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Qualified Person for Pharmacovigilance
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101	Draft COMMISSION REGULATION (EC) No …/.. of […] on the conditional marketing authorisation for medicinal products falling within the scope of Regulation (EC) No[removed]of the European Parliament and the Council of Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:24:03 Pharmaceutical sciences Health European Medicines Agency Directive 2001/83/EC Summary of Product Characteristics Supplementary protection certificate Qualified Person Responsible For Pharmacovigilance Clinical research Pharmaceuticals policy Research
102	Microsoft Word - introduction and orientation.doc Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:24:09 Pharmaceuticals policy Health Pharmacology Pharmacy Pharmacovigilance European Medicines Agency EudraVigilance Qualified Person Responsible For Pharmacovigilance Pharmaceutical sciences Clinical research Drug safety
103	Microsoft PowerPoint - PVig ENTR[removed]ppt Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:51:38 Pharmaceutical sciences Pharmacovigilance Patient safety Adverse effect Pharmaceutical drug Qualified Person Responsible For Pharmacovigilance Medicine Pharmacology Health
104	Microsoft PowerPoint - 13 HOLM Anja (EMA) EMA.ppt [Mode de compatibilité] Add to Reading List Source URL: www.rr-africa.oie.int Language: English - Date: 2010-11-24 09:14:54 Pharmaceutical sciences Pharmacology European Medicines Agency EudraLex European Directorate for the Quality of Medicines Pharmacovigilance Qualified Person Qualified Person Responsible For Pharmacovigilance Good Clinical Practice Directive Clinical research Pharmaceuticals policy Research
105	EUROPEAN COMMISSION Brussels, XXX […](2013) XXX draft Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-11-21 02:55:10 Quality Pharmacology Good distribution practice Pharmaceutics Clinical research Quality management system European Medicines Agency Qualified Person for Pharmacovigilance Pharmaceutical industry Pharmaceuticals policy Pharmaceutical sciences
106	EUROPEAN COMMISSION HEALTH AND CONSUMERS DIRECTORATE-GENERAL Health systems and products Medicinal products – authorisations, EMA PHARM 618 Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 08:48:36 Pharmaceutical sciences Health EudraLex Directive 2001/83/EC Pharmacovigilance Qualified Person Responsible For Pharmacovigilance Regulation Directive Medicinal product Pharmaceuticals policy Clinical research Research
107	EUROPEAN COMMISSION HEALTH AND CONSUMERS DIRECTORATE-GENERAL Health systems and products Medicinal products – authorisations, European Medicines Agency PHARM 626 Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-30 04:50:13 Pharmaceuticals policy Health Drug safety Pharmacy European Medicines Agency Pharmacovigilance Albert Borschette Biosimilar Qualified Person Responsible For Pharmacovigilance Pharmaceutical sciences Pharmacology Clinical research
108	2011_09_21_public_consultation.doc Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:35:30 Health Drug safety Pharmacy Pharmacovigilance Medical device Systems engineering process Qualified Person for Pharmacovigilance Medicine Pharmaceutical sciences Pharmacology
109	EUROPEAN COMMISSION HEALTH AND CONSUMERS DIRECTORATE-GENERAL Health systems and products Medicinal products – authorisations, European Medicines Agency PHARM 648 Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2014-05-05 07:48:08 Pharmacology Health Drug safety Pharmacy European Medicines Agency Pharmacovigilance Directive 2001/83/EC Qualified Person Responsible For Pharmacovigilance Supplementary protection certificate Pharmaceuticals policy Clinical research Pharmaceutical sciences
110	EUROPEAN COMMISSION HEALTH AND CONSUMERS DIRECTORATE-GENERAL Health systems and products Medicinal products – authorisations, EMA PHARM 635 Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-30 04:33:16 Pharmacology Health Drug safety Pharmacy Pharmacovigilance European Medicines Agency Directive 2001/83/EC Qualified Person Responsible For Pharmacovigilance Qualified Person for Pharmacovigilance Pharmaceutical sciences Clinical research Pharmaceuticals policy