IRB: Ethics - PDFSEARCH.IO - Document Search Engine

IRB: Ethics
Results: 397

#	Item
231	To IRB, or Not to IRB? That Is the Question Add to Reading List Source URL: www.collin.edu Language: English - Date: 2010-05-07 12:46:12 Ethics Applied ethics Institutional review board Belmont Report Declaration of Helsinki Human subject research Informed consent Tuskegee syphilis experiment Common Rule Medical ethics Clinical research Research
232	IRB Update Part 2 October 18, 2012 George Gasparis Executive Director, CU HRPP Add to Reading List Source URL: cumc.columbia.edu Language: English - Date: 2013-01-08 12:20:46 Research Clinical research Clinical pharmacology Food and Drug Administration Therapeutics United States Public Health Service Consent Institutional review board Ethics Pharmacology Pharmaceutical sciences
233	D2[removed]University of Kentucky Policy on Prompt Reporting For Unanticipated Problems, Serious or Life-Threatening Events, and Anticipated or Unanticipated Related Deaths to the Institutional Review Board (IRB) and Insti Add to Reading List Source URL: www.research.uky.edu Language: English - Date: 2012-09-14 14:44:36 Drug safety Scientific method Pharmacology Science Medical ethics Adverse event Serious adverse event Institutional review board Clinical research coordinator Clinical research Pharmaceutical industry Research
234	F5.0000 Modification Request Form University of Kentucky Institutional Review Board (IRB) F5.0000 Modification Request Form Add to Reading List Source URL: www.research.uky.edu Language: English - Date: 2014-06-13 11:14:52 Research Design of experiments Pharmacology Medicine Drug safety Institutional review board Health Insurance Portability and Accountability Act Informed consent Clinical research coordinator Clinical research Medical ethics Ethics
235	RESEARCH SUBJECTS INFORMATION UPDATED CUMC INSTITUTIONAL REVIEW BOARD (IRB) CONTACT INFORMATION The Columbia University Medical Center (CUMC) Institutional Review Board (IRB) is a committee that independently conducts on Add to Reading List Source URL: cumc.columbia.edu Language: English - Date: 2013-10-16 13:32:07 Medical ethics Applied ethics Design of experiments Pharmacology Drug safety Institutional review board Informed consent Human subject research Clinical research coordinator Clinical research Research Ethics
236	South Carolina Department of Mental Health Institutional Review Board (IRB) OFFICE OF GENERAL COUNSEL 2414 Bull Street, Columbia, South Carolina[removed]FWA #[removed]) Add to Reading List Source URL: www.state.sc.us Language: English - Date: 2012-05-29 13:42:26 Privacy Data privacy Health Insurance Portability and Accountability Act Internet privacy Institutional review board Protected health information Medical privacy Ethics Health Privacy law
237	Human Research Protection Office Barnes Jewish Hospital St. Louis Children’s Hospital Washington University IRB ID #: Add to Reading List Source URL: gep.wustl.edu Language: English - Date: 2014-08-17 14:06:26 Ethics Medical ethics Design of experiments Pharmacology Pharmaceutical industry Institutional review board Clinical trial Informed consent Deception Clinical research Research Science
238	Revised: [removed]Application for Review of Cornell University Training Programs and Cornell University Classes Requiring the Use of Human Participants in Research CORNELL UNIVERSITY Institutional Review Board – Hum Add to Reading List Source URL: www.irb.cornell.edu Language: English - Date: 2013-09-18 12:22:40 Institutional review board Pharmacology Cornell University Ethics New York Applied ethics Clinical research Design of experiments Drug safety
239	Microsoft PowerPoint - Goldman Presentation IRB and Genetics.ppt Add to Reading List Source URL: www.azdhs.gov Language: English - Date: 2011-08-05 15:03:32 Clinical research Science Informed consent Human subject research Biobanks Cooperative Human Tissue Network Biological specimen Ethics Medicine Medical ethics
240	IHS Institutional Review Board (IRB) Checklist Add to Reading List Source URL: www.npaihb.org Language: English - Date: 2006-06-15 22:17:00 Science Design of experiments Pharmacology Medical ethics Pharmaceutical industry Institutional review board Clinical trial Informed consent Risk Clinical research Ethics Research

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