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Results: 263

#	Item
231	EUROPEAN COMMISSION HEALTH AND CONSUMERS DIRECTORATE-GENERAL Public Health and Risk Assessment Pharmaceuticals Brussels, Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:37:29 Quality Pharmaceutical sciences Business Research Good manufacturing practice Quality assurance Good distribution practice Validation EudraLex Pharmaceuticals policy Pharmaceutical industry Clinical research
232	eu_gdpguidline_publicconsultation.doc Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:37:42 Pharmaceutical sciences Quality Pharmacology Pharmaceutics Food safety Good manufacturing practice Validation EudraLex Good distribution practice Pharmaceutical industry Pharmaceuticals policy Clinical research
233	EUROPEAN COMMISSION Brussels, [removed]SWD[removed]final VOLUME II (Annexes) Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:29:42 Clinical Trials Directive EudraLex Clinical trial Good Clinical Practice Pharmacovigilance EudraCT Ethics Committee Medical research Serious adverse event Clinical research Research Health
234	SUBMISSION OF COMMENTS ON DRAFT DIRECTIVE OF THE EUROPEAN PARLIAMENT AND OF THE COUNCIL AMENDING DIRECTIVE[removed]EC AND DIRECTIVE[removed]EC AS REGARDS AMENDMENTS TO THE TERMS OF MARKETING AUTHORISATIONS FOR MEDICAL P Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:06:35 Health Pharmaceutical sciences European Medicines Agency Directive EudraLex Directive 75/319/EEC Pharmaceuticals policy Clinical research Research
235	Microsoft Word - 2005_12_GMP Part I Chapter 8 Final.doc Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:09:44 Pharmaceutical industry Health policy Product liability Product recall Health Qualified Person Recall EudraLex Good manufacturing practice Pharmaceuticals policy Clinical research Research
236	EUROPEAN COMMISSION HEALTH AND CONSUMERS DIRECTORATE-GENERAL Health systems and products Pharmaceuticals Brussels, [removed] Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:46:17 Research Pharmaceutics Pharmaceutical sciences European Union law Food safety Good manufacturing practice Validation EudraLex European Medicines Agency Clinical research Pharmaceutical industry Pharmaceuticals policy
237	Microsoft Word - Chapter[removed]final.doc Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:37:47 Pharmaceutical industry Pharmaceutical sciences Health European Medicines Agency Pharmacology EudraLex Test data exclusivity Validation Summary of Product Characteristics Clinical research Pharmaceuticals policy Research
238	EUROPEAN COMMISSION Brussels, [removed]COM[removed]final Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2014-04-01 08:56:22 Pharmaceutical sciences Health European Medicines Agency EudraLex Pharmacovigilance Cell therapy Medical device Directive 2001/83/EC Alternative medicine Pharmaceuticals policy Clinical research Medicine
239	CHAPTER 3 COMMUNITY REFERRAL Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2014-05-26 08:08:04 Research Pharmacology Health Drug safety Pharmacy European Medicines Agency EudraLex Summary of Product Characteristics Pharmacovigilance Clinical research Pharmaceuticals policy Pharmaceutical sciences
240	EUROPEAN COMMISSION HEALTH AND CONSUMERS DIRECTORATE-GENERAL Health systems and products Medicinal products – quality, safety and efficacy Brussels, [removed] Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:37:30 European Union Law Health EudraLex Directive 2001/83/EC Medicinal product Qualified Person Clinical Trials Directive Good Clinical Practice Directive Clinical research Pharmaceuticals policy European Union directives

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