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Trial practice
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#	Item
441	REPUBLIQUE FRANÇAISE Comments on the Commission’s review of the clinical trials directive Afssaps, as the French National Competent Authority (NCA) for clinical trials (CT), would like to thank the Commission for hav Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:33:22 Pharmaceutical sciences Pharmaceutics Pharmaceuticals policy Pharmacology Good Clinical Practice Clinical trial Clinical Trials Directive Marketing authorization Ethics Committee Clinical research Pharmaceutical industry Research
442	EPF’s RESPONSE TO THE COMMISSION PUBLIC CONSULTATION ON THE CLINICAL TRIALS DIRECTIVE[removed]EC 19 January 2009 Introduction The European Patients’ Forum (EPF) welcomes the Commission’s initiative to Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:33:39 Science Health Design of experiments Pharmacology Medical ethics Clinical trial Declaration of Helsinki Good Clinical Practice Institutional review board Clinical research Research Pharmaceutical industry
443	Statement of the „Deutsche Gesellschaft für Medizinische Informatik, Biometrie und Epidemiologie e.V. GMDS” ( German Association for Medical Informatics, Biometry and Epidemiology) concerning the Public Consultation Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:31:20 Design of experiments Pharmacology Pharmaceutical sciences Pharmaceutical industry Medical statistics Clinical trial Pharmacovigilance Clinical Trials Directive Good Clinical Practice Clinical research Research Science
444	FACULTY OF PHARMACEUTICAL MEDICINE OF THE ROYAL COLLEGES OF PHYSICIANS OF THE UNITED KINGDOM 1 St Andrews Place, Regent?s Park, London. NW1 4LB Telephone + [removed]0343 – Fax +[removed]5381 Email: [removed] Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:33:46 Good Clinical Practice Clinical Trials Directive Clinical trial Ethics Committee Declaration of Helsinki Pharmaceutical industry Clinical research Research Pharmaceutical sciences
445	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
446	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
447	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
448	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
449	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
450	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

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