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Results: 263

#	Item
171	Association Européenne des Spécialités Pharmaceutiques Grand Public Association of the European Self-Medication Industry Europäischer Verband der Arzneimittel-Hersteller AESGP comments on the European Commission’s Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:30:30 Drug safety Pharmaceuticals policy Pharmacy Clinical research Pharmacovigilance EudraLex Pharmaceutical drug European Medicines Agency Regulation of therapeutic goods Pharmaceutical sciences Pharmacology Health
172	Microsoft Word - DGentr-PH-COM_2002_735-F2PH311medicame_EN_ACTE.doc Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:06:39 Research Pharmacology European Medicines Agency Pharmaceutical industry Pharmacovigilance Directive 2001/83/EC Good Laboratory Practice Qualified Person Responsible For Pharmacovigilance EudraLex Clinical research Pharmaceutical sciences Pharmaceuticals policy
173	European Medicines Agency Human Medicines Evaluation Unit London, 5 February 2007 CPMP[removed], Revision 5 Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:51:35 Pharmaceutical industry Pharmaceutical sciences Pharmacology Health European Medicines Agency EudraLex Committee for Medicinal Products for Human Use Validation Summary of Product Characteristics Clinical research Research Pharmaceuticals policy
174	EUROPEAN COMMISSION HEALTH AND CONSUMERS DIRECTORATE-GENERAL Public health and Risk assessment Pharmaceuticals Brussels, 01 June 2010 Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:30:22 Health Pharmaceutical sciences Pharmaceutical industry Pharmacology EudraLex European Union law Good manufacturing practice Clinical trial Qualified Person Clinical research Pharmaceuticals policy Research
175	technical_guidance_en.doc Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:30:21 EudraCT ClinicalTrials.gov Clinical trials registry European Medicines Agency Clinical Trials Directive Clinical trial EudraLex Regulatory requirement Clinical research Research Health
176	RTF Document Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:37:37 Pharmacology Research Pharmaceuticals policy Pharmaceutics Pharmacopoeias EudraLex European Pharmacopoeia Validation Excipient Pharmaceutical industry Clinical research Pharmaceutical sciences
177	Microsoft Word - HMA_text_for_website_on_botanicals_2012_fin.docx Add to Reading List Source URL: www.hma.eu Language: English - Date: 2012-12-21 06:17:00 Technology European Directive on Traditional Herbal Medicinal Products European Union Nutrition Clinical research Dietary supplement Alternative medicine Health claims on food labels EudraLex Health Medicine Packaging
178	[removed]EN Official Journal of the European Union Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:24:06 Pharmaceutical sciences Health European Medicines Agency Directive 2001/83/EC EudraLex Council Implementing Regulation (EU) No 282/2011 Clinical research Pharmaceuticals policy Research
179	[removed]EN Official Journal of the European Communities Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:45:15 Health Pharmaceutical sciences European Medicines Agency Directive 65/65/EEC Directive 75/319/EEC Supplementary protection certificate EudraLex Pharmaceuticals policy Clinical research Research
180	Microsoft Word - Rev July[removed]doc Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 08:55:14 Health Pharmacology Pharmaceutical industry Drug safety Qualified Person EudraLex Good manufacturing practice Pharmacovigilance Supplementary protection certificate Pharmaceuticals policy Pharmaceutical sciences Clinical research

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