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Results: 263

#	Item
251	BETTER REGULATION OF PHARMACEUTICALS: TOWARDS A SIMPLER, CLEARER AND MORE FLEXIBLE FRAMEWORK ON VARIATIONS Public consultation on the ‘co-decision’ part What is the purpose of this consultation? The Commission has an Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:06:34 Health Pharmaceutical sciences European Medicines Agency Directive 2001/83/EC Directive 75/319/EEC EudraLex Pharmaceuticals policy Clinical research Research
252	eu_gdpguidline_publicconsultation.doc Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 08:56:13 Pharmaceutical sciences Quality Pharmacology Pharmaceutics Food safety Good manufacturing practice Validation EudraLex Good distribution practice Pharmaceutical industry Pharmaceuticals policy Clinical research
253	06.06a D - Draft Annex 16 Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:08:24 Research Health Pharmaceutical sciences Qualified Person Good manufacturing practice European Medicines Agency EudraLex European Directive on Traditional Herbal Medicinal Products Supplementary protection certificate Pharmaceuticals policy Clinical research Pharmaceutical industry
254	30 April[removed]Submission of comments on GDP APIs Comments from: Name of organisation or individual Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-11-07 08:55:20 Research Pharmaceutical sciences Pharmaceutics Good manufacturing practice EudraLex Directive European Medicines Agency Comment Personal digital assistant Clinical research Pharmaceuticals policy Pharmaceutical industry
255	SPECIFIC PRIVACY STATEMENT PUBLIC CONSULTATION ON REVISION OF ANNEX 15 OF GOOD MANUFACTURING PRACTICE GUIDELINES, EUDRALEX, VOL. 4 1. Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2014-02-06 02:57:35 Personally identifiable information Information privacy Security Ethics Human behavior Privacy European Data Protection Supervisor Data privacy
256	COMMISSION OF THE EUROPEAN COMMUNITIES Brussels, 10 December 2008 SEC[removed]Volume I Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:28:13 Medicine Clinical research Pharmaceuticals policy Drug safety Pharmacy Pharmacovigilance European Medicines Agency EudraLex European Directive on Traditional Herbal Medicinal Products Pharmaceutical sciences Pharmacology Health
257	Association Européenne des Spécialités Pharmaceutiques Grand Public Association of the European Self-Medication Industry Europäischer Verband der Arzneimittel-Hersteller AESGP comments on the Commission Guidelines on Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-11-07 08:55:17 Quality European Union law Health policy Health Technology EudraLex Good manufacturing practice Good distribution practice Medicinal product Pharmaceuticals policy Pharmaceutical industry Clinical research
258	Better Medicines for Children Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:12:28 Pharmacology European Medicines Agency Supplementary protection certificate EudraLex EudraCT Paediatric-use marketing authorisation Clinical research Research Pharmaceutical sciences
259	Guideline on good pharmacovigilance practices (GVP), Module VII PSUR Add to Reading List Source URL: www.ema.europa.eu Language: English - Date: 2013-12-12 06:09:27 Clinical research Pharmaceuticals policy Pharmaceutical industry Pharmacology Drug safety European Medicines Agency Pharmacovigilance Marketing authorization EudraLex Medicine Health Pharmaceutical sciences
260	PDF Document Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:04:19 EudraLex Qualified Person European Union Conformity assessment Evaluation Science Sociology Pharmaceuticals policy Clinical research Israel–European Union relations

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