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61	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
62	Microsoft Word - ACRO Response to EU Commission on the Clinical Trials Directive 8 January 2010 Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:33:26 Science Clinical trial Clinical Trials Directive EudraLex EudraCT Pharmacovigilance Ethics Committee Directive Institutional review board Clinical research Research Pharmaceutical sciences
63	Microsoft PowerPoint - 4.H3_van Gool(差替)[removed]ICORD Session 2 Van Gool2 Add to Reading List Source URL: icord.se Language: English - Date: 2012-07-24 07:32:40 Research Drug discovery Epidemiology Pharmaceutical industry Pharmaceuticals policy EudraCT Clinical trial Orphan drug Immunotherapy Medicine Clinical research Health
64	Serious Adverse Event Report Form Add to Reading List Source URL: www.khpcto.co.uk Language: English - Date: 2012-11-26 10:34:17 Health Pharmaceutics Pharmacology Design of experiments Epidemiology Serious adverse event Clinical trial EudraCT Adverse effect Clinical research Pharmaceutical industry Research
65	Microsoft Word - EUCROF_Consultation_2001_20_EC_20100108.doc Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:32:46 Health Ethics Committee Pharmacovigilance Institutional review board Clinical trial Declaration of Helsinki EudraCT EudraVigilance Clinical Trials Directive Clinical research Research Medicine
66	EUROPEAN COMMISSION: ASSESSMENT OF THE FUNCTIONING OF THE “CLINICAL TRIALS DIRECTIVE” [removed]EC PUBLIC CONSULTATION PAPER dated[removed] Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:33:42 EudraCT Clinical Trials Directive Clinical trial Pharmacovigilance Ethics Committee Clinical research Research Pharmaceutical sciences
67	01 October 2014 Information and Communications Technology EudraCT Public Web Report for September 2014 Introduction: The following statistics were taken from the EudraCT Database on 30 September 2014. Add to Reading List Source URL: eudract.ema.europa.eu Language: English - Date: 2014-12-17 09:16:35 Clinical Data Management Health EudraCT European Medicines Agency Clinical trial Telephone numbers in the United Kingdom Clinical research Research Pharmaceutical industry
68	01 September 2014 Information and Communications Technology EudraCT Public Web Report for August 2014 Introduction: The following statistics were taken from the EudraCT Database on 31 August 2014. Add to Reading List Source URL: eudract.ema.europa.eu Language: English - Date: 2014-12-17 09:16:35 Clinical Data Management Health EudraCT European Medicines Agency Clinical trial Telephone numbers in the United Kingdom Clinical research Research Pharmaceutical industry
69	04 August 2014 Information and Communications Technology EudraCT Public Web Report for July 2014 Introduction: The following statistics were taken from the EudraCT Database on 31 July 2014. Add to Reading List Source URL: eudract.ema.europa.eu Language: English - Date: 2014-12-17 09:16:35 Clinical Data Management Health EudraCT European Medicines Agency Clinical trial Telephone numbers in the United Kingdom Clinical research Research Pharmaceutical industry
70	Annex 1: Clinical trial Application Form REQUEST FOR AUTHORISATION OF A CLINICAL TRIAL ON A MEDICINAL PRODUCT FOR HUMAN USE TO THE COMPETENT AUTHORITIES AND FOR OPINION OF THE ETHICS COMMITTEES IN THE COMMUNITY For offi Add to Reading List Source URL: eudract.ema.europa.eu Language: English - Date: 2014-12-17 09:16:30 Science Clinical trial Design of experiments Drug discovery Pharmacology Geometric dimensioning and tolerancing Pharmaceutical sciences Clinical research Pharmaceutical industry Research

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