IRB: Ethics - PDFSEARCH.IO - Document Search Engine

IRB: Ethics
Results: 397

#	Item
321	Human Research Subject Protection and Institutional Review Boards (IRB) Standard Operating Policies and Procedures (SOPP) Office of Regulatory Research Compliance Add to Reading List Source URL: www.orrchoward.com Language: English - Date: 2014-07-08 13:36:46 Science Pharmaceutical sciences Design of experiments Medical ethics Pharmaceutical industry Institutional review board Clinical trial Informed consent Food and Drug Administration Pharmacology Research Clinical research
322	INDIANA UNIVERSITY SOUTHEAST INSTITUTIONAL REVIEW BOARD (IRB) REVIEW REQUEST FORM FOR THE INCLUSION OF PRISONERS IN RESEARCH Principal Investigator: IRB Study: Add to Reading List Source URL: www.ius.edu Language: English - Date: 2009-01-12 09:20:28 Applied ethics Criminal law Medical ethics Design of experiments Pharmacology Institutional review board Human subject research Prison Parole Ethics Clinical research Research
323	THIS DOCUMENT HAS BEEN ARCHIVED BECAUSE ITS CONTENT IS NO LONGER APPLICABLE UNDER FEDERALWIDE ASSURANCES APPROVED BY OHRP. August 27, [removed]Updated July 21, 2000] Add to Reading List Source URL: www.hhs.gov Language: English - Date: 2012-08-01 16:06:27 Science Institutional review board Office for Human Research Protections Human subject research Cooperative Human Tissue Network Certified IRB Professional Clinical research Research Ethics
324	INDIANA UNIVERSITY SOUTHEAST INSTITUTIONAL REVIEW BOARD (IRB) REVIEW DOCUMENTATION OF REVIEW AND APPROVAL (DRA) IU Southeast IRB STUDY NUMBER:______________ (IRB Office will assign) Add to Reading List Source URL: www.ius.edu Language: English - Date: 2010-09-01 10:59:59 Science Design of experiments Pharmacology Scientific method Drug safety Institutional review board Informed consent Clinical research coordinator Clinical trial Clinical research Research Medical ethics
325	Human Subjects Protection Final Report Add to Reading List Source URL: www.hhs.gov Language: English - Date: 2004-06-21 08:58:56 Clinical research Pharmacology Design of experiments Drug safety Medical ethics Institutional review board Public Responsibility in Medicine and Research National Institutes of Health Certified IRB Professional Research Medicine Health
326	Office for Human Research Protections (OHRP) NOTE: THIS GUIDANCE HAS BEEN REPLACED BY OHRP’s JULY 1, 2011 GUIDANCE. THIS GUIDANCE REPLACES OHRP’S JULY 11, 2002 GUIDANCE ENTITLED “GUIDANCE ON WRITTEN IRB PROCEDURES. Add to Reading List Source URL: www.hhs.gov Language: English - Date: 2014-09-11 00:35:39 Science Design of experiments Pharmacology Drug safety Medical ethics Institutional review board Clinical trial Investigational New Drug Office for Human Research Protections Clinical research Research Medicine
327	Columbia University Human Subjects Protection Training Course The Columbia Human Subjects Protection Training Course requires completion of five individual modules within the online CITI (Collaborative IRB Training Initi Add to Reading List Source URL: cumc.columbia.edu Language: English - Date: 2013-01-08 12:21:20 Ethics Health Pharmacology Research ethics Medical statistics Informed consent Belmont Report Food and Drug Administration Human subject research Research Clinical research Medical ethics
328	Clarification of Public Use Data Files Add to Reading List Source URL: www.hhs.gov Language: English - Date: 2004-06-21 09:25:57 Pharmacology Medical ethics Ethics Research Drug safety Institutional review board Data sharing Certified IRB Professional Cooperative Human Tissue Network Science Clinical research Design of experiments
329	Guide to the Institutional Review Board (IRB) at the University of Nebraska–Lincoln Add to Reading List Source URL: research.unl.edu Language: English - Date: 2012-08-21 10:23:40 Science Institutional review board Belmont Report Office for Human Research Protections Clinical trial Public Responsibility in Medicine and Research Common Rule Human subject research Grant Clinical research Research Ethics
330	INDIANA UNIVERSITY SOUTHEAST INSTITUTIONAL REVIEW BOARD (IRB) REVIEW REQUEST FORM FOR THE INCLUSION OF PREGNANT WOMEN, HUMAN FETUSES, AND NEONATES IN RESEARCH Principal Investigator: Add to Reading List Source URL: www.ius.edu Language: English - Date: 2009-01-12 09:21:06 Obstetrics Health Applied ethics Clinical research Abortion Informed consent Pregnancy Institutional review board Miscarriage Medicine Medical ethics Fertility

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