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Final good
Results: 556

#	Item
511	ega-pos-pap[removed]ec-consultation-counterfeit medicines &慭瀻 api gmp-FINAL Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2011-09-02 06:31:46 Pharmacology Health Pharmacy Clinical research Good manufacturing practice Good distribution practice Counterfeit medications Traceability Directive 2001/83/EC Pharmaceuticals policy Pharmaceutical sciences Pharmaceutical industry
512	GMP Guide Chapter 1 Q10 implementation final Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:07:51 Pharmaceutical industry Pharmacology Pharmaceutical sciences Research European Union directives Good manufacturing practice Biologic Validation Biotechnology Biology Pharmaceuticals policy Clinical research
513	Microsoft Word - 2008_09_Annex 3 final public.doc Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:03:00 Pharmaceutical industry Validity Food safety Radiopharmaceuticals Validation Nuclear medicine Good manufacturing practice Radioactive contamination Radiopharmacology Medicine Health Radiobiology
514	EUROPEAN COMMISSION Brussels, [removed]SWD[removed]final VOLUME I Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:29:39 Pharmaceutical sciences Pharmaceuticals policy Science Pharmacology Evaluation methods Clinical Trials Directive European Forum for Good Clinical Practice Regulatory requirement European Medicines Agency Clinical research Research Pharmaceutical industry
515	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
516	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
517	Microsoft Word - Annex15 final.doc Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:10:42 Systems engineering Science Technology Quality Validation Business Verification and validation Verification Good manufacturing practice Pharmaceutical industry Validity Food safety
518	Microsoft Word - Good_practice_report_final_ETC.doc Add to Reading List Source URL: icm.eionet.europa.eu Language: English - Date: 2009-09-01 05:18:50 Effects of global warming Adaptation to global warming Global warming Climate change policy United Nations Framework Convention on Climate Change River Basin Management Plans Intergovernmental Panel on Climate Change Current sea level rise Water crisis Environment Earth Climate change
519	GMP Guide Chapter 1 Q10 implementation final Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:08:23 Quality Technology Pharmaceutics Clinical research Pharmaceuticals policy Good manufacturing practice Corrective and preventive action Validation ISO Pharmaceutical industry Quality management Business
520	Chapter 7 final version[removed] Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:08:40 Clinical research International economics Contract law Health Good manufacturing practice Law Outsourcing EudraLex Contract Pharmaceuticals policy Pharmaceutical industry Business

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