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European Directorate for the Quality of Medicines
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31	page 1/5 Counterfeit medecines and similar crimes Counterfeit medecines and similar crimes Key points Add to Reading List Source URL: www.coe.int Language: English - Date: 2012-05-18 10:30:48 Crime Pharmaceutical industry Business Counterfeit medications Public health Counterfeit European Directorate for the Quality of Medicines Organized crime Council of Europe Counterfeit consumer goods Pharmaceuticals policy Health
32	Regulatory acceptance of 3Rs testing methods for medicinal products – EMA perspective Dr. Sonja Beken EMA Joint Expert Group on the application of 3Rs EMA Safety Working Party Add to Reading List Source URL: circabc.europa.eu Language: English Pharmaceutical sciences Pharmaceutics European Medicines Agency EMA Validation European Directorate for the Quality of Medicines Committee for Medicinal Products for Human Use Clinical trial Clinical research Pharmaceutical industry Research
33	Ref. Ares[removed][removed]EUROPEAN COMMISSION HEALTH AND CONSUMERS DIRECTORATE-GENERAL Directorate D - Health systems and products D4 – Substances of Human Origin and Tobacco Control Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2015-01-28 11:48:08 Transfusion medicine Hematology Blood donation West Nile virus Plasmapheresis MSM blood donor controversy European Directorate for the Quality of Medicines Blood bank Blood transfusion Medicine Anatomy Blood
34	IMI indicative Call topic All information regarding future IMI Call topics is indicative and subject to change. Final information about the IMI’s future Calls will be communicated after approval by the IMI Governing Bo Add to Reading List Source URL: www.imi.europa.eu Language: English - Date: 2014-09-29 03:43:19 Virology European Directorate for the Quality of Medicines Biology Vaccination Microbiology Vaccine
35	[removed]November 2014 EMA/CMDh[removed]COORDINATION GROUP FOR MUTUAL RECOGNITION AND DECENTRALISED PROCEDURES - HUMAN MEETING Add to Reading List Source URL: www.hma.eu Language: English - Date: 2014-11-26 05:36:03 Research Pharmaceutical industry Agenda Minutes Validation Electronic Common Technical Document European Directorate for the Quality of Medicines Business Meetings Clinical research Parliamentary procedure
36	BRIEFING PAPER SUBJECT: EGA POSITION ON THE API CMDh MEETING (18 NOV[removed]DATE: SUPPLY Add to Reading List Source URL: www.hma.eu Language: English - Date: 2014-12-02 08:15:28 Health Marketing authorization European Directorate for the Quality of Medicines EudraLex Government Pharmaceuticals policy Pharmaceutical industry Good manufacturing practice
37	Doc. Ref: CMDh[removed]November 2013 Working Group on Active Substance Master File Procedures The work sharing procedure for the assessment of Active Substance Master File (ASMF) Add to Reading List Source URL: www.hma.eu Language: English - Date: 2013-12-02 08:26:42 Strasbourg European Medicines Agency Pharmaceutics Research Pharmaceutical sciences Pharmaceutical industry Council of Europe European Directorate for the Quality of Medicines
38	Report from the CMDh meeting held on 18th, 19th and 20th July 2011 CMDh/EMA Sub-Group on Paediatric Regulation The CMDh would like to remind marketing authorisation holders to check the CMDh press release and website for Add to Reading List Source URL: www.hma.eu Language: English - Date: 2011-07-28 10:21:34 Council of Europe European Directorate for the Quality of Medicines Strasbourg Pharmacovigilance Paroxetine Pascal European Medicines Agency Pharmaceutical sciences Chemistry Pharmacology
39	CMDh BEST PRACTICE GUIDE ON THE COMPILATION OF THE DOSSIER FOR NEW APPLICATIONS SUBMITTED IN MUTUAL RECOGNITION & DECENTRALISED PROCEDURES Doc. Ref.: CMDh[removed]Rev.1 September 2014 Add to Reading List Source URL: www.hma.eu Language: English - Date: 2014-10-10 05:13:04 Research Pharmacology Summary of Product Characteristics EudraLex Bioequivalence Test data exclusivity European Directorate for the Quality of Medicines Supplementary protection certificate Pharmaceuticals policy Clinical research Pharmaceutical sciences
40	Microsoft Word - E.01 CMDv RfR Feb-Mar10 EMEA-CMDv[removed]doc Add to Reading List Source URL: www.hma.eu Language: English - Date: 2010-05-19 12:55:25 Pharmaceutical sciences European Medicines Agency Pharmaceuticals policy Health Pharmacology European Directorate for the Quality of Medicines Referral marketing Veterinary physician Medicinal product Clinical research Pharmaceutical industry Research