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Qualified person
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#	Item
411	Name of Recipient F11 to next Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:37:44 Quality Research Good distribution practice Validation Health Qualified Person Medicine European Directive on Traditional Herbal Medicinal Products European Medicines Agency Pharmaceuticals policy Clinical research Pharmaceutical industry
412	Form for submission of comments Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:37:40 Qualified Person Stakeholder Comment Received Pronunciation States of Germany Agency Data Computing Clinical research Information Pharmaceuticals policy
413	Microsoft Word - 2005_12_GMP Part I Chapter 8 Final.doc Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:09:44 Pharmaceutical industry Health policy Product liability Product recall Health Qualified Person Recall EudraLex Good manufacturing practice Pharmaceuticals policy Clinical research Research
414	Ref. Ares[removed][removed]EUROPEAN COMMISSION HEALTH AND CONSUMERS DIRECTORATE-GENERAL Health systems and products Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:37:36 Research Pharmaceutical sciences Pharmaceutical industry Health policy European Union Good manufacturing practice Medicinal product Qualified Person Biologic Pharmaceuticals policy Clinical research Pharmacology
415	Public Consultation on the Commission Guidelines on Good Distribution Practice of Medicinal Products for Human Use Comments from the Czech Republic General remarks on batch number The new 2010 legislation strengthens the Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:37:40 Pharmacy Marketing Qualified Person Health Good distribution practice Shelf life Business Distribution Pharmaceuticals policy Clinical research Pharmaceutical industry
416	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
417	Ref. Ares[removed][removed]Rue de La Loi 26, Box U 1040 Brussels, Belgium the vītallink in heatīhcare — — Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:37:36 Pharmaceutical sciences Pharmaceutics Quality Research Good distribution practice Good manufacturing practice Validation Qualified Person European Medicines Agency Pharmaceutical industry Pharmaceuticals policy Clinical research
418	Microsoft Word - QPAssociation_Comment_Draft EU GDP Guide_Letter.doc Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:37:37 Qualified Person Quality Validation Science Business Technology Clinical research Pharmaceutical industry Pharmaceuticals policy
419	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
420	Comments from the European Industrial Pharmacists Group on the Commission’s Revised Guidelines on Good Distribution Practice of Medicinal Products for Human Use The updating of the Guidelines on Good Distribution Pract Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:37:36 Research Health Pharmaceutical industry Good distribution practice Quality EudraLex Qualified Person Electronic cigarette Gross domestic product Pharmaceuticals policy Clinical research Pharmaceutical sciences

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