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Serious adverse event
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61	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
62	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
63	All trials registered. All results reported. September 2013 The AllTrials campaign calls for all past and present clinical trials to be registered and their results reported. Clinical trials are investigations designed t Add to Reading List Source URL: www.alltrials.net Language: English - Date: 2014-05-26 10:34:05 Science Scientific method Clinical trials Design of experiments Epidemiology ClinicalTrials.gov Adverse event Serious adverse event Randomized controlled trial Clinical research Research Pharmaceutical industry
64	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
65	EUCOPE comments regarding Clinical Trials Directive 2001_20_EC_fin Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:33:21 Health Clinical Trials Directive Pharmacovigilance Ethics Committee Serious adverse event Clinical trial Clinical research Research Pharmaceutical sciences
66	The Joint Clinical Trials Office A partnership for clinical research SAE From Completion Guidelines Serious Adverse Events Reporting Form Completion Guidelines Add to Reading List Source URL: www.khpcto.co.uk Language: English - Date: 2012-05-15 11:50:37 Pharmaceutics Pharmaceutical sciences Serious adverse event Clinical trial IMP Horsepower Adverse event EudraCT Clinical research Pharmaceutical industry Research
67	Single-site MOOP APPENDICES.docx Add to Reading List Source URL: www.niams.nih.gov Language: English - Date: 2014-11-14 11:54:48 Pharmaceutics Science Serious adverse event Clinical trial Adverse event Methadone X Window System Function Clinical research Pharmaceutical industry Research
68	Multi-site MOOP APPENDICES_1.docx Add to Reading List Source URL: www.niams.nih.gov Language: English - Date: 2014-11-14 14:28:14 Pharmaceutics Science Serious adverse event Clinical trial Adverse event Methadone X Window System Function Clinical research Pharmaceutical industry Research
69	National Institute of Arthritis and Musculoskeletal and Skin Diseases Add to Reading List Source URL: www.niams.nih.gov Language: English - Date: 2014-11-14 11:54:20 Science Scientific method Design of experiments Pharmacology Clinical trial Adverse event Institutional review board Case report form Serious adverse event Clinical research Pharmaceutical industry Research
70	National Institute of Arthritis and Musculoskeletal and Skin Diseases Add to Reading List Source URL: www.niams.nih.gov Language: English - Date: 2014-11-14 14:26:51 Science Scientific method Design of experiments Pharmacology Clinical trial Adverse event Institutional review board Case report form Serious adverse event Clinical research Pharmaceutical industry Research

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