EudraVigilance - PDFSEARCH.IO - Document Search Engine

EudraVigilance
Results: 183

#	Item
61	Microsoft PowerPoint[removed]Coding_with_MedDRA.pptx Add to Reading List Source URL: www.meddra.org Language: English - Date: 2014-09-23 11:53:36 Health MedDRA EudraVigilance Pharmacovigilance Adverse effect Mental disorder Serious adverse event Pharmaceutical industry Pharmacology Pharmaceutical sciences Medicine
62	Microsoft PowerPoint[removed]100_Getting_started_with_MedDRA.pptx Add to Reading List Source URL: www.meddra.org Language: English - Date: 2014-09-23 11:33:39 Clinical research Pharmaceuticals policy Drug safety Pharmacy MedDRA EudraVigilance Uppsala Monitoring Centre Pharmacovigilance International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use Pharmacology Pharmaceutical sciences Health
63	Microsoft PowerPoint[removed]1701_Safety_Data_Analysis_and_SMQs.pptx Add to Reading List Source URL: www.meddra.org Language: English - Date: 2014-04-03 13:58:20 MedDRA Health Pharmaceuticals policy Medicine EudraVigilance Pharmacovigilance Pharmacology Drug safety Pharmaceutical sciences
64	Microsoft PowerPoint[removed]Intro_Data_Analysis_SMQs_Physicians.pptx Add to Reading List Source URL: www.meddra.org Language: English - Date: 2014-09-23 12:14:27 Health MedDRA Pharmaceutical sciences Pharmaceuticals policy Psychopathology EudraVigilance Pharmacovigilance Mental disorder Immune system Pharmacology Medicine Drug safety
65	08 January 2010 EMA[removed]European Medicines Agency response to the European Commission’s “ASSESSMENT OF THE FUNCTIONING OF THE “CLINICAL TRIALS DIRECTIVE” [removed]EC” launched in October 2009. Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:33:24 Pharmaceutical sciences European Medicines Agency EudraVigilance EudraCT Clinical trial Clinical Trials Directive Good Clinical Practice Ethics Committee EudraLex Clinical research Research Health
66	REASONED OPINION[removed]OF THE JOINT COMMITTEE FOR THE EUROPEAN UNION OF 24 SEPTEMBER 2013 ON INFRINGEMENT OF THE PRINCIPLE OF SUBSIDIARITY BY THE PROPOSAL FOR A REGULATION OF THE EUROPEAN PARLIAMENT AND OF THE COUNCIL O Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2015-01-07 06:16:51 Health Law Drug safety Pharmacology Pharmacy European Medicines Agency Pharmacovigilance EudraVigilance Subsidiarity Clinical research Pharmaceuticals policy Pharmaceutical sciences
67	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
68	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
69	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
70	ICH STEERING COMMITTEE November 9-10, 2011 Seville, Spain SUMMARY 1. Opening Discussions The ICH Steering Committee (SC) meeting in Seville was chaired by the EU. The Add to Reading List Source URL: www.ich.org Language: English - Date: 2014-11-11 11:03:12 Drug safety Health Medicine Pharmacology Clinical Data Management Electronic Common Technical Document MedDRA Environmental Working Group EudraVigilance Clinical research Research Pharmaceuticals policy

UPDATE