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EudraGMP
Results: 7

#	Item
1	2012–2013 Annual Report of the HMA Strategy Postal address: Heads of Medicines Agencies Permanent Secretariat, Add to Reading List Source URL: www.hma.eu Language: English - Date: 2013-07-05 09:59:50 Health Drug safety Pharmaceuticals policy Pharmacy European Medicines Agency Pharmacovigilance European Directorate for the Quality of Medicines EudraVigilance EudraGMP Pharmaceutical sciences Pharmacology Clinical research
2	Introduction to the EU telematics programme Add to Reading List Source URL: www.hma.eu Language: English - Date: 2012-06-08 09:27:42 Pharmaceutical sciences Research Drug safety EudraGMP European Medicines Agency EUDRANET EudraPharm EudraVigilance Telematics Pharmaceuticals policy Health clinical research
3	EUROPEAN COMMISSION HEALTH AND CONSUMERS DIRECTORATE-GENERAL Health systems and products Medicinal products – authorisations, EMA Head of Unit Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 08:47:49 Health Clinical research Drug safety Council of Europe Pharmacy European Directorate for the Quality of Medicines Pharmacovigilance EudraGMP European Pharmacopoeia Pharmaceuticals policy Pharmaceutical sciences Medicine
4	EUROPEAN COMMISSION HEALTH AND CONSUMERS DIRECTORATE-GENERAL Health systems and products Medicinal products – Quality, safety and efficacy PHARM 633 Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-11-21 03:31:56 Research Pharmaceutical sciences Health European Union directives European Medicines Agency EudraLex EudraGMP Good manufacturing practice Clinical Trials Directive Pharmaceuticals policy Clinical research Pharmaceutical industry
5	Submission of comments on TEMPLATE FOR THE QUALIFIED PERSON’S DECLARATION CONCERNING GMP COMPLIANCE OF INVESTIGATIONAL MEDICINAL PRODUCTS MANUFACTURED IN NON-EU COUNTRIES Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:30:25 Pharmaceutical industry Health Pharmaceutical sciences Clinical Data Management EudraCT Qualified Person EudraGMP European Medicines Agency Audit Clinical research Pharmaceuticals policy Research
6	Batch Certificate Rev 5 Final _Adopted during 62th GMDP IWG meeting in May 2011 Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:07:53 Food safety Good manufacturing practice Health EudraGMP Medicine Pharmaceuticals policy Pharmaceutical industry clinical research
7	Work Plan for GMP/GDP Inspectors Working Group for 2013 Add to Reading List Source URL: www.ema.europa.eu Language: English - Date: 2013-07-21 04:58:08 Pharmaceutics Quality Pharmaceutical sciences Pharmacology Validation Validity European Medicines Agency EudraGMP Good distribution practice Pharmaceutical industry Pharmaceuticals policy Clinical research

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