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Directive 2001 83 EC
Results: 312

#	Item
211	Q&A TRADITIONAL HERBAL MEDICINAL PRODUCTS Doc. Ref.: CMDh[removed]Rev.1 February 2013 Question 1 What is the meaning of a “Community monograph” in the context of MRP/DCP of traditional Add to Reading List Source URL: www.hma.eu Language: English - Date: 2013-03-07 04:51:57 Research Pharmaceuticals policy Pharmaceutical industry European Union European Medicines Agency Herbalism Herbal Directive 2001/83/EC Alternative medicine Clinical research Medicine Health
212	COUNCIL OF THE EUROPEAN UNION Brussels, 23 April[removed]OR. en[removed] Add to Reading List Source URL: www.europarl.europa.eu Language: English - Date: 2013-05-29 03:10:12 Law Medical Devices Directive Directive 2001/83/EC European Union Clinical research Pharmaceuticals policy
213	Microsoft Word - HERBALS - DRAFT REPORT[removed]final.doc Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:25:59 Health Pharmaceuticals policy European Directive on Traditional Herbal Medicinal Products European Union Pharmaceutical industry European Medicines Agency Herbalism Directive 2001/83/EC Herbal Clinical research Medicine Alternative medicine
214	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
215	Microsoft Word - counterfeitscommissionreplymay08.doc Add to Reading List Source URL: www.mhra.gov.uk Language: English - Date: 2008-05-24 08:46:05 European Union Food safety Good manufacturing practice Directive 2001/83/EC Health Pharmaceuticals policy Clinical research Pharmaceutical industry
216	[removed]Official Journal of the European Union EN Add to Reading List Source URL: www.eubis-europe.eu Language: English - Date: 2012-02-15 15:06:11 Research Health European Medicines Agency Good Clinical Practice Directive Directive 2001/83/EC Clinical Trials Directive Medicinal product Medical Devices Directive Medical device Clinical research Pharmaceuticals policy Medicine
217	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
218	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
219	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
220	EUROPEAN COMMISSION Brussels, C[removed]final Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2012-12-05 10:12:40 Research Health Drug safety Pharmacology Pharmacy Pharmacovigilance Directive 2001/83/EC Italian Senate Clinical research Pharmaceuticals policy Pharmaceutical sciences

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