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EudraCT
Results: 165

#	Item
51	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
52	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
53	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
54	26082_VHP report_VHP200903 x Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:33:25 Medicine Pharmaceutical industry Clinical Data Management EudraCT Pharmacology European Organisation for Research and Treatment of Cancer Clinical trial Clinical research Research Health
55	Cover letter Copenhagen, January[removed]Sirs, Thanks for providing us with the opportunity to express our concerns and Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:31:20 Clinical Trials Directive Clinical trial Good Clinical Practice EudraCT Declaration of Helsinki Ethics Committee Institutional review board Adverse event EudraVigilance Clinical research Research Health
56	100108_Clinical_Trials_Directiv_BPI_Comments_endx Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:33:28 Pharmacology Health Pharmaceutical industry Medical statistics Pharmacy Pharmacovigilance Clinical trial EudraCT Ethics Committee Clinical research Research Pharmaceutical sciences
57	DGPharMed response to EC Consultation on Clinical Trials Directive DGPharMed e.V. Geschäftsstelle . Olschewskibogen 7 . D[removed]München Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:33:34 Ethics Committee EudraCT Good Clinical Practice Clinical trial Clinical Trials Clinical research Research Clinical Trials Directive
58	Administrative regulation[removed][removed]2012 Finnish Medicines Agency Administrative Regulation Add to Reading List Source URL: www.fimea.fi Language: English - Date: 2013-08-16 02:23:12 Health Clinical Trials Directive Clinical trial European Medicines Agency EudraCT Serious adverse event Good Clinical Practice EudraVigilance Qualified Person Clinical research Research Pharmaceutical sciences
59	EORTC-ConsultationCTDpublicpaper05012010_ finalx Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:33:34 Pharmaceutical sciences Medicine Design of experiments Drug safety Pharmaceutical industry European Organisation for Research and Treatment of Cancer Clinical trial EudraCT Pharmacovigilance Clinical research Research Pharmacology
60	EORTC- PositionstatementCTD06012010_final Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:33:39 Clinical trial European Organisation for Research and Treatment of Cancer Ethics Committee EudraCT Pharmacovigilance Clinical research Research Pharmaceutical sciences

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