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151	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
152	Better regulation of veterinary pharmaceuticals: how to put in place a simpler legal framework, safeguarding public and animal Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 08:10:17 Pharmacology Health Drug safety Pharmacy European Medicines Agency Pharmacovigilance Test data exclusivity Summary of Product Characteristics EudraLex Pharmaceuticals policy Pharmaceutical sciences Clinical research
153	Better regulation of veterinary pharmaceuticals: how to put in place a simpler legal framework, safeguarding public and animal Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 08:05:58 Pharmacology Health Drug safety Pharmacy European Medicines Agency Pharmacovigilance Test data exclusivity Summary of Product Characteristics EudraLex Pharmaceuticals policy Pharmaceutical sciences Clinical research
154	Microsoft Word - Vol 8 october[removed]doc Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 08:59:14 Research European Medicines Agency Pharmaceutical industry Maximum Residue Limit Pharmaceutical sciences Pharmacology Ammonium bituminosulfonate EudraLex Clinical research Pesticides Soil contamination
155	[removed]EN Official Journal of the European Communities Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:11:10 Veterinary physician Aspirin Milk Pharmacology Research EudraLex Directive 93/41/EEC Clinical research Pharmaceuticals policy Medicine
156	Better regulation of veterinary pharmaceuticals: how to put in place a simpler legal framework, safeguarding public and animal Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 08:18:33 Pharmacology Health Drug safety Pharmacy European Medicines Agency Pharmacovigilance Test data exclusivity Summary of Product Characteristics EudraLex Pharmaceuticals policy Pharmaceutical sciences Clinical research
157	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
158	Better regulation of veterinary pharmaceuticals: how to put in place a simpler legal framework, safeguarding public and animal Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 08:22:28 Pharmacology Health Drug safety Pharmacy European Medicines Agency Pharmacovigilance Test data exclusivity Summary of Product Characteristics EudraLex Pharmaceuticals policy Pharmaceutical sciences Clinical research
159	Better regulation of veterinary pharmaceuticals: how to put in place a simpler legal framework, safeguarding public and animal Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 08:14:52 Pharmacology Health Drug safety Pharmacy European Medicines Agency Pharmacovigilance Test data exclusivity Summary of Product Characteristics EudraLex Pharmaceuticals policy Pharmaceutical sciences Clinical research
160	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