33 results
Keyword Bronchenolo Gola Remove keyword
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National expert: Ivana Golabova, State Institute for Drug Control (updated)
- Declaration of interests - 79.77 KB | PDF
- Curriculum Vitae - 16.42 KB | PDF
Vitae PERSONAL INFORMATION Ivana Golabova WORK EXPERIENCE September … Golabova 2020-12-21 Classified as … declaration of interests I, Ivana Golabova Organisation/Company: State … -
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National expert: Renata Golasikova, State Institute for Drug Control
- Declaration of interests - 79.09 KB | PDF
- Curriculum Vitae - 16.24 KB | PDF
vitae PERSONAL INFORMATION Renata Golasikova WORK EXPERIENCE June 2015–Present … Golasikova 2020-09-07 Classified as … declaration of interests I, Renata Golasikova Organisation/Company: State … -
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National expert: Jolanta Grygielska, European Medicines Agency (updated)
- Declaration of interests - 79.75 KB | PDF
- Curriculum Vitae - 22.8 KB | PDF
Sochocka-Bykowska, M., Zo-Giebel, A., Gola, Z., Guzera, Z., Maliska … -
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National expert: Martina Weise, Federal Institute for Drugs and Medical Devices (updated)
- Declaration of interests - 80.14 KB | PDF
- Curriculum Vitae - 24.72 KB | PDF
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National expert: Marina Martano, Ministry for Health (updated)
- Declaration of interests - 81.1 KB | PDF
- Curriculum Vitae - 37.98 KB | PDF
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National expert: Dariusz Sladowski, The Office for Registration of Medicinal Products, Medical Devices and Biocides (updated)
- Declaration of interests - 81.57 KB | PDF
- Curriculum Vitae - 31.24 KB | PDF
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Human medicine European public assessment report (EPAR): Elonva (updated)
corifollitropin alfa, Reproductive Techniques, Assisted, Ovulation Induction
Date of authorisation: 25/01/2010, Revision: 17, Authorised, Last updated: 26/02/2021 -
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Human medicine European public assessment report (EPAR): Gazyvaro
Obinutuzumab, Leukemia, Lymphocytic, Chronic, B-Cell
Date of authorisation: 22/07/2014,
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, Revision: 11, Authorised, Last updated: 29/01/2021
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Human medicine European public assessment report (EPAR): Rapamune
Sirolimus, Graft Rejection, Kidney Transplantation
Date of authorisation: 13/03/2001, Revision: 40, Authorised, Last updated: 07/01/2021 -
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National expert: Ewa Balkowiec Iskra, The Office for Registration of Medicinal Products, Medical Devices and Biocides (updated)
- Declaration of interests - 80 KB | PDF
- Curriculum Vitae - 22.78 KB | PDF
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Human medicine European public assessment report (EPAR): Rekovelle
follitropin delta, Anovulation
Date of authorisation: 12/12/2016,, Revision: 1, Authorised, Last updated: 29/06/2017
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National expert: Robin Ristl, Austrian Medicines and Medical Devices Agency (updated)
- Declaration of interests - 80.95 KB | PDF
- Curriculum Vitae - 37.54 KB | PDF
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National expert: Edo Richard, European Medicines Agency (updated)
- Declaration of interests - 79.76 KB | PDF
- Curriculum Vitae - 46.38 KB | PDF
Chappell MA, van Osch MJP, Golay X, Thomas DL, De Vita E … -
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Herbal medicinal product: Anisi aetheroleum
Pimpinella anisum L., Anise Oil, F: Assessment finalised, Last updated: 06/10/2016 -
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Herbal medicinal product: Anisi fructus
Pimpinella anisum L., Aniseed, F: Assessment finalised, Last updated: 06/10/2016 -
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Herbal medicinal product: Hyperici herba
Hypericum perforatum L., St. John's Wort, P: Draft published, Last updated: 08/03/2018 -
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National expert: Livia Puljak, Agency for Medicinal Products and Medical Devices of Croatia (updated)
- Declaration of interests - 79.77 KB | PDF
- Curriculum Vitae - 49.37 KB | PDF
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National expert: Saskia de Wildt, European Medicines Agency (updated)
- Declaration of interests - 81.8 KB | PDF
- Curriculum Vitae - 49.18 KB | PDF
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Referral: Quinolones
quinolones, Article 35
Status: European Commission final decision, opinion/position date: 09/03/2010, EC decision date: 01/07/2010, Last updated: 16/07/2010 -
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Referral: Ambroxol and bromhexine-containing medicines
ambroxol and bromhexine, Article 31 referrals
Status: European Commission final decision, opinion/position date: 18/11/2015, EC decision date: 14/01/2016, Last updated: 05/02/2016 -
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National expert: Flora Peyvandi, European Medicines Agency (updated)
- Declaration of interests - 87.57 KB | PDF
- Curriculum Vitae - 237.45 KB | PDF
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Referral: Renin-angiotensin-system (RAS)-acting agents
captopril, imidapril, zofenopril, candesartan, delapril, telmisartan, aliskiren, moexipril, enalapril, valsartan, fosinopril, irbesartan, perindopril, quinapril, ramipril, eprosartan, olmesartan, trandolapril, losartan, azilsartan, lisinopril, spirapril, benazepril, cilazapril, associated names: Tolucombi, Telmisartan Teva, Telmisartan Teva Pharma, Tolura, Onduarp, Twynsta, Actelsar HCT, Kinzalkomb, MicardisPlus, PritorPlus, Copalia HCT, Dafiro HCT, Exforge HCT, Rasilamlo, Rasilez, Rasilez HCT, Rasitrio, Edarbi, Ipreziv, Aprovel, Ifirmasta (previously Irbesartan Krka), Irbesartan Teva, Irbesartan Zentiva (previously Irbesartan Winthrop), Karvea, Sabervel, CoAprovel, Ifirmacombi, Irbesartan/Hydrochlorothiazide Teva, Irbesartan Hydrochlorothiazide Zentiva (previously Irbesartan Hydrochlorothiazide Winthrop), Karvezide, Kinzalmono (previously Telmisartan Boehringer Ingelheim Pharma KG), Micardis, Pritor, Telmisartan Actavis, Article 31 referrals
Status: European Commission final decision, opinion/position date: 22/05/2014, EC decision date: 04/09/2014, Last updated: 08/10/2014 -
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Orphan designation: Vascular endothelial growth factor-D gene in an adenoviral vector for use with a collagen collar for: Prevention of stenosis in synthetic grafts used in haemodialysis
Date of first decision: 08/06/2004, Positive, Last updated: 03/04/2014 -
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EU Telematics
Last updated: 27/01/2021