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Directive 2001 83 EC
Results: 312

#	Item
191	EUROPEAN COMMISSION HEALTH AND CONSUMERS DIRECTORATE-GENERAL Health systems and products Medicinal products – authorisations, EMA PHARM 635 Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-30 04:33:16 Pharmacology Health Drug safety Pharmacy Pharmacovigilance European Medicines Agency Directive 2001/83/EC Qualified Person Responsible For Pharmacovigilance Qualified Person for Pharmacovigilance Pharmaceutical sciences Clinical research Pharmaceuticals policy
192	EUROPEAN COMMISSION HEALTH AND CONSUMERS DIRECTORATE-GENERAL Health systems and products Medicinal products – authorisations, EMA PHARM 641 Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2014-05-05 07:48:07 European Medicines Agency Pharmaceutical industry Pharmaceutical sciences Health Directive 2001/83/EC Octapharma Research exemption Supplementary protection certificate Clinical research Pharmaceuticals policy Research
193	EUROPEAN COMMISSION HEALTH AND CONSUMERS DIRECTORATE-GENERAL Health systems and products Medicinal products – authorisations, European Medicines Agency PHARM 656 Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2014-05-05 07:45:56 Pharmaceutical sciences Pharmacology European Union Pharmaceutical industry European Medicines Agency Directive 2001/83/EC Clinical Trials Directive EudraLex Clinical research Pharmaceuticals policy Research
194	EUROPA-ENTERPRISE-2008 ICT Standardisation Work Programme Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2012-10-18 12:06:43 Law European Union Privacy law Public law Data Retention Directive Clinical Trials Directive Data Protection Directive Government procurement in the European Union Directive 2001/83/EC European Union directives Clinical research Pharmaceuticals policy
195	Consultation Paper Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:02:34 Medicine Research Good Laboratory Practice Directive 2001/83/EC Medical device Cell therapy Qualified Person Biologic Electronic cigarette Pharmaceuticals policy Clinical research Biology
196	Notes for applicants and holders of a Wholesale Dealer’s Licence (WDA(H)) or Broker Registration MHRA Guidance Note 6 1 Add to Reading List Source URL: www.mhra.gov.uk Language: English - Date: 2014-07-03 12:41:38 Pharmacy Health Pharmaceutical industry Executive agencies of the United Kingdom government Qualified Person Good distribution practice Medical device Veterinary Medicines Directorate Directive 2001/83/EC Pharmaceuticals policy Clinical research Medicine
197	IN GENERAL Comment 1: The ATMP Regulation should urgently be revised to focus on delivering affordable therapies to all those who are in need, without necessarily “placing these products on the European market”. The Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:02:50 Research Health European Union Directive 2001/83/EC Medicinal product Medical device European Directive on Traditional Herbal Medicinal Products Clinical Trials Directive Clinical research Pharmaceuticals policy Medicine
198	March 29, 2013 European Commission DG Health and Consumers Unit D5 ‘Medicinal products – authorisations, EMA’ [removed] In Re: Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:02:32 Pharmaceuticals policy Clinical research American Association of Tissue Banks Medical research Allotransplantation Tissue bank Directive 2001/83/EC Medicinal product Certified Tissue Bank Specialist Medicine Transplantation medicine Health
199	Directive[removed]EC of the European Parliament and of the Council of 18 June 2009 amending Directive[removed]EC and Directive[removed]EC, as regards variations to the terms of marketing authorisations for medicinal pro Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 08:52:57 European Union Health policy Health Directive 2001/83/EC European Medicines Agency Directive 75/318/EEC Directive on intra-EU-transfers of defence-related products Pharmaceuticals policy Clinical research Research
200	[removed]BPI Comments Public Consultation ATMP Regulation Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:02:18 Research Pharmaceuticals policy Pharmaceutical industry European Medicines Agency Pharmacovigilance ATMP Food and Drug Administration Directive 2001/83/EC Advances in Theoretical and Mathematical Physics Pharmaceutical sciences Pharmacology Clinical research

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