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Results: 263

#	Item
211	Microsoft Word - Summary record 12th meeting VETPHARM 223 final.doc Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:25:44 Research Health Pharmacovigilance Directive 75/318/EEC European Directorate for the Quality of Medicines Directive 2001/83/EC EudraLex European Medicines Agency Pharmaceuticals policy Clinical research Pharmaceutical sciences
212	SG[removed]-EN-TRA-00 (IT) Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2012-09-19 10:54:00 Research Health European Medicines Agency Directive 2001/83/EC Pharmacovigilance European Directive on Traditional Herbal Medicinal Products EudraLex Clinical research Pharmaceuticals policy Pharmaceutical sciences
213	CHAPTER 1 AL Good Clinical Practice Principles: Legal Background and Applicability Add to Reading List Source URL: media.wiley.com Language: English - Date: 2013-08-29 07:14:50 Pharmaceuticals policy Health Good Clinical Practice Good Clinical Laboratory Practice Clinical research associate Institutional review board EudraLex Clinical Trials Directive Clinical trial Clinical research Research Pharmaceutical industry
214	Microsoft Word - Final record 11th Veterinary Pharmaceutical Committee 1 Ju. Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:26:09 Pharmaceuticals policy Pharmacology Pharmaceutical industry Drug safety Pharmacovigilance Validation European Directorate for the Quality of Medicines European Medicines Agency EudraLex Clinical research Pharmaceutical sciences Research
215	Microsoft Word - Minutes of 18 th meeting FINAL.doc Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:25:48 European Union European Union law Health Law EudraLex Clinical Trials Directive Pharmaceuticals policy Clinical research European Union directives
216	Microsoft Word - 2007_03_20_Flash report Final-rev.doc Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:25:59 Transposition European Union European Union directives Law Europe EudraLex Pharmaceuticals policy European Union law Clinical research
217	j277 Index 510(k) – abbreviated 203 – de novo 203 Add to Reading List Source URL: www.wiley-vch.de Language: English - Date: 2008-09-12 03:09:45 Medicine Health Pharmacology Pharmaceuticals policy Drug safety Good manufacturing practice Validation EudraLex European Medicines Agency Pharmaceutical sciences Pharmaceutical industry Clinical research
218	Communication from the Commission — Detailed guidance on the request to the competent authorities for authorisation of a clinical trial on a medicinal product for human use, the notification of substantial amendments a Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:00:38 Pharmaceutical sciences Health Pharmacology Pharmaceutical industry European Union European Medicines Agency Clinical Trials Directive EudraLex EudraCT Clinical research Research Pharmaceuticals policy
219	EUROPEAN COMMISSION HEALTH AND CONSUMERS DIRECTORATE-GENERAL Health products and systems Medicinal products – quality, safety and efficacy Brussels, [removed] Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 08:59:05 Medicine Health Clinical Trials Directive EudraLex Good Clinical Practice Directive Medicinal product Medical device Ethics Committee Clinical trial Clinical research Pharmaceuticals policy Research
220	EUROPEAN COMMISSION HEALTH AND CONSUMERS DIRECTORATE-GENERAL Health products and systems Pharmaceuticals Brussels, [removed] Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:30:25 Medicine Health Clinical Trials Directive EudraLex Good Clinical Practice Directive Medicinal product Medical device Ethics Committee Clinical trial Clinical research Pharmaceuticals policy Research

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