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Good Clinical Practice Directive
Results: 216

#	Item
131	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
132	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
133	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
134	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
135	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
136	090166e584a29a9e[removed]doc Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:00:27 Health EudraLex Clinical Trials Directive Good Clinical Practice Directive Clinical trial IMP Good Clinical Practice Ethics Committee EudraCT Clinical research Research Pharmaceutical sciences
137	ClinicalTrials_BIS_8p.Nov.11.indd Add to Reading List Source URL: www.esf.org Language: English - Date: 2012-01-27 09:43:23 Pharmaceutical sciences Pharmaceutics Pharmaceuticals policy Pharmacology European Science Foundation Science and technology in Europe Clinical Trials Directive EudraLex Good Clinical Practice Clinical research Pharmaceutical industry Research
138	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
139	Regulation (EC) No [removed]of the European Parliament and of the Council of 6 May 2009 laying down Community procedures for the establishment of residue limits of pharmacologically active substances in foodstuffs of a Add to Reading List Source URL: www.fve.org Language: English - Date: 2014-06-03 16:50:42 European Medicines Agency Pharmaceutical industry Biocidal Products Directive European Union Government Good Laboratory Practice European Chemicals Bureau Clinical research European Union directives Research
140	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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