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#	Item
31	EUROPEAN COMMISSION HEALTH AND CONSUMERS DIRECTORATE-GENERAL Health systems and products Medicinal products – authorisations, European Medicines Agency PHARM 675 Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2014-10-24 08:51:03 European Medicines Agency Pharmaceutical sciences Research Pharmacology EudraLex Clinical research Directorate-General for Health and Consumers Pharmaceuticals policy
32	EUROPEAN COMMISSION Brussels, [removed]COM[removed]final[removed]COD) Add to Reading List Source URL: www.parlament.gv.at Language: English - Date: 2012-07-18 02:09:49 Health Pharmaceutical sciences Pharmaceutical industry Pharmacology European Union Clinical Trials Directive EudraLex Good Clinical Practice Directive European Medicines Agency Clinical research Research Pharmaceuticals policy
33	European Commission - Statement Commissioner Andriukaitis hails half a century of European pharmaceutical legislation Brussels, 30 January 2015 This year marks the 50th anniversary of the birth of pharmaceutical legisla Add to Reading List Source URL: europa.eu Language: English Health Pharmaceutical industry European Union Federalism European Medicines Agency EudraLex Pharmaceuticals policy Pharmaceutical sciences Pharmacology
34	RECOMMENDATION FOR IMPLEMENTATION OF COMMISSION DECISIONS OR CMDh AGREEMENTS FOLLOWING UNION REFERRAL PROCEDURES WHERE THE MARKETING AUTHORISATION IS MAINTAINED OR VARIED Doc. Ref.: CMDh[removed]September 2014 Add to Reading List Source URL: www.hma.eu Language: English - Date: 2014-10-09 13:06:26 Referral marketing EudraLex Clinical research Pharmaceuticals policy Internet marketing
35	CMD(h) AGREEMENT POSITION PAPER ON SUNSET CLAUSE AND ITS APPLICATION TO MARKETING AUTHORISATIONS GRANTED IN MORE THAN ONE MEMBER STATE Doc. Ref.: CMDh[removed]Rev 1 December 2006March 2011 Legal background Add to Reading List Source URL: www.hma.eu Language: English - Date: 2011-03-28 10:49:34 Pharmaceutical sciences EudraLex Article One of the United States Constitution Research Health Pharmacology Pharmaceutical industry Supplementary protection certificate Qualified Person for Pharmacovigilance Pharmaceuticals policy Clinical research European Union law
36	PERF III Acquis Working Group Doc. Ref.: EMEA/PERF/Acq[removed]en/Final This document sets out discussions held in the PERF III Acquis Group. It intends to facilitate preparation and implementation of the relevant EC leg Add to Reading List Source URL: www.hma.eu Language: English - Date: 2007-02-25 18:38:59 EudraLex European Union Political philosophy Europe Supplementary protection certificate European Medicines Agency Pharmaceuticals policy Clinical research European Union law
37	08 January 2010 EMA[removed]European Medicines Agency response to the European Commission’s “ASSESSMENT OF THE FUNCTIONING OF THE “CLINICAL TRIALS DIRECTIVE” [removed]EC” launched in October 2009. Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:33:24 Pharmaceutical sciences European Medicines Agency EudraVigilance EudraCT Clinical trial Clinical Trials Directive Good Clinical Practice Ethics Committee EudraLex Clinical research Research Health
38	Policy Forum The Unintended Consequences of Clinical Trials Regulations Alex D. McMahon1, David I. Conway1, Tom M. MacDonald2, Gordon T. McInnes3 1 Dental School, Faculty of Medicine, University of Glasgow, Glasgow, Sc Add to Reading List Source URL: ec.europa.eu Language: English* - Date: 2013-10-09 09:33:26 Good Clinical Practice EudraLex Clinical Trials Directive Clinical trial Adverse event Pharmaceutical industry Institutional review board Ethics Committee European Organisation for Research and Treatment of Cancer Clinical research Research Pharmaceutical sciences
39	Comments E C C O 8 Jan 2010_...tioning of CTD[removed]EC.pdf Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:33:40 European Union European Union directives Europe Research Clinical Trials Directive Directive Internal Market Good Clinical Practice Directive EudraLex Pharmaceuticals policy Clinical research European Union law
40	MINISTERIO DE SANIDAD Y POLÍTICA SOCIAL COMMENTS ON THE ASSESSMENT OF THE FUNCTIONING OF THE “CLINICAL TRIALS DIRECTIVE” [removed]EC (ENTR/F/2/SF D[removed]) Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:32:43 Ethics Committee Clinical trial EudraLex Good Clinical Practice Clinical research Research Clinical Trials Directive

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