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Qualified Person for Pharmacovigilance
Results: 136

#	Item
41	Administrative regulation[removed]Dnro[removed][removed]UNOFFICIAL TRANSLATION Add to Reading List Source URL: www.fimea.fi Language: English Research Health European Medicines Agency European Directive on Traditional Herbal Medicinal Products Directive 2001/83/EC Pharmacovigilance Qualified Person Qualified Person Responsible For Pharmacovigilance Supplementary protection certificate Pharmaceuticals policy Clinical research Pharmaceutical sciences
42	L[removed]EN Official Journal of the European Union Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 08:52:52 Research Health Pharmacology European Union Pharmaceutical industry European Medicines Agency Supplementary protection certificate Qualified Person Responsible For Pharmacovigilance Clinical Trials Directive Pharmaceuticals policy Clinical research Pharmaceutical sciences
43	CONTACT INFORMATION The person responsible for pharmacovigilance (EU QPPV) and possible contact person in Finland (Administrative regulations of the Finnish Medicines Agency (Fimea[removed], [removed]and[removed]) Add to Reading List Source URL: www.fimea.fi Language: English Health Pharmacy Pharmaceuticals policy Pharmacovigilance Clinical research Qualified Person Responsible For Pharmacovigilance Qualified Person for Pharmacovigilance Pharmaceutical sciences Pharmacology Drug safety
44	AESGP Workshop London \| 23-24 October 2013 Making the European marketing authorisation procedures work for non-prescription medicines European and national regulators and industry representatives participated at the AESG Add to Reading List Source URL: www.aesgp.eu Language: English Health Pharmaceutical industry Drug safety Pharmacy European Medicines Agency Pharmacovigilance Medicines and Healthcare products Regulatory Agency Veterinary Medicines Directorate Qualified Person Responsible For Pharmacovigilance Pharmaceutical sciences Pharmacology Clinical research
45	HEADS OF AGENCIES AD HOC WORKING GROUP - ESTABLISHING A EUROPEAN RISK MANAGEMENT STRATEGY Add to Reading List Source URL: www.hma.eu Language: English - Date: 2007-03-07 07:36:46 Drug safety Clinical research Pharmaceuticals policy Pharmacy Pharmacovigilance EudraVigilance European Medicines Agency Pharmacoepidemiology Qualified Person Responsible For Pharmacovigilance Pharmaceutical sciences Pharmacology Health
46	EUROPEAN COMMISSION Brussels, [removed]COM[removed]final[removed]COD) Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2014-10-02 03:33:14 Health European Medicines Agency Directive 2001/83/EC Qualified Person Responsible For Pharmacovigilance Supplementary protection certificate Pharmaceuticals policy Clinical research Research
47	POSITION PAPER ON THE TRANSPARENCY POLICY OF THE COORDINATION GROUP FOR MUTUAL RECOGNITION AND DECENTRALISED PROCEDURES – HUMAN (CMDh) Doc. Ref.: CMDh[removed], Rev1 December 2012Rev.2 March 2014 Add to Reading List Source URL: www.hma.eu Language: English - Date: 2014-04-14 11:57:50 Drug safety Pharmacy Pharmaceuticals policy Pharmacovigilance Magnetic resonance imaging Clinical research Qualified Person Responsible For Pharmacovigilance European Medicines Agency Pharmaceutical sciences Pharmacology Health
48	POSITION PAPER ON THE TRANSPARENCY POLICY OF THE COORDINATION GROUP FOR MUTUAL RECOGNITION AND DECENTRALISED PROCEDURES – HUMAN (CMDh) Doc. Ref.: CMDh[removed], Rev.2 March 2014 Introduction Add to Reading List Source URL: www.hma.eu Language: English - Date: 2014-04-14 11:57:49 Pharmacy Health Pharmaceuticals policy Pharmacovigilance Clinical research European Medicines Agency Qualified Person Responsible For Pharmacovigilance Pharmaceutical sciences Pharmacology Drug safety
49	EUROPEAN COMMISSION Brussels, [removed]COM[removed]final[removed]COD) Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2014-10-02 03:41:28 Research Health Pharmacology European Medicines Agency Pharmaceutical industry Pharmacovigilance Directive 65/65/EEC Summary of Product Characteristics Qualified Person Responsible For Pharmacovigilance Clinical research Pharmaceutical sciences Pharmaceuticals policy
50	EUROPEAN COMMISSION Brussels, XXX […](2014) XXX draft Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2014-09-10 03:22:40 Health European Medicines Agency Directive 2001/83/EC Qualified Person Responsible For Pharmacovigilance Supplementary protection certificate Pharmaceuticals policy Clinical research Research

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