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Qualified person
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#	Item
321	BPIs Comments on GMP Draft Annex 16 Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-11-28 04:09:47 Qualified Person Computing QP Software Pharmaceuticals policy Clinical research
322	Form for submission of comments Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-11-28 04:09:49 Clinical research Pharmaceuticals policy Qualified Person
323	Form for submission of comments Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-11-28 04:09:49 Research Pharmaceutical sciences Health Qualified Person European Medicines Agency Good manufacturing practice EudraLex European Union Directive Clinical research Pharmaceuticals policy Pharmaceutical industry
324	Form for submission of comments Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-11-28 04:09:46 Electronic cigarette Requirement Technology Human behavior Clinical research Pharmaceuticals policy Qualified Person
325	Form for submission of comments Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-11-28 04:09:48 Food safety Good manufacturing practice Qualified Person Health Pharmaceuticals policy Pharmaceutical industry Clinical research
326	Form for submission of comments Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-11-28 04:09:46 Clinical research Pharmaceuticals policy Qualified Person
327	Form for submission of comments Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-11-28 04:09:45 Research Pharmaceutical sciences Pharmaceutics Qualified Person Good manufacturing practice Requirement European Medicines Agency Systems engineering process Clinical research Pharmaceutical industry Pharmaceuticals policy
328	Ref. Ares[removed][removed]Warsaw, November 5, 2013 European Commission Directorate General for Health and Consumers, Unit SANCO/D/6 Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-11-28 04:09:47 Pharmaceutical sciences Pharmaceutics Research Food safety Quality Good manufacturing practice Qualified Person European Medicines Agency Specification Pharmaceutical industry Pharmaceuticals policy Clinical research
329	Ref. Ares[removed][removed]LFB Biotechnologies Comments regarding EC Public Consultation on the Revision of EU Commission guideline on Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-11-28 04:09:47 Qualified Person Good manufacturing practice Health Science Pharmaceuticals policy Clinical research Pharmaceutical industry
330	PRACTICAL LAW MULTI-JURISDICTIONAL GUIDE 2013 LIFE SCIENCES The law and leading lawyers worldwide Add to Reading List Source URL: www.franzosi.com Language: English - Date: 2013-09-13 08:19:40 Pharmacology Research Pharmacy Intellectual property law Supplementary protection certificate European Medicines Agency Summary of Product Characteristics Qualified Person Responsible For Pharmacovigilance Good Clinical Practice Directive Pharmaceutical sciences Pharmaceuticals policy Clinical research

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