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Clinical Trials Directive
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#	Item
121	8 janvier 2010 Consultation on "Clinical Trials Directive" [removed]EC Analyse de la consultation publique sur la Directive Européenne. CONTRIBUTION DU GROUPE DE TRAVAIL EUROPEEN DE LA CNCP (CONFERENCE NATIONALE FRANCAIS Add to Reading List Source URL: ec.europa.eu Language: French - Date: 2013-10-09 09:33:26
122	Comments on the Public Consultation Document Assessment of the functioning of the ‘Clinical Trials Directive’ [removed]EC The Clinical Trial Service Unit ( CTSU) is part of Oxford University and is an academic unit co Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:33:25 Science Medicine Pharmacology Design of experiments Medical ethics Clinical trial Good Clinical Practice Pharmacovigilance Serious adverse event Clinical research Research Pharmaceutical industry
123	CONSOLIDATED COMMENTS OF THE CLINICAL TRIALS FACILITATION GROUP (CTFG) ON THE ASSESSMENT OF THE FUNCTIONING OF THE “CLINICAL TRIALS DIRECTIVE” [removed]EC ENTR/F/2/SF D[removed]Table of Contents: 1.1. Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:33:23 Clinical Trials Directive Ethics Committee Clinical trial Clinical research Research Good Clinical Practice
124	Information provided by Farmaindustria (Spain) in relation to the delays mentioned under Section 3.2 Weaknesses of the Consultation Paper on the Functioning of the Clinical Trials Directive The time period from the submi Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:31:22 Scientific method Clinical trial Clinical Trials Directive Ethics Committee Clinical research Research Science
125	UK RESPONSE TO THE COMMISSION’S CONSULTATION ON REVIEW OF THE CLINICAL TRIALS DIRECTIVE General points (consultation items[removed]The introduction of legislation aimed at harmonising the way in which clinical trials c Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:33:50 Health Ethics Committee Clinical Trials Directive Good Clinical Practice Pharmacovigilance Clinical trial European Medicines Agency Clinical research Research Pharmaceutical sciences
126	ASSESSMENT OF DIRECTIVE[removed]EC OPEN CONSULTATION OF THE EUROPEAN COMMISSION REPLY OF THE HUNGARIAN HEALTH ADMINISTRATION General considerations Directive[removed]EC of the European Parliament and of the Council of 4 Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:31:20 Scientific method Clinical trial Good Clinical Practice Clinical Trials Directive Clinical site Institutional review board EudraCT Good Clinical Practice Directive Clinical research Research Science
127	London, 01 February 2010 Doc. Ref. EMA[removed]EUDRAVIGILANCE EXPERT WORKING GROUP COMMENTS ON THE EUROPEAN COMMISSION PUBLIC CONSULTATION PAPER – “ASSESSMENT OF THE FUNCTIONING OF THE “CLINICAL TRIALS Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:32:49 Pharmaceutical sciences EudraVigilance Serious adverse event Clinical Trials Directive Pharmacovigilance European Medicines Agency Adverse event Clinical trial EudraCT Clinical research Research Health
128	Association Européenne des Spécialités Pharmaceutiques Grand Public Association of the European Self-Medication Industry Europäischer Verband der Arzneimittel-Hersteller AESGP RESPONSE TO THE COMMISSION’S CONSULTAT Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:33:22 Science Clinical trial Clinical Trials Directive Ethics Committee Institutional review board Pharmacovigilance Adverse event Good Clinical Practice Clinical research Research Pharmaceutical sciences
129	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
130	Consultation paper of the European Commission: Assessment of the Functioning of the “Clinical Trials Directive” [removed]EC European Commission has launched a consultation paper about functioning of the Clinical Trial Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:33:25 Scientific method Clinical Trials Directive Ethics Committee Clinical trial EudraCT Institutional review board Good Clinical Practice Clinical research Research Science

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