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Serious adverse event
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51	Serious Adverse Events Report Form: (not occurring at the local site) Add to Reading List Source URL: www.health.qld.gov.au Language: English - Date: 2012-02-27 18:26:30 Serious adverse event Adverse event Clinical research Pharmaceutical industry Research
52	PHARMACY AND POISONS ORDINANCE (Cap[removed]APPLICATION FOR A CLINICAL TRIAL/MEDICINAL TEST CERTIFICATE PART A: TRIAL INFORMATION A1. Add to Reading List Source URL: www.drugoffice.gov.hk Language: English - Date: 2014-01-09 07:33:31 Clinical research Research Health Pharmacy Drug safety Adverse event Serious adverse event Clinical trial Adverse effect Pharmaceutical sciences Pharmacology Pharmaceutical industry
53	CITI Offers More Than Basics in Responsible Conduct of Research Did you know there are more than the required human subjects protection courses available online through the Collaborative Institutional Training Initiative Add to Reading List Source URL: www.its.utmb.edu Language: English - Date: 2014-01-03 10:49:11 Pharmaceutical sciences Health Clinical trial Good Clinical Practice Adverse event Serious adverse event Food and Drug Administration Citigroup Medical research Clinical research Pharmaceutical industry Research
54	University of Central Oklahoma Add to Reading List Source URL: www.uco.edu Language: English - Date: 2014-09-12 09:25:53 Ethics Science Pharmacology Drug safety Design of experiments Institutional review board Adverse event Serious adverse event Risk Clinical research Research Pharmaceutical industry
55	Sydney University Human Research Ethics Committee REPORTING Form: Adverse events In clinical trials THIS FORM SHOULD BE USED TO REPORT: Adverse Events (AEs), Serious Adverse Events (SAEs), Serious Unexpected Suspected Dr Add to Reading List Source URL: sydney.edu.au Language: English - Date: 2014-10-03 02:00:37 Pharmaceutics Pharmaceutical sciences Adverse event Clinical trial Serious adverse event Communications protocol Research ethics Clinical research Pharmaceutical industry Research
56	Sydney University Human Research Ethics Committee REPORTING Form: SUMMARY REPORT FORM OF ADVERSE EVENTS FOR CLINICAL TRIALS THIS FORM SHOULD BE USED TO REPORT: For Annual Serious Adverse Events (SAEs) And Quarterly/Six M Add to Reading List Source URL: sydney.edu.au Language: English - Date: 2014-10-03 02:00:37 Pharmacology Health Pharmaceutical sciences Adverse effect Serious adverse event Adverse event Irma Clinical trial Clinical research Pharmaceutical industry Research
57	REPORTING SERIOUS ADVERSE EVENTS (SAEs) AND PROBLEMS INVOLVING RISKS TO SUBJECTS OR OTHERS IN VA RESEARCH A Serious Adverse Advent (SAE) or a Problem Involving Risks to Subjects or Others occurs in VA research. The SAE o Add to Reading List Source URL: www.va.gov Language: English - Date: 2011-12-20 08:33:53 Adverse event Serious adverse event Clinical research Pharmaceutical industry Research
58	The Wright State University IRBs – EVENT REPORTING FORM FOR UNANTICIPATED PROBLEMS, ADVERSE EVENTS, ETC. ADVERSE EVENT/UNANTICIPATED PROBLEM REPORTING FORM The Wright State University Institutional Review Board Office Add to Reading List Source URL: www.wright.edu Language: English - Date: 2008-12-12 14:39:41 Pharmaceutical sciences Medicine Adverse event Serious adverse event Intervention Clinical research coordinator Clinical trial Clinical research Pharmaceutical industry Research
59	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
60	Federation of the European Academies of Medicine Palais des Académies Rue Ducale 1 B[removed]Brussels Tel: +[removed] Fax: +[removed]65 [removed] www.feam.eu.com FEAM Response to Consultation on Fun Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:33:50 Science Ethics Committee Clinical trial Clinical Trials Directive Institutional review board EudraCT Serious adverse event Declaration of Helsinki Clinical trial management Clinical research Research Scientific method

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