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Results: 263

#	Item
201	EUROPEAN COMMISSION HEALTH AND CONSUMERS DIRECTORATE-GENERAL Health systems and products Medicinal products – authorisations, EMA PHARM 631 Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-30 04:33:16 Pharmaceutical sciences Pharmacology Pharmaceutical industry Executive agencies of the United Kingdom government Drug safety European Medicines Agency EudraLex Clinical research Pharmaceuticals policy Research
202	EUROPEAN COMMISSION HEALTH AND CONSUMERS DIRECTORATE-GENERAL Health systems and products Medicinal products – authorisations, European Medicines Agency PHARM 656 Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2014-05-05 07:45:56 Pharmaceutical sciences Pharmacology European Union Pharmaceutical industry European Medicines Agency Directive 2001/83/EC Clinical Trials Directive EudraLex Clinical research Pharmaceuticals policy Research
203	Notes for applicants and holders of a Manufacturer’s Licence MHRA Guidance Note 5 1 Add to Reading List Source URL: www.mhra.gov.uk Language: English - Date: 2014-07-03 12:41:08 Pharmaceutical industry Clinical research Health Good manufacturing practice European Directive on Traditional Herbal Medicinal Products Qualified Person European Medicines Agency Medical device EudraLex Pharmaceuticals policy Medicine Pharmaceutical sciences
204	Headquarters Executive Office Gyle Square 1 South Gyle Crescent EDINBURGH EH12 9EB Telephone[removed] Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:02:41 Stem cells Pharmaceuticals policy Cell biology European Medicines Agency Cell therapy EudraLex European Directorate for the Quality of Medicines Directive 2001/83/EC Embryonic stem cell Biology Clinical research Biotechnology
205	CMDh QUESTIONS & ANSWERS PRODUCT INFORMATION / INFORMATION ON MEDICINAL PRODUCTS Doc. Ref.: CMDh[removed], Rev0 October 2012 Add to Reading List Source URL: www.hma.eu Language: English - Date: 2013-08-08 03:51:36 Health policy Health EudraLex Directive 2001/83/EC Pharmaceuticals policy Clinical research Research
206	CMDv/MAN[removed]EMEA/CMDv[removed]CMDv/ NOTICE TO APPLICANTS SUB-GROUP BACKGROUND Add to Reading List Source URL: www.hma.eu Language: English - Date: 2011-03-30 10:51:07 European Union law Veterinary physician Health Pharmaceuticals policy Clinical research EudraLex
207	EUROPEAN COMMISSION Brussels, XXX […](2013) XXX draft Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:36:08 Research Health Pharmacology Pharmaceutical industry Drug safety European Medicines Agency EudraLex Pharmacovigilance Directive 2001/83/EC Pharmaceuticals policy Clinical research Pharmaceutical sciences
208	SUMMARY OF FEES in accordance with Article 25 of the Royal Decree of 3 July 1969 as amended by the Royal Decree of 17 December 2008 and in accordance with the Royal Decree of 14 December 2006 and adapted to indexation Ve Add to Reading List Source URL: www.fagg-afmps.be Language: English - Date: 2012-09-18 08:55:20 Economy of the European Union Euro EudraLex Europe Pharmaceuticals policy Clinical research European Union
209	Microsoft Word - VETPHARM 253-revised_Final minutes of 14th VetpharmCom me… Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:25:58 Pharmaceutical sciences Pharmacology EudraLex European Directorate for the Quality of Medicines Directive 2001/83/EC Pharmacovigilance Validation Clinical research Pharmaceuticals policy Research
210	Microsoft Word - final minutes 13th vetpharm com.doc Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:22:02 Health Pharmaceutical sciences Qualified Person Responsible For Pharmacovigilance Directive 2001/83/EC Pharmacovigilance Qualified Person European Directorate for the Quality of Medicines European Medicines Agency EudraLex Pharmaceuticals policy Clinical research Research

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