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Directive 2001 83 EC
Results: 312

#	Item
141	COUNCIL OF THE EUROPEAN UNION Brussels, 22 September[removed]OR. en[removed] Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:22:04 Research Health Directive 2001/83/EC European Medicines Agency Clinical Trials Directive Pharmacovigilance Medicinal product Medical device European Directive on Traditional Herbal Medicinal Products Clinical research Pharmaceuticals policy Medicine
142	Microsoft Word - Comments from AssICC on EC Concept paper Sanco.ddg.1.d.6_2… Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:41:50 European Union Law Directive 2001/83/EC EudraLex Europe Good Clinical Practice Directive Battery Directive Clinical research Pharmaceuticals policy European Union directives
143	[removed]EN Official Journal of the European Communities Add to Reading List Source URL: www.fve.org Language: English - Date: 2014-06-03 16:50:49 Health Pharmaceutical sciences Pharmacology Pharmaceutical industry European Union Directive 93/41/EEC Directive 2001/83/EC Marketing authorization Homeopathy Pharmaceuticals policy Clinical research Medicine
144	[removed]EN Official Journal of the European Union Add to Reading List Source URL: www.fve.org Language: English - Date: 2014-06-03 16:50:47 Pharmaceutical sciences Health European Medicines Agency Directive 93/41/EEC Clinical Trials Directive Directive 2001/83/EC Pharmacovigilance Summary of Product Characteristics Supplementary protection certificate Clinical research Pharmaceuticals policy Research
145	EIPG COMMENTS on Sanco.ddg1.d[removed]Extension of the Directive on GMP for medicinal products to active substances Consultation Item No 1: Do you agree with this appraisal and approach? Yes, we agree with this app Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:44:17 EudraLex Medicinal product Qualified Person Law Government Clinical Trials Directive Directive 2001/83/EC Pharmaceuticals policy Clinical research Health
146	Comments on the Concept Paper submitted for Public Consultation concerning the Delegated Act on Principles and Guidelines of Good Manufacturing Practice for Active Substances in Medicinal Products for Human use. Ref: San Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:41:49 Pharmaceutical sciences Health policy EudraLex Good manufacturing practice Qualified Person Medicinal product Directive 2001/83/EC Validation Qualified Person for Pharmacovigilance Pharmaceuticals policy Clinical research Research
147	REGULATION (EEC) No[removed]Council Regulation (EEC) No[removed]of 22 July 1993 laying down Community procedures for the authorization and supervision of medicinal products for human and veterinary use and establishing a Add to Reading List Source URL: www.fve.org Language: English - Date: 2014-06-03 16:50:49 Research Pharmacy Directive 75/318/EEC Directive 75/319/EEC Good Laboratory Practice Directive 93/41/EEC Marketing authorization Directive 65/65/EEC Directive 2001/83/EC Pharmaceuticals policy Clinical research Health policy
148	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: www.fve.org Language: English - Date: 2014-06-03 16:50:48 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
149	L[removed]EN Official Journal of the European Union Add to Reading List Source URL: www.fve.org Language: English - Date: 2014-06-03 16:50:48 Pharmacology Research Health Pharmaceutical industry European Medicines Agency Good Laboratory Practice Pharmacovigilance Summary of Product Characteristics Directive 2001/83/EC Clinical research Pharmaceutical sciences Pharmaceuticals policy
150	L[removed]EN Official Journal of the European Union Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:22:07 Health policy Health Clinical Trials Directive Directive 2001/83/EC Good manufacturing practice Qualified Person Good Clinical Practice Directive EudraLex Pharmaceuticals policy Clinical research Research

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