Press Office
| Committee for Medicinal Products for Human Use (CHMP) Press Archive | ||
| 2010 | ||
| 28/01/10 | CHMP/35712/2010 | Monthly report from the January meeting |
| 22/01/10 | CHMP/32068/2010 | Press Release from the January meeting |
| 07/01/10 | CHMP/834035/2009 | Monthly report from the December meeting Corr. (published 13/01/10) |
| 2009 | ||
| 18/12/09 | CHMP/833104/2009 | Press Release from the December meeting Corr. (published 06/01/10) |
| 27/11/09 | CHMP/745639/2009 | Monthly report from the CHMP November meeting |
| 20/11/09 | CHMP/752431/2009 | Press Release from the November meeting |
| 20/11/09 | CHMP/739818/2009 | Press Release - EMEA makes recommendations to minimise risk of nephrogenic systemic fibrosis with gadolinium-containing contrast agents |
| 30/10/09 | CHMP/674356/2009 | Monthly report from the CHMP October meeting |
| 23/10/09 | CHMP/671190/2009 | Press Release from the October meeting Corr. (published 27/10/09) |
| 02/10/09 | CHMP/599418/2009 | Monthly Report from the September meeting |
| 25/09/09 | CHMP/606274/2009 | Press Release from the September meeting Corr. (published 29/09/09) |
| 30/07/09 | CHMP/473955/2009 | Monthly Report from the July meeting Corr. (published 31/07/09) |
| 24/07/09 | CHMP/468553/2009 | Press release from the July meeting Corr. (published 27/10/09) |
| 03/07/09 | CHMP/389326/2009 | Monthly Report from the June meeting |
| 30/06/09 | CHMP/367523/2009 | Public statement on the recommendation to lift the suspension of the marketing authorisation for Optison (perflutren) |
| 26/06/09 | CHMP/397215/2009 | Press Release from the June meeting Corr. (published 27/10/09) |
| 26/06/09 | CHMP/394741/2009 | Press Release - EMEA recommends first marketing authorisation for an advanced therapy medicinal product |
| 05/06/09 | CHMP/330510/2009 | Monthly Report from the May meeting |
| 02/06/09 | EMEA/328956/2009 | Public statement on possible interaction between clopidogrel and proton pump inhibitors |
| 29/05/09 | CHMP/330580/2009 | Press Release from the May meeting |
| 29/05/09 | CHMP/322964/2009 | Press Release - EMEA recommends lifting of supply and treatment restrictions for Neupro |
| 30/04/09 | CHMP/271292/2009 | Monthly report from the April meeting |
| 23/04/09 | CHMP/249660/2009 | Press Release from the April meeting |
| 26/03/09 | CHMP/174243/2009 | Monthly report from the March meeting |
| 19/03/09 | CHMP/172797/2009 | Press Release from the March meeting |
| 26/02/09 | CHMP/97795/2009 | Monthly report from the February meeting |
| 19/02/09 | CHMP/107282/2009 | Press Release from the February meeting |
| 19/02/09 | CHMP/20857/2009 | Press Release
- EMEA recommends suspension of the marketing authorisation of Raptiva (efalizumab) - See also - Questions and Answers on Raptiva |
| 30/01/09 | EMEA/39660/2009 | Monthly Report from the January meeting |
| 22/01/09 | EMEA/37933/2009 | Press Release from the January meeting Corr. |
| 22/01/09 | CHMP/22315/2009 | Press Release -
EMEA makes recommendations for safer use of Ritalin and other methylphenidate-containing medicines in the EU See also - Questions and answers on the review of medicines containing methylphenidate |
| 22/01/09 | EMEA/27603/2009 | Press Release -
EMEA recommends new contraindication for Fareston (toremifene) See also - Questions and answers on the addition of contraindications for Fareston (toremifene) |
| 16/01/09 | EMEA/13509/09 | Press Release - Priority access for children during Myozyme supply shortage |
| 07/01/09 | EMEA/679401/08 | Monthly Report from the December meeting Corr. |
| 2008 | ||
| 19/12/08 | EMEA/CHMP/670724/08 | Press Release from the December meeting Corr. |
| 17/12/08 | EMEA/683633/2008 | Press Release - Janssen-Cilag International N.V. withdraws its application for an extension of indication for Invega (paliperidone) |
| 04/12/08 | EMEA/645579/2008 | Press Release - Oncoscience AG withdraws its application for Theraloc (nimotuzumab) |
| 28/11/08 | EMEA/612074/2008 | Monthly Report from the November meeting |
| 27/11/08 | EMEA/CHMP/590563/2008 | Opinion of the committee for medicinal products for human use pursuant to article 5(3) of regulation (EC) No 726/2004, on
conventional antipsychotics See also - Appendix I - CHMP Assessment Report On Conventional Antipsychotics and - Questions and answers on the review of the use of conventional antipsychotic medicines in elderly patients with dementia |
| 21/11/08 | EMEA/CHMP/606566/2008 | Press Release from the November meeting Corr. 2 |
| 20/11/08 | EMEA/CHMP/613852/2008 | Press Release-
European Medicines Agency recommends the suspension of the marketing authorisation of Ionsys (fentanyl hydrochloride) - See also - Questions and answers on Ionsys |
| 31/10/08 | EMEA/CHMP/539474/2008 | Monthly report from the October meeting |
| 31/10/08 | EMEA/CHMP/550206/2008 | Press Release from the October meeting (Rev 2) |
| 23/10/08 | EMEA/CHMP/537777/2008 | Press Release - The European Medicines Agency recommends suspension of the marketing authorisation of Acomplia - See also - Questions and answers on Acomplia |
| 23/10/08 | EMEA/CHMP/493770/2008 | Press Release - European Medicines Agency recommends first switch from prescription-only to non-prescription for a centrally authorised medicine |
| 08/10/08 | EMEA/CHMP/505537/2008 | Monthly report from the September meeting |
| 25/09/08 | EMEA/CHMP/503956/2008 | Press Release from the September meeting |
| 25/09/08 | EMEA/CHMP/496612/08 | European Medicines Agency recommends update of product information of Tysabri and risk of progressive multifocal leukoencephalopathy (PML) |
| 13/08/08 | EMEA/CHMP/424554/2008 | Press Release - European Medicines Agency update on progressive multifocal leukoencephalopathy (PML) and Tysabri |
| 05/08/08 | EMEA/417535/2008 | Press Release - Pharmion Ltd withdraws its marketing authorisation application for Orplatna (INN: satraplatin) |
| 01/08/08 | EMEA/CHMP/390768/2008 | Monthly Report from the July meeting |
| 28/07/08 | EMEA/388064/2008 | Press Release from the July meeting (Rev. 1) |
| 24/07/08 | EMEA/CHMP/382927/2008 | Press Release - European Medicines Agency recommends restricting the use of oral moxifloxacin-containing medicines |
| 24/07/08 | EMEA/CHMP/382256/2008 | Press Release - Studies assessed by the EMEA indicate no increased risk of developing cancer for patients who have taken Viracept contaminated with ethyl mesilate See also - Questions and Answers on Viracept |
| 03/07/08 | EMEA/CHMP/327265/2008 | Monthly Report from the June meeting |
| 01/07/08 | EMEA/CHMP/333963/2008 | Press Release - EMEA recommends a new warning for epoetins for their use in cancer patients (Corr.) |
| 26/06/08 | EMEA/CHMP/333636/2008 | Press Release - EMEA recommends strengthening warnings and contraindications for etoricoxib-containing medicines used in the treatment of rheumatoid arthritis and ankylosing spondylitis |
| 26/06/08 | EMEA/CHMP/322395/2008 | Press Release - EMEA recommends new warnings and contraindications for ergot-derived dopamine agonists |
| 26/06/08 | EMEA/CHMP/332645/2008 | Press Release from the June meeting |
| 19/06/08 | EMEA/CHMP/323118/2008 | Press Release - Euro Nippon Kayaku GmbH withdraws its marketing authorisation application for Spanidin (gusperimus) |
| 06/06/08 | EMEA/CHMP/279235/2008 | Monthly report from the May meeting |
| 05/06/08 | EMEA/CHMP/277722/2008 | Press Release - European Medicines Agency recommends measures to manage contamination of heparin-containing medicines - See also Questions & Answers on Heparins |
| 02/06/08 | EMEA/CHMP/278126/2008 | Press Release from the May meeting |
| 01/05/08 | EMEA/CHMP/213268/2008 | Monthly report from the April meeting (Corr.) |
| 30/04/08 | EMEA/CHMP/205947/2008 | Press Release from the April meeting (Corr.) |
| 24/04/08 | EMEA/215870/2008 | Press release - Wyeth withdraws its application to extend the marketing authorisation for Tygacil |
| 02/04/08 | EMEA/142888/2008 | Press release - Further data needed to determine risk of heart attack with abacavir - See also Q&A on Abacavir and the risk of heart attack |
| 28/03/08 | EMEA/136288/2008 | Public Statement on Bextra (valdecoxib) - Non-renewal of the Marketing Authorisation in the European Union |
| 27/03/08 | EMEA/137943/2008 | Monthly report from the March meeting |
| 20/03/08 | EMEA/CHMP/139489/2008 | Press release EMEA concludes new advice to doctors and patients for Tysabri (natalizumab) needed - See also Q&A on Tysabri and liver injury |
| 20/03/08 | EMEA/139443/2008 | Press release - EMEA recommends new contraindication for Velcade (bortezomib) - See also Q&A on the addition of a contraindication for Velcade (bortezomib) |
| 20/03/08 | EMEA/CHMP/140780/2008 | Press release from the March meeting |
| 04/03/08 | EMEA/CHMP/95268/2008 | Monthly report from the February meeting |
| 25/02/08 | EMEA/95140/2008 | Press release - Actelion withdraws its application for an extension of indication for Zavesca |
| 21/02/08 | EMEA/CHMP/87277/2008 | Press release from the February meeting |
| 21/02/08 | EMEA/CHMP/90694/2008 | Press release - EMEA recommends authorisation of first pre-pandemic influenza vaccine |
| 14/02/08 | EMEA/60439/08 | Public Statement on Risk of peripheral neuropathy with Sebivo (telbivudine) |
| 11/02/08 | EMEA/599866/07 | Questions and Answers on the withdrawal of the marketing application for Sinerem |
| 05/02/08 | EMEA/37124/08 | Monthly report from the January meeting |
| 04/02/08 | EMEA/4193/08 | Questions and Answers on the withdrawal of the Marketing Authorisation Application for Insulin Human Rapid Marvel, Insulin Human Long Marvel and Insulin Human 30/70 Mix Marvel |
| 01/02/08 | EMEA/44714/2008 | Letter from European Medicines Agency to all concerned Market Authorisation Holders on the actions needed to mitigate possible risks of contamination by alkyl mesilates, (di)isetionates, tosilates and besilates. |
| 28/01/08 | EMEA/45635/2008 | Press release - Ipsen Ltd withdraws its application for an extension of indication for NutropinAq |
| 25/01/08 | EMEA/CHMP/26421/2008 | Public Statement on Levviax (Telithromycin) Withdrawal of the Marketing Authorisation in the European Union |
| 24/01/08 | EMEA/CHMP/28614/2008 | Press release from the January meeting |
| 24/01/08 | EMEA/33024/2008 | Press release - European Medicines Agency recommends the approval of thalidomide for the treatment of rare bone-marrow cancer |
| 24/01/08 | EMEA/42232/2008 | Press release - EMEA recommends new warnings and contraindications for rosiglitazone |
| 24/01/08 | EMEA/37479/2008 | Press release - EMEA statement on the safety of Gardasil |
| 16/01/08 | EMEA/2435/2008 | Press release - Marvel LifeSciences Ltd withdraws its marketing authorisation applications for Insulin Human Rapid Marvel, Insulin Human Long Marvel and Insulin Human 30/70 Mix Marvel |
| 2007 | ||
| 21/12/07 | EMEA/CHMP/585637/07 | Monthly Report from the December meeting |
| 14/12/07 | EMEA/583851/07 | Press Release from the December meeting |
| 27/11/07 | EMEA/522109/07 | Monthly Report from the November meeting |
| 20/11/07 | EMEA/541192/07 | Press release - Novartis withdraws its application to extend the marketing authorisation for Zometa |
| 21/11/07 | EMEA/534678/07 | Press release - European Medicines Agency recommends suspension of marketing authorisation of aprotinin-containing medicines for systemic use - See also Q&A on the EMEA recommendation to suspend the marketing authorisation of aprotinin-containing medicines (Corr) |
| 19/11/07 | EMEA/522741/07 | Public Statement on the cessation of marketing of Exubera (Insulin human) |
| 16/11/07 | EMEA/521472/07 | Press release - INFAI withdraws its marketing authorisation application for Gastromotal - See also Q&A on the withdrawal of the Marketing Application |
| 16/11/07 | EMEA/CHMP/522566/07 | Press release from the November meeting (Corr. 20/11/07) |
| 16/11/07 | EMEA/5020463/07 | Press release - European Medicines Agency recommends suspension of Marketing Authorisations for Carisoprodol-containing medicinal products - See also Q&A on the recommendation to suspend the Marketing Auhorisations for Carisoprodol-containing products |
| 16/11/07 | EMEA/417458/07 | Press release - EMEA recommends changes in the product information for Protelos/Osseor due to the risk of severe hypersensitivity reactions See also Q&A on the safety of Protelos/Osseor |
| 25/10/07 | EMEA/473066/07 | Monthly Report from the October meeting |
| 23/10/07 | EMEA/496188/07 | Public Statement - Epoetins and the risk of tumour growth progression and thromboembolic events in cancer patients and cardiovascular risks in patients with chronic kidney disease |
| 18/10/07 | EMEA/479200/07 | Press Release from the October meeting |
| 28/09/07 | EMEA/427480/07 | Monthly Report from the September meeting |
| 21/09/07 | EMEA/323703/07 | Press Release from the September meeting (Corr. 27/09/07) |
| 26/07/07 | EMEA/CHMP/285833/07 | Public Statement on Trudexa (adalimumab) Withdrawal of the Marketing Authorisation in the European Union |
| 25/07/07 | EMEA/318931/07 | Monthly Report from the July meeting |
| 19/07/07 | EMEA/431407/07 | Press Release from the July meeting |
| 29/06/07 | EMEA/267656/07 | Monthly Report from the June meeting |
| 22/06/07 | EMEA/267556/07 | Press Release from the June meeting |
| 25/06/07 | EMEA/265144/07 | European Medicines Agency recommends restricted use for Piroxicam - See also Q&A on the review of Piroxicam |
| 22/06/07 | EMEA/CHMP/267556/07 | CHMP Press Release from the June meeting |
| 21/06/07 | EMEA/275367/07 | European Medicines Agency agrees on action plan following the recall of Viracept and recommends suspension of the Marketing Authorisation - See also Q&A on the follow-up to the Viracept recall |
| 06/06/07 | EMEA/251283/07 | European Medicines Agency announces recall of Viracept - See also Q&A on the recall of Viracept |
| 05/06/07 | EMEA/CHMP/222371/07 | Monthly Report from the May meeting |
| 29/05/07 | EMEA/235491/07 | Protherics withdraws its marketing authorisation application for Voraxaze |
| 25/05/07 | EMEA/CHMP/231382/07 | Press Release from the May meeting (Corr. 05/06/07) |
| 24/05/07 | EMEA/218760/07 | Questions and Answers document on Bicalutamide 150 mg tablets |
| 04/05/07 | EMEA/CHMP/181739/07 | Monthly Report from the April meeting |
| 30/04/07 | EMEA/193194/07 | ISTA Pharma Ltd withdraws its marketing authorisation application for Vitragan |
| 27/04/07 | EMEA/184876/07 | EMEA concludes first accelerated assessment for a medicine for human use |
| 27/04/07 | EMEA/CHMP/186566/07 | Press Release from the April meeting |
| 29/03/07 | EMEA/CHMP/144134/07 | Monthly Report from the March meeting |
| 23/03/07 | EMEA/CHMP/132706/07 | Press Release from the March meeting |
| 05/03/07 | EMEA/79902/07 | Public Statement - Baraclude (entecavir) Occurrence of a resistant HIV variant in a patient co-infected with HIV and HBV |
| 02/03/07 | EMEA/CHMP/85096/07 | Monthly Report from the February meeting |
| 23/02/07 | EMEA/CHMP/82850/07 | Press Release from the February meeting |
| 02/02/07 | EMEA/CHMP/521168/07 | Monthly Report from the January meeting |
| 25/01/07 | EMEA/CHMP/39118/07 | Press Release from the January meeting |
| 2006 | ||
| 20/12/06 | EMEA/CHMP/488156/06 | Monthly Report from the December Meeting |
| 15/12/06 | EMEA/CHMP/506977/06 | Press Release from the December meeting (Corrected 15/12/06, 15:30 hrs) |
| 29/11/06 | EMEA/CHMP/484273/06 | Monthly Report from the November meeting |
| 17/11/06 | EMEA/CHMP/460883/06 | Press Release from the November meeting (correction. Active substance corrected for two products) |
| 27/10/06 | EMEA/CHMP/410526/06 | Monthly Report from the October Plenary Session |
| 25/10/06 | EMEA/CHMP/416788/06 | EMEA Workshop on Neonates: Development of medicines for neonates needs multi-disciplinary cooperation |
| 24/10/06 | EMEA/CHMP/746469/06 | European Medicines Agency review concludes positive benefit-risk balance for non-selective NSAIDs - See also Q&A on the review of non-selective NSAIDs |
| 19/10/06 | EMEA/CHMP/421027/06 | Press Release from the October Plenary Session |
| 29/09/06 | EMEA/CHMP/325128/06 | Monthly Report from the September Plenary Session |
| 21/09/06 | EMEA/CHMP/376832/06 | Press Release from the September Plenary session correction |
| 04/08/06 | EMEA/CHMP/296185/06 | Monthly Report from the July Plenary Session |
| 28/07/06 | EMEA/CHMP/289040/06 | Press Release from the July Plenary session |
| 12/07/06 | EMEA/CHMP/222629/06 | Monthly Report from the June 2006 Plenary Session |
| 29/06/06 | EMEA/CHMP/243602/06 | Press Release from the June Plenary session |
| 14/06/06 | EMEA/CHMP/209537/06 | Monthly Report from the May 2006 Plenary Session |
| 06/06/06 | EMEA/CHMP/202554/06 | European Medicines Agency adopts a positive opinion for the use of Prozac in the treatment of children and adolescents suffering from depression - See also Q&A on PROZAC for use in children and adolescents |
| 02/06/06 | EMEA/CHMP/204606/06 | Press Release from the May Plenary Session |
| 01/06/06 | EMEA/CHMP/192804/06 | Public Statement on Infergen (Interferon alfacon-1) Withdrawal of the Marketing Authorisatoin in the European Union |
| 12/05/06 | EMEA/CHMP/111495/06 | Monthly Report from the April 2006 Plenary Session Rev 1 |
| 28/04/06 | EMEA/CHMP/152608/06 | Press Release from the April Plenary Session |
| 06/04/06 | EMEA/CHMP/102937/06 | Monthly Report from the March 2006 Plenary Session Rev 1 |
| 24/03/06 | EMEA/CHMP/106554/06 | Press Release from the March Plenary Session - See also Q&A on ZELNORM |
| 17/03/06 | EMEA/CHMP/70961/06 | Monthly Report from the February 2006 Plenary Session Rev 1 |
| 23/02/06 | EMEA/CHMP/69276/06 | Press Release from the February Plenary Session |
| 17/02/06 | EMEA/CHMP/35006/06 | Monthly Report from the January 2006 Plenary Session |
| 27/01/06 | EMEA/CHMP/32796/06 | Press Release from the January Plenary Session |
| 2005 | ||
| 16/01/06 | EMEA/CHMP/420100/05 | Monthly Report from the December 2005 Plenary Session Rev 1 |
| 15/12/05 | EMEA/CHMP/420087/05 | European Medicines Agency recommends no changes for Tamiflu safety information |
| 15/12/05 | EMEA/CHMP/421484/05 | Press Release from the December Plenary Session |
| 01/12/05 | EMEA/CHMP/364660/05 | Monthly Report from the November 2005 Plenary Session |
| 17/11/05 | EMEA/CHMP/384581/05 | Press Release from the November Plenary Session |
| 17/11/05 | EMEA/CHMP/362348/05 | Revised Monthly Report from the October 2005 Plenary Session |
| 13/10/05 | EMEA/CHMP/341463/05 | Press Release from the October Plenary Session Rev 1 |
| 28/09/05 | EMEA/CHMP/295298/05 | Monthly Report from the September 2005 Plenary Session |
| 22/09/05 | EMEA/CHMP/312626/05 | European Medicines Agency statement on Herceptin |
| 20/09/05 | EMEA/CHMP/29736/05 | European Medicines Agency recommends suspension of Hexavac |
| 20/09/05 | EMEA/CHMP/304888/05 | Questions and Answers on the suspension of Hexavac |
| 15/09/05 | EMEA/CHMP/303099/05 | Press Release from the September Plenary Session |
| 12/08/05 | EMEA/CHMP/262135/05 | EMEA consulting on a draft guideline on pharmacovigilance for medicines used in children |
| 04/08/05 | EMEA/CHMP/229460/05 | Monthly Report from the July 2005 Plenary Session |
| 02/08/05 | EMEA/CHMP/250423/05 | Questions and Answers on non-selective NSAIDs European Medicines Agency concludes action on COX-2 inhibitors correction |
| 27/07/05 | EMEA/CHMP/246640/05 | Press Release from the July Plenary Session |
| 08/07/05 | EMEA/CHMP/207020/05 | Monthly Report from the June 2005 Plenary Session |
| 27/06/05 | EMEA/CHMP/207407/05 | Press Release from the June Plenary Session |
| 07/06/05 | EMEA/CHMP/160895/05 | Monthly Report from the May 2005 Plenary Session correction |
| 25/05/05 | EMEA/CHMP/176508/05 | Press Release from the May Plenary Session |
| 25/05/05 | EMEA/CHMP/176508/05 | Press Release from the May Plenary Session |
| 03/05/05 | EMEA/CHMP/121307/05 | Monthly Report from the April 2005 Plenary Session |
| 25/04/05 | EMEA/CHMP/128918/05 | Press Release and Q&A correction- European Medicines Agency finalises review of antidepressants in children and adolescents |
| 21/04/05 | CHMP/138444/05 | Press Release from the April Plenary Session |
| 01/04/05 | EMEA/CHMP/82984/05 | Monthly Report from the March 2005 Plenary Session corr 2 |
| 17/03/05 | EMEA/CHMP/96995/05 | Press Release from the March Plenary Session |
| 25/02/05 | EMEA/CHMP/45462/05 | Monthly Report from the February 2005 Plenary Session |
| 17/02/05 | EMEA/CHMP/59424/05 | Press Release from the February Plenary Session |
| 01/02/05 | EMEA/CHMP/22735/05 | Monthly Report from the January 2005 Plenary Session corr in Annex I |
| 20/01/05 | EMEA/CHMP/21979/05 | Press Release from the January Plenary Session |
| 2004 | ||
| 06/01/05 | EMEA/CHMP/203834/04 | Monthly Report from the December 2004 Plenary Session |
| 16/12/04 | EMEA/CHMP/199703/04 | Press Release from the 13-15 December Plenary Meeting |
| 30/11/04 | EMEA/CHMP/160431/04 | Monthly Report from the November Plenary Meeting |
| 18/11/04 | EMEA/CHMP/152989/04 | Press Release from the 15 - 18 November Plenary Session |
| 29/10/04 | EMEA/CHMP/119155/04 | Monthly Report from the October Plenary Meeting |
| 19/10/04 | EMEA/CHMP/116066/04 | Press Release from the 15 -18 October 2004 Plenary Session |
| 19/10/04 | EMEA/CHMP/269/04 | Monthly Report from the September Plenary Meeting |
| 18/10/04 | EMEA/CHMP/1214/04 | Monthly Report from the July Plenary Meeting Corrigendum |
| 16/09/04 | EMEA/CHMP/74329/04 | Press Release from the 13-16 September 2004 Plenary Session |
| 29/07/04 | EMEA/CHMP/21550/04 | Press Release from the 27th -29th July 2004 Plenary Session |
| 04/07/04 | EMEA/CHMP/651/04 | Monthly Report from the 22-23 June Plenary Meeting |
| 24/06/04 | EMEA/CHMP/17587/04 | Press Release from the 22nd -23rd June 2004 Plenary Session |
| 11/06/04 | EMEA/CHMP/409/04 | Monthly report from the 1st -3rd June 2004 Plenary Session |
| 04/06/04 | EMEA/CHMP/15358/04 | Press Release from the June 2004 Plenary Session |
| 30/04/04 | EMEA/CPMP/11951/04 | Monthly report from the April 2004 Plenary session |
| 22/04/04 | EMEA/CPMP/11206/04 | Press Release from the April 2004 Plenary session |
| 01/04/04 | EMEA/CPMP/1238/04 | Monthly report from the March 2004 Plenary session |
| 25/03/04 | EMEA/CPMP/1303/04 | Press Release from the March 2004 session |
| 04/03/04 | EMEA/CPMP/0537/04 | Monthly report from the February 2004 Plenary session |
| 27/02/04 | EMEA/CPMP/ 857/04 | Press Release from the February 2004 session |
| 29/01/04 | EMEA/CPMP/269/04 | Monthly report from the January 2004 Plenary session |
| 22/01/04 | EMEA/CPMP/406/04 | Press Release from the January 2004 session |
| 20/01/04 | EMEA/CPMP/1476/04 | CPMP elects new chair and vice-chair at its 100th meeting |
| 2003 | ||
| 23/12/03 | EMEA/CPMP/6016/03 | Monthly report from the December session |
| 18/12/03 | EMEA/CPMP/6199/03 | Press Release from the December session |
| 03/12/03 | EMEA/CPMP/5728/03 | Monthly report from the November session Revision 1 |
| 20/11/03 | EMEA/CPMP/5732/03 | Press Release from the November session |
| 05/11/03 | EMEA/CPMP/4482/03 | Monthly report from the September session Revision 2 |
| 24/10/03 | EMEA/CPMP/5020/03 | Monthly report
from the October session See also Presentation from the EFPIA Info Day on Performance Indicators on Pre-and Post Authorisation activities in the Centralised Procedure (Large file, 950KB) |
| 23/10/03 | EMEA/CPMP/5259/03 | Press Release from the October session |
| 25/09/03 | EMEA/CPMP/4817/03 | Press Release from the September session |
| 04/09/03 | EMEA/23230/03 | Extraordinary meeting 3 September |
| 01/08/03 | EMEA/CPMP/3754/03 | Monthly report from the July session |
| 25/07/03 | EMEA/CPMP/3971/03 | Press Release from the July session |
| 04/07/03 | EMEA/CPMP/3297/03 | Monthly report from the June session |
| 27/06/03 | EMEA/CPMP/16832/03 | Press Release from the June session |
| 05/06/03 | EMEA/CPMP/2568/03 | Monthly report from the May session Revised |
| 22/05/03 | EMEA/CPMP/2848/03 | Press Release from the May session |
| 02/05/03 | EMEA/CPMP/2347/03 | Monthly report from the April session |
| 28/04/03 | EMEA/CPMP/2376/03 | Press Release from the April session |
| 28/03/03 | EMEA/CPMP/1358/03 | Monthly report from the March session |
| 20/03/03 | EMEA/CPMP/1611/03 | Press Release from the March session |
| 03/03/03 | EMEA/CPMP/3794/03 | Monthly report from the February session Corrigendum |
| 24/02/03 | EMEA/CPMP/0890/03 | Press Release from the February session Revised |
| 30/01/03 | EMEA/CPMP/0209/03 | Monthly report from the January session |
| 23/01/03 | EMEA/CPMP/0294/03 | Press Release from the January session |
| 2002 | ||
| 06/01/03 | EMEA/CPMP/6248/02 | Monthly report from the December session |
| 19/12/02 | EMEA/CPMP/6589/02 | Press Release from the December session |
| 28/11/02 | EMEA/CPMP/5857/02 | Monthly report from the November session |
| 21/11/02 | EMEA/CPMP/5802/02 | Press Release from the November session |
| 24/10/02 | EMEA/CPMP/4979/02 | Monthly report from the October session |
| 18/10/02 | EMEA/CPMP/5203/02 | Press Release from the October session |
| 01/10/02 | EMEA/CPMP/4634/02 | Monthly report from the September session |
| 19/09/02 | EMEA/CPMP/4698/02 | Press Release from the September session |
| 31/07/02 | EMEA/CPMP/3473/02 | Monthly report from the July session |
| 25/07/02 | EMEA/CPMP/3677/02 | Press Release from the July session |
| 10/07/02 | EMEA/CPMP/2749/02 | Monthly report from the June session |
| 27/06/02 | EMEA/CPMP/3065/02 | Press Release from the June session |
| 06/06/02 | EMEA/CPMP/2348/02 | Press
Release from the 1st CPMP Workshop for Patients' Organisations on
the theme ' Information and participation' - See also Participants' List |
| 06/06/02 | EMEA/CPMP/2222/02 | Monthly report from the May session |
| 31/05/02 | EMEA/CPMP/2341/02 | Press Release from the May session |
| 28/04/02 | EMEA/CPMP/8204/02 | Monthly report from the April session |
| 26/04/02 | EMEA/CPMP/1747/02 | Press Release from the April session |
| 25/03/02 | EMEA/CPMP/1110/02 | Monthly report from the March session |
| 21/03/02 | EMEA/CPMP/7412/02 | Press Release from CPMP March session |
| 01/03/02 | EMEA/CPMP/590/02 | Monthly report from the February session |
| 21/02/02 | EMEA/CPMP/561/02 | Press Release from CPMP February session |
| 24/01/02 | EMEA/CPMP/197/02 | Monthly report from CPMP January session |
| 17/01/02 | EMEA/CPMP/4025/02 | Press Release from CPMP January session |
| 2001 | ||
| 19/12/01 | EMEA/CPMP/3926/01 | Monthly Report from December CPMP session |
| 13/12/01 | EMEA/CPMP/4025/01 | Press Release from December CPMP session |
| 04/12/01 | EMEA/32158/01 | First EMEA Workshop on Ethics in Clinical Trials |
| 21/11/01 | EMEA/CPMP/3636/01 | Monthly Report from November CPMP session |
| 16/11/01 | EMEA/CPMP/3658/01 | Press Release from November CPMP session |
| 24/10/01 | EMEA/CPMP/3310/01 | Monthly Report from October CPMP session |
| 19/10/01 | EMEA/CPMP/3297/01 | Press Release from the October CPMP Session |
| 25/09/01 | EMEA/CPMP/2936/01 | Technical Report fromSeptember CPMP session |
| 25/09/01 | EMEA/CPMP/2973/01 | Press Release from the September CPMP Session |
| 31/07/01 | EMEA/CPMP/2358/01 | Technical Report from July CPMP session |
| 27/07/01 | EMEA/CPMP/2341/01 | Press Release from the July CPMP Session |
| 26/06/01 | EMEA/CPMP/2020/01 | Technical Report from June CPMP session |
| 28/06/01 | EMEA/CPMP/1935/01 | Press Release from June CPMP session |
| 07/06/01 | EMEA/CPMP/1577/01 | Technical Report from May CPMP session |
| 02/05/01 | EMEA/CPMP/1252/01 | From April CPMP session (Full Meeting Report) |
| 26/04/01 | EMEA/CPMP/1262/01 | Press Release from CPMP session (Summary) |
| 27/03/01 | EMEA/CPMP/906/01 | Press Release from CPMP session |
| 27/02/01 | EMEA/CPMP/521/01 | Press Release from CPMP session |
| 31/01/01 | EMEA/CPMP/250/01 | Press Release from CPMP session |
| 23/01/01 | Press Release | EMEA announces new CPMP chairman and vice-chairman |
| 18/01/01 | Extraordinary CPMP press release |
CPMP Members |
| 18/01/01 | EMEA/CPMP/39663/00 | Press Release: SIAMED 2000 - Speeding up drug regulation in Europe |
| 2000 | ||
| 18/12/00 | EMEA/CPMP/4305/00 | Press Release |
| 21/11/00 | EMEA/CPMP/2901/00 | Press Release |
| 23/10/00 | EMEA/CPMP/2849/00 | Press Release |
| 09/10/00 | EMEA/22213/00 | Announcement of Seminar on Pre-Clinical Safety Evaluation of Vaccines |
| 25/09/00 | EMEA/CPMP/2522/00 | Press Release |
| 27/07/00 | EMEA/CPMP/1964/00 | Press Release |
| 25/07/00 | EMEA/20840/00 | Nomination of new Head of the Human Unit |
| 27/06/00 | EMEA/CPMP/1586/00 | Press Release |
| 31/05/00 | EMEA/CPMP/1304/00 | Press Release |
| 11/04/00 | EMEA/CPMP/941/00 | Press Release |
| 20/03/00 | EMEA/CPMP/543/00 | Press Release |
| 15/02/00 | EMEA/CPMP/316/00 | Press Release |
| 18/01/00 | EMEA/CPMP/122/00 | Press Release |
| 1999 | ||
| 20/12/99 | EMEA/CPMP/3323/99 | Press Release |
| 22/11/99 | EMEA/CPMP/3091/99 | Press Release |
| 25/10/99 | EMEA/CPMP/2769/99 | Press Release |
| 27/09/99 | EMEA/CPMP/2590/99 | Press Release |
| 09/09/99 | EMEA/CPMP/2325/99 | Extraordinary meeting to finalise review of Anorectic Agents |
| 30/07/99 | EMEA/CPMP/2137/99 | Press Release |
| 25/06/99 | EMEA/CPMP/1817/99 | Press Release |
| 25/05/99 | EMEA/CPMP/1434/99 | Press Release |
| 26/04/99 | EMEA/CPMP/1150/99 | Press Release |
| 29/03/99 | EMEA/CPMP/841/99 | Press Release |
| 01/03/99 | EMEA/CPMP/566/99 | Press Release |
| 01/02/99 | EMEA/CPMP/159/99 | Press Release |
| 1998 | ||
| 21/12/98 | EMEA/CPMP/2866/98 | Press Release |
| 24/11/98 | EMEA/CPMP/2572/98 | Press Release |
| 26/10/98 | EMEA/CPMP/2244/98 | Press Release |
| 21/09/98 | EMEA/CPMP/2010/98 | Press Release |
| 27/07/98 | EMEA/CPMP/1342/98 | Press Release |
| 29/06/98 | EMEA/CPMP/1150/98 | Press Release |
| 29/05/98 | EMEA/CPMP/975/98 | Press Release |
| 22/04/98 | EMEA/CPMP/808/98 | Press Release |
| 27/03/98 | EMEA/CPMP/438/98 | Press Release |
| 27/02/98 | EMEA/CPMP/209/98 | Press Release |
| 30/01/98 | EMEA/CPMP/069/98 | Press Release |
| 1997 | ||
| 19/12/97 | EMEA/CPMP/1138/97 | Press Release Rev. |
| 20/11/97 | EMEA/CPMP/1056/97 | Press Release |
| 24/10/97 | EMEA/CPMP/921/97 | Press Release |
| 25/09/97 | EMEA/CPMP/813/97 | Press Release |
| 25/07/97 | EMEA/CPMP/651/97 | Press Release |
| 20/06/97 | EMEA/CPMP/502/97 | Press Release |
| 16/05/97 | EMEA/CPMP/389/97 | Press Release |
| 18/04/97 | EMEA/CPMP/341/97 | Press Release |
| 21/03/97 | EMEA/CPMP/234/97 | Press Release |
| 20/02/97 | EMEA/CPMP/182/97 | Press Release |
| 24/01/97 | EMEA/CPMP/045/97 | Press Release |
| 1996 | ||
| 18/12/96 | EMEA/CPMP/1095/96 | Press Release |
| 20/11/96 | EMEA/CPMP/960/96 | Press Release |
| 16/10/96 | EMEA/CPMP/871/96 | Press Release |
| 11/09/96 | EMEA/CPMP/741/96 | Press Release |
| 18/07/96 | EMEA/CPMP/644/96 | Press Release |
| 20/06/96 | EMEA/CPMP/513/96 | Press Release |
| 23/05/96 | EMEA/CPMP/426/96 | Press Release - See also Annex Community Marketing Authorisations of Medicinal Products: Status on the 23rd May 1996 |
| 19/04/96 | EMEA/CPMP/351/96 | Press Release |
| 14/03/96 | EMEA/CPMP/285/96 | Press Release |
| 15/02/96 | EMEA/CPMP/179/96 | Press Release |
| 18/01/96 | EMEA/CPMP/023/96 | Press Release |
| 1995 | ||
| 21/12/95 | EMEA/CPMP/938/95 | Press Release |
| 29/11/95 | EMEA/CPMP/832/95 | Press Release |
| 19/10/95 | EMEA/CPMP/656/95 | Press Release - See also Annex |

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