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GMP
Results: 1048

#	Item
971	Microsoft Word[removed]EMA comments form_IMP_GMP declaration 3rd countries_comments EQPA.doc Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:30:28 Audit Auditing Clinical research Pharmaceuticals policy Qualified Person
972	Vienna, 27 March[removed]SANCO/D/6/SF/mg/ddg1.d[removed]PHARMIG response to the European Commission Draft: Template for the Qualified Person’s Declaration Concerning GMP Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:30:26 Audit Qualified Person Auditing Pharmaceuticals policy Information technology audit Clinical research
973	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
974	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
975	[removed]:14 From: Audny Stenbråten [[removed]] Sent: vendredi 30 décembre[removed]:59 To: SANCO GMP Subject: Public consultation Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:37:36 Pharmaceuticals policy Clinical research
976	[removed]:12 From: Koen VINCENT (DHL EUHQ) [[removed]] Sent: lundi 24 octobre[removed]:08 To: SANCO GMP; [removed]! Subject: Draft GDP Guidelines - comments Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:37:42 Broward County Florida DHL Express Express mail North Rhine-Westphalia Transport hub Consignee Transport Technology Business
977	GMP_chapter6_final [removed]GMP_chapter6_final Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2014-03-31 10:03:22 Pharmaceutical industry Validity Quality Tests Test method Protocol Validation Verification and validation Specification Science Technology Evaluation
978	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
979	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
980	[removed]:08 From: Belsky, Kimberly [[removed]] Sent: mercredi 28 décembre[removed]:13 To: SANCO GMP; [removed] Subject: Regarding: Public consultation of the revised Commission guideline Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:37:44 Business Management Validation Validity Security Systems engineering process Risk management Science Quality Pharmaceutical industry Clinical research

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