt.pdf","nl":"https://www.ema.europa.eu/nl/documents/overview/onbevzi-epar-medicine-overview_nl.pdf","pl":"https://www.ema.europa.eu/pl/documents/overview/onbevzi-epar-medicine-overview_pl.pdf","pt":"https://www.ema.europa.eu/pt/documents/overview/onbevzi-epar-medicine-overview_pt.pdf","ro":"https://www.ema.europa.eu/ro/documents/overview/onbevzi-epar-medicine-overview_ro.pdf","sk":"https://www.ema.europa.eu/sk/documents/overview/onbevzi-epar-medicine-overview_sk.pdf","sl":"https://www.ema.europa.eu/sl/documents/overview/onbevzi-epar-medicine-overview_sl.pdf","fi":"https://www.ema.europa.eu/fi/documents/overview/onbevzi-epar-medicine-overview_fi.pdf","sv":"https://www.ema.europa.eu/sv/documents/overview/onbevzi-epar-medicine-overview_sv.pdf"}},
    {"id":"50490","name":"Lumoxiti : EPAR - Medicine overview","type":"overview","status":"unknown","consultation_date":"","first_published_date":"2021-03-09T09:10:00Z","last_updated_date":"2021-08-11T16:52:00Z","reference_number":"EMA/691967/2020","document_url":"https://www.ema.europa.eu/en/documents/overview/lumoxiti-epar-medicine-overview_en.pdf","translations":{"bg":"https://www.ema.europa.eu/bg/documents/overview/lumoxiti-epar-medicine-overview_bg.pdf","es":"https://www.ema.europa.eu/es/documents/overview/lumoxiti-epar-medicine-overview_es.pdf","cs":"https://www.ema.europa.eu/cs/documents/overview/lumoxiti-epar-medicine-overview_cs.pdf","da":"https://www.ema.europa.eu/da/documents/overview/lumoxiti-epar-medicine-overview_da.pdf","de":"https://www.ema.europa.eu/de/documents/overview/lumoxiti-epar-medicine-overview_de.pdf","et":"https://www.ema.europa.eu/et/documents/overview/lumoxiti-epar-medicine-overview_et.pdf","el":"https://www.ema.europa.eu/el/documents/overview/lumoxiti-epar-medicine-overview_el.pdf","fr":"https://www.ema.europa.eu/fr/documents/overview/lumoxiti-epar-medicine-overview_fr.pdf","hr":"https://www.ema.europa.eu/hr/documents/overview/lumoxiti-epar-medicine-overview_hr.pdf","it":"https://www.ema.europa.eu/it/documents/overview/lumoxiti-epar-medicine-overview_it.pdf","lv":"https://www.ema.europa.eu/lv/documents/overview/lumoxiti-epar-medicine-overview_lv.pdf","lt":"https://www.ema.europa.eu/lt/documents/overview/lumoxiti-epar-medicine-overview_lt.pdf","hu":"https://www.ema.europa.eu/hu/documents/overview/lumoxiti-epar-medicine-overview_hu.pdf","mt":"https://www.ema.europa.eu/mt/documents/overview/lumoxiti-epar-medicine-overview_mt.pdf","nl":"https://www.ema.europa.eu/nl/documents/overview/lumoxiti-epar-medicine-overview_nl.pdf","pl":"https://www.ema.europa.eu/pl/documents/overview/lumoxiti-epar-medicine-overview_pl.pdf","pt":"https://www.ema.europa.eu/pt/documents/overview/lumoxiti-epar-medicine-overview_pt.pdf","ro":"https://www.ema.europa.eu/ro/documents/overview/lumoxiti-epar-medicine-overview_ro.pdf","sk":"https://www.ema.europa.eu/sk/documents/overview/lumoxiti-epar-medicine-overview_sk.pdf","sl":"https://www.ema.europa.eu/sl/documents/overview/lumoxiti-epar-medicine-overview_sl.pdf","fi":"https://www.ema.europa.eu/fi/documents/overview/lumoxiti-epar-medicine-overview_fi.pdf","sv":"https://www.ema.europa.eu/sv/documents/overview/lumoxiti-epar-medicine-overview_sv.pdf"}},
    {"id":"50529","name":"Jcovden (previously COVID-19 Vaccine Janssen) : EPAR - Medicine overview","type":"overview","status":"unknown","consultation_date":"","first_published_date":"2021-03-11T17:54:00Z","last_updated_date":"2024-08-09T11:51:00Z","reference_number":"EMA/10056/2023","document_url":"https://www.ema.europa.eu/en/documents/overview/jcovden-previously-covid-19-vaccine-janssen-epar-medicine-overview_en.pdf","translations":{"bg":"https://www.ema.europa.eu/bg/documents/overview/jcovden-previously-covid-19-vaccine-janssen-epar-medicine-overview_bg.pdf","es":"https://www.ema.europa.eu/es/documents/overview/jcovden-previously-covid-19-vaccine-janssen-epar-medicine-overview_es.pdf","cs":"https://www.ema.europa.eu/cs/documents/overview/jcovden-previously-covid-19-vaccine-janssen-epar-medicine-overview_cs.pdf","da":"https://www.ema.europa.eu/da/documents/overview/jcovden-previously-covid-19-vaccine-janssen-epar-medicine-overview_da.pdf","de":"https://www.ema.europa.eu/de/documents/overview/jcovden-previously-covid-19-vaccine-janssen-epar-medicine-overview_de.pdf","et":"https://www.ema.europa.eu/et/documents/overview/jcovden-previously-covid-19-vaccine-janssen-epar-medicine-overview_et.pdf","el":"https://www.ema.europa.eu/el/documents/overview/jcovden-previously-covid-19-vaccine-janssen-epar-medicine-overview_el.pdf","fr":"https://www.ema.europa.eu/fr/documents/overview/jcovden-previously-covid-19-vaccine-janssen-epar-medicine-overview_fr.pdf","hr":"https://www.ema.europa.eu/hr/documents/overview/jcovden-previously-covid-19-vaccine-janssen-epar-medicine-overview_hr.pdf","it":"https://www.ema.europa.eu/it/documents/overview/jcovden-previously-covid-19-vaccine-janssen-epar-medicine-overview_it.pdf","lv":"https://www.ema.europa.eu/lv/documents/overview/jcovden-previously-covid-19-vaccine-janssen-epar-medicine-overview_lv.pdf","lt":"https://www.ema.europa.eu/lt/documents/overview/jcovden-previously-covid-19-vaccine-janssen-epar-medicine-overview_lt.pdf","hu":"https://www.ema.europa.eu/hu/documents/overview/jcovden-previously-covid-19-vaccine-janssen-epar-medicine-overview_hu.pdf","mt":"https://www.ema.europa.eu/mt/documents/overview/jcovden-previously-covid-19-vaccine-janssen-epar-medicine-overview_mt.pdf","nl":"https://www.ema.europa.eu/nl/documents/overview/jcovden-previously-covid-19-vaccine-janssen-epar-medicine-overview_nl.pdf","pl":"https://www.ema.europa.eu/pl/documents/overview/jcovden-previously-covid-19-vaccine-janssen-epar-medicine-overview_pl.pdf","pt":"https://www.ema.europa.eu/pt/documents/overview/jcovden-previously-covid-19-vaccine-janssen-epar-medicine-overview_pt.pdf","ro":"https://www.ema.europa.eu/ro/documents/overview/jcovden-previously-covid-19-vaccine-janssen-epar-medicine-overview_ro.pdf","sk":"https://www.ema.europa.eu/sk/documents/overview/jcovden-previously-covid-19-vaccine-janssen-epar-medicine-overview_sk.pdf","sl":"https://www.ema.europa.eu/sl/documents/overview/jcovden-previously-covid-19-vaccine-janssen-epar-medicine-overview_sl.pdf","fi":"https://www.ema.europa.eu/fi/documents/overview/jcovden-previously-covid-19-vaccine-janssen-epar-medicine-overview_fi.pdf","sv":"https://www.ema.europa.eu/sv/documents/overview/jcovden-previously-covid-19-vaccine-janssen-epar-medicine-overview_sv.pdf"}},
    {"id":"50548","name":"Rexxolide : EPAR - Medicine overview","type":"overview","status":"unknown","consultation_date":"","first_published_date":"2021-03-12T15:24:00Z","last_updated_date":"2025-10-14T11:11:11Z","reference_number":"EMA/555704/2020","document_url":"https://www.ema.europa.eu/en/documents/overview/rexxolide-epar-medicine-overview_en.pdf","translations":{"bg":"https://www.ema.europa.eu/bg/documents/overview/rexxolide-epar-medicine-overview_bg.pdf","es":"https://www.ema.europa.eu/es/documents/overview/rexxolide-epar-medicine-overview_es.pdf","cs":"https://www.ema.europa.eu/cs/documents/overview/rexxolide-epar-medicine-overview_cs.pdf","da":"https://www.ema.europa.eu/da/documents/overview/rexxolide-epar-medicine-overview_da.pdf","de":"https://www.ema.europa.eu/de/documents/overview/rexxolide-epar-medicine-overview_de.pdf","et":"https://www.ema.europa.eu/et/documents/overview/rexxolide-epar-medicine-overview_et.pdf","el":"https://www.ema.europa.eu/el/documents/overview/rexxolide-epar-medicine-overview_el.pdf","fr":"https://www.ema.europa.eu/fr/documents/overview/rexxolide-epar-medicine-overview_fr.pdf","ga":"https://www.ema.europa.eu/ga/documents/overview/rexxolide-epar-medicine-overview_ga.pdf","hr":"https://www.ema.europa.eu/hr/documents/overview/rexxolide-epar-medicine-overview_hr.pdf","it":"https://www.ema.europa.eu/it/documents/overview/rexxolide-epar-medicine-overview_it.pdf","lv":"https://www.ema.europa.eu/lv/documents/overview/rexxolide-epar-medicine-overview_lv.pdf","lt":"https://www.ema.europa.eu/lt/documents/overview/rexxolide-epar-medicine-overview_lt.pdf","hu":"https://www.ema.europa.eu/hu/documents/overview/rexxolide-epar-medicine-overview_hu.pdf","mt":"https://www.ema.europa.eu/mt/documents/overview/rexxolide-epar-medicine-overview_mt.pdf","nl":"https://www.ema.europa.eu/nl/documents/overview/rexxolide-epar-medicine-overview_nl.pdf","pl":"https://www.ema.europa.eu/pl/documents/overview/rexxolide-epar-medicine-overview_pl.pdf","pt":"https://www.ema.europa.eu/pt/documents/overview/rexxolide-epar-medicine-overview_pt.pdf","ro":"https://www.ema.europa.eu/ro/documents/overview/rexxolide-epar-medicine-overview_ro.pdf","sk":"https://www.ema.europa.eu/sk/documents/overview/rexxolide-epar-medicine-overview_sk.pdf","sl":"https://www.ema.europa.eu/sl/documents/overview/rexxolide-epar-medicine-overview_sl.pdf","fi":"https://www.ema.europa.eu/fi/documents/overview/rexxolide-epar-medicine-overview_fi.pdf","sv":"https://www.ema.europa.eu/sv/documents/overview/rexxolide-epar-medicine-overview_sv.pdf","is":"https://www.ema.europa.eu/is/documents/overview/rexxolide-epar-medicine-overview_is.pdf","no":"https://www.ema.europa.eu/no/documents/overview/rexxolide-epar-medicine-overview_no.pdf"}},
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    {"id":"60923","name":"Ebglyss : EPAR -  Medicine overview","type":"overview","status":"unknown","consultation_date":"","first_published_date":"2023-11-21T16:18:18Z","last_updated_date":"2023-11-21T16:18:18Z","reference_number":"EMA/424720/2023","document_url":"https://www.ema.europa.eu/en/documents/overview/ebglyss-epar-medicine-overview_en.pdf","translations":{"bg":"https://www.ema.europa.eu/bg/documents/overview/ebglyss-epar-medicine-overview_bg.pdf","es":"https://www.ema.europa.eu/es/documents/overview/ebglyss-epar-medicine-overview_es.pdf","cs":"https://www.ema.europa.eu/cs/documents/overview/ebglyss-epar-medicine-overview_cs.pdf","da":"https://www.ema.europa.eu/da/documents/overview/ebglyss-epar-medicine-overview_da.pdf","de":"https://www.ema.europa.eu/de/documents/overview/ebglyss-epar-medicine-overview_de.pdf","et":"https://www.ema.europa.eu/et/documents/overview/ebglyss-epar-medicine-overview_et.pdf","el":"https://www.ema.europa.eu/el/documents/overview/ebglyss-epar-medicine-overview_el.pdf","fr":"https://www.ema.europa.eu/fr/documents/overview/ebglyss-epar-medicine-overview_fr.pdf","hr":"https://www.ema.europa.eu/hr/documents/overview/ebglyss-epar-medicine-overview_hr.pdf","it":"https://www.ema.europa.eu/it/documents/overview/ebglyss-epar-medicine-overview_it.pdf","lv":"https://www.ema.europa.eu/lv/documents/overview/ebglyss-epar-medicine-overview_lv.pdf","lt":"https://www.ema.europa.eu/lt/documents/overview/ebglyss-epar-medicine-overview_lt.pdf","hu":"https://www.ema.europa.eu/hu/documents/overview/ebglyss-epar-medicine-overview_hu.pdf","mt":"https://www.ema.europa.eu/mt/documents/overview/ebglyss-epar-medicine-overview_mt.pdf","nl":"https://www.ema.europa.eu/nl/documents/overview/ebglyss-epar-medicine-overview_nl.pdf","pl":"https://www.ema.europa.eu/pl/documents/overview/ebglyss-epar-medicine-overview_pl.pdf","pt":"https://www.ema.europa.eu/pt/documents/overview/ebglyss-epar-medicine-overview_pt.pdf","ro":"https://www.ema.europa.eu/ro/documents/overview/ebglyss-epar-medicine-overview_ro.pdf","sk":"https://www.ema.europa.eu/sk/documents/overview/ebglyss-epar-medicine-overview_sk.pdf","sl":"https://www.ema.europa.eu/sl/documents/overview/ebglyss-epar-medicine-overview_sl.pdf","fi":"https://www.ema.europa.eu/fi/documents/overview/ebglyss-epar-medicine-overview_fi.pdf","sv":"https://www.ema.europa.eu/sv/documents/overview/ebglyss-epar-medicine-overview_sv.pdf"}},
    {"id":"60938","name":"Jaypirca : EPAR - Medicine overview","type":"overview","status":"unknown","consultation_date":"","first_published_date":"2023-11-20T15:12:53Z","last_updated_date":"2025-04-25T10:38:00Z","reference_number":"EMA/96088/2025","document_url":"https://www.ema.europa.eu/en/documents/overview/jaypirca-epar-medicine-overview_en.pdf","translations":{"bg":"https://www.ema.europa.eu/bg/documents/overview/jaypirca-epar-medicine-overview_bg.pdf","es":"https://www.ema.europa.eu/es/documents/overview/jaypirca-epar-medicine-overview_es.pdf","cs":"https://www.ema.europa.eu/cs/documents/overview/jaypirca-epar-medicine-overview_cs.pdf","da":"https://www.ema.europa.eu/da/documents/overview/jaypirca-epar-medicine-overview_da.pdf","de":"https://www.ema.europa.eu/de/documents/overview/jaypirca-epar-medicine-overview_de.pdf","et":"https://www.ema.europa.eu/et/documents/overview/jaypirca-epar-medicine-overview_et.pdf","el":"https://www.ema.europa.eu/el/documents/overview/jaypirca-epar-medicine-overview_el.pdf","fr":"https://www.ema.europa.eu/fr/documents/overview/jaypirca-epar-medicine-overview_fr.pdf","hr":"https://www.ema.europa.eu/hr/documents/overview/jaypirca-epar-medicine-overview_hr.pdf","it":"https://www.ema.europa.eu/it/documents/overview/jaypirca-epar-medicine-overview_it.pdf","lv":"https://www.ema.europa.eu/lv/documents/overview/jaypirca-epar-medicine-overview_lv.pdf","lt":"https://www.ema.europa.eu/lt/documents/overview/jaypirca-epar-medicine-overview_lt.pdf","hu":"https://www.ema.europa.eu/hu/documents/overview/jaypirca-epar-medicine-overview_hu.pdf","mt":"https://www.ema.europa.eu/mt/documents/overview/jaypirca-epar-medicine-overview_mt.pdf","nl":"https://www.ema.europa.eu/nl/documents/overview/jaypirca-epar-medicine-overview_nl.pdf","pl":"https://www.ema.europa.eu/pl/documents/overview/jaypirca-epar-medicine-overview_pl.pdf","pt":"https://www.ema.europa.eu/pt/documents/overview/jaypirca-epar-medicine-overview_pt.pdf","ro":"https://www.ema.europa.eu/ro/documents/overview/jaypirca-epar-medicine-overview_ro.pdf","sk":"https://www.ema.europa.eu/sk/documents/overview/jaypirca-epar-medicine-overview_sk.pdf","sl":"https://www.ema.europa.eu/sl/documents/overview/jaypirca-epar-medicine-overview_sl.pdf","fi":"https://www.ema.europa.eu/fi/documents/overview/jaypirca-epar-medicine-overview_fi.pdf","sv":"https://www.ema.europa.eu/sv/documents/overview/jaypirca-epar-medicine-overview_sv.pdf"}},
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    {"id":"66224","name":"Purevax RCP FeLV : EPAR - Medicine overview","type":"overview","status":"unknown","consultation_date":"","first_published_date":"2010-01-26T12:03:15Z","last_updated_date":"2024-12-19T10:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/overview/purevax-rcp-felv-epar-medicine-overview_en.pdf","translations":{"bg":"https://www.ema.europa.eu/bg/documents/overview/purevax-rcp-felv-epar-medicine-overview_bg.pdf","es":"https://www.ema.europa.eu/es/documents/overview/purevax-rcp-felv-epar-medicine-overview_es.pdf","cs":"https://www.ema.europa.eu/cs/documents/overview/purevax-rcp-felv-epar-medicine-overview_cs.pdf","da":"https://www.ema.europa.eu/da/documents/overview/purevax-rcp-felv-epar-medicine-overview_da.pdf","de":"https://www.ema.europa.eu/de/documents/overview/purevax-rcp-felv-epar-medicine-overview_de.pdf","et":"https://www.ema.europa.eu/et/documents/overview/purevax-rcp-felv-epar-medicine-overview_et.pdf","el":"https://www.ema.europa.eu/el/documents/overview/purevax-rcp-felv-epar-medicine-overview_el.pdf","fr":"https://www.ema.europa.eu/fr/documents/overview/purevax-rcp-felv-epar-medicine-overview_fr.pdf","ga":"https://www.ema.europa.eu/ga/documents/overview/purevax-rcp-felv-epar-medicine-overview_ga.pdf","hr":"https://www.ema.europa.eu/hr/documents/overview/purevax-rcp-felv-epar-medicine-overview_hr.pdf","it":"https://www.ema.europa.eu/it/documents/overview/purevax-rcp-felv-epar-medicine-overview_it.pdf","lv":"https://www.ema.europa.eu/lv/documents/overview/purevax-rcp-felv-epar-medicine-overview_lv.pdf","lt":"https://www.ema.europa.eu/lt/documents/overview/purevax-rcp-felv-epar-medicine-overview_lt.pdf","hu":"https://www.ema.europa.eu/hu/documents/overview/purevax-rcp-felv-epar-medicine-overview_hu.pdf","mt":"https://www.ema.europa.eu/mt/documents/overview/purevax-rcp-felv-epar-medicine-overview_mt.pdf","nl":"https://www.ema.europa.eu/nl/documents/overview/purevax-rcp-felv-epar-medicine-overview_nl.pdf","pl":"https://www.ema.europa.eu/pl/documents/overview/purevax-rcp-felv-epar-medicine-overview_pl.pdf","pt":"https://www.ema.europa.eu/pt/documents/overview/purevax-rcp-felv-epar-medicine-overview_pt.pdf","ro":"https://www.ema.europa.eu/ro/documents/overview/purevax-rcp-felv-epar-medicine-overview_ro.pdf","sk":"https://www.ema.europa.eu/sk/documents/overview/purevax-rcp-felv-epar-medicine-overview_sk.pdf","sl":"https://www.ema.europa.eu/sl/documents/overview/purevax-rcp-felv-epar-medicine-overview_sl.pdf","fi":"https://www.ema.europa.eu/fi/documents/overview/purevax-rcp-felv-epar-medicine-overview_fi.pdf","sv":"https://www.ema.europa.eu/sv/documents/overview/purevax-rcp-felv-epar-medicine-overview_sv.pdf","is":"https://www.ema.europa.eu/is/documents/overview/purevax-rcp-felv-epar-medicine-overview_is.pdf","no":"https://www.ema.europa.eu/no/documents/overview/purevax-rcp-felv-epar-medicine-overview_no.pdf"}},
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    {"id":"70338","name":"Usrenty : EPAR - Medicine overview","type":"overview","status":"unknown","consultation_date":"","first_published_date":"2025-09-30T09:22:48Z","last_updated_date":"2025-09-30T09:22:48Z","reference_number":"EMA/82162/2025","document_url":"https://www.ema.europa.eu/en/documents/overview/usrenty-epar-medicine-overview_en.pdf","translations":{"bg":"https://www.ema.europa.eu/bg/documents/overview/usrenty-epar-medicine-overview_bg.pdf","es":"https://www.ema.europa.eu/es/documents/overview/usrenty-epar-medicine-overview_es.pdf","cs":"https://www.ema.europa.eu/cs/documents/overview/usrenty-epar-medicine-overview_cs.pdf","da":"https://www.ema.europa.eu/da/documents/overview/usrenty-epar-medicine-overview_da.pdf","de":"https://www.ema.europa.eu/de/documents/overview/usrenty-epar-medicine-overview_de.pdf","et":"https://www.ema.europa.eu/et/documents/overview/usrenty-epar-medicine-overview_et.pdf","el":"https://www.ema.europa.eu/el/documents/overview/usrenty-epar-medicine-overview_el.pdf","fr":"https://www.ema.europa.eu/fr/documents/overview/usrenty-epar-medicine-overview_fr.pdf","hr":"https://www.ema.europa.eu/hr/documents/overview/usrenty-epar-medicine-overview_hr.pdf","it":"https://www.ema.europa.eu/it/documents/overview/usrenty-epar-medicine-overview_it.pdf","lv":"https://www.ema.europa.eu/lv/documents/overview/usrenty-epar-medicine-overview_lv.pdf","lt":"https://www.ema.europa.eu/lt/documents/overview/usrenty-epar-medicine-overview_lt.pdf","hu":"https://www.ema.europa.eu/hu/documents/overview/usrenty-epar-medicine-overview_hu.pdf","mt":"https://www.ema.europa.eu/mt/documents/overview/usrenty-epar-medicine-overview_mt.pdf","nl":"https://www.ema.europa.eu/nl/documents/overview/usrenty-epar-medicine-overview_nl.pdf","pl":"https://www.ema.europa.eu/pl/documents/overview/usrenty-epar-medicine-overview_pl.pdf","pt":"https://www.ema.europa.eu/pt/documents/overview/usrenty-epar-medicine-overview_pt.pdf","ro":"https://www.ema.europa.eu/ro/documents/overview/usrenty-epar-medicine-overview_ro.pdf","sk":"https://www.ema.europa.eu/sk/documents/overview/usrenty-epar-medicine-overview_sk.pdf","sl":"https://www.ema.europa.eu/sl/documents/overview/usrenty-epar-medicine-overview_sl.pdf","fi":"https://www.ema.europa.eu/fi/documents/overview/usrenty-epar-medicine-overview_fi.pdf","sv":"https://www.ema.europa.eu/sv/documents/overview/usrenty-epar-medicine-overview_sv.pdf"}},
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    {"id":"10272","name":"Rezolsta : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2014-12-12T01:00:00Z","last_updated_date":"2025-08-04T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/rezolsta-epar-risk-management-plan_en.pdf"},
    {"id":"10425","name":"Lenvima : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2015-06-25T02:00:00Z","last_updated_date":"2024-04-30T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/lenvima-epar-risk-management-plan_en.pdf"},
    {"id":"10989","name":"Yescarta : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2018-09-10T02:00:00Z","last_updated_date":"2026-05-19T12:30:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/yescarta-epar-risk-management-plan_en.pdf"},
    {"id":"12092","name":"Jardiance : EPAR - Risk Management Plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2023-05-16T02:00:00Z","last_updated_date":"2025-06-25T14:20:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/jardiance-epar-risk-management-plan_en.pdf"},
    {"id":"12204","name":"Triumeq : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2014-10-15T02:00:00Z","last_updated_date":"2025-11-14T15:57:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/triumeq-epar-risk-management-plan_en.pdf"},
    {"id":"13230","name":"Jinarc : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2015-06-12T02:00:00Z","last_updated_date":"2026-06-01T14:32:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/jinarc-epar-risk-management-plan_en.pdf"},
    {"id":"13518","name":"Revlimid : EPAR - Risk Management Plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2022-12-06T02:00:00Z","last_updated_date":"2025-09-09T14:03:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/revlimid-epar-risk-management-plan_en.pdf"},
    {"id":"17170","name":"Opdivo : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2015-07-16T02:00:00Z","last_updated_date":"2026-06-02T11:19:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/opdivo-epar-risk-management-plan_en.pdf"},
    {"id":"19831","name":"Anoro : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2014-06-16T02:00:00Z","last_updated_date":"2025-03-27T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/anoro-epar-risk-management-plan_en.pdf"},
    {"id":"20612","name":"Entyvio : EPAR - Risk-management-plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2014-06-16T02:00:00Z","last_updated_date":"2026-03-03T09:17:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/entyvio-epar-risk-management-plan_en.pdf"},
    {"id":"21156","name":"Latuda : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2014-05-13T02:00:00Z","last_updated_date":"2024-12-13T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/latuda-epar-risk-management-plan_en.pdf"},
    {"id":"22789","name":"Intuniv : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2015-10-06T02:00:00Z","last_updated_date":"2024-06-10T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/intuniv-epar-risk-management-plan_en.pdf"},
    {"id":"23500","name":"Pregabalin Sandoz : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2015-07-16T02:00:00Z","last_updated_date":"2025-10-06T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/pregabalin-sandoz-epar-risk-management-plan_en.pdf"},
    {"id":"23615","name":"Gazyvaro : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2014-08-20T02:00:00Z","last_updated_date":"2025-09-04T12:30:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/gazyvaro-epar-risk-management-plan_en.pdf"},
    {"id":"24009","name":"Bosulif : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2018-05-07T02:00:00Z","last_updated_date":"2025-08-26T15:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/bosulif-epar-risk-management-plan_en.pdf"},
    {"id":"24465","name":"Xarelto : EPAR - Risk-management-plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2022-12-06T02:00:00Z","last_updated_date":"2024-06-03T17:52:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/xarelto-epar-risk-management-plan_en.pdf"},
    {"id":"24674","name":"Gilenya : EPAR - Risk Management Plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2023-06-01T02:00:00Z","last_updated_date":"2025-09-23T17:58:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/gilenya-epar-risk-management-plan_en.pdf"},
    {"id":"25177","name":"Harvoni : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2014-12-04T01:00:00Z","last_updated_date":"2026-01-09T16:44:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/harvoni-epar-risk-management-plan_en.pdf"},
    {"id":"25590","name":"Nucala : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2015-12-03T01:00:00Z","last_updated_date":"2026-03-09T15:10:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/nucala-epar-risk-management-plan_en.pdf"},
    {"id":"26093","name":"Imlygic : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2025-09-25T01:00:00Z","last_updated_date":"2025-09-25T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/imlygic-epar-risk-management-plan_en.pdf"},
    {"id":"26389","name":"Hefiya : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2018-08-06T16:44:00Z","last_updated_date":"2026-02-16T16:44:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/hefiya-epar-risk-management-plan_en.pdf"},
    {"id":"26643","name":"Mekinist : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2014-07-09T02:00:00Z","last_updated_date":"2026-05-19T14:11:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/mekinist-epar-risk-management-plan_en.pdf"},
    {"id":"26693","name":"Cerdelga : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2015-02-13T01:00:00Z","last_updated_date":"2026-05-20T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/cerdelga-epar-risk-management-plan_en.pdf"},
    {"id":"26775","name":"Adempas : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2014-05-13T02:00:00Z","last_updated_date":"2025-08-05T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/adempas-epar-risk-management-plan_en.pdf"},
    {"id":"27357","name":"Lucentis : EPAR - Risk Management Plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2018-08-31T02:00:00Z","last_updated_date":"2023-05-17T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/lucentis-epar-risk-management-plan_en.pdf"},
    {"id":"27641","name":"Imnovid : EPAR - Risk Management Plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2023-06-29T15:34:00Z","last_updated_date":"2026-01-20T16:26:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/imnovid-epar-risk-management-plan_en.pdf"},
    {"id":"28260","name":"Keytruda : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2015-07-30T02:00:00Z","last_updated_date":"2026-04-22T10:32:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/keytruda-epar-risk-management-plan_en.pdf"},
    {"id":"28386","name":"Riximyo : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2018-08-10T15:50:00Z","last_updated_date":"2025-08-05T17:33:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/riximyo-epar-risk-management-plan_en.pdf"},
    {"id":"29040","name":"Ultibro Breezhaler : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2018-05-02T02:00:00Z","last_updated_date":"2025-02-11T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/ultibro-breezhaler-epar-risk-management-plan_en.pdf"},
    {"id":"29956","name":"Plegridy : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2014-07-31T02:00:00Z","last_updated_date":"2025-11-14T10:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/plegridy-epar-risk-management-plan_en.pdf"},
    {"id":"30002","name":"Tagrisso : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2018-11-30T11:00:00Z","last_updated_date":"2025-01-09T18:03:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/tagrisso-epar-risk-management-plan_en.pdf"},
    {"id":"30892","name":"Neuraceq : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2014-05-13T02:00:00Z","last_updated_date":"2025-11-21T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/neuraceq-epar-risk-management-plan_en.pdf"},
    {"id":"30921","name":"Moventig : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2014-12-17T01:00:00Z","last_updated_date":"2025-01-15T15:40:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/moventig-epar-risk-management-plan_en.pdf"},
    {"id":"32488","name":"Juluca : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2024-12-10T16:29:00Z","last_updated_date":"2025-11-14T10:44:04Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/juluca-epar-risk-management-plan_en.pdf"},
    {"id":"32525","name":"Aimovig : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2018-08-08T02:00:00Z","last_updated_date":"2025-12-10T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/aimovig-epar-risk-management-plan_en.pdf"},
    {"id":"34051","name":"Ikervis : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2015-05-07T02:00:00Z","last_updated_date":"2026-01-15T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/ikervis-epar-risk-management-plan_en.pdf"},
    {"id":"35658","name":"Edistride : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2015-12-10T01:00:00Z","last_updated_date":"2024-09-24T13:34:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/edistride-epar-risk-management-plan_en.pdf"},
    {"id":"37036","name":"Tafinlar : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2018-09-11T02:00:00Z","last_updated_date":"2026-05-19T17:14:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/tafinlar-epar-risk-management-plan_en.pdf"},
    {"id":"37291","name":"Vargatef : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2015-01-08T01:00:00Z","last_updated_date":"2026-03-19T12:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/vargatef-epar-risk-management-plan_en.pdf"},
    {"id":"38457","name":"Laventair : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2014-06-13T02:00:00Z","last_updated_date":"2025-03-27T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/laventair-epar-risk-management-plan_en.pdf"},
    {"id":"38510","name":"Scenesse : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2015-02-12T01:00:00Z","last_updated_date":"2025-10-17T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/scenesse-epar-risk-management-plan_en.pdf"},
    {"id":"38578","name":"Zykadia : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2015-06-04T02:00:00Z","last_updated_date":"2025-09-03T15:23:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/zykadia-epar-risk-management-plan_en.pdf"},
    {"id":"39507","name":"Ofev : EPAR - Risk Management Plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2023-06-26T11:51:00Z","last_updated_date":"2025-03-10T09:03:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/ofev-epar-risk-management-plan_en.pdf"},
    {"id":"39896","name":"Vokanamet : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2014-05-15T02:00:00Z","last_updated_date":"2024-12-18T14:06:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/vokanamet-epar-risk-management-plan_en.pdf"},
    {"id":"40225","name":"Genvoya : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2015-12-01T01:00:00Z","last_updated_date":"2026-01-28T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/genvoya-epar-risk-management-plan_en.pdf"},
    {"id":"40446","name":"Cresemba : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2015-10-29T01:00:00Z","last_updated_date":"2024-10-01T01:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/cresemba-epar-risk-management-plan_en.pdf"},
    {"id":"40643","name":"Saxenda : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2015-04-16T02:00:00Z","last_updated_date":"2025-07-31T16:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/saxenda-epar-risk-management-plan_en.pdf"},
    {"id":"40665","name":"Rixathon : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2018-08-07T02:00:00Z","last_updated_date":"2025-10-06T15:35:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/rixathon-epar-risk-management-plan_en.pdf"},
    {"id":"41402","name":"Zavicefta : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2018-09-05T12:05:00Z","last_updated_date":"2025-11-13T12:05:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/zavicefta-epar-risk-management-plan_en.pdf"},
    {"id":"41739","name":"Hyrimoz : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2018-08-02T02:00:00Z","last_updated_date":"2026-02-13T10:09:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/hyrimoz-epar-risk-management-plan_en.pdf"},
    {"id":"42082","name":"Veyvondi : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2018-09-20T02:00:00Z","last_updated_date":"2026-01-20T16:54:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/veyvondi-epar-risk-management-plan_en.pdf"},
    {"id":"42125","name":"Darzalex : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2018-09-21T02:00:00Z","last_updated_date":"2025-08-29T17:33:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/darzalex-epar-risk-management-plan_en.pdf"},
    {"id":"42133","name":"Abilify Maintena : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2018-09-14T17:25:00Z","last_updated_date":"2024-04-10T17:25:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/abilify-maintena-epar-risk-management-plan_en.pdf"},
    {"id":"42179","name":"Invokana : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2018-10-03T11:48:00Z","last_updated_date":"2025-12-18T11:54:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/invokana-epar-risk-management-plan_en.pdf"},
    {"id":"42232","name":"Xerava : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2018-10-08T15:09:00Z","last_updated_date":"2026-03-13T17:49:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/xerava-epar-risk-management-plan_en.pdf"},
    {"id":"42281","name":"Slenyto : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2018-10-10T16:45:00Z","last_updated_date":"2025-04-01T17:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/slenyto-epar-risk-management-plan_en.pdf"},
    {"id":"42309","name":"Mektovi : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2018-10-12T12:43:00Z","last_updated_date":"2024-09-05T15:45:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/mektovi-epar-risk-management-plan_en.pdf"},
    {"id":"42314","name":"Braftovi : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2018-10-12T13:00:00Z","last_updated_date":"2024-09-05T11:10:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/braftovi-epar-risk-management-plan_en.pdf"},
    {"id":"42413","name":"Simponi : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2018-10-23T10:06:00Z","last_updated_date":"2026-01-30T12:16:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/simponi-epar-risk-management-plan_en.pdf"},
    {"id":"42478","name":"Verzenios : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2018-10-29T18:22:00Z","last_updated_date":"2026-02-25T10:16:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/verzenios-epar-risk-management-plan_en.pdf"},
    {"id":"42560","name":"Venclyxto : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2018-11-06T17:08:00Z","last_updated_date":"2025-10-22T16:51:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/venclyxto-epar-risk-management-plan_en.pdf"},
    {"id":"42695","name":"Viread : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2018-11-15T15:23:00Z","last_updated_date":"2025-11-18T11:04:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/viread-epar-risk-management-plan_en.pdf"},
    {"id":"42853","name":"RoActemra : EPAR - Risk-management-plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2018-11-28T10:06:00Z","last_updated_date":"2026-04-01T11:01:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/roactemra-epar-risk-management-plan_en.pdf"},
    {"id":"43008","name":"Remicade : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2018-12-12T11:20:00Z","last_updated_date":"2025-02-05T14:48:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/remicade-epar-risk-management-plan_en.pdf"},
    {"id":"43111","name":"Lyrica : EPAR - Risk Management Plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2023-05-26T17:06:00Z","last_updated_date":"2025-05-02T11:12:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/lyrica-epar-risk-management-plan_en.pdf"},
    {"id":"43203","name":"Flucelvax Tetra : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2018-12-20T15:36:00Z","last_updated_date":"2026-02-27T11:05:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/flucelvax-tetra-epar-risk-management-plan_en.pdf"},
    {"id":"43336","name":"Luxturna : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2019-01-11T12:01:00Z","last_updated_date":"2026-02-16T14:15:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/luxturna-epar-risk-management-plan_en.pdf"},
    {"id":"43378","name":"Ziextenzo : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2019-01-16T17:06:00Z","last_updated_date":"2026-03-27T11:55:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/ziextenzo-epar-risk-management-plan_en.pdf"},
    {"id":"43389","name":"Ocrevus : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2023-11-10T15:51:00Z","last_updated_date":"2026-04-16T16:08:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/ocrevus-epar-risk-management-plan_en.pdf"},
    {"id":"43428","name":"Yervoy : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2019-11-13T11:22:00Z","last_updated_date":"2025-11-21T11:28:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/yervoy-epar-risk-management-plan_en.pdf"},
    {"id":"43439","name":"Trumenba : EPAR Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2019-01-22T13:03:00Z","last_updated_date":"2025-06-02T11:02:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/trumenba-epar-risk-management-plan_en.pdf"},
    {"id":"43440","name":"Sivextro : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2019-01-22T13:09:00Z","last_updated_date":"2025-03-20T10:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/sivextro-epar-risk-management-plan_en.pdf"},
    {"id":"43489","name":"Poteligeo : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2019-01-28T11:00:00Z","last_updated_date":"2026-01-20T12:38:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/poteligeo-epar-risk-management-plan_en.pdf"},
    {"id":"43494","name":"Xtandi : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2019-01-25T17:44:00Z","last_updated_date":"2024-04-25T15:22:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/xtandi-epar-risk-management-plan_en.pdf"},
    {"id":"43507","name":"Jivi : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2019-01-28T12:41:00Z","last_updated_date":"2025-11-04T16:20:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/jivi-epar-risk-management-plan_en.pdf"},
    {"id":"43553","name":"Kisqali :  EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2019-01-30T12:43:00Z","last_updated_date":"2026-01-26T11:48:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/kisqali-epar-risk-management-plan_en.pdf"},
    {"id":"43618","name":"Namuscla : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2019-02-01T18:02:00Z","last_updated_date":"2026-06-03T11:11:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/namuscla-epar-risk-management-plan_en.pdf"},
    {"id":"43779","name":"Sovaldi : EPAR - Risk-management-plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2019-02-18T16:11:00Z","last_updated_date":"2026-01-09T16:30:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/sovaldi-epar-risk-management-plan_en.pdf"},
    {"id":"43795","name":"Rubraca : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2019-02-19T13:14:00Z","last_updated_date":"2023-11-30T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/rubraca-epar-risk-management-plan_en.pdf"},
    {"id":"43812","name":"Oniyde : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2019-02-20T11:13:00Z","last_updated_date":"2024-05-17T09:48:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/oniyde-epar-risk-management-plan_en.pdf"},
    {"id":"44018","name":"Adcetris : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2019-03-13T10:44:00Z","last_updated_date":"2025-10-01T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/adcetris-epar-risk-management-plan_en.pdf"},
    {"id":"44060","name":"Erleada : EPAR - Risk-management-plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2025-01-09T09:47:00Z","last_updated_date":"2026-03-31T13:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/erleada-epar-risk-management-plan_en.pdf"},
    {"id":"44114","name":"Ferriprox : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2019-03-26T17:27:00Z","last_updated_date":"2023-02-27T12:49:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/ferriprox-epar-risk-management-plan_en.pdf"},
    {"id":"44169","name":"Neulasta : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2019-04-03T16:33:00Z","last_updated_date":"2025-12-08T13:09:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/neulasta-epar-risk-management-plan_en.pdf"},
    {"id":"44181","name":"Forxiga : EPAR - Risk Management Plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2023-06-28T13:06:00Z","last_updated_date":"2024-09-24T17:14:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/forxiga-epar-risk-management-plan_en.pdf"},
    {"id":"44258","name":"Orencia : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2019-04-12T15:59:00Z","last_updated_date":"2026-05-11T13:52:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/orencia-epar-risk-management-plan_en.pdf"},
    {"id":"44298","name":"Idacio : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2019-04-17T15:22:00Z","last_updated_date":"2025-10-21T17:14:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/idacio-epar-risk-management-plan_en.pdf"},
    {"id":"44309","name":"Ajovy : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2019-04-17T17:05:00Z","last_updated_date":"2024-05-17T14:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/ajovy-epar-risk-management-plan_en.pdf"},
    {"id":"44325","name":"Tarceva : EPAR - Risk-management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2019-04-24T09:35:00Z","last_updated_date":"2019-04-24T09:35:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/tarceva-epar-risk-management-plan_en.pdf"},
    {"id":"44344","name":"Amgevita : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2019-04-25T11:34:00Z","last_updated_date":"2024-05-22T12:21:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/amgevita-epar-risk-management-plan_en.pdf"},
    {"id":"44409","name":"Kineret : EPAR - Risk-management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2023-03-29T15:43:00Z","last_updated_date":"2026-01-30T11:08:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/kineret-epar-risk-management-plan_en.pdf"},
    {"id":"44470","name":"Besremi : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2019-05-08T14:59:00Z","last_updated_date":"2025-10-21T15:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/besremi-epar-risk-management-plan_en.pdf"},
    {"id":"44489","name":"Aranesp : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2019-05-14T09:46:00Z","last_updated_date":"2026-01-13T12:34:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/aranesp-epar-risk-management-plan_en.pdf"},
    {"id":"44496","name":"Truvada : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2019-05-14T16:59:00Z","last_updated_date":"2025-11-18T15:16:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/truvada-epar-risk-management-plan_en.pdf"},
    {"id":"44538","name":"Waylivra : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2019-05-20T10:47:00Z","last_updated_date":"2025-07-14T14:25:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/waylivra-epar-risk-management-plan_en.pdf"},
    {"id":"44682","name":"Dectova : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2024-12-11T09:40:00Z","last_updated_date":"2024-12-11T09:40:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/dectova-epar-risk-management-plan_en.pdf"},
    {"id":"44719","name":"Lorviqua : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2019-06-17T14:56:00Z","last_updated_date":"2026-04-15T10:07:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/lorviqua-epar-risk-management-plan_en.pdf"},
    {"id":"44761","name":"Ilaris : EPAR - Risk management plan ","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2024-12-11T11:54:00Z","last_updated_date":"2024-12-11T11:54:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/ilaris-epar-risk-management-plan_en.pdf"},
    {"id":"44900","name":"Skyrizi : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2024-07-29T17:17:00Z","last_updated_date":"2025-06-11T11:08:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/skyrizi-epar-risk-management-plan_en.pdf"},
    {"id":"44956","name":"Esperoct : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2019-06-28T14:41:00Z","last_updated_date":"2024-12-05T16:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/esperoct-epar-risk-management-plan_en.pdf"},
    {"id":"44961","name":"Dupixent : EPAR - Risk-management-plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2019-06-28T16:36:00Z","last_updated_date":"2026-04-10T14:42:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/dupixent-epar-risk-management-plan_en.pdf"},
    {"id":"44992","name":"Edurant : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2019-07-04T16:14:00Z","last_updated_date":"2024-10-23T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/edurant-epar-risk-management-plan_en.pdf"},
    {"id":"44994","name":"Benlysta : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2019-07-05T11:29:00Z","last_updated_date":"2025-07-30T16:32:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/benlysta-epar-risk-management-plan_en.pdf"},
    {"id":"45002","name":"Libtayo : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2019-07-05T14:54:00Z","last_updated_date":"2025-12-10T09:50:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/libtayo-epar-risk-management-plan_en.pdf"},
    {"id":"45005","name":"Talzenna : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2019-07-08T10:26:00Z","last_updated_date":"2024-09-11T15:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/talzenna-epar-risk-management-plan_en.pdf"},
    {"id":"45019","name":"Xromi : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2019-07-08T16:40:00Z","last_updated_date":"2025-11-03T11:55:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/xromi-epar-risk-management-plan_en.pdf"},
    {"id":"45051","name":"Humira : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2019-07-12T14:05:00Z","last_updated_date":"2026-05-07T17:25:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/humira-epar-risk-management-plan_en.pdf"},
    {"id":"45067","name":"Mycamine : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2019-07-16T10:38:00Z","last_updated_date":"2025-10-13T12:27:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/mycamine-epar-risk-management-plan_en.pdf"},
    {"id":"45091","name":"Prolia : EPAR - Risk Management Plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2023-10-24T11:09:00Z","last_updated_date":"2024-01-10T08:33:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/prolia-epar-risk-management-plan_en.pdf"},
    {"id":"45122","name":"Exjade : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2019-07-25T14:54:00Z","last_updated_date":"2026-05-21T12:15:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/exjade-epar-risk-management-plan_en.pdf"},
    {"id":"45145","name":"Cufence : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2019-07-29T11:54:00Z","last_updated_date":"2025-07-02T11:15:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/cufence-epar-risk-management-plan_en.pdf"},
    {"id":"45152","name":"Aflunov : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2019-07-30T10:34:00Z","last_updated_date":"2024-11-04T13:29:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/aflunov-epar-risk-management-plan_en.pdf"},
    {"id":"45156","name":"LysaKare : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2019-07-30T14:50:00Z","last_updated_date":"2025-04-28T15:41:57Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/lysakare-epar-risk-management-plan_en.pdf"},
    {"id":"45192","name":"Striascan : EPAR - Risk Management Plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2019-08-02T13:30:00Z","last_updated_date":"2024-03-12T15:07:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/striascan-epar-risk-management-plan_en.pdf"},
    {"id":"45207","name":"Adenuric : EPAR - Risk Management Plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2023-04-20T16:48:00Z","last_updated_date":"2026-02-26T12:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/adenuric-epar-risk-management-plan_en.pdf"},
    {"id":"45256","name":"Rotarix : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2019-08-14T14:58:00Z","last_updated_date":"2025-12-19T15:27:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/rotarix-epar-risk-management-plan_en.pdf"},
    {"id":"45330","name":"Avastin : EPAR - Risk Management Plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2022-12-06T10:57:00Z","last_updated_date":"2022-12-06T10:57:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/avastin-epar-risk-management-plan_en.pdf"},
    {"id":"45341","name":"Posaconazole Accord : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2019-08-28T11:21:00Z","last_updated_date":"2024-04-22T11:10:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/posaconazole-accord-epar-risk-management-plan_en.pdf"},
    {"id":"45348","name":"Xigduo : EPAR - Risk Management Plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2023-05-26T14:19:00Z","last_updated_date":"2025-12-18T10:32:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/xigduo-epar-risk-management-plan_en.pdf"},
    {"id":"45372","name":"Prevymis : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2019-09-03T14:49:00Z","last_updated_date":"2025-05-27T09:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/prevymis-epar-risk-management-plan_en.pdf"},
    {"id":"45374","name":"Soliris : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2019-09-04T17:40:00Z","last_updated_date":"2025-06-19T17:46:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/soliris-epar-risk-management-plan_en.pdf"},
    {"id":"45376","name":"Dovato : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2024-12-10T15:35:00Z","last_updated_date":"2025-09-26T16:45:25Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/dovato-epar-risk-management-plan_en.pdf"},
    {"id":"45383","name":"Vimpat : EPAR - Risk Management Plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2019-09-05T11:00:00Z","last_updated_date":"2023-11-07T17:07:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/vimpat-epar-risk-management-plan_en.pdf"},
    {"id":"45430","name":"Stelara : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2019-09-12T15:17:00Z","last_updated_date":"2026-04-24T14:15:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/stelara-epar-risk-management-plan_en.pdf"},
    {"id":"45437","name":"Lacosamide UCB : EPAR - Risk-management-plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2019-09-12T17:14:00Z","last_updated_date":"2023-11-07T11:05:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/lacosamide-ucb-epar-risk-management-plan_en.pdf"},
    {"id":"45556","name":"Emtricitabine/Tenofovir disoproxil Zentiva : EPAR - Risk-management-plan summary","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2019-10-03T11:32:00Z","last_updated_date":"2024-02-28T14:15:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/emtricitabine-tenofovir-disoproxil-zentiva-epar-risk-management-plan-summary_en.pdf"},
    {"id":"45559","name":"Remsima : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2019-10-03T13:31:00Z","last_updated_date":"2025-11-19T13:41:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/remsima-epar-risk-management-plan_en.pdf"},
    {"id":"45594","name":"Lonsurf : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2019-10-08T15:13:00Z","last_updated_date":"2024-04-05T11:33:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/lonsurf-epar-risk-management-plan_en.pdf"},
    {"id":"45625","name":"Spinraza : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2019-10-09T13:34:00Z","last_updated_date":"2026-01-29T10:18:16Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/spinraza-epar-risk-management-plan_en.pdf"},
    {"id":"45769","name":"Noxafil : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2019-10-22T15:35:00Z","last_updated_date":"2026-03-24T10:30:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/noxafil-epar-risk-management-plan_en.pdf"},
    {"id":"45771","name":"Tecentriq : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2024-09-04T12:21:00Z","last_updated_date":"2026-04-28T10:44:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/tecentriq-epar-risk-management-plan_en.pdf"},
    {"id":"45782","name":"Vitrakvi : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2024-08-27T12:19:00Z","last_updated_date":"2024-08-27T12:19:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/vitrakvi-epar-risk-management-plan_en.pdf"},
    {"id":"45861","name":"Erelzi : EPAR - Risk-management-plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2019-10-30T16:50:00Z","last_updated_date":"2025-12-16T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/erelzi-epar-risk-management-plan_en.pdf"},
    {"id":"45875","name":"Jylamvo : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2019-10-31T17:07:00Z","last_updated_date":"2024-06-24T14:10:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/jylamvo-epar-risk-management-plan_en.pdf"},
    {"id":"45879","name":"Bavencio : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2019-11-04T11:37:00Z","last_updated_date":"2026-05-21T11:40:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/bavencio-epar-risk-management-plan_en.pdf"},
    {"id":"46036","name":"Eliquis : EPAR - Risk Management Plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2022-12-06T09:49:00Z","last_updated_date":"2026-04-01T16:22:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/eliquis-epar-risk-management-plan_en.pdf"},
    {"id":"46216","name":"Rhokiinsa : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2019-12-03T11:16:00Z","last_updated_date":"2026-01-15T16:22:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/rhokiinsa-epar-risk-management-plan_en.pdf"},
    {"id":"46277","name":"Jentadueto : EPAR - Risk-management-plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2019-12-10T11:30:00Z","last_updated_date":"2026-02-12T13:28:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/jentadueto-epar-risk-management-plan_en.pdf"},
    {"id":"46279","name":"Trajenta : EPAR - Risk Management Plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2019-12-10T12:19:00Z","last_updated_date":"2026-02-12T15:40:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/trajenta-epar-risk-management-plan_en.pdf"},
    {"id":"46282","name":"Glyxambi : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2019-12-10T15:53:00Z","last_updated_date":"2026-02-12T13:32:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/glyxambi-epar-risk-management-plan_en.pdf"},
    {"id":"46334","name":"Rinvoq : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2019-12-18T14:31:00Z","last_updated_date":"2025-04-14T09:54:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/rinvoq-epar-risk-management-plan_en.pdf"},
    {"id":"46340","name":"Xeljanz : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2019-12-19T12:04:00Z","last_updated_date":"2025-01-20T11:42:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/xeljanz-epar-risk-management-plan_en.pdf"},
    {"id":"46352","name":"Brinavess : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2019-12-19T16:41:00Z","last_updated_date":"2025-05-19T16:45:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/brinavess-epar-risk-management-plan_en.pdf"},
    {"id":"46385","name":"VeraSeal : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2020-01-06T15:06:00Z","last_updated_date":"2024-03-05T12:39:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/veraseal-epar-risk-management-plan_en.pdf"},
    {"id":"46412","name":"Kuvan : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2020-01-10T15:56:00Z","last_updated_date":"2025-04-22T14:20:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/kuvan-epar-risk-management-plan_en.pdf"},
    {"id":"46502","name":"Mayzent : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2020-01-23T14:43:00Z","last_updated_date":"2025-11-24T12:40:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/mayzent-epar-risk-management-plan_en.pdf"},
    {"id":"46572","name":"Clopidogrel / Acetylsalicylic acid Mylan : EPAR - Risk-management-plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2020-01-24T17:11:00Z","last_updated_date":"2024-03-04T12:46:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/clopidogrel-acetylsalicylic-acid-mylan-epar-risk-management-plan_en.pdf"},
    {"id":"46665","name":"Kalydeco : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2020-02-03T17:21:00Z","last_updated_date":"2025-07-02T16:52:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/kalydeco-epar-risk-management-plan_en.pdf"},
    {"id":"46683","name":"Baqsimi : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2020-02-06T13:11:00Z","last_updated_date":"2025-09-15T17:23:33Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/baqsimi-epar-risk-management-plan_en.pdf"},
    {"id":"46707","name":"Revestive : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2020-02-11T13:11:00Z","last_updated_date":"2024-03-06T16:41:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/revestive-epar-risk-management-plan_en.pdf"},
    {"id":"46720","name":"Votubia : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2020-02-12T16:07:00Z","last_updated_date":"2024-10-30T17:30:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/votubia-epar-risk-management-plan_en.pdf"},
    {"id":"46721","name":"Glivec : EPAR - Risk-management-plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2020-02-12T16:07:00Z","last_updated_date":"2024-02-22T18:21:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/glivec-epar-risk-management-plan_en.pdf"},
    {"id":"46728","name":"Sunosi : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2020-02-12T12:31:00Z","last_updated_date":"2025-09-05T17:15:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/sunosi-epar-risk-management-plan_en.pdf"},
    {"id":"46764","name":"Amsparity : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2020-02-14T17:34:00Z","last_updated_date":"2025-08-20T15:20:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/amsparity-epar-risk-management-plan_en.pdf"},
    {"id":"46769","name":"Tecfidera : EPAR - Risk Management Plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2022-11-30T15:04:00Z","last_updated_date":"2024-09-26T14:12:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/tecfidera-epar-risk-management-plan_en.pdf"},
    {"id":"46783","name":"Beovu : EPAR - Risk Management Plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2023-05-26T12:39:00Z","last_updated_date":"2024-11-29T15:35:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/beovu-epar-risk-management-plan_en.pdf"},
    {"id":"46799","name":"Isturisa : EPAR - Risk-management-plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2020-02-18T16:07:00Z","last_updated_date":"2024-05-29T09:48:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/isturisa-epar-risk-management-plan_en.pdf"},
    {"id":"46814","name":"Vyndaqel : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2020-02-21T09:38:00Z","last_updated_date":"2024-11-22T11:45:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/vyndaqel-epar-risk-management-plan_en.pdf"},
    {"id":"46827","name":"Azacitidine Accord : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2020-02-21T14:37:00Z","last_updated_date":"2025-10-08T15:40:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/azacitidine-accord-epar-risk-management-plan_en.pdf"},
    {"id":"46842","name":"Evenity : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2020-02-24T17:02:00Z","last_updated_date":"2025-02-17T14:01:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/evenity-epar-risk-management-plan_en.pdf"},
    {"id":"46878","name":"Aubagio : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2022-11-10T10:34:00Z","last_updated_date":"2024-06-12T11:28:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/aubagio-epar-risk-management-plan_en.pdf"},
    {"id":"47098","name":"Cubicin : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2020-03-23T11:50:00Z","last_updated_date":"2025-01-16T15:58:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/cubicin-epar-risk-management-plan_en.pdf"},
    {"id":"47119","name":"Qtern : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2020-03-25T14:46:00Z","last_updated_date":"2025-12-18T10:25:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/qtern-epar-risk-management-plan_en.pdf"},
    {"id":"47258","name":"Nubeqa : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2020-04-01T11:31:00Z","last_updated_date":"2025-07-28T15:51:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/nubeqa-epar-risk-management-plan_en.pdf"},
    {"id":"47298","name":"Kaletra : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2020-04-02T15:28:00Z","last_updated_date":"2025-01-20T12:18:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/kaletra-epar-risk-management-plan_en.pdf"},
    {"id":"47362","name":"Ruxience : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2020-04-07T11:23:00Z","last_updated_date":"2025-07-14T15:28:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/ruxience-epar-risk-management-plan_en.pdf"},
    {"id":"47371","name":"GoResp Digihaler (previously Budesonide/Formoterol Teva Pharma B.V.) : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2020-04-07T14:31:00Z","last_updated_date":"2024-04-16T16:50:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/goresp-digihaler-previously-budesonide-formoterol-teva-pharma-bv-epar-risk-management-plan_en.pdf"},
    {"id":"47392","name":"Trepulmix : EPAR - Risk management plan ","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2020-04-08T17:32:00Z","last_updated_date":"2024-05-17T15:31:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/trepulmix-epar-risk-management-plan_en.pdf"},
    {"id":"47412","name":"Cinacalcet Accordpharma : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2020-04-15T14:00:00Z","last_updated_date":"2024-06-27T12:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/cinacalcet-accordpharma-epar-risk-management-plan_en.pdf"},
    {"id":"47475","name":"Nustendi : EPAR - Risk management plan ","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2020-04-24T10:17:00Z","last_updated_date":"2026-02-27T11:44:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/nustendi-epar-risk-management-plan_en.pdf"},
    {"id":"47491","name":"Nilemdo : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2020-04-24T16:01:00Z","last_updated_date":"2026-02-27T12:12:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/nilemdo-epar-risk-management-plan_en.pdf"},
    {"id":"47586","name":"Lokelma : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2020-05-07T11:23:00Z","last_updated_date":"2025-08-13T15:29:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/lokelma-epar-risk-management-plan_en.pdf"},
    {"id":"47660","name":"Ruconest : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2020-05-18T09:20:00Z","last_updated_date":"2026-05-20T13:45:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/ruconest-epar-risk-management-plan_en.pdf"},
    {"id":"47770","name":"Imvanex : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2024-10-16T12:45:00Z","last_updated_date":"2026-05-18T16:13:14Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/imvanex-epar-risk-management-plan_en.pdf"},
    {"id":"47783","name":"Zeposia: EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2020-05-27T16:32:00Z","last_updated_date":"2026-03-03T16:22:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/zeposia-epar-risk-management-plan_en.pdf"},
    {"id":"47831","name":"Fluad Tetra : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2020-05-29T16:29:00Z","last_updated_date":"2026-02-26T13:53:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/fluad-tetra-epar-risk-management-plan_en.pdf"},
    {"id":"47860","name":"Jorveza : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2020-06-04T15:24:00Z","last_updated_date":"2026-04-15T12:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/jorveza-epar-risk-management-plan_en.pdf"},
    {"id":"47926","name":"Zejula : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2020-06-10T12:43:00Z","last_updated_date":"2025-05-07T12:59:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/zejula-epar-risk-management-plan_en.pdf"},
    {"id":"47949","name":"Taltz : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2020-06-11T10:45:00Z","last_updated_date":"2026-02-26T02:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/taltz-epar-risk-management-plan_en.pdf"},
    {"id":"48003","name":"Sarclisa : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2020-06-12T15:43:00Z","last_updated_date":"2025-03-12T15:44:46Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/sarclisa-epar-risk-management-plan_en.pdf"},
    {"id":"48037","name":"Refixia : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2020-06-17T12:33:00Z","last_updated_date":"2025-11-25T14:32:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/refixia-epar-risk-management-plan_en.pdf"},
    {"id":"48105","name":"Opsumit : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2020-06-24T12:39:00Z","last_updated_date":"2024-11-26T11:18:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/opsumit-epar-risk-management-plan_en.pdf"},
    {"id":"48173","name":"Eviplera : EPAR - Risk-management-plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2020-06-26T15:30:00Z","last_updated_date":"2025-12-09T10:28:08Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/eviplera-epar-risk-management-plan_en.pdf"},
    {"id":"48217","name":"Fingolimod Accord : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2020-07-03T11:30:00Z","last_updated_date":"2026-03-02T16:32:47Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/fingolimod-accord-epar-risk-management-plan_en.pdf"},
    {"id":"48267","name":"Reblozyl : EPAR - Risk-management-plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2020-07-08T16:58:00Z","last_updated_date":"2024-05-13T10:18:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/reblozyl-epar-risk-management-plan_en.pdf"},
    {"id":"48284","name":"Verkazia : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2020-07-10T16:08:00Z","last_updated_date":"2026-01-15T14:47:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/verkazia-epar-risk-management-plan_en.pdf"},
    {"id":"48355","name":"Veklury : EPAR – Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2020-07-22T16:27:00Z","last_updated_date":"2025-06-26T11:10:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/veklury-epar-risk-management-plan_en.pdf"},
    {"id":"48359","name":"Mvabea : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2020-07-23T09:58:00Z","last_updated_date":"2025-03-25T11:11:11Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/mvabea-epar-risk-management-plan_en.pdf"},
    {"id":"48365","name":"Zabdeno : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2020-07-23T10:23:00Z","last_updated_date":"2025-03-25T15:17:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/zabdeno-epar-risk-management-plan_en.pdf"},
    {"id":"48436","name":"Zercepac : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2020-07-28T10:53:00Z","last_updated_date":"2024-06-25T13:52:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/zercepac-epar-risk-management-plan_en.pdf"},
    {"id":"48453","name":"Enbrel : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2020-07-28T12:32:00Z","last_updated_date":"2025-08-13T09:39:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/enbrel-epar-risk-management-plan_en.pdf"},
    {"id":"48460","name":"Suboxone : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2020-07-28T16:11:00Z","last_updated_date":"2024-06-03T13:37:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/suboxone-epar-risk-management-plan_en.pdf"},
    {"id":"48469","name":"Perjeta : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2020-07-29T11:10:00Z","last_updated_date":"2024-04-05T13:02:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/perjeta-epar-risk-management-plan_en.pdf"},
    {"id":"48505","name":"Piqray : EPAR - Risk-management-plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2020-07-30T16:58:00Z","last_updated_date":"2025-11-04T12:10:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/piqray-epar-risk-management-plan_en.pdf"},
    {"id":"48511","name":"Ecalta : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2023-03-21T10:05:00Z","last_updated_date":"2023-03-21T10:05:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/ecalta-epar-risk-management-plan_en.pdf"},
    {"id":"48562","name":"Apixaban Accord : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2020-08-06T16:32:00Z","last_updated_date":"2026-02-24T15:50:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/apixaban-accord-epar-risk-management-plan_en.pdf"},
    {"id":"48597","name":"Hepcludex : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2020-08-12T14:42:00Z","last_updated_date":"2026-03-31T16:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/hepcludex-epar-risk-management-plan_en.pdf"},
    {"id":"48681","name":"Kaftrio : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2020-08-21T15:08:00Z","last_updated_date":"2025-11-11T16:05:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/kaftrio-epar-risk-management-plan_en.pdf"},
    {"id":"48712","name":"Idefirix : EPAR - Risk-management-plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2020-08-28T11:01:00Z","last_updated_date":"2025-07-02T14:25:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/idefirix-epar-risk-management-plan_en.pdf"},
    {"id":"48832","name":"Blenrep : EPAR - Risk Management Plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2023-10-25T11:39:00Z","last_updated_date":"2024-03-13T12:21:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/blenrep-epar-risk-management-plan_en.pdf"},
    {"id":"48900","name":"Shingrix : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2020-09-28T14:21:00Z","last_updated_date":"2025-12-19T11:47:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/shingrix-epar-risk-management-plan_en.pdf"},
    {"id":"48915","name":"Ayvakyt : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2020-09-30T18:03:00Z","last_updated_date":"2026-01-09T14:55:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/ayvakyt-epar-risk-management-plan_en.pdf"},
    {"id":"48929","name":"Arsenic trioxide medac : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2020-10-01T14:36:00Z","last_updated_date":"2026-04-21T13:12:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/arsenic-trioxide-medac-epar-risk-management-plan_en.pdf"},
    {"id":"49002","name":"Erivedge : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2020-10-13T11:53:00Z","last_updated_date":"2026-01-22T22:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/erivedge-epar-risk-management-plan_en.pdf"},
    {"id":"49136","name":"Olumiant : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2020-10-27T11:27:00Z","last_updated_date":"2026-05-07T09:34:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/olumiant-epar-risk-management-plan_en.pdf"},
    {"id":"49215","name":"Calquence : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2020-11-11T17:34:00Z","last_updated_date":"2025-07-15T10:18:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/calquence-epar-risk-management-plan_en.pdf"},
    {"id":"49276","name":"Arikayce liposomal : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2020-11-18T16:20:00Z","last_updated_date":"2025-07-10T11:52:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/arikayce-liposomal-epar-risk-management-plan_en.pdf"},
    {"id":"49364","name":"Supemtek Tetra : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2020-11-25T15:38:00Z","last_updated_date":"2025-04-10T13:55:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/supemtek-tetra-epar-risk-management-plan_en.pdf"},
    {"id":"49386","name":"MenQuadfi : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2020-11-27T09:24:00Z","last_updated_date":"2024-04-18T15:50:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/menquadfi-epar-risk-management-plan_en.pdf"},
    {"id":"49452","name":"Neparvis : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2020-12-07T16:52:00Z","last_updated_date":"2025-03-10T14:45:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/neparvis-epar-risk-management-plan_en.pdf"},
    {"id":"49668","name":"Palforzia : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2020-12-21T13:33:00Z","last_updated_date":"2025-07-04T10:19:19Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/palforzia-epar-risk-management-plan_en.pdf"},
    {"id":"49669","name":"Comirnaty : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2020-12-23T14:29:00Z","last_updated_date":"2026-05-29T11:43:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/comirnaty-epar-risk-management-plan_en.pdf"},
    {"id":"49677","name":"Libmeldy : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2020-12-22T11:10:00Z","last_updated_date":"2025-12-10T16:36:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/libmeldy-epar-risk-management-plan_en.pdf"},
    {"id":"49697","name":"Spikevax (previously COVID-19 Vaccine Moderna): EPAR - Risk-management-plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2021-01-20T11:50:00Z","last_updated_date":"2026-02-24T09:44:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/spikevax-previously-covid-19-vaccine-moderna-epar-risk-management-plan_en.pdf"},
    {"id":"49704","name":"Rekambys : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2021-01-04T14:41:00Z","last_updated_date":"2025-11-04T15:51:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/rekambys-epar-risk-management-plan_en.pdf"},
    {"id":"49715","name":"Vocabria : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2021-01-05T11:55:00Z","last_updated_date":"2025-10-30T11:43:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/vocabria-epar-risk-management-plan_en.pdf"},
    {"id":"49720","name":"Trixeo Aerosphere : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2021-01-05T15:04:00Z","last_updated_date":"2025-09-19T15:51:28Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/trixeo-aerosphere-epar-risk-management-plan_en.pdf"},
    {"id":"49732","name":"Livogiva : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2021-01-06T12:43:00Z","last_updated_date":"2025-12-10T15:30:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/livogiva-epar-risk-management-plan_en.pdf"},
    {"id":"49785","name":"Fycompa : EPAR - Risk-management-plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2021-01-13T12:29:00Z","last_updated_date":"2023-02-24T10:50:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/fycompa-epar-risk-management-plan_en.pdf"},
    {"id":"49803","name":"Valdoxan : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2021-01-14T11:26:00Z","last_updated_date":"2025-01-06T14:10:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/valdoxan-epar-risk-management-plan_en.pdf"},
    {"id":"49831","name":"Incruse Ellipta : Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2021-01-18T16:46:00Z","last_updated_date":"2025-03-28T15:06:28Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/incruse-ellipta-risk-management-plan_en.pdf"},
    {"id":"49870","name":"Roclanda : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2021-01-21T10:34:00Z","last_updated_date":"2026-01-15T12:45:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/roclanda-epar-risk-management-plan_en.pdf"},
    {"id":"49890","name":"Tremfya : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2021-01-22T10:29:00Z","last_updated_date":"2025-12-19T11:36:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/tremfya-epar-risk-management-plan_en.pdf"},
    {"id":"49894","name":"Vaxzevria (previously COVID-19 Vaccine AstraZeneca) : EPAR - Risk-management-plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2021-02-18T09:50:00Z","last_updated_date":"2024-05-07T10:58:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/vaxzevria-previously-covid-19-vaccine-astrazeneca-epar-risk-management-plan_en.pdf"},
    {"id":"49896","name":"Xofluza : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2021-01-22T11:21:00Z","last_updated_date":"2025-06-02T16:57:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/xofluza-epar-risk-management-plan_en.pdf"},
    {"id":"50060","name":"Nplate : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2021-02-03T01:00:00Z","last_updated_date":"2024-05-16T14:48:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/nplate-epar-risk-management-plan_en.pdf"},
    {"id":"50065","name":"Tivicay : EPAR - Risk management plan ","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2024-12-10T16:22:00Z","last_updated_date":"2025-11-14T10:26:06Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/tivicay-epar-risk-management-plan_en.pdf"},
    {"id":"50108","name":"Enhertu : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2021-02-08T17:23:00Z","last_updated_date":"2025-12-03T16:35:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/enhertu-epar-risk-management-plan_en.pdf"},
    {"id":"50144","name":"Uptravi : EPAR - Risk-management-plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2021-02-11T15:31:00Z","last_updated_date":"2026-02-19T14:20:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/uptravi-epar-risk-management-plan_en.pdf"},
    {"id":"50156","name":"Rukobia : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2021-02-12T14:27:00Z","last_updated_date":"2025-03-31T10:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/rukobia-epar-risk-management-plan_en.pdf"},
    {"id":"50159","name":"Iscover : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2021-02-12T15:32:00Z","last_updated_date":"2025-04-16T12:34:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/iscover-epar-risk-management-plan_en.pdf"},
    {"id":"50161","name":"Plavix : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2021-02-12T16:11:00Z","last_updated_date":"2025-04-16T10:44:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/plavix-epar-risk-management-plan_en.pdf"},
    {"id":"50240","name":"Tukysa : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2021-02-18T16:02:00Z","last_updated_date":"2025-11-14T08:42:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/tukysa-epar-risk-management-plan_en.pdf"},
    {"id":"50299","name":"Yuflyma : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2021-02-26T16:09:00Z","last_updated_date":"2026-02-05T16:13:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/yuflyma-epar-risk-management-plan_en.pdf"},
    {"id":"50306","name":"Ogluo : EPAR - Risk Management Plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2021-02-26T16:57:00Z","last_updated_date":"2023-05-26T15:49:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/ogluo-epar-risk-management-plan_en.pdf"},
    {"id":"50324","name":"Heplisav B : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2021-03-01T13:42:00Z","last_updated_date":"2024-05-13T08:38:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/heplisav-b-epar-risk-management-plan_en.pdf"},
    {"id":"50375","name":"Inrebic : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2021-03-03T09:25:00Z","last_updated_date":"2025-03-05T12:30:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/inrebic-epar-risk-management-plan_en.pdf"},
    {"id":"50526","name":"COVID-19 Vaccine Janssen : EPAR - Risk-management-plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2021-03-11T15:05:00Z","last_updated_date":"2024-08-09T11:52:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/covid-19-vaccine-janssen-epar-risk-management-plan_en.pdf"},
    {"id":"50806","name":"Ontozry : EPAR - Risk-management-plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2021-04-13T15:37:00Z","last_updated_date":"2024-04-23T16:02:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/ontozry-epar-risk-management-plan_en.pdf"},
    {"id":"50835","name":"Yondelis : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2021-04-14T16:06:00Z","last_updated_date":"2025-04-03T10:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/yondelis-epar-risk-management-plan_en.pdf"},
    {"id":"50973","name":"Retsevmo : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2021-04-23T16:08:00Z","last_updated_date":"2025-12-15T11:32:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/retsevmo-epar-risk-management-plan_en.pdf"},
    {"id":"50995","name":"HyQvia : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2021-04-28T15:42:00Z","last_updated_date":"2025-05-05T11:40:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/hyqvia-epar-risk-management-plan_en.pdf"},
    {"id":"51040","name":"Jemperli : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2021-05-03T12:00:00Z","last_updated_date":"2025-01-21T15:08:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/jemperli-epar-risk-management-plan_en.pdf"},
    {"id":"51057","name":"Evrysdi : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2021-05-04T11:35:00Z","last_updated_date":"2026-04-17T16:36:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/evrysdi-epar-risk-management-plan_en.pdf"},
    {"id":"51066","name":"Abiraterone Accord : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2021-05-05T09:54:00Z","last_updated_date":"2024-04-19T10:57:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/abiraterone-accord-epar-risk-management-plan_en.pdf"},
    {"id":"51346","name":"Ponvory : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2021-06-02T13:33:00Z","last_updated_date":"2025-10-15T14:24:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/ponvory-epar-risk-management-plan_en.pdf"},
    {"id":"51518","name":"Evkeeza : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2021-06-21T14:59:00Z","last_updated_date":"2025-01-07T10:45:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/evkeeza-epar-risk-management-plan_en.pdf"},
    {"id":"51527","name":"Adtralza : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2025-10-27T15:24:00Z","last_updated_date":"2025-10-27T15:24:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/adtralza-epar-risk-management-plan_en.pdf"},
    {"id":"52008","name":"Imcivree : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2021-07-22T10:36:00Z","last_updated_date":"2026-05-27T11:56:17Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/imcivree-epar-risk-management-plan_en.pdf"},
    {"id":"52116","name":"Votrient : EPAR - Risk Management Plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2021-07-28T11:07:00Z","last_updated_date":"2023-04-25T05:08:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/votrient-epar-risk-management-plan_en.pdf"},
    {"id":"52200","name":"Jakavi : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2021-08-04T18:01:00Z","last_updated_date":"2025-08-29T11:50:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/jakavi-epar-risk-management-plan_en.pdf"},
    {"id":"52259","name":"Bimzelx : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2021-08-24T09:17:00Z","last_updated_date":"2026-03-17T16:52:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/bimzelx-epar-risk-management-plan_en.pdf"},
    {"id":"52274","name":"Abecma : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2021-08-25T15:55:00Z","last_updated_date":"2025-12-09T11:41:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/abecma-epar-risk-management-plan_en.pdf"},
    {"id":"52309","name":"Fingolimod Mylan : EPAR - Risk management plan","type":"rmp","status":"Adopted","consultation_date":"","first_published_date":"2021-08-31T15:50:00Z","last_updated_date":"2025-11-28T11:06:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/fingolimod-mylan-epar-risk-management-plan_en.pdf"},
    {"id":"52370","name":"Byooviz  : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2021-09-08T14:43:00Z","last_updated_date":"2026-01-23T15:06:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/byooviz-epar-risk-management-plan_en.pdf"},
    {"id":"52382","name":"Minjuvi : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2021-09-08T15:09:00Z","last_updated_date":"2026-01-27T12:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/minjuvi-epar-risk-management-plan_en.pdf"},
    {"id":"52529","name":"Zinplava : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2021-09-21T12:42:00Z","last_updated_date":"2024-03-01T15:43:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/zinplava-epar-risk-management-plan_en.pdf"},
    {"id":"52572","name":"Esbriet : EPAR - Risk Management Plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2023-05-17T16:17:00Z","last_updated_date":"2023-09-08T09:03:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/esbriet-epar-risk-management-plan_en.pdf"},
    {"id":"52821","name":"Janumet : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2022-11-18T17:24:00Z","last_updated_date":"2022-11-18T17:24:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/janumet-epar-risk-management-plan_en.pdf"},
    {"id":"52889","name":"Mavenclad : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2021-10-20T17:19:00Z","last_updated_date":"2026-01-13T14:14:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/mavenclad-epar-risk-management-plan_en.pdf"},
    {"id":"52931","name":"Deltyba : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2021-10-28T12:29:00Z","last_updated_date":"2026-03-18T14:53:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/deltyba-epar-risk-management-plan_en.pdf"},
    {"id":"52961","name":"Galvus : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2021-10-29T14:50:00Z","last_updated_date":"2025-02-19T10:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/galvus-epar-risk-management-plan_en.pdf"},
    {"id":"53112","name":"Regkirona : EPAR - Risk-management-plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2021-11-12T15:00:00Z","last_updated_date":"2025-04-24T16:22:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/regkirona-epar-risk-management-plan_en.pdf"},
    {"id":"53166","name":"Ronapreve : EPAR - Risk-management-plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2021-11-19T15:00:00Z","last_updated_date":"2026-01-23T14:06:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/ronapreve-epar-risk-management-plan_en.pdf"},
    {"id":"53256","name":"Vumerity : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2021-11-24T12:52:00Z","last_updated_date":"2024-09-26T15:02:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/vumerity-epar-risk-management-plan_en.pdf"},
    {"id":"53264","name":"Trodelvy : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2021-11-24T14:34:00Z","last_updated_date":"2024-06-06T11:08:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/trodelvy-epar-risk-management-plan_en.pdf"},
    {"id":"53312","name":"Rivaroxaban Viatris : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2021-11-29T13:25:00Z","last_updated_date":"2025-07-23T10:38:33Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/rivaroxaban-viatris-epar-risk-management-plan_en.pdf"},
    {"id":"53433","name":"Gavreto : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2021-12-09T11:00:00Z","last_updated_date":"2025-01-17T10:07:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/gavreto-epar-risk-management-plan_en.pdf"},
    {"id":"53519","name":"Brukinsa : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2021-12-15T09:31:00Z","last_updated_date":"2025-10-02T17:51:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/brukinsa-epar-risk-management-plan_en.pdf"},
    {"id":"53543","name":"Aspaveli : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2021-12-16T10:15:00Z","last_updated_date":"2026-05-13T11:12:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/aspaveli-epar-risk-management-plan_en.pdf"},
    {"id":"53567","name":"Xevudy : EPAR - Risk-management-plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2021-12-16T17:12:00Z","last_updated_date":"2026-03-04T17:13:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/xevudy-epar-risk-management-plan_en.pdf"},
    {"id":"53586","name":"Nuvaxovid : EPAR - Risk-management-plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2021-12-20T14:14:00Z","last_updated_date":"2024-10-16T11:10:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/nuvaxovid-epar-risk-management-plan_en.pdf"},
    {"id":"53595","name":"Cibinqo : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2021-12-17T15:07:00Z","last_updated_date":"2026-02-06T11:53:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/cibinqo-epar-risk-management-plan_en.pdf"},
    {"id":"53675","name":"Firazyr : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2025-10-15T08:36:00Z","last_updated_date":"2025-10-15T08:36:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/firazyr-epar-risk-management-plan_en.pdf"},
    {"id":"53789","name":"Hukyndra : EPAR - Risk management plan ","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2025-01-21T18:44:00Z","last_updated_date":"2025-01-21T18:44:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/hukyndra-epar-risk-management-plan_en.pdf"},
    {"id":"53931","name":"Tavneos : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2022-01-26T17:09:00Z","last_updated_date":"2025-01-06T16:35:51Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/tavneos-epar-risk-management-plan_en.pdf"},
    {"id":"53960","name":"Paxlovid : EPAR - Risk-management-plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2022-01-27T16:37:00Z","last_updated_date":"2025-12-04T11:04:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/paxlovid-epar-risk-management-plan_en.pdf"},
    {"id":"54004","name":"Tecovirimat SIGA - EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2022-01-28T12:07:00Z","last_updated_date":"2025-11-10T10:18:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/tecovirimat-siga-epar-risk-management-plan_en.pdf"},
    {"id":"54148","name":"Bridion : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2022-02-14T12:38:00Z","last_updated_date":"2025-02-10T10:19:36Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/bridion-epar-risk-management-plan_en.pdf"},
    {"id":"54237","name":"Saphnelo : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2022-02-21T14:20:00Z","last_updated_date":"2025-12-18T13:36:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/saphnelo-epar-risk-management-plan_en.pdf"},
    {"id":"54264","name":"Ozempic : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2022-02-23T14:07:00Z","last_updated_date":"2026-03-25T17:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/ozempic-epar-risk-management-plan_en.pdf"},
    {"id":"54428","name":"Kerendia : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2022-03-11T15:03:00Z","last_updated_date":"2026-05-07T10:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/kerendia-epar-risk-management-plan_en.pdf"},
    {"id":"54496","name":"Sapropterin Dipharma : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2022-03-16T17:40:00Z","last_updated_date":"2025-10-17T10:48:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/sapropterin-dipharma-epar-risk-management-plan_en.pdf"},
    {"id":"54596","name":"Daxas : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2022-03-25T16:39:00Z","last_updated_date":"2026-02-25T14:36:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/daxas-epar-risk-management-plan_en.pdf"},
    {"id":"54709","name":"Breyanzi : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2022-04-08T15:31:00Z","last_updated_date":"2025-12-18T17:30:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/breyanzi-epar-risk-management-plan_en.pdf"},
    {"id":"54843","name":"Kapruvia : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2022-04-28T09:43:00Z","last_updated_date":"2026-06-01T09:36:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/kapruvia-epar-risk-management-plan_en.pdf"},
    {"id":"54901","name":"Evusheld : EPAR - Risk-management-plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2022-05-05T15:24:00Z","last_updated_date":"2025-10-14T12:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/evusheld-epar-risk-management-plan_en.pdf"},
    {"id":"54906","name":"Padcev : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2022-05-05T17:19:00Z","last_updated_date":"2025-07-17T10:42:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/padcev-epar-risk-management-plan_en.pdf"},
    {"id":"54917","name":"Modigraf : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2022-05-06T15:31:00Z","last_updated_date":"2024-11-05T12:25:01Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/modigraf-epar-risk-management-plan_en.pdf"},
    {"id":"54936","name":"Kevzara : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2022-05-11T12:19:00Z","last_updated_date":"2025-01-31T10:53:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/kevzara-epar-risk-management-plan_en.pdf"},
    {"id":"54942","name":"Iclusig : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2022-05-11T15:23:00Z","last_updated_date":"2026-03-25T16:31:44Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/iclusig-epar-risk-management-plan_en.pdf"},
    {"id":"55001","name":"Uplizna : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2022-05-19T09:28:00Z","last_updated_date":"2026-02-17T12:35:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/uplizna-epar-risk-management-plan_en.pdf"},
    {"id":"55059","name":"Zessly : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2022-05-23T13:22:00Z","last_updated_date":"2024-05-29T13:05:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/zessly-epar-risk-management-plan_en.pdf"},
    {"id":"55062","name":"Halaven : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2023-10-23T16:32:00Z","last_updated_date":"2023-10-23T16:32:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/halaven-epar-risk-management-plan_en.pdf"},
    {"id":"55105","name":"Mysimba : EPAR - Risk management plan","type":"rmp","status":"Adopted","consultation_date":"","first_published_date":"2022-05-30T08:58:00Z","last_updated_date":"2026-04-10T13:15:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/mysimba-epar-risk-management-plan_en.pdf"},
    {"id":"55157","name":"Cabometyx : EPAR - Risk-management-plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2022-06-09T08:51:00Z","last_updated_date":"2025-09-17T14:57:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/cabometyx-epar-risk-management-plan_en.pdf"},
    {"id":"55199","name":"Carvykti : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2022-06-13T09:46:00Z","last_updated_date":"2026-03-13T14:51:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/carvykti-epar-risk-management-plan_en.pdf"},
    {"id":"55297","name":"Camcevi : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2022-06-20T11:28:00Z","last_updated_date":"2026-05-11T15:22:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/camcevi-epar-risk-management-plan_en.pdf"},
    {"id":"55340","name":"COVID-19 Vaccine (inactivated, adjuvanted) Valneva : EPAR - Risk-management-plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2022-06-23T16:00:00Z","last_updated_date":"2022-07-01T12:22:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/covid-19-vaccine-inactivated-adjuvanted-valneva-epar-risk-management-plan_en.pdf"},
    {"id":"55442","name":"Yselty : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2022-07-01T15:22:00Z","last_updated_date":"2025-11-21T14:46:17Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/yselty-epar-risk-management-plan_en.pdf"},
    {"id":"55446","name":"Filsuvez : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2022-07-04T12:09:00Z","last_updated_date":"2025-07-11T12:42:20Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/filsuvez-epar-risk-management-plan_en.pdf"},
    {"id":"55537","name":"Dexdor : EPAR - Risk Management Plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2023-06-20T09:22:00Z","last_updated_date":"2025-06-11T11:20:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/dexdor-epar-risk-management-plan_en.pdf"},
    {"id":"55618","name":"Sugammadex Fresenius Kabi : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2022-07-21T14:45:00Z","last_updated_date":"2025-07-11T14:32:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/sugammadex-fresenius-kabi-epar-risk-management-plan_en.pdf"},
    {"id":"55700","name":"Xenpozyme : EPAR - Risk-management-plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2022-07-27T14:53:00Z","last_updated_date":"2025-05-27T17:08:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/xenpozyme-epar-risk-management-plan_en.pdf"},
    {"id":"55708","name":"Nexviadyme : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2022-07-27T16:44:00Z","last_updated_date":"2026-01-23T14:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/nexviadyme-epar-risk-management-plan_en.pdf"},
    {"id":"55858","name":"Pepaxti : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2022-08-22T14:30:00Z","last_updated_date":"2024-10-24T15:03:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/pepaxti-epar-risk-management-plan_en.pdf"},
    {"id":"55875","name":"Sunlenca : EPAR - Risk management plan ","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2022-08-25T14:46:00Z","last_updated_date":"2025-07-14T16:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/sunlenca-epar-risk-management-plan_en.pdf"},
    {"id":"56000","name":"Roctavian : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2022-09-06T15:38:00Z","last_updated_date":"2026-01-14T12:33:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/roctavian-epar-risk-management-plan_en.pdf"},
    {"id":"56008","name":"Scemblix : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2022-09-07T11:57:00Z","last_updated_date":"2026-04-30T16:33:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/scemblix-epar-risk-management-plan_en.pdf"},
    {"id":"56025","name":"Procysbi : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2022-09-08T08:57:00Z","last_updated_date":"2026-05-19T12:12:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/procysbi-epar-risk-management-plan_en.pdf"},
    {"id":"56062","name":"Vyvgart : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2022-09-12T10:52:00Z","last_updated_date":"2026-01-23T13:39:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/vyvgart-epar-risk-management-plan_en.pdf"},
    {"id":"56141","name":"Opdualag : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2022-09-20T15:14:00Z","last_updated_date":"2026-04-07T13:50:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/opdualag-epar-risk-management-plan_en.pdf"},
    {"id":"56146","name":"Lupkynis : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2022-09-20T15:53:00Z","last_updated_date":"2024-07-25T10:35:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/lupkynis-epar-risk-management-plan_en.pdf"},
    {"id":"56157","name":"Illuzyce : EPAR - Risk Management Plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2023-06-07T15:22:00Z","last_updated_date":"2023-06-07T15:22:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/illuzyce-epar-risk-management-plan_en.pdf"},
    {"id":"56162","name":"Tezspire : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2022-09-21T12:01:00Z","last_updated_date":"2025-10-22T15:57:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/tezspire-epar-risk-management-plan_en.pdf"},
    {"id":"56259","name":"Nulibry : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2022-09-29T15:35:00Z","last_updated_date":"2022-09-29T15:35:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/nulibry-epar-risk-management-plan_en.pdf"},
    {"id":"56308","name":"Ranivisio : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2022-10-04T11:53:00Z","last_updated_date":"2025-05-27T11:21:46Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/ranivisio-epar-risk-management-plan_en.pdf"},
    {"id":"56369","name":"Amvuttra : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2022-10-12T12:31:00Z","last_updated_date":"2025-06-12T15:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/amvuttra-epar-risk-management-plan_en.pdf"},
    {"id":"56373","name":"Ritonavir Mylan : EPAR - Risk Management Plan ","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2022-10-12T14:48:00Z","last_updated_date":"2026-03-26T10:33:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/ritonavir-mylan-epar-risk-management-plan_en.pdf"},
    {"id":"56386","name":"Tecvayli : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2022-10-13T11:32:00Z","last_updated_date":"2025-06-04T14:55:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/tecvayli-epar-risk-management-plan_en.pdf"},
    {"id":"56395","name":"Vabysmo : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2022-10-13T12:00:00Z","last_updated_date":"2025-07-14T17:12:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/vabysmo-epar-risk-management-plan_en.pdf"},
    {"id":"56445","name":"Thalidomide Lipomed : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2022-10-20T14:11:00Z","last_updated_date":"2025-09-15T14:47:32Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/thalidomide-lipomed-epar-risk-management-plan_en.pdf"},
    {"id":"56553","name":"VidPrevtyn Beta : EPAR - Risk-management-plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2022-11-11T14:54:00Z","last_updated_date":"2024-03-20T13:20:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/vidprevtyn-beta-epar-risk-management-plan_en.pdf"},
    {"id":"56619","name":"Teriflunomide Accord : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2022-11-14T16:17:00Z","last_updated_date":"2024-05-02T15:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/teriflunomide-accord-epar-risk-management-plan_en.pdf"},
    {"id":"56629","name":"Beyfortus : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2022-11-15T15:39:00Z","last_updated_date":"2024-10-07T11:47:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/beyfortus-epar-risk-management-plan_en.pdf"},
    {"id":"56697","name":"Enjaymo : EPAR - Risk Management Plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2022-11-17T17:03:00Z","last_updated_date":"2022-11-17T17:03:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/enjaymo-epar-risk-management-plan_en.pdf"},
    {"id":"56772","name":"Livtencity : EPAR - Risk Management Plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2022-11-24T10:25:00Z","last_updated_date":"2025-10-22T12:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/livtencity-epar-risk-management-plan_en.pdf"},
    {"id":"56781","name":"Mounjaro : EPAR - Risk Management Plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2022-11-25T09:07:00Z","last_updated_date":"2024-02-21T10:06:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/mounjaro-epar-risk-management-plan_en.pdf"},
    {"id":"56786","name":"Sorafenib Accord : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2025-09-30T09:46:00Z","last_updated_date":"2025-09-30T09:46:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/sorafenib-accord-epar-risk-management-plan_en.pdf"},
    {"id":"56818","name":"Biktarvy : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2022-11-28T16:36:00Z","last_updated_date":"2025-02-27T09:46:07Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/biktarvy-epar-risk-management-plan_en.pdf"},
    {"id":"56857","name":"Xalkori : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2022-12-02T10:06:00Z","last_updated_date":"2026-01-08T15:38:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/xalkori-epar-risk-management-plan_en.pdf"},
    {"id":"56874","name":"Pyrukynd : EPAR - Risk Management Plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2022-12-05T10:54:00Z","last_updated_date":"2026-05-21T16:30:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/pyrukynd-epar-risk-management-plan_en.pdf"},
    {"id":"56885","name":"Nexavar : EPAR - Risk Management Plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2022-12-06T11:13:00Z","last_updated_date":"2025-03-28T12:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/nexavar-epar-risk-management-plan_en.pdf"},
    {"id":"56886","name":"Zytiga : EPAR - Risk Management Plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2022-12-06T11:18:00Z","last_updated_date":"2023-12-06T15:12:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/zytiga-epar-risk-management-plan_en.pdf"},
    {"id":"56999","name":"Livmarli : EPAR - Risk Management Plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2022-12-14T11:52:00Z","last_updated_date":"2026-04-17T16:07:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/livmarli-epar-risk-management-plan_en.pdf"},
    {"id":"57085","name":"Qdenga : EPAR - Risk Management Plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2022-12-16T13:37:00Z","last_updated_date":"2024-12-11T12:04:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/qdenga-epar-risk-management-plan_en.pdf"},
    {"id":"57120","name":"Pluvicto : EPAR - Risk-management-plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2022-12-21T17:02:00Z","last_updated_date":"2022-12-21T17:02:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/pluvicto-epar-risk-management-plan_en.pdf"},
    {"id":"57126","name":"Locametz: EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2022-12-21T17:41:00Z","last_updated_date":"2025-09-15T14:47:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/locametz-epar-risk-management-plan_en.pdf"},
    {"id":"57142","name":"Mycapssa: EPAR - Risk-management-plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2022-12-22T12:58:00Z","last_updated_date":"2025-03-21T10:40:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/mycapssa-epar-risk-management-plan_en.pdf"},
    {"id":"57150","name":"Eladynos : EPAR - Risk-management-plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2022-12-22T17:30:00Z","last_updated_date":"2022-12-22T17:30:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/eladynos-epar-risk-management-plan_en.pdf"},
    {"id":"57224","name":"Ebvallo : EPAR - Risk Management Plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2023-01-11T15:27:00Z","last_updated_date":"2023-01-11T15:27:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/ebvallo-epar-risk-management-plan_en.pdf"},
    {"id":"57292","name":"Sugammadex Amomed : EPAR - Risk Management Plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2023-01-13T16:33:00Z","last_updated_date":"2025-06-25T13:35:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/sugammadex-amomed-epar-risk-management-plan_en.pdf"},
    {"id":"57315","name":"Pirfenidone Viatris : EPAR - Risk Management Plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2023-01-17T17:19:00Z","last_updated_date":"2023-11-28T18:12:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/pirfenidone-viatris-epar-risk-management-plan_en.pdf"},
    {"id":"57402","name":"Zynlonta : EPAR - Risk Management Plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2023-01-26T13:55:00Z","last_updated_date":"2023-01-26T13:55:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/zynlonta-epar-risk-management-plan_en.pdf"},
    {"id":"57510","name":"Stribild : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2023-02-02T14:47:00Z","last_updated_date":"2025-08-13T15:32:52Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/stribild-epar-risk-management-plan_en.pdf"},
    {"id":"57576","name":"Spevigo : EPAR - Risk Management Plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2023-02-08T15:41:00Z","last_updated_date":"2025-08-21T12:52:08Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/spevigo-epar-risk-management-plan_en.pdf"},
    {"id":"57813","name":"Aloxi : EPAR - Risk-management-plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2023-02-24T10:41:00Z","last_updated_date":"2023-02-24T10:41:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/aloxi-epar-risk-management-plan_en.pdf"},
    {"id":"57838","name":"Hemgenix : EPAR - Risk Management Plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2023-02-28T12:31:00Z","last_updated_date":"2023-02-28T12:31:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/hemgenix-epar-risk-management-plan_en.pdf"},
    {"id":"57865","name":"Imjudo : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2023-03-02T15:56:00Z","last_updated_date":"2023-03-02T15:56:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/imjudo-epar-risk-management-plan_en.pdf"},
    {"id":"58121","name":"NovoRapid : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2023-03-22T13:39:00Z","last_updated_date":"2024-02-27T11:53:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/novorapid-epar-risk-management-plan_en.pdf"},
    {"id":"58239","name":"Bimervax : EPAR - Risk-management-plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2023-03-31T08:45:00Z","last_updated_date":"2025-06-11T11:07:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/bimervax-epar-risk-management-plan_en.pdf"},
    {"id":"58266","name":"Sotyktu : EPAR - Risk Management Plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2023-03-31T17:23:00Z","last_updated_date":"2026-06-03T13:16:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/sotyktu-epar-risk-management-plan_en.pdf"},
    {"id":"58275","name":"Tremelimumab AstraZeneca : EPAR - Risk Management Plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2023-04-04T10:13:00Z","last_updated_date":"2024-08-22T10:39:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/tremelimumab-astrazeneca-epar-risk-management-plan_en.pdf"},
    {"id":"58487","name":"Opzelura : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2023-04-20T15:04:00Z","last_updated_date":"2025-07-28T14:44:15Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/opzelura-epar-risk-management-plan_en.pdf"},
    {"id":"58554","name":"Emend : EPAR - Risk Management Plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2023-04-28T16:46:00Z","last_updated_date":"2023-04-28T16:46:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/emend-epar-risk-management-plan_en.pdf"},
    {"id":"58596","name":"Elfabrio : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2023-05-08T15:02:00Z","last_updated_date":"2026-03-17T15:40:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/elfabrio-epar-risk-management-plan_en.pdf"},
    {"id":"58653","name":"Tibsovo : EPAR - Risk Management Plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2023-05-12T12:14:00Z","last_updated_date":"2025-09-03T15:58:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/tibsovo-epar-risk-management-plan_en.pdf"},
    {"id":"58664","name":"TachoSil : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2023-05-12T15:22:00Z","last_updated_date":"2025-06-17T13:52:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/tachosil-epar-risk-management-plan_en.pdf"},
    {"id":"58699","name":"Xofigo : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2023-05-16T12:02:00Z","last_updated_date":"2025-07-28T14:01:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/xofigo-epar-risk-management-plan_en.pdf"},
    {"id":"58822","name":"Epysqli : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2023-05-31T11:04:00Z","last_updated_date":"2024-03-18T10:14:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/epysqli-epar-risk-management-plan_en.pdf"},
    {"id":"58830","name":"Dabigatran Etexilate Accord : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2023-05-31T13:45:00Z","last_updated_date":"2026-04-22T15:28:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/dabigatran-etexilate-accord-epar-risk-management-plan_en.pdf"},
    {"id":"58836","name":"Vafseo: EPAR - Risk-management-plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2023-05-31T14:11:00Z","last_updated_date":"2023-05-31T14:11:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/vafseo-epar-risk-management-plan_en.pdf"},
    {"id":"58887","name":"Omvoh : EPAR - Risk Management Plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2023-06-08T12:12:00Z","last_updated_date":"2025-02-21T12:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/omvoh-epar-risk-management-plan_en.pdf"},
    {"id":"58940","name":"Rxulti : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2023-06-14T14:38:00Z","last_updated_date":"2025-04-04T09:35:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/rxulti-epar-risk-management-plan_en.pdf"},
    {"id":"59098","name":"Cymbalta : EPAR - Risk-management-plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2023-06-27T08:58:00Z","last_updated_date":"2023-06-27T08:58:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/cymbalta-epar-risk-management-plan_en.pdf"},
    {"id":"59320","name":"Vipdomet : EPAR - Risk Management Plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2023-07-11T12:25:00Z","last_updated_date":"2024-01-31T10:10:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/vipdomet-epar-risk-management-plan_en.pdf"},
    {"id":"59348","name":"Briumvi : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2023-07-13T14:17:00Z","last_updated_date":"2023-12-15T15:19:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/briumvi-epar-risk-management-plan_en.pdf"},
    {"id":"59360","name":"Xgeva : Risk-managment-plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2023-07-17T09:47:00Z","last_updated_date":"2026-03-19T12:22:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/xgeva-risk-managment-plan_en.pdf"},
    {"id":"59378","name":"Columvi : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2023-07-18T11:53:00Z","last_updated_date":"2025-06-11T09:51:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/columvi-epar-risk-management-plan_en.pdf"},
    {"id":"59386","name":"Lytgobi : EPAR - Risk-management-plan","type":"rmp","status":"Adopted","consultation_date":"","first_published_date":"2023-07-18T12:36:00Z","last_updated_date":"2023-07-18T12:36:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/lytgobi-epar-risk-management-plan_en.pdf"},
    {"id":"59548","name":"Ebymect : EPAR - Risk-management-plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2015-11-23T14:19:00Z","last_updated_date":"2025-12-18T15:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/ebymect-epar-risk-management-plan_en.pdf"},
    {"id":"59631","name":"Aquipta : EPAR - Risk Management Plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2023-08-25T10:48:00Z","last_updated_date":"2024-06-28T12:38:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/aquipta-epar-risk-management-plan_en.pdf"},
    {"id":"60007","name":"Abrysvo : EPAR - Risk Management Plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2023-09-15T09:00:00Z","last_updated_date":"2025-06-02T19:03:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/abrysvo-epar-risk-management-plan_en.pdf"},
    {"id":"60050","name":"Litfulo : EPAR - Risk Management Plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2023-09-18T15:48:00Z","last_updated_date":"2025-03-03T13:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/litfulo-epar-risk-management-plan_en.pdf"},
    {"id":"60080","name":"Apretude : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2023-09-20T15:57:00Z","last_updated_date":"2025-02-19T13:38:20Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/apretude-epar-risk-management-plan_en.pdf"},
    {"id":"60088","name":"Talvey : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2023-09-21T11:28:00Z","last_updated_date":"2025-10-22T15:19:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/talvey-epar-risk-management-plan_en.pdf"},
    {"id":"60190","name":"Tyruko : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2023-09-28T08:53:00Z","last_updated_date":"2026-03-06T10:23:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/tyruko-epar-risk-management-plan_en.pdf"},
    {"id":"60217","name":"Lyfnua : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2023-09-29T15:16:00Z","last_updated_date":"2023-09-29T15:16:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/lyfnua-epar-risk-management-plan_en.pdf"},
    {"id":"60228","name":"Tevimbra : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2023-10-02T15:34:00Z","last_updated_date":"2025-12-02T10:27:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/tevimbra-epar-risk-management-plan_en.pdf"},
    {"id":"60241","name":"Yesafili : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2023-10-03T13:31:00Z","last_updated_date":"2025-07-18T22:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/yesafili-epar-risk-management-plan_en.pdf"},
    {"id":"60263","name":"Tepkinly : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2023-10-05T09:27:00Z","last_updated_date":"2024-10-30T10:25:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/tepkinly-epar-risk-management-plan_en.pdf"},
    {"id":"60293","name":"Orserdu : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2023-10-09T10:52:00Z","last_updated_date":"2023-10-09T10:52:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/orserdu-epar-risk-management-plan_en.pdf"},
    {"id":"60450","name":"Fintepla : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2023-10-18T16:01:00Z","last_updated_date":"2026-05-07T11:48:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/fintepla-epar-risk-management-plan_en.pdf"},
    {"id":"60509","name":"Sprycel : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2023-10-30T15:08:00Z","last_updated_date":"2025-06-18T16:55:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/sprycel-epar-risk-management-plan_en.pdf"},
    {"id":"60571","name":"Otezla : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2015-02-16T01:00:00Z","last_updated_date":"2024-10-22T08:47:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/otezla-epar-risk-management-plan_en.pdf"},
    {"id":"60698","name":"Pradaxa : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2023-03-22T14:24:00Z","last_updated_date":"2025-12-16T14:02:24Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/pradaxa-epar-risk-management-plan_en.pdf"},
    {"id":"60716","name":"Vidaza : EPAR - Risk-management-plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2023-06-15T14:24:00Z","last_updated_date":"2023-06-15T14:24:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/vidaza-epar-risk-management-plan_en.pdf"},
    {"id":"60854","name":"Zoonotic Influenza Vaccine Seqirus: EPAR - Risk-management-plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2023-11-10T12:05:00Z","last_updated_date":"2025-06-27T12:30:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/zoonotic-influenza-vaccine-seqirus-epar-risk-management-plan_en.pdf"},
    {"id":"60924","name":"Ebglyss : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2023-11-21T16:21:52Z","last_updated_date":"2026-03-20T10:14:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/ebglyss-epar-risk-management-plan_en.pdf"},
    {"id":"60941","name":"Jaypirca : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2023-11-20T15:18:56Z","last_updated_date":"2025-04-25T09:45:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/jaypirca-epar-risk-management-plan_en.pdf"},
    {"id":"60951","name":"Vanflyta : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2023-11-21T11:25:20Z","last_updated_date":"2023-11-21T11:25:20Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/vanflyta-epar-risk-management-plan_en.pdf"},
    {"id":"61060","name":"Takhzyro : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2023-11-22T10:44:01Z","last_updated_date":"2025-06-02T15:49:06Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/takhzyro-epar-risk-management-plan_en.pdf"},
    {"id":"61082","name":"Inaqovi : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2023-11-30T16:06:31Z","last_updated_date":"2023-11-30T16:06:31Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/inaqovi-epar-risk-management-plan_en.pdf"},
    {"id":"61107","name":"Cialis : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2023-12-01T11:01:39Z","last_updated_date":"2024-09-11T10:16:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/cialis-epar-risk-management-plan_en.pdf"},
    {"id":"61262","name":"Yorvipath : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2023-12-06T09:23:09Z","last_updated_date":"2023-12-06T09:23:09Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/yorvipath-epar-risk-management-plan_en.pdf"},
    {"id":"61331","name":"Zilbrysq : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2023-12-08T11:25:57Z","last_updated_date":"2023-12-08T11:25:57Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/zilbrysq-epar-risk-management-plan_en.pdf"},
    {"id":"61343","name":"Faslodex : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2023-12-08T16:47:19Z","last_updated_date":"2023-12-08T16:47:19Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/faslodex-epar-risk-management-plan_en.pdf"},
    {"id":"61383","name":"Brineura : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2023-12-12T13:15:50Z","last_updated_date":"2023-12-12T13:15:50Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/brineura-epar-risk-management-plan_en.pdf"},
    {"id":"61608","name":"Loargys: EPAR - Risk Management Plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2023-12-22T16:35:24Z","last_updated_date":"2025-12-09T10:43:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/loargys-epar-risk-management-plan_en.pdf"},
    {"id":"61626","name":"Agamree : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2024-01-04T14:25:00Z","last_updated_date":"2024-11-15T15:07:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/agamree-epar-risk-management-plan_en.pdf"},
    {"id":"61680","name":"Renvela : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2024-01-10T08:57:19Z","last_updated_date":"2024-01-10T08:57:19Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/renvela-epar-risk-management-plan_en.pdf"},
    {"id":"61757","name":"Leflunomide Zentiva (previously Leflunomide Winthrop) : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2024-01-15T12:05:29Z","last_updated_date":"2024-01-15T12:05:29Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/leflunomide-zentiva-previously-leflunomide-winthrop-epar-risk-management-plan_en.pdf"},
    {"id":"61777","name":"Veltassa : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2024-01-16T12:17:42Z","last_updated_date":"2024-01-16T12:17:42Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/veltassa-epar-risk-management-plan_en.pdf"},
    {"id":"61796","name":"Spexotras : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2024-01-17T14:28:40Z","last_updated_date":"2025-02-18T15:27:13Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/spexotras-epar-risk-management-plan_en.pdf"},
    {"id":"61881","name":"Elrexfio : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2024-01-25T11:36:14Z","last_updated_date":"2025-07-16T16:30:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/elrexfio-epar-risk-management-plan_en.pdf"},
    {"id":"61964","name":"Rimmyrah : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2024-01-31T11:12:23Z","last_updated_date":"2024-01-31T11:12:23Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/rimmyrah-epar-risk-management-plan_en.pdf"},
    {"id":"62023","name":"Uzpruvo : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2024-02-07T15:03:36Z","last_updated_date":"2025-03-11T13:55:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/uzpruvo-epar-risk-management-plan_en.pdf"},
    {"id":"62037","name":"Omjjara : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2024-02-08T11:26:54Z","last_updated_date":"2024-02-08T11:26:54Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/omjjara-epar-risk-management-plan_en.pdf"},
    {"id":"62043","name":"Elucirem : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2024-02-08T12:01:52Z","last_updated_date":"2026-02-10T14:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/elucirem-epar-risk-management-plan_en.pdf"},
    {"id":"62092","name":"Vueway : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2024-02-13T11:33:44Z","last_updated_date":"2026-02-10T13:42:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/vueway-epar-risk-management-plan_en.pdf"},
    {"id":"62176","name":"Mevlyq : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2024-02-15T12:26:28Z","last_updated_date":"2024-02-15T12:26:28Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/mevlyq-epar-risk-management-plan_en.pdf"},
    {"id":"62194","name":"Besponsa : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2024-02-15T14:17:13Z","last_updated_date":"2026-05-18T12:38:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/besponsa-epar-risk-management-plan_en.pdf"},
    {"id":"62241","name":"Tysabri : EPAR - Risk-management-plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2024-02-21T15:30:01Z","last_updated_date":"2026-05-26T13:01:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/tysabri-epar-risk-management-plan_en.pdf"},
    {"id":"62250","name":"Herceptin : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2024-02-22T10:09:52Z","last_updated_date":"2026-03-02T11:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/herceptin-epar-risk-management-plan_en.pdf"},
    {"id":"62258","name":"Azacitidine Kabi : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2024-02-22T14:48:20Z","last_updated_date":"2024-02-22T14:48:20Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/azacitidine-kabi-epar-risk-management-plan_en.pdf"},
    {"id":"62296","name":"Skyclarys : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2024-02-26T12:21:21Z","last_updated_date":"2024-02-26T12:21:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/skyclarys-epar-risk-management-plan_en.pdf"},
    {"id":"62301","name":"Rystiggo : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2024-02-26T14:37:11Z","last_updated_date":"2024-12-11T11:02:54Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/rystiggo-epar-risk-management-plan_en.pdf"},
    {"id":"62335","name":"Casgevy : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2024-02-28T12:57:05Z","last_updated_date":"2026-02-19T11:11:01Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/casgevy-epar-risk-management-plan_en.pdf"},
    {"id":"62359","name":"Spravato : EPAR - Risk-management-plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2024-02-29T14:35:00Z","last_updated_date":"2025-09-10T14:22:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/spravato-epar-risk-management-plan_en.pdf"},
    {"id":"62432","name":"Aclasta : EPAR - Risk-management-plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2024-03-04T17:20:26Z","last_updated_date":"2024-03-04T17:20:26Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/aclasta-epar-risk-management-plan_en.pdf"},
    {"id":"62551","name":"Ibuprofen Gen.Orph : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2024-03-12T13:00:03Z","last_updated_date":"2024-03-12T13:00:03Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/ibuprofen-genorph-epar-risk-management-plan_en.pdf"},
    {"id":"62559","name":"Prevenar 20 (previously Apexxnar) : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2024-03-12T15:26:30Z","last_updated_date":"2024-04-26T17:49:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/prevenar-20-previously-apexxnar-epar-risk-management-plan_en.pdf"},
    {"id":"62589","name":"Krazati : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2024-03-13T11:20:53Z","last_updated_date":"2025-12-02T10:35:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/krazati-epar-risk-management-plan_en.pdf"},
    {"id":"62672","name":"Dabigatran Etexilate Leon Farma : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2024-03-21T12:16:56Z","last_updated_date":"2024-09-26T11:18:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/dabigatran-etexilate-leon-farma-epar-risk-management-plan_en.pdf"},
    {"id":"62716","name":"Exblifep : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2024-03-22T16:28:14Z","last_updated_date":"2024-03-22T16:28:14Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/exblifep-epar-risk-management-plan_en.pdf"},
    {"id":"62817","name":"Niapelf : EPAR - Risk Management Plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2024-04-04T15:01:52Z","last_updated_date":"2024-04-04T15:01:52Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/niapelf-epar-risk-management-plan_en.pdf"},
    {"id":"62889","name":"Abraxane : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2024-04-10T13:35:48Z","last_updated_date":"2024-04-10T13:35:48Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/abraxane-epar-risk-management-plan_en.pdf"},
    {"id":"63028","name":"Nintedanib Accord : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2024-04-22T10:30:28Z","last_updated_date":"2025-08-29T10:39:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/nintedanib-accord-epar-risk-management-plan_en.pdf"},
    {"id":"63113","name":"Kisplyx : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2024-04-30T12:58:00Z","last_updated_date":"2025-05-23T13:59:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/kisplyx-epar-risk-management-plan_en.pdf"},
    {"id":"63124","name":"Zynyz : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2024-05-02T09:30:00Z","last_updated_date":"2026-03-18T12:30:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/zynyz-epar-risk-management-plan_en.pdf"},
    {"id":"63138","name":"Celldemic : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2024-05-02T13:07:00Z","last_updated_date":"2024-05-02T13:07:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/celldemic-epar-risk-management-plan_en.pdf"},
    {"id":"63144","name":"Incellipan : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2024-05-02T14:13:00Z","last_updated_date":"2024-05-02T14:13:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/incellipan-epar-risk-management-plan_en.pdf"},
    {"id":"63179","name":"Emblaveo : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2024-05-07T09:33:00Z","last_updated_date":"2024-05-07T09:33:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/emblaveo-epar-risk-management-plan_en.pdf"},
    {"id":"63257","name":"Voydeya : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2024-05-17T14:35:00Z","last_updated_date":"2024-05-17T14:35:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/voydeya-epar-risk-management-plan_en.pdf"},
    {"id":"63277","name":"Apremilast Accord : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2024-05-21T11:06:00Z","last_updated_date":"2024-05-21T11:06:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/apremilast-accord-epar-risk-management-plan_en.pdf"},
    {"id":"63307","name":"Tizveni : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2024-05-23T14:56:00Z","last_updated_date":"2024-08-02T11:25:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/tizveni-epar-risk-management-plan_en.pdf"},
    {"id":"63334","name":"Betmiga : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2024-05-28T11:28:00Z","last_updated_date":"2024-09-05T11:11:01Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/betmiga-epar-risk-management-plan_en.pdf"},
    {"id":"63346","name":"Filspari : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2024-05-28T15:27:00Z","last_updated_date":"2025-04-30T10:55:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/filspari-epar-risk-management-plan_en.pdf"},
    {"id":"63359","name":"Omlyclo : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2024-05-29T11:32:00Z","last_updated_date":"2025-04-24T15:05:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/omlyclo-epar-risk-management-plan_en.pdf"},
    {"id":"63365","name":"Jyseleca : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2024-05-29T13:22:00Z","last_updated_date":"2024-05-29T13:22:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/jyseleca-epar-risk-management-plan_en.pdf"},
    {"id":"63390","name":"Orgalutran : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2024-05-30T10:00:00Z","last_updated_date":"2024-05-30T10:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/orgalutran-epar-risk-management-plan_en.pdf"},
    {"id":"63441","name":"Lytenava : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2024-05-31T15:50:00Z","last_updated_date":"2024-05-31T15:50:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/lytenava-epar-risk-management-plan_en.pdf"},
    {"id":"63453","name":"Awiqli : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2024-06-03T12:52:00Z","last_updated_date":"2025-11-17T16:18:59Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/awiqli-epar-risk-management-plan_en.pdf"},
    {"id":"63508","name":"Jubbonti : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2024-06-06T11:17:00Z","last_updated_date":"2024-06-06T11:17:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/jubbonti-epar-risk-management-plan_en.pdf"},
    {"id":"63531","name":"Parsabiv : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2024-06-07T11:01:00Z","last_updated_date":"2024-06-07T11:01:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/parsabiv-epar-risk-management-plan_en.pdf"},
    {"id":"63560","name":"Pyzchiva : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2024-06-11T12:40:00Z","last_updated_date":"2025-10-30T10:53:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/pyzchiva-epar-risk-management-plan_en.pdf"},
    {"id":"63600","name":"Fabhalta : EPAR - Risk-management-plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2024-06-14T12:00:00Z","last_updated_date":"2025-04-11T14:22:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/fabhalta-epar-risk-management-plan_en.pdf"},
    {"id":"63610","name":"Qalsody : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2024-06-14T12:22:17Z","last_updated_date":"2026-05-11T09:34:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/qalsody-epar-risk-management-plan_en.pdf"},
    {"id":"63647","name":"Wyost : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2024-06-17T12:56:00Z","last_updated_date":"2024-06-17T12:56:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/wyost-epar-risk-management-plan_en.pdf"},
    {"id":"63679","name":"Neoatricon : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2024-06-19T11:45:00Z","last_updated_date":"2024-06-19T11:45:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/neoatricon-epar-risk-management-plan_en.pdf"},
    {"id":"63684","name":"Alecensa : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2024-06-19T12:42:00Z","last_updated_date":"2024-06-19T12:42:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/alecensa-epar-risk-management-plan_en.pdf"},
    {"id":"63724","name":"Constella : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2024-06-24T13:00:00Z","last_updated_date":"2024-06-24T13:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/constella-epar-risk-management-plan_en.pdf"},
    {"id":"63756","name":"Fluenz : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2024-06-26T14:24:00Z","last_updated_date":"2024-06-26T14:24:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/fluenz-epar-risk-management-plan_en.pdf"},
    {"id":"63780","name":"Xydalba : EPAR - Risk-management-plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2024-06-27T11:11:01Z","last_updated_date":"2025-05-06T15:27:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/xydalba-epar-risk-management-plan_en.pdf"},
    {"id":"63824","name":"Agilus : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2024-07-01T14:59:00Z","last_updated_date":"2024-07-01T14:59:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/agilus-epar-risk-management-plan_en.pdf"},
    {"id":"64023","name":"Truqap : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2024-07-11T11:11:01Z","last_updated_date":"2025-03-07T12:20:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/truqap-epar-risk-management-plan_en.pdf"},
    {"id":"64199","name":"Ixchiq : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2024-07-18T11:39:00Z","last_updated_date":"2025-09-24T11:36:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/ixchiq-epar-risk-management-plan_en.pdf"},
    {"id":"64453","name":"Durveqtix : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2024-08-01T09:26:49Z","last_updated_date":"2025-06-04T11:42:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/durveqtix-epar-risk-management-plan_en.pdf"},
    {"id":"64458","name":"Dasatinib Accord Healthcare : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2024-08-01T09:50:57Z","last_updated_date":"2025-11-13T09:25:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/dasatinib-accord-healthcare-epar-risk-management-plan_en.pdf"},
    {"id":"64463","name":"Pomalidomide Krka : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2024-08-01T10:13:09Z","last_updated_date":"2024-08-01T10:13:09Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/pomalidomide-krka-epar-risk-management-plan_en.pdf"},
    {"id":"64469","name":"Pomalidomide Zentiva : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2024-08-01T10:54:16Z","last_updated_date":"2026-05-26T15:46:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/pomalidomide-zentiva-epar-risk-management-plan_en.pdf"},
    {"id":"64480","name":"Velsipity : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2024-08-01T17:17:25Z","last_updated_date":"2025-06-17T16:33:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/velsipity-epar-risk-management-plan_en.pdf"},
    {"id":"64487","name":"Apexelsin : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2024-08-02T12:30:31Z","last_updated_date":"2024-08-02T12:30:31Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/apexelsin-epar-risk-management-plan_en.pdf"},
    {"id":"64617","name":"GalliaPharm : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2024-08-22T13:50:18Z","last_updated_date":"2024-08-22T13:50:18Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/galliapharm-epar-risk-management-plan_en.pdf"},
    {"id":"64625","name":"Zegalogue : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2024-08-23T15:20:32Z","last_updated_date":"2024-08-23T15:20:32Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/zegalogue-epar-risk-management-plan_en.pdf"},
    {"id":"64657","name":"Balversa : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2024-08-29T13:36:19Z","last_updated_date":"2024-08-29T13:36:19Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/balversa-epar-risk-management-plan_en.pdf"},
    {"id":"64667","name":"Piasky : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2024-08-30T11:26:59Z","last_updated_date":"2026-02-10T10:30:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/piasky-epar-risk-management-plan_en.pdf"},
    {"id":"64691","name":"Pegasys : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2024-09-04T09:09:48Z","last_updated_date":"2024-09-04T09:09:48Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/pegasys-epar-risk-management-plan_en.pdf"},
    {"id":"64703","name":"Reagila : EPAR - Risk Management Plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2024-09-05T09:24:00Z","last_updated_date":"2024-09-05T09:24:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/reagila-epar-risk-management-plan_en.pdf"},
    {"id":"64721","name":"Eurneffy : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2024-09-05T13:27:23Z","last_updated_date":"2026-06-01T10:30:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/eurneffy-epar-risk-management-plan_en.pdf"},
    {"id":"64729","name":"mResvia : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2024-09-06T09:38:54Z","last_updated_date":"2026-04-30T11:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/mresvia-epar-risk-management-plan_en.pdf"},
    {"id":"64733","name":"Cholestagel : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2024-09-06T11:15:00Z","last_updated_date":"2024-09-06T11:15:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/cholestagel-epar-risk-management-plan_en.pdf"},
    {"id":"64755","name":"Viagra : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2024-09-06T16:00:00Z","last_updated_date":"2024-09-06T16:00:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/viagra-epar-risk-management-plan_en.pdf"},
    {"id":"64785","name":"Tadalafil Lilly : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2024-09-11T10:20:00Z","last_updated_date":"2024-09-11T10:20:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/tadalafil-lilly-epar-risk-management-plan_en.pdf"},
    {"id":"64789","name":"Steqeyma : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2024-09-11T12:50:00Z","last_updated_date":"2025-09-23T16:56:14Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/steqeyma-epar-risk-management-plan_en.pdf"},
    {"id":"64798","name":"Nilotinib Accord : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2024-09-11T15:48:00Z","last_updated_date":"2024-09-11T15:48:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/nilotinib-accord-epar-risk-management-plan_en.pdf"},
    {"id":"64850","name":"Tauvid : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2024-09-13T14:43:00Z","last_updated_date":"2024-09-13T14:43:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/tauvid-epar-risk-management-plan_en.pdf"},
    {"id":"64860","name":"Bondronat : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2024-09-16T14:47:00Z","last_updated_date":"2024-09-16T14:47:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/bondronat-epar-risk-management-plan_en.pdf"},
    {"id":"64863","name":"Bonviva : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2024-09-16T14:50:00Z","last_updated_date":"2024-09-16T14:50:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/bonviva-epar-risk-management-plan_en.pdf"},
    {"id":"64879","name":"Inflectra : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2024-09-17T15:18:00Z","last_updated_date":"2026-02-17T11:11:01Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/inflectra-epar-risk-management-plan_en.pdf"},
    {"id":"64910","name":"Ibrance : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2024-09-18T15:35:00Z","last_updated_date":"2024-09-18T15:35:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/ibrance-epar-risk-management-plan_en.pdf"},
    {"id":"64971","name":"Iqirvo : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2024-09-20T12:06:00Z","last_updated_date":"2024-09-20T12:06:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/iqirvo-epar-risk-management-plan_en.pdf"},
    {"id":"64988","name":"Kayfanda : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2024-09-23T11:43:00Z","last_updated_date":"2025-07-11T10:36:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/kayfanda-epar-risk-management-plan_en.pdf"},
    {"id":"65008","name":"Anzupgo : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2024-09-24T12:27:00Z","last_updated_date":"2024-09-24T12:27:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/anzupgo-epar-risk-management-plan_en.pdf"},
    {"id":"65013","name":"Eksunbi : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2024-09-24T12:54:00Z","last_updated_date":"2025-09-08T10:59:39Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/eksunbi-epar-risk-management-plan_en.pdf"},
    {"id":"65018","name":"Loqtorzi : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2024-09-24T13:16:00Z","last_updated_date":"2024-09-24T13:16:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/loqtorzi-epar-risk-management-plan_en.pdf"},
    {"id":"65022","name":"Amlodipine / Valsartan Mylan : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2024-09-24T13:44:00Z","last_updated_date":"2024-09-24T13:44:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/amlodipine-valsartan-mylan-epar-risk-management-plan_en.pdf"},
    {"id":"65028","name":"Winrevair : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2024-09-25T11:20:00Z","last_updated_date":"2026-03-09T09:52:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/winrevair-epar-risk-management-plan_en.pdf"},
    {"id":"65038","name":"Tuznue : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2024-09-25T15:31:00Z","last_updated_date":"2024-09-25T15:31:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/tuznue-epar-risk-management-plan_en.pdf"},
    {"id":"65104","name":"Axitinib Accord : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2024-10-02T08:54:00Z","last_updated_date":"2024-12-19T12:21:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/axitinib-accord-epar-risk-management-plan_en.pdf"},
    {"id":"65112","name":"Otulfi : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2024-10-02T14:06:00Z","last_updated_date":"2026-05-12T16:20:08Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/otulfi-epar-risk-management-plan_en.pdf"},
    {"id":"65197","name":"Fymskina : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2024-10-07T09:10:21Z","last_updated_date":"2025-07-17T12:13:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/fymskina-epar-risk-management-plan_en.pdf"},
    {"id":"65204","name":"Yuvanci : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2024-10-07T10:44:00Z","last_updated_date":"2024-10-07T10:44:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/yuvanci-epar-risk-management-plan_en.pdf"},
    {"id":"65252","name":"Enzalutamide Viatris : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2024-10-09T14:12:00Z","last_updated_date":"2024-10-09T14:12:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/enzalutamide-viatris-epar-risk-management-plan_en.pdf"},
    {"id":"65255","name":"Arexvy : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2024-10-09T14:40:00Z","last_updated_date":"2026-02-17T11:11:01Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/arexvy-epar-risk-management-plan_en.pdf"},
    {"id":"65272","name":"Dynastat : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2024-10-10T15:29:00Z","last_updated_date":"2024-10-10T15:29:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/dynastat-epar-risk-management-plan_en.pdf"},
    {"id":"65276","name":"Pergoveris : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2024-10-11T09:05:00Z","last_updated_date":"2024-10-11T09:05:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/pergoveris-epar-risk-management-plan_en.pdf"},
    {"id":"65464","name":"Akantior : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2024-10-29T09:17:50Z","last_updated_date":"2024-10-29T09:17:50Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/akantior-epar-risk-management-plan_en.pdf"},
    {"id":"65470","name":"Epruvy (previously Ranibizumab Midas) : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2024-10-29T09:46:53Z","last_updated_date":"2025-05-27T09:42:40Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/epruvy-previously-ranibizumab-midas-epar-risk-management-plan_en.pdf"},
    {"id":"65539","name":"Cejemly : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2024-11-05T09:20:07Z","last_updated_date":"2025-11-27T08:55:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/cejemly-epar-risk-management-plan_en.pdf"},
    {"id":"65571","name":"Vevizye : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2024-11-08T11:57:28Z","last_updated_date":"2024-11-08T11:57:28Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/vevizye-epar-risk-management-plan_en.pdf"},
    {"id":"65602","name":"Buccolam : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2024-11-13T09:30:21Z","last_updated_date":"2024-11-13T09:30:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/buccolam-epar-risk-management-plan_en.pdf"},
    {"id":"65714","name":"Ordspono : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2024-11-19T16:13:27Z","last_updated_date":"2024-11-19T16:13:27Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/ordspono-epar-risk-management-plan_en.pdf"},
    {"id":"65745","name":"Zubsolv : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2024-11-21T11:00:48Z","last_updated_date":"2024-11-21T11:00:48Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/zubsolv-epar-risk-management-plan_en.pdf"},
    {"id":"65849","name":"Pomalidomide Teva : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2024-11-28T09:44:02Z","last_updated_date":"2026-05-28T17:02:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/pomalidomide-teva-epar-risk-management-plan_en.pdf"},
    {"id":"65868","name":"Flucelvax : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2024-11-28T15:02:55Z","last_updated_date":"2025-04-15T12:45:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/flucelvax-epar-risk-management-plan_en.pdf"},
    {"id":"65917","name":"Fluad : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2024-12-03T12:05:25Z","last_updated_date":"2024-12-03T12:05:25Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/fluad-epar-risk-management-plan_en.pdf"},
    {"id":"65935","name":"Menveo : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2024-12-04T08:49:05Z","last_updated_date":"2024-12-04T08:49:05Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/menveo-epar-risk-management-plan_en.pdf"},
    {"id":"65961","name":"Fosavance : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2024-12-05T10:44:15Z","last_updated_date":"2024-12-05T10:44:15Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/fosavance-epar-risk-management-plan_en.pdf"},
    {"id":"65968","name":"Theralugand : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2024-12-05T12:41:38Z","last_updated_date":"2024-12-05T12:41:38Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/theralugand-epar-risk-management-plan_en.pdf"},
    {"id":"65998","name":"Adrovance : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2024-12-05T16:59:15Z","last_updated_date":"2024-12-05T16:59:15Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/adrovance-epar-risk-management-plan_en.pdf"},
    {"id":"66005","name":"Vantavo : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2024-12-05T17:21:46Z","last_updated_date":"2024-12-05T17:21:46Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/vantavo-epar-risk-management-plan_en.pdf"},
    {"id":"66042","name":"Opuviz: EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2024-12-10T11:59:00Z","last_updated_date":"2024-12-10T11:59:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/opuviz-epar-risk-management-plan_en.pdf"},
    {"id":"66060","name":"Elahere : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2024-12-10T16:37:34Z","last_updated_date":"2024-12-10T16:37:34Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/elahere-epar-risk-management-plan_en.pdf"},
    {"id":"66075","name":"Grepid : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2024-12-12T10:43:10Z","last_updated_date":"2024-12-12T10:43:10Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/grepid-epar-risk-management-plan_en.pdf"},
    {"id":"66080","name":"Penbraya :  EPAR - Risk-management-plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2024-12-12T11:08:38Z","last_updated_date":"2025-02-05T12:44:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/penbraya-epar-risk-management-plan_en.pdf"},
    {"id":"66194","name":"Firdapse : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2024-12-18T11:11:24Z","last_updated_date":"2024-12-18T11:11:24Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/firdapse-epar-risk-management-plan_en.pdf"},
    {"id":"66202","name":"Absimky : EPAR - Risk Management Plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2024-12-18T13:23:35Z","last_updated_date":"2025-12-18T12:05:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/absimky-epar-risk-management-plan_en.pdf"},
    {"id":"66207","name":"Hympavzi : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2024-12-18T14:10:26Z","last_updated_date":"2025-11-25T15:05:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/hympavzi-epar-risk-management-plan_en.pdf"},
    {"id":"66213","name":"Imuldosa : EPAR - Risk Management Plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2024-12-18T14:34:40Z","last_updated_date":"2024-12-18T14:34:40Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/imuldosa-epar-risk-management-plan_en.pdf"},
    {"id":"66275","name":"Buprenorphine Neuraxpharm : EPAR - Risk Management Plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2025-01-09T13:44:29Z","last_updated_date":"2025-01-09T13:44:29Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/buprenorphine-neuraxpharm-epar-risk-management-plan_en.pdf"},
    {"id":"66280","name":"ellaOne :  EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2025-01-09T15:11:14Z","last_updated_date":"2025-01-09T15:11:14Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/ellaone-epar-risk-management-plan_en.pdf"},
    {"id":"66325","name":"Erbitux : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2025-01-16T11:01:00Z","last_updated_date":"2025-02-19T09:42:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/erbitux-epar-risk-management-plan_en.pdf"},
    {"id":"66362","name":"Alhemo : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2025-01-17T15:51:19Z","last_updated_date":"2025-09-25T17:43:40Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/alhemo-epar-risk-management-plan_en.pdf"},
    {"id":"66379","name":"Afqlir : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2025-01-20T15:17:30Z","last_updated_date":"2025-01-20T15:17:30Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/afqlir-epar-risk-management-plan_en.pdf"},
    {"id":"66388","name":"Eltrombopag Viatris : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2025-01-21T10:24:23Z","last_updated_date":"2025-01-21T10:24:23Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/eltrombopag-viatris-epar-risk-management-plan_en.pdf"},
    {"id":"66459","name":"Ahzantive : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2025-01-24T16:48:48Z","last_updated_date":"2025-01-24T16:48:48Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/ahzantive-epar-risk-management-plan_en.pdf"},
    {"id":"66490","name":"Augtyro : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2025-01-28T16:58:45Z","last_updated_date":"2025-01-28T16:58:45Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/augtyro-epar-risk-management-plan_en.pdf"},
    {"id":"66519","name":"Nexium Control : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2025-01-30T09:34:45Z","last_updated_date":"2025-01-30T09:34:45Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/nexium-control-epar-risk-management-plan_en.pdf"},
    {"id":"66569","name":"Gohibic : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2025-02-03T12:08:20Z","last_updated_date":"2025-02-03T12:08:20Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/gohibic-epar-risk-management-plan_en.pdf"},
    {"id":"66653","name":"Ituxredi : EPAR - Risk Management Plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2025-02-10T16:08:31Z","last_updated_date":"2025-07-09T10:07:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/ituxredi-epar-risk-management-plan_en.pdf"},
    {"id":"66661","name":"Hetronifly : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2025-02-11T09:22:08Z","last_updated_date":"2026-05-13T14:05:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/hetronifly-epar-risk-management-plan_en.pdf"},
    {"id":"66671","name":"Korjuny : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2025-02-11T12:30:10Z","last_updated_date":"2025-02-11T12:30:10Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/korjuny-epar-risk-management-plan_en.pdf"},
    {"id":"66793","name":"Fasenra : EPAR - Risk Management Plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2025-02-14T16:04:43Z","last_updated_date":"2025-02-27T09:41:52Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/fasenra-epar-risk-management-plan_en.pdf"},
    {"id":"66817","name":"CellCept : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2025-02-17T11:29:41Z","last_updated_date":"2025-02-17T11:29:41Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/cellcept-epar-risk-management-plan_en.pdf"},
    {"id":"66860","name":"Siiltibcy : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2025-02-19T09:19:43Z","last_updated_date":"2025-02-19T09:19:43Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/siiltibcy-epar-risk-management-plan_en.pdf"},
    {"id":"66865","name":"Nemluvio : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2025-02-19T09:39:22Z","last_updated_date":"2025-02-19T09:39:22Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/nemluvio-epar-risk-management-plan_en.pdf"},
    {"id":"66898","name":"Yesintek : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2025-02-20T11:48:10Z","last_updated_date":"2026-05-27T16:08:52Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/yesintek-epar-risk-management-plan_en.pdf"},
    {"id":"66929","name":"Kavigale : EPAR - Risk Management Plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2026-02-25T15:18:28Z","last_updated_date":"2026-02-25T15:18:28Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/kavigale-epar-risk-management-plan_en.pdf"},
    {"id":"66950","name":"Seladelpar Gilead : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2025-02-25T13:58:44Z","last_updated_date":"2026-02-20T10:30:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/seladelpar-gilead-epar-risk-management-plan_en.pdf"},
    {"id":"66996","name":"Kostaive: EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2025-02-26T14:53:49Z","last_updated_date":"2026-06-03T14:12:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/kostaive-epar-risk-management-plan_en.pdf"},
    {"id":"67011","name":"Welireg : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2025-02-27T13:31:47Z","last_updated_date":"2025-02-27T13:31:47Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/welireg-epar-risk-management-plan_en.pdf"},
    {"id":"67076","name":"Beyonttra : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2025-03-03T14:22:46Z","last_updated_date":"2025-03-03T14:22:46Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/beyonttra-epar-risk-management-plan_en.pdf"},
    {"id":"67084","name":"Obodence : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2025-03-03T15:29:18Z","last_updated_date":"2025-03-03T15:29:18Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/obodence-epar-risk-management-plan_en.pdf"},
    {"id":"67096","name":"Baiama : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2025-03-04T13:21:22Z","last_updated_date":"2025-03-04T13:21:22Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/baiama-epar-risk-management-plan_en.pdf"},
    {"id":"67103","name":"Ibandronic acid Accord : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2025-03-04T14:48:52Z","last_updated_date":"2025-03-04T14:48:52Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/ibandronic-acid-accord-epar-risk-management-plan_en.pdf"},
    {"id":"67105","name":"Ryzodeg : EPAR - Risk Management Plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2025-03-04T15:09:19Z","last_updated_date":"2025-03-04T15:09:19Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/ryzodeg-epar-risk-management-plan_en.pdf"},
    {"id":"67133","name":"Emcitate : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2025-03-11T10:54:11Z","last_updated_date":"2025-03-11T10:54:11Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/emcitate-epar-risk-management-plan_en.pdf"},
    {"id":"67171","name":"Zefylti : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2025-03-10T15:18:35Z","last_updated_date":"2025-03-10T15:18:35Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/zefylti-epar-risk-management-plan_en.pdf"},
    {"id":"67189","name":"Andembry : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2025-03-11T14:54:43Z","last_updated_date":"2025-03-11T14:54:43Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/andembry-epar-risk-management-plan_en.pdf"},
    {"id":"67197","name":"Paxneury : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2025-03-11T15:28:58Z","last_updated_date":"2025-03-11T15:28:58Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/paxneury-epar-risk-management-plan_en.pdf"},
    {"id":"67199","name":"Rytelo : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2025-03-11T15:51:07Z","last_updated_date":"2025-03-11T15:51:07Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/rytelo-epar-risk-management-plan_en.pdf"},
    {"id":"67220","name":"Wainzua : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2025-03-12T10:32:32Z","last_updated_date":"2025-03-12T10:32:32Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/wainzua-epar-risk-management-plan_en.pdf"},
    {"id":"67310","name":"Lazcluze : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2025-03-17T15:29:38Z","last_updated_date":"2026-03-26T12:40:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/lazcluze-epar-risk-management-plan_en.pdf"},
    {"id":"67355","name":"Leflunomide ratiopharm : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2025-03-19T16:16:16Z","last_updated_date":"2025-03-19T16:16:16Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/leflunomide-ratiopharm-epar-risk-management-plan_en.pdf"},
    {"id":"67408","name":"Vimkunya : EPAR - Risk Management Plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2025-03-24T10:40:44Z","last_updated_date":"2025-03-24T10:40:44Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/vimkunya-epar-risk-management-plan_en.pdf"},
    {"id":"67437","name":"EndolucinBeta : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2025-03-25T13:17:40Z","last_updated_date":"2025-03-25T13:17:40Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/endolucinbeta-epar-risk-management-plan_en.pdf"},
    {"id":"67458","name":"Kadcyla : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2025-03-26T12:44:45Z","last_updated_date":"2025-03-26T12:44:45Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/kadcyla-epar-risk-management-plan_en.pdf"},
    {"id":"67493","name":"Eydenzelt : EPAR - Risk Management Plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2025-03-27T13:35:24Z","last_updated_date":"2025-03-27T13:35:24Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/eydenzelt-epar-risk-management-plan_en.pdf"},
    {"id":"67614","name":"Osenvelt : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2025-04-03T12:46:14Z","last_updated_date":"2025-04-03T12:46:14Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/osenvelt-epar-risk-management-plan_en.pdf"},
    {"id":"67635","name":"Avtozma : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2025-04-04T13:21:14Z","last_updated_date":"2025-04-04T13:21:14Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/avtozma-epar-risk-management-plan_en.pdf"},
    {"id":"67645","name":"Stoboclo : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2025-04-04T15:22:53Z","last_updated_date":"2025-04-04T15:22:53Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/stoboclo-epar-risk-management-plan_en.pdf"},
    {"id":"67662","name":"Tivdak : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2025-04-07T12:03:00Z","last_updated_date":"2025-04-07T12:03:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/tivdak-epar-risk-management-plan_en.pdf"},
    {"id":"67686","name":"Pavblu : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2025-04-08T12:13:58Z","last_updated_date":"2025-04-08T12:13:58Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/pavblu-epar-risk-management-plan_en.pdf"},
    {"id":"67799","name":"Capvaxive : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2025-04-14T16:27:53Z","last_updated_date":"2026-06-01T15:08:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/capvaxive-epar-risk-management-plan_en.pdf"},
    {"id":"67884","name":"Dyrupeg : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2025-04-16T16:43:14Z","last_updated_date":"2025-04-16T16:43:14Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/dyrupeg-epar-risk-management-plan_en.pdf"},
    {"id":"67924","name":"Eltrombopag Accord : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2025-04-23T09:55:14Z","last_updated_date":"2026-02-25T14:22:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/eltrombopag-accord-epar-risk-management-plan_en.pdf"},
    {"id":"68020","name":"Spedra : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2025-04-28T16:46:09Z","last_updated_date":"2025-04-28T16:46:09Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/spedra-epar-risk-management-plan_en.pdf"},
    {"id":"68063","name":"Lynozyfic : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2025-05-02T13:18:40Z","last_updated_date":"2025-05-02T13:18:40Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/lynozyfic-epar-risk-management-plan_en.pdf"},
    {"id":"68094","name":"Leqembi : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2025-05-05T16:15:40Z","last_updated_date":"2026-02-04T14:20:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/leqembi-epar-risk-management-plan_en.pdf"},
    {"id":"68129","name":"Vyjuvek : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2025-05-06T16:47:22Z","last_updated_date":"2025-05-06T16:47:22Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/vyjuvek-epar-risk-management-plan_en.pdf"},
    {"id":"68147","name":"Finlee : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2025-05-07T15:38:33Z","last_updated_date":"2025-05-07T15:38:33Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/finlee-epar-risk-management-plan_en.pdf"},
    {"id":"68205","name":"Tuzulby : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2025-05-08T16:48:13Z","last_updated_date":"2025-05-08T16:48:13Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/tuzulby-epar-risk-management-plan_en.pdf"},
    {"id":"68247","name":"Datroway : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2025-05-13T09:59:40Z","last_updated_date":"2025-05-13T09:59:40Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/datroway-epar-risk-management-plan_en.pdf"},
    {"id":"68312","name":"Deqsiga : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2025-05-16T11:05:11Z","last_updated_date":"2025-05-16T11:05:11Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/deqsiga-epar-risk-management-plan_en.pdf"},
    {"id":"68337","name":"Bylvay : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2025-05-19T11:05:14Z","last_updated_date":"2025-07-11T10:33:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/bylvay-epar-risk-management-plan_en.pdf"},
    {"id":"68430","name":"Zoledronic Acid Accord : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2025-05-23T16:16:23Z","last_updated_date":"2025-05-23T16:16:23Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/zoledronic-acid-accord-epar-risk-management-plan_en.pdf"},
    {"id":"68635","name":"Qoyvolma : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2025-06-10T12:28:08Z","last_updated_date":"2025-09-09T11:28:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/qoyvolma-epar-risk-management-plan_en.pdf"},
    {"id":"68770","name":"Xbryk : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2025-06-16T15:11:54Z","last_updated_date":"2025-06-16T15:11:54Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/xbryk-epar-risk-management-plan_en.pdf"},
    {"id":"68810","name":"Cinryze : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2025-06-18T14:02:34Z","last_updated_date":"2025-06-18T14:02:34Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/cinryze-epar-risk-management-plan_en.pdf"},
    {"id":"68873","name":"Lemtrada : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2025-06-20T15:04:54Z","last_updated_date":"2025-06-20T15:04:54Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/lemtrada-epar-risk-management-plan_en.pdf"},
    {"id":"69084","name":"Ziihera : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2025-07-03T10:49:05Z","last_updated_date":"2025-07-03T10:49:05Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/ziihera-epar-risk-management-plan_en.pdf"},
    {"id":"69103","name":"Leflunomide medac : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2025-07-04T11:58:49Z","last_updated_date":"2025-07-04T11:58:49Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/leflunomide-medac-epar-risk-management-plan_en.pdf"},
    {"id":"69194","name":"Duvyzat : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2025-07-09T15:36:50Z","last_updated_date":"2025-07-09T15:36:50Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/duvyzat-epar-risk-management-plan_en.pdf"},
    {"id":"69237","name":"Levetiracetam Accord : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2025-07-11T10:29:07Z","last_updated_date":"2025-07-11T10:29:07Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/levetiracetam-accord-epar-risk-management-plan_en.pdf"},
    {"id":"69266","name":"Tepezza : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2025-07-14T15:50:51Z","last_updated_date":"2025-07-14T15:50:51Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/tepezza-epar-risk-management-plan_en.pdf"},
    {"id":"69281","name":"Natpar : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2025-07-15T10:06:06Z","last_updated_date":"2025-07-15T10:06:06Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/natpar-epar-risk-management-plan_en.pdf"},
    {"id":"69289","name":"Trabectedin Accord : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2025-07-15T11:53:42Z","last_updated_date":"2025-07-15T11:53:42Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/trabectedin-accord-epar-risk-management-plan_en.pdf"},
    {"id":"69427","name":"Benepali : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2025-07-24T11:13:49Z","last_updated_date":"2025-12-01T15:30:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/benepali-epar-risk-management-plan_en.pdf"},
    {"id":"69529","name":"Jubereq : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2025-07-28T13:00:04Z","last_updated_date":"2025-07-28T13:00:04Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/jubereq-epar-risk-management-plan_en.pdf"},
    {"id":"69537","name":"Sephience : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2025-07-28T14:21:30Z","last_updated_date":"2025-07-28T14:21:30Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/sephience-epar-risk-management-plan_en.pdf"},
    {"id":"69546","name":"Osvyrti : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2025-07-28T15:26:31Z","last_updated_date":"2025-07-28T15:26:31Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/osvyrti-epar-risk-management-plan_en.pdf"},
    {"id":"69629","name":"Blenrep : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2025-08-01T15:22:28Z","last_updated_date":"2025-08-01T15:22:28Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/blenrep-epar-risk-management-plan_en.pdf-0"},
    {"id":"69660","name":"Emtricitabine / Tenofovir alafenamide Viatris : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2025-08-05T11:59:41Z","last_updated_date":"2025-08-05T11:59:41Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/emtricitabine-tenofovir-alafenamide-viatris-epar-risk-management-plan_en.pdf"},
    {"id":"69687","name":"Cystadrops : EPAR - Risk Management Plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2025-08-08T13:42:25Z","last_updated_date":"2025-08-08T13:42:25Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/cystadrops-epar-risk-management-plan_en.pdf"},
    {"id":"69692","name":"Wezenla : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2025-08-11T12:27:08Z","last_updated_date":"2025-08-11T12:27:08Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/wezenla-epar-risk-management-plan_en.pdf"},
    {"id":"69693","name":"Zometa : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2025-08-11T17:37:52Z","last_updated_date":"2025-08-11T17:37:52Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/zometa-epar-risk-management-plan_en.pdf"},
    {"id":"69715","name":"Dazublys: EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2025-08-12T17:37:07Z","last_updated_date":"2025-08-12T17:37:07Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/dazublys-epar-risk-management-plan_en.pdf"},
    {"id":"69770","name":"Aucatzyl: EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2025-08-19T15:23:35Z","last_updated_date":"2025-08-19T15:23:35Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/aucatzyl-epar-risk-management-plan_en.pdf"},
    {"id":"69775","name":"Usymro: EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2025-08-19T19:18:34Z","last_updated_date":"2025-08-19T19:18:34Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/usymro-epar-risk-management-plan_en.pdf"},
    {"id":"69782","name":"Ezmekly: EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2025-08-20T11:04:57Z","last_updated_date":"2025-08-20T11:04:57Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/ezmekly-epar-risk-management-plan_en.pdf"},
    {"id":"69814","name":"Evfraxy : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2025-08-21T12:01:13Z","last_updated_date":"2025-08-21T12:01:13Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/evfraxy-epar-risk-management-plan_en.pdf"},
    {"id":"69815","name":"Truxima : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2025-08-21T13:41:27Z","last_updated_date":"2025-08-21T13:41:27Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/truxima-epar-risk-management-plan_en.pdf"},
    {"id":"69821","name":"Vevzuo : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2025-08-21T14:48:39Z","last_updated_date":"2025-08-21T14:48:39Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/vevzuo-epar-risk-management-plan_en.pdf"},
    {"id":"69873","name":"Itovebi : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2025-08-27T16:25:14Z","last_updated_date":"2025-08-27T16:25:14Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/itovebi-epar-risk-management-plan_en.pdf"},
    {"id":"69896","name":"Attrogy : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2025-08-28T16:28:04Z","last_updated_date":"2025-09-17T09:08:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/attrogy-epar-risk-management-plan_en.pdf"},
    {"id":"69929","name":"Yeytuo : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2025-09-03T09:54:45Z","last_updated_date":"2025-09-03T09:54:45Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/yeytuo-epar-risk-management-plan_en.pdf"},
    {"id":"69935","name":"Junod : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2025-09-03T10:20:46Z","last_updated_date":"2025-09-03T10:20:46Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/junod-epar-risk-management-plan_en.pdf"},
    {"id":"69958","name":"Nintedanib Viatris : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2025-09-05T08:53:48Z","last_updated_date":"2025-09-05T08:53:48Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/nintedanib-viatris-epar-risk-management-plan_en.pdf"},
    {"id":"69971","name":"Zemcelpro : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2025-09-05T15:06:22Z","last_updated_date":"2025-09-05T15:06:22Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/zemcelpro-epar-risk-management-plan_en.pdf"},
    {"id":"70003","name":"Yaxwer : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2025-09-08T16:36:14Z","last_updated_date":"2025-09-08T16:36:14Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/yaxwer-epar-risk-management-plan_en.pdf"},
    {"id":"70057","name":"Ryjunea : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2025-09-11T09:18:32Z","last_updated_date":"2025-09-11T09:18:32Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/ryjunea-epar-risk-management-plan_en.pdf"},
    {"id":"70097","name":"Riulvy : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2025-09-16T17:10:43Z","last_updated_date":"2025-09-16T17:10:43Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/riulvy-epar-risk-management-plan_en.pdf"},
    {"id":"70117","name":"Bomyntra : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2025-09-17T11:56:31Z","last_updated_date":"2025-09-17T11:56:31Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/bomyntra-epar-risk-management-plan_en.pdf"},
    {"id":"70129","name":"Conexxence : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2025-09-17T15:48:24Z","last_updated_date":"2025-09-17T15:48:24Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/conexxence-epar-risk-management-plan_en.pdf"},
    {"id":"70205","name":"Romvimza : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2025-09-22T11:52:39Z","last_updated_date":"2025-09-22T11:52:39Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/romvimza-epar-risk-management-plan_en.pdf"},
    {"id":"70226","name":"Alyftrek : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2025-09-23T13:52:54Z","last_updated_date":"2025-09-23T13:52:54Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/alyftrek-epar-risk-management-plan_en.pdf"},
    {"id":"70259","name":"Emtricitabine / Rilpivirine / Tenofovir Alafenamide Viatris : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2025-09-25T09:37:49Z","last_updated_date":"2025-09-25T09:37:49Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/emtricitabine-rilpivirine-tenofovir-alafenamide-viatris-epar-risk-management-plan_en.pdf"},
    {"id":"70300","name":"Voranigo : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2025-09-26T14:46:26Z","last_updated_date":"2025-11-12T15:40:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/voranigo-epar-risk-management-plan_en.pdf"},
    {"id":"70323","name":"Zurzuvae : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2025-09-29T15:43:41Z","last_updated_date":"2025-09-29T15:43:41Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/zurzuvae-epar-risk-management-plan_en.pdf"},
    {"id":"70339","name":"Usrenty : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2025-09-30T09:27:30Z","last_updated_date":"2026-05-18T10:32:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/usrenty-epar-risk-management-plan_en.pdf"},
    {"id":"70368","name":"Maapliv : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2025-09-30T14:47:25Z","last_updated_date":"2025-09-30T14:47:25Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/maapliv-epar-risk-management-plan_en.pdf"},
    {"id":"70376","name":"Micardis : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2025-09-30T16:27:56Z","last_updated_date":"2025-09-30T16:27:56Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/micardis-epar-risk-management-plan_en.pdf"},
    {"id":"70414","name":"Vivlipeg : EPAR - Risk Management Plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2025-10-02T15:49:49Z","last_updated_date":"2025-10-02T15:49:49Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/vivlipeg-epar-risk-management-plan_en.pdf"},
    {"id":"70435","name":"Ogsiveo : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2025-10-03T11:55:19Z","last_updated_date":"2025-10-03T11:55:19Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/ogsiveo-epar-risk-management-plan_en.pdf"},
    {"id":"70483","name":"Ekterly : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2025-10-08T08:48:43Z","last_updated_date":"2025-10-08T08:48:43Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/ekterly-epar-risk-management-plan_en.pdf"},
    {"id":"70501","name":"Zadenvi : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2025-10-09T11:25:21Z","last_updated_date":"2025-10-09T11:25:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/zadenvi-epar-risk-management-plan_en.pdf"},
    {"id":"70518","name":"Denbrayce : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2025-10-09T16:54:34Z","last_updated_date":"2025-10-09T16:54:34Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/denbrayce-epar-risk-management-plan_en.pdf"},
    {"id":"70639","name":"Mynzepli : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2025-10-17T14:54:45Z","last_updated_date":"2025-10-17T14:54:45Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/mynzepli-epar-risk-management-plan_en.pdf"},
    {"id":"70644","name":"Izamby : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2025-10-17T15:17:39Z","last_updated_date":"2025-10-17T15:17:39Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/izamby-epar-risk-management-plan_en.pdf"},
    {"id":"70651","name":"Tryngolza : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2025-10-17T15:43:21Z","last_updated_date":"2025-10-17T15:43:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/tryngolza-epar-risk-management-plan_en.pdf"},
    {"id":"70773","name":"Rolcya : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2025-10-23T09:22:42Z","last_updated_date":"2025-10-23T09:22:42Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/rolcya-epar-risk-management-plan_en.pdf"},
    {"id":"70830","name":"Bilprevda : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2025-10-27T09:52:16Z","last_updated_date":"2025-10-27T09:52:16Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/bilprevda-epar-risk-management-plan_en.pdf"},
    {"id":"70838","name":"Bildyos : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2025-10-27T10:18:02Z","last_updated_date":"2025-10-27T10:18:02Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/bildyos-epar-risk-management-plan_en.pdf"},
    {"id":"70872","name":"Kisunla : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2025-10-28T12:27:50Z","last_updated_date":"2025-10-28T12:27:50Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/kisunla-epar-risk-management-plan_en.pdf"},
    {"id":"70987","name":"Vgenfli : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2025-11-04T08:48:40Z","last_updated_date":"2025-11-04T08:48:40Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/vgenfli-epar-risk-management-plan_en.pdf"},
    {"id":"71024","name":"Xoanacyl : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2025-11-06T09:10:11Z","last_updated_date":"2025-11-06T09:10:11Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/xoanacyl-epar-risk-management-plan_en.pdf"},
    {"id":"71065","name":"Rezdiffra : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2025-11-10T10:33:19Z","last_updated_date":"2025-11-10T10:33:19Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/rezdiffra-epar-risk-management-plan_en.pdf"},
    {"id":"71110","name":"Eyluxvi : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2025-11-12T16:20:32Z","last_updated_date":"2025-11-12T16:20:32Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/eyluxvi-epar-risk-management-plan_en.pdf"},
    {"id":"71153","name":"Afiveg : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2025-11-13T16:50:18Z","last_updated_date":"2025-11-13T16:50:18Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/afiveg-epar-risk-management-plan_en.pdf"},
    {"id":"71192","name":"Imreplys : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2025-11-17T12:56:39Z","last_updated_date":"2025-11-17T12:56:39Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/imreplys-epar-risk-management-plan_en.pdf"},
    {"id":"71217","name":"Enwylma : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2025-11-18T13:07:33Z","last_updated_date":"2025-11-18T13:07:33Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/enwylma-epar-risk-management-plan_en.pdf"},
    {"id":"71260","name":"Gobivaz : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2025-11-20T14:07:45Z","last_updated_date":"2025-11-20T14:07:45Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/gobivaz-epar-risk-management-plan_en.pdf"},
    {"id":"71268","name":"Usgena : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2025-11-21T09:21:06Z","last_updated_date":"2025-11-21T09:21:06Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/usgena-epar-risk-management-plan_en.pdf"},
    {"id":"71279","name":"Eiyzey : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2025-11-21T11:23:11Z","last_updated_date":"2025-11-21T11:23:11Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/eiyzey-epar-risk-management-plan_en.pdf"},
    {"id":"71311","name":"SonoVue : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2025-11-24T13:44:25Z","last_updated_date":"2025-11-24T13:44:25Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/sonovue-epar-risk-management-plan_en.pdf"},
    {"id":"71373","name":"Lynkuet : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2025-11-27T15:19:23Z","last_updated_date":"2025-11-27T15:19:23Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/lynkuet-epar-risk-management-plan_en.pdf"},
    {"id":"71499","name":"Brinsupri : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2025-12-04T12:36:07Z","last_updated_date":"2025-12-04T12:36:07Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/brinsupri-epar-risk-management-plan_en.pdf"},
    {"id":"71504","name":"Denosumab Intas : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2025-12-04T13:58:56Z","last_updated_date":"2025-12-04T13:58:56Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/denosumab-intas-epar-risk-management-plan_en.pdf"},
    {"id":"71729","name":"Imaavy : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2025-12-12T13:50:24Z","last_updated_date":"2025-12-12T13:50:24Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/imaavy-epar-risk-management-plan_en.pdf"},
    {"id":"71769","name":"Ventavis : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2025-12-16T09:51:58Z","last_updated_date":"2025-12-16T09:51:58Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/ventavis-epar-risk-management-plan_en.pdf"},
    {"id":"71790","name":"Rivaroxaban Koanaa : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2025-12-17T08:34:11Z","last_updated_date":"2025-12-17T08:34:11Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/rivaroxaban-koanaa-epar-risk-management-plan_en.pdf"},
    {"id":"71794","name":"Rapiscan : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2025-12-17T09:25:16Z","last_updated_date":"2025-12-17T09:25:16Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/rapiscan-epar-risk-management-plan_en.pdf"},
    {"id":"71857","name":"Macitentan Accord : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2025-12-19T08:39:28Z","last_updated_date":"2025-12-19T08:39:28Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/macitentan-accord-epar-risk-management-plan_en.pdf"},
    {"id":"71866","name":"Methylthioninium chloride Proveblue : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2025-12-19T11:32:51Z","last_updated_date":"2025-12-19T11:32:51Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/methylthioninium-chloride-proveblue-epar-risk-management-plan_en.pdf"},
    {"id":"71876","name":"Macitentan AccordPharma : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2025-12-19T13:09:15Z","last_updated_date":"2025-12-19T13:09:15Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/macitentan-accordpharma-epar-risk-management-plan_en.pdf"},
    {"id":"71913","name":"Zvogra : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2026-01-05T13:01:55Z","last_updated_date":"2026-01-05T13:01:55Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/zvogra-epar-risk-management-plan_en.pdf"},
    {"id":"71921","name":"Kefdensis : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2026-01-05T14:20:39Z","last_updated_date":"2026-01-05T14:20:39Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/kefdensis-epar-risk-management-plan_en.pdf"},
    {"id":"71980","name":"Norvir : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2026-01-07T16:12:44Z","last_updated_date":"2026-01-07T16:12:44Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/norvir-epar-risk-management-plan_en.pdf"},
    {"id":"71988","name":"Wayrilz : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2026-01-08T12:52:06Z","last_updated_date":"2026-01-08T12:52:06Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/wayrilz-epar-risk-management-plan_en.pdf"},
    {"id":"72027","name":"Winlevi : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2026-01-13T14:04:28Z","last_updated_date":"2026-01-13T14:04:28Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/winlevi-epar-risk-management-plan_en.pdf"},
    {"id":"72032","name":"GalenVita : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2026-01-13T14:38:36Z","last_updated_date":"2026-01-13T14:38:36Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/galenvita-epar-risk-management-plan_en.pdf"},
    {"id":"72111","name":"Victoza : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2026-01-16T13:50:45Z","last_updated_date":"2026-01-16T13:50:45Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/victoza-epar-risk-management-plan_en.pdf"},
    {"id":"72135","name":"Teduglutide Viatris : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2026-01-19T13:29:31Z","last_updated_date":"2026-01-19T13:29:31Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/teduglutide-viatris-epar-risk-management-plan_en.pdf"},
    {"id":"72155","name":"Ponlimsi : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2026-01-20T11:37:38Z","last_updated_date":"2026-01-20T11:37:38Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/ponlimsi-epar-risk-management-plan_en.pdf"},
    {"id":"72161","name":"Degevma : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2026-01-20T12:05:23Z","last_updated_date":"2026-01-20T12:05:23Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/degevma-epar-risk-management-plan_en.pdf"},
    {"id":"72188","name":"VacPertagen : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2026-01-21T14:51:37Z","last_updated_date":"2026-01-21T14:51:37Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/vacpertagen-epar-risk-management-plan_en.pdf"},
    {"id":"72211","name":"Inluriyo : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2026-01-23T09:45:06Z","last_updated_date":"2026-01-23T09:45:06Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/inluriyo-epar-risk-management-plan_en.pdf"},
    {"id":"72236","name":"Austedo : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2026-01-23T16:58:21Z","last_updated_date":"2026-01-23T16:58:21Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/austedo-epar-risk-management-plan_en.pdf"},
    {"id":"72243","name":"Zypadhera : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2026-01-26T10:16:25Z","last_updated_date":"2026-01-26T10:16:25Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/zypadhera-epar-risk-management-plan_en.pdf"},
    {"id":"72317","name":"Zavesca : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2026-01-28T13:22:14Z","last_updated_date":"2026-01-28T13:22:14Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/zavesca-epar-risk-management-plan_en.pdf"},
    {"id":"72347","name":"INOmax : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2026-01-29T13:02:30Z","last_updated_date":"2026-01-29T13:02:30Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/inomax-epar-risk-management-plan_en.pdf"},
    {"id":"72389","name":"Trisenox : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2026-01-30T14:53:16Z","last_updated_date":"2026-01-30T14:53:16Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/trisenox-epar-risk-management-plan_en.pdf"},
    {"id":"72409","name":"Enzalutamide Accordpharma  : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2026-02-03T15:07:31Z","last_updated_date":"2026-02-03T15:07:31Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/enzalutamide-accordpharma-epar-risk-management-plan_en.pdf"},
    {"id":"72413","name":"Imraldi : EPAR - Risk-management-plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2026-02-04T11:49:49Z","last_updated_date":"2026-02-04T11:49:49Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/imraldi-epar-risk-management-plan_en.pdf"},
    {"id":"72425","name":"Clopidogrel Zentiva : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2026-02-05T14:21:22Z","last_updated_date":"2026-02-05T14:21:22Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/clopidogrel-zentiva-epar-risk-management-plan_en.pdf"},
    {"id":"72529","name":"Kyinsu : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2026-02-12T12:37:48Z","last_updated_date":"2026-02-12T12:37:48Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/kyinsu-epar-risk-management-plan_en.pdf"},
    {"id":"72572","name":"Pregabalin Zentiva : EPAR - Risk-management-plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2026-02-16T15:34:55Z","last_updated_date":"2026-02-16T15:34:55Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/pregabalin-zentiva-epar-risk-management-plan_en.pdf"},
    {"id":"72613","name":"Tasigna : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2026-02-19T17:25:58Z","last_updated_date":"2026-02-19T17:25:58Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/tasigna-epar-risk-management-plan_en.pdf"},
    {"id":"72629","name":"Teizeild : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2026-02-20T15:12:05Z","last_updated_date":"2026-04-13T12:58:08Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/teizeild-epar-risk-management-plan_en.pdf"},
    {"id":"72635","name":"Osqay : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2026-02-20T15:59:30Z","last_updated_date":"2026-02-20T15:59:30Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/osqay-epar-risk-management-plan_en.pdf"},
    {"id":"72643","name":"Dawnzera : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2026-02-20T16:40:41Z","last_updated_date":"2026-02-20T16:40:41Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/dawnzera-epar-risk-management-plan_en.pdf"},
    {"id":"72664","name":"Ranluspec : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2026-02-24T10:44:11Z","last_updated_date":"2026-02-24T10:44:11Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/ranluspec-epar-risk-management-plan_en.pdf"},
    {"id":"72670","name":"Acvybra : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2026-02-24T12:06:44Z","last_updated_date":"2026-02-24T12:06:44Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/acvybra-epar-risk-management-plan_en.pdf"},
    {"id":"72674","name":"mNexspike : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2026-03-04T12:33:18Z","last_updated_date":"2026-03-04T12:33:18Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/mnexspike-epar-risk-management-plan_en.pdf"},
    {"id":"72689","name":"Gotenfia : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2026-02-25T12:27:00Z","last_updated_date":"2026-02-25T12:27:00Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/gotenfia-epar-risk-management-plan_en.pdf"},
    {"id":"72751","name":"Aumseqa : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2026-02-27T13:25:10Z","last_updated_date":"2026-02-27T13:25:10Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/aumseqa-epar-risk-management-plan_en.pdf"},
    {"id":"72762","name":"Xbonzy : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2026-03-02T09:57:27Z","last_updated_date":"2026-03-02T09:57:27Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/xbonzy-epar-risk-management-plan_en.pdf"},
    {"id":"72792","name":"Aqneursa : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2026-03-03T11:17:40Z","last_updated_date":"2026-03-03T11:17:40Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/aqneursa-epar-risk-management-plan_en.pdf"},
    {"id":"72801","name":"Myqorzo : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2026-03-03T14:12:02Z","last_updated_date":"2026-03-03T14:12:02Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/myqorzo-epar-risk-management-plan_en.pdf"},
    {"id":"72867","name":"Waskyra : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2026-03-05T16:43:12Z","last_updated_date":"2026-03-05T16:43:12Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/waskyra-epar-risk-management-plan_en.pdf"},
    {"id":"72980","name":"Exdensur : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2026-03-12T15:28:06Z","last_updated_date":"2026-03-12T15:28:06Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/exdensur-epar-risk-management-plan_en.pdf"},
    {"id":"73008","name":"Anktiva : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2026-03-13T13:15:09Z","last_updated_date":"2026-03-13T13:15:09Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/anktiva-epar-risk-management-plan_en.pdf"},
    {"id":"73171","name":"Stivarga : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2026-03-24T15:16:25Z","last_updated_date":"2026-03-24T15:16:25Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/stivarga-epar-risk-management-plan_en.pdf"},
    {"id":"73304","name":"Ilumira : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2026-04-01T16:36:56Z","last_updated_date":"2026-04-01T16:36:56Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/ilumira-epar-risk-management-plan_en.pdf"},
    {"id":"73330","name":"Rezurock : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2026-04-07T14:12:23Z","last_updated_date":"2026-04-07T14:12:23Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/rezurock-epar-risk-management-plan_en.pdf"},
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    {"id":"73720","name":"Xolremdi : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2026-05-12T11:36:14Z","last_updated_date":"2026-05-12T11:36:14Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/xolremdi-epar-risk-management-plan_en.pdf"},
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    {"id":"73808","name":"Zoledronic acid Teva : EPAR - Risk management plan","type":"rmp","status":"unknown","consultation_date":"","first_published_date":"2026-05-21T15:29:17Z","last_updated_date":"2026-05-21T15:29:17Z","reference_number":"","document_url":"https://www.ema.europa.eu/en/documents/rmp/zoledronic-acid-teva-epar-risk-management-plan_en.pdf"},
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