Adverse event - PDFSEARCH.IO - Document Search Engine

Adverse event
Results: 2359

#	Item
451	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
452	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
453	NIAMS DSM Reports Closed_Single-site_1[removed]docx Add to Reading List Source URL: www.niams.nih.gov Language: English - Date: 2014-11-24 15:58:55 Safety monitoring Adverse event Science Technology Business Clinical research Pharmaceutical industry Data monitoring committees
454	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
455	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
456	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
457	Ref. Ares[removed][removed]EUROPEAN COMMISSION HEALTH AND CONSUMERS DIRECTORATE-GENERAL Directorate D - Health systems and products D4 – Substances of Human Origin and Tobacco Control Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2014-12-09 06:48:24 Patient safety Hematology Clinical research Pharmacology Blood donation Blood transfusion Pharmacovigilance Adverse effect Adverse event Medicine Health Transfusion medicine
458	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
459	Shore Design Consultancy Ltd MEDICAL TRAINING DEVICES IN THE HOME As home-managed disease states, medical devices and user groups diversify and proliferate helping ever more people, Ian Scrimgeour, MEng, User Centred De Add to Reading List Source URL: www.ondrugdelivery.com Language: English - Date: 2014-09-25 04:30:33 Medical equipment Medical device Medical technology E-learning Use error Adverse event Kinesthetic learning Education Medicine Learning
460	Food and Drug Administration Office of the Commissioner / Office of Planning Risk Communication Staff SUMMARY MINUTES RISK COMMUNICATION ADVISORY COMMITTEE (RCAC) Add to Reading List Source URL: www.fda.gov Language: English MedWatch Pharmacology Adverse Event Reporting System Food and Drug Administration Pharmaceutical sciences Clinical research

UPDATE