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Results: 263

#	Item
221	7th May[removed]Contribution from Groupement des Pharmaciens de L’Industrie en Europe (European Industrial Pharmacists’ Group), to the Public Consultation in Preparation of a legal proposal to combat Counterfeit Medici Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:46:45 Pharmaceutical industry Research Health EudraLex Good distribution practice Directive 2001/83/EC Qualified Person Medicinal product Good manufacturing practice Pharmaceuticals policy Clinical research Pharmaceutical sciences
222	Commission Guideline — Guidance on posting and publication of result-related information on clinical trials in relation to the implementation of Article[removed]of Regulation (EC) No[removed]and Article[removed]of Regulat Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:02:34 EudraCT ClinicalTrials.gov European Medicines Agency Clinical Trials Directive Clinical trials registry Good Clinical Practice Ethics Committee Clinical trial EudraLex Clinical research Research Science
223	John Dalli Member of the European Commission, responsible for Health and Consumer Policy Commissioner Dalli delivers speech on "Clinical Trials Directive – Meeting Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2012-03-08 08:36:32 Health Clinical Trials Directive Clinical trial Ethics Committee Pharmaceutical industry Regulatory requirement EudraLex Pharmacovigilance Clinical research Research Pharmaceutical sciences
224	[removed]EUROGROUP FOR ANIMALS PHARMACEUTICALS Current situation The pharmaceutical sector is extensively regulated at the European Union’s level in the dual interest of ensuring the highest possible level of public h Add to Reading List Source URL: eurogroupforanimals.org Language: English - Date: 2011-09-06 07:17:01 Research Health European Medicines Agency International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use Regulatory requirement Directive 65/65/EEC Pharmaceutical industry Pharmacopoeia EudraLex Pharmaceuticals policy Clinical research Pharmaceutical sciences
225	Microsoft Word - 2008_03_11_Consultation Document FINAL _public_.doc Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:25:50 Pharmaceutical sciences Health Pharmacology Good distribution practice Good manufacturing practice European Medicines Agency EudraLex Counterfeit consumer goods Counterfeit medications Pharmaceuticals policy Pharmaceutical industry Clinical research
226	What you Need to Know about Biosimilar Medicinal Products Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-04-22 02:55:35 Pharmaceuticals policy Clinical research Pharmaceutical industry Biotechnology European Medicines Agency Biosimilar Biologic Pharmacovigilance EudraLex Pharmaceutical sciences Pharmacology Health
227	Proposal for revision of guideline_Track changes March 2012 Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:02:33 Pharmaceutical sciences Biology Pharmaceutical industry European Medicines Agency European Union Alternative medicine Directive 2001/83/EC Cell therapy EudraLex Clinical research Research Pharmaceuticals policy
228	EUROPEAN COMMISSION HEALTH AND CONSUMERS DIRECTORATE-GENERAL Health systems and products Medicinal products – quality, safety and efficacy Implementation Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2014-03-28 08:54:56 European Union directives Law European Union Directive 2001/83/EC EudraLex Government Framework decision European labour law Pharmaceuticals policy Clinical research European Union law
229	Guidelines on the details of the various categories of variations, on the operation of the procedures laid down in Chapters II, IIa, III and IV of Commission Regulation (EC) No[removed]of 24 November 2008 concerning t Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 08:55:16 Research Health Pharmacology European Union Pharmaceutical industry European Medicines Agency Supplementary protection certificate EudraLex Clinical Trials Directive Clinical research Pharmaceuticals policy Pharmaceutical sciences
230	Brussels, xx December 2009 F2/2009/D/2102 Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 08:56:16 Hematology Pharmaceuticals policy Biology Transfusion medicine Pharmaceutical industry EudraLex Plasmapheresis Blood bank Qualified Person Medicine Clinical research Anatomy

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