Good Clinical Laboratory Practice - PDFSEARCH.IO - Document Search Engine

Good Clinical Laboratory Practice
Results: 226

#	Item
191	Disclaimer: This document is intended for use as a documentation tool and the Institutions do not assume any liability for its content. Working document Version 6 – (4 May[removed]List of Legislation Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2012-03-20 13:51:52 Evaluation Reference Standards Directive 93/41/EEC Good Laboratory Practice Pharmaceuticals policy European Union directives Clinical research
192	Anifeed/O-sanco/crendbref 9-10 juillet[removed]SUMMARY MINUTES OF THE MEETING OF THE STANDING COMMITTEE FOR FEEDINGSTUFFS 9-10 July 2001 CHAIRMAN: W. Penning Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2012-03-20 14:29:41 Clinical research Pharmaceuticals policy European Union law European Union directives Good Laboratory Practice Evaluation Reference Standards
193	SUMMARY MINUTES OF THE MEETING OF THE STANDING COMMITTEE ON THE FOOD CHAIN AND ANIMAL HEALTH Animal Nutrition Section 20 November 2003 STANDING COMMITTEE 1. Discussion and possible request for an opinion on a Draft Commi Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2012-03-20 14:40:45 Evaluation Reference Standards European Union law Law Good Laboratory Practice Clinical Trials Directive Pharmaceuticals policy Clinical research European Union directives
194	Microsoft PowerPoint - 11 SMITH Merton (FDA) VICH.ppt [Mode de compatibilité] Add to Reading List Source URL: www.rr-africa.oie.int Language: English - Date: 2010-11-24 09:13:32 Pharmacology Clinical research Health Food and Drug Administration United States Public Health Service Good manufacturing practice Good Laboratory Practice Good Clinical Practice Regulatory requirement Pharmaceuticals policy Pharmaceutical sciences Pharmaceutical industry
195	COMMISSION OF THE EUROPEAN COMMUNITIES Brussels, [removed]COM[removed]final REPORT FROM THE COMMISSION TO THE COUNCIL AND THE EUROPEAN Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2012-03-20 14:36:18 Standards Pharmaceuticals policy European Union Clinical research ISIRI Good Laboratory Practice European Union directives Evaluation Reference
196	L[removed]EN Official Journal of the European Union Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 08:59:37 Pharmacology Research Health Pharmaceutical industry European Medicines Agency Good Laboratory Practice Pharmacovigilance Summary of Product Characteristics Directive 2001/83/EC Clinical research Pharmaceutical sciences Pharmaceuticals policy
197	Consultation Paper Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:02:34 Medicine Research Good Laboratory Practice Directive 2001/83/EC Medical device Cell therapy Qualified Person Biologic Electronic cigarette Pharmaceuticals policy Clinical research Biology
198	Corporate Plan[removed] Add to Reading List Source URL: www.mhra.gov.uk Language: English - Date: 2013-04-11 11:41:47 Clinical research Pharmaceutical industry Pharmacology Pharmacy Department of Health Medicines and Healthcare products Regulatory Agency Pharmacovigilance Medical device Good Laboratory Practice Medicine Health Pharmaceutical sciences
199	Canada-EC Regulatory Cooperation Roadmap[removed]March 2009 Chemicals Cooperation between the European Commission and Canada regarding: (1) the regulation of substances, and (2) the effective implementation of their Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2012-10-18 11:44:01 Pharmaceutical sciences Research Good Laboratory Practice Organisation for Economic Co-operation and Development European Directorate for the Quality of Medicines Environment Canada European Medicines Agency Validation Pharmacovigilance Clinical research Government Pharmaceutical industry
200	Microsoft Word - Annex 1 EU-NETVAL-EligibilityCriteria Januari 2013 for web.docx Add to Reading List Source URL: ihcp.jrc.ec.europa.eu Language: English - Date: 2014-01-20 06:09:09 Evaluation Standards Quality Pharmaceutical industry Validity ISO/IEC 17025 Good Clinical Laboratory Practice Validation Good Laboratory Practice Quality management Technology Science

UPDATE