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Qualified Person for Pharmacovigilance
Results: 136

#	Item
21	Authorisations by the Department of Agriculture and Rural Development (DARDNI) as the Competent Authority for Northern Ireland under Regulation (ECand Commission Regulation (EUCertain authorisation Add to Reading List Source URL: www.dardni.gov.uk Language: English - Date: 2014-08-13 06:40:07 European Union Council Implementing Regulation (EU) No 282/2011 Qualified Person Responsible For Pharmacovigilance Pharmaceuticals policy European Union directives Clinical research
22	Ref. AresEUROPEAN COMMISSION HEALTH AND CONSUMERS DIRECTORATE-GENERAL Health systems and products Medicinal products – authorisations, EMA Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:30:39 Pharmacology Clinical research Pharmacy Pharmaceuticals policy Pharmacovigilance European Medicines Agency EudraVigilance Qualified Person Responsible For Pharmacovigilance Pharmaceutical sciences Drug safety Health
23	JUDGMENT OF THE COURT 9 April 2015 (Veterinary medicinal products – Supplementary protection certificate – Regulation (EEC) No – Concept of “first authorisation to place a product on the market” in t Add to Reading List Source URL: www.eftacourt.int Language: English - Date: 2015-04-09 05:16:30 Intellectual property law Patent law of the European Union Supplementary protection certificate Pharmaceutical sciences Government European Medicines Agency Directive 65/65/EEC Term of patent Qualified Person Responsible For Pharmacovigilance Clinical research Pharmaceuticals policy Research
24	Information for Applicants / Holders of Marketing Authorisation for Veterinary Medicinal Products with respect to the implementation of the Commission Regulation (EC) No[removed]concerning the examination of variation Add to Reading List Source URL: www.uskvbl.cz Language: English - Date: 2010-02-11 03:34:07 Research Health Pharmaceutical industry EudraLex European Union law Pharmacology Marketing authorization European Medicines Agency Qualified Person Responsible For Pharmacovigilance Pharmaceuticals policy Clinical research Pharmaceutical sciences
25	L[removed]EN Official Journal of the European Union Add to Reading List Source URL: www.biosafety.be Language: English - Date: 2004-04-30 11:18:54 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
26	L[removed]EN Official Journal of the European Union Add to Reading List Source URL: www.biosafety.be Language: English - Date: 2004-04-30 11:18:54 Research Health Pharmacology European Medicines Agency Qualified Person Responsible For Pharmacovigilance Directive 2001/83/EC Pharmacovigilance Qualified Person Summary of Product Characteristics Pharmaceuticals policy Clinical research Pharmaceutical sciences
27	Regulation[removed][removed]2014 Regulation of the Finnish Medicines Agency Add to Reading List Source URL: www.fimea.fi Language: English - Date: 2014-02-20 10:01:55 Health Pharmaceuticals policy Drug safety Clinical research Pharmacovigilance Pharmaceutical industry European Medicines Agency Qualified Person Responsible For Pharmacovigilance Pharmaceutical sciences Pharmacology Pharmacy
28	Under the auspices of The League of Arab State Guideline on good pharmacovigilance practices (GVP) Add to Reading List Source URL: www.jfda.jo Language: English - Date: 2014-11-30 02:08:03 Medicine Pharmaceuticals policy Drug safety Pharmacy Pharmacovigilance Qualified Person Responsible For Pharmacovigilance Pharmaceutical drug Adverse effect Pharmacology Health Pharmaceutical sciences
29	European Commission [removed]European Commission Add to Reading List Source URL: www.medicinenaturali.net Language: English - Date: 2013-04-03 10:18:59 Pharmaceutical sciences Pharmaceuticals policy Drug safety Pharmacy Clinical research Pharmacovigilance Patient safety Adverse effect Qualified Person for Pharmacovigilance Medicine Health Pharmacology
30	E-ALERT \| Food & Drug October 27, 2014 EU COURT OF JUSTICE STRENGTHENS RIGHTS OF ORIGINATORS TOWARDS GENERIC APPROVALS In a ruling of 23 October 2014, 1 the EU Court of Justice concluded that the Medicines Directive Add to Reading List Source URL: www.cov.com Language: English - Date: 2014-10-27 09:49:11 Supplementary protection certificate Qualified Person for Pharmacovigilance Pharmaceuticals policy Test data exclusivity Health