Directive 2001 83 EC - PDFSEARCH.IO - Document Search Engine

Directive 2001 83 EC
Results: 312

#	Item
251	Microsoft Word - Report 2010.doc Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:12:00 Pharmacology Pharmaceutical industry European Medicines Agency Pharmaceuticals policy Supplementary protection certificate Summary of Product Characteristics Directive 2001/83/EC Food and Drug Administration Clinical research Pharmaceutical sciences Research
252	Microsoft Word[removed]Non-paper annex[removed]doc Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:02:24 Cell biology Clinical research Pharmaceuticals policy Emerging technologies Cell therapy Tissue engineering Allotransplantation Directive 2001/83/EC Medical device Biology Medicine Stem cells
253	EUROPEAN COMMISSION HEALTH AND CONSUMERS DIRECTORATE-GENERAL Health systems and products Medicinal products – quality, safety and efficacy Brussels, [removed] Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:46:52 Directive 2001/83/EC Medicinal product Medicine European Union Good Clinical Practice Directive European Directive on Traditional Herbal Medicinal Products Clinical research Pharmaceuticals policy Health
254	Microsoft Word - Report 2009.doc Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:11:59 Pharmaceutical sciences Pharmaceuticals policy European Medicines Agency Government Supplementary protection certificate Summary of Product Characteristics Directive 2001/83/EC Clinical research Research Pharmaceutical industry
255	EUROPEAN COMMISSION HEALTH AND CONSUMERS DIRECTORATE-GENERAL Health systems and products Pharmaceuticals Brussels, [removed] Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:46:52 European Union Law Clinical research Pharmaceuticals policy Directive 2001/83/EC
256	EUROPEAN COMMISSION Brussels, [removed]COM[removed]final Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2014-04-01 08:56:22 Pharmaceutical sciences Health European Medicines Agency EudraLex Pharmacovigilance Cell therapy Medical device Directive 2001/83/EC Alternative medicine Pharmaceuticals policy Clinical research Medicine
257	Microsoft Word - EMEA comments on draft Regulation Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:07:11 European Medicines Agency Government Pharmaceutical sciences Directive 2001/83/EC Qualified Person Responsible For Pharmacovigilance Supplementary protection certificate Clinical research Pharmaceuticals policy Research
258	Biennial report (Article 21 of Regulation (EC[removed]) Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2012-03-13 12:02:50 Law European Union Consumer protection law Directive 2001/83/EC Unfair Commercial Practices Directive Directive on Privacy and Electronic Communications Consumer protection Council Implementing Regulation (EU) No 282/2011 Clinical Trials Directive European Union directives Pharmaceuticals policy Clinical research
259	<Date of submission> Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:37:28 Research Pharmaceutical sciences Pharmaceutics Quality Good distribution practice European Medicines Agency Directive 2001/83/EC Alternative medicine Clinical research Pharmaceuticals policy Pharmaceutical industry
260	EUROPEAN COMMISSION HEALTH AND CONSUMERS DIRECTORATE-GENERAL Health systems and products Medicinal products – quality, safety and efficacy Brussels, [removed] Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:37:30 European Union Law Health EudraLex Directive 2001/83/EC Medicinal product Qualified Person Clinical Trials Directive Good Clinical Practice Directive Clinical research Pharmaceuticals policy European Union directives

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