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51	ADVISORY Advice on the implementation of EU-Directive[removed]EU Add to Reading List Source URL: www.egagenerics.com Language: English - Date: 2014-12-27 09:47:51 Research European Union Law EudraLex Directive 2001/83/EC Clinical Trials Directive European Medicines Agency Clinical research Pharmaceuticals policy European Union directives
52	L[removed]EN Official Journal of the European Union Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:46:09 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
53	CMDh BEST PRACTICE GUIDE ON THE PROCESSING OF RENEWALS IN THE MUTUAL RECOGNITION AND DECENTRALISED PROCEDURES CMDh[removed]Rev.10 November 2014 Add to Reading List Source URL: www.hma.eu Language: English - Date: 2014-12-02 06:50:38 Risk Pharmacology Drug safety Clinical research Pharmacy Pharmacovigilance Maintenance fee Risk assessment EudraLex Pharmaceuticals policy Pharmaceutical sciences Statistics
54	Ref. Ares[removed][removed]EUROPEAN COMMISSION HEALTH AND CONSUMERS DIRECTORATE-GENERAL Health systems and products Medicinal products – authorisations, European Medicines Agency Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2014-08-26 06:09:08 Health Pharmaceutical industry European Medicines Agency Pharmaceuticals policy Medical device Pharmacovigilance EudraLex Medicine Pharmaceutical sciences Clinical research
55	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 08:10:19 Pharmacology Health Drug safety Pharmacy European Medicines Agency Pharmacovigilance Test data exclusivity Summary of Product Characteristics EudraLex Pharmaceuticals policy Pharmaceutical sciences Clinical research
56	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 08:06:56 Pharmacology Health Drug safety Pharmacy European Medicines Agency Pharmacovigilance Test data exclusivity Summary of Product Characteristics EudraLex Pharmaceuticals policy Pharmaceutical sciences Clinical research
57	Formatted: Font: 14 pt, Bold Formatted: Font: 14 pt, Bold VETERINARY MEDICINES GUIDANCE NOTE Add to Reading List Source URL: www.vmd.defra.gov.uk Language: English - Date: 2014-09-11 04:34:34 Clinical research Health Pharmacology Quality Veterinary Medicines Directorate Qualified Person Good manufacturing practice EudraLex Validation Pharmaceuticals policy Pharmaceutical sciences Pharmaceutical industry
58	Microsoft Word - PCDOCS-#[removed]v4-VMGN_008_Wholesale_Dealers_Authorisations_-_CONSULTATION_Version.doc Add to Reading List Source URL: www.vmd.defra.gov.uk Language: English Research Pharmaceutical sciences Pharmacy Veterinary Medicines Directorate Pharmaceuticals policy Medicines and Healthcare products Regulatory Agency EudraLex Validation Veterinary physician Clinical research Executive agencies of the United Kingdom government Pharmaceutical industry
59	Microsoft Word - PCDOCS-#[removed]v3-VMGN_15_Manufacturing_Authorisations_-_CONSULTATION_VERSION.doc Add to Reading List Source URL: www.vmd.defra.gov.uk Language: English - Date: 2014-09-11 04:34:35 Clinical research Health Pharmacology Quality Veterinary Medicines Directorate Qualified Person Good manufacturing practice EudraLex Validation Pharmaceuticals policy Pharmaceutical sciences Pharmaceutical industry
60	Microsoft Word - PCDOCS-#[removed]v2-DRAFT_VMGN_9_Guidance_on_appeals_against_regulatory_decisions.doc Add to Reading List Source URL: www.vmd.defra.gov.uk Language: English Health Pharmacology Veterinary Medicines Directorate Pharmaceuticals policy European Medicines Agency EudraLex Pharmacovigilance Veterinary physician Pharmaceutical sciences Clinical research Medicine

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