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IRB: Ethics
Results: 397

#	Item
181	47898059525File Number: 00File Number: 4789805247650Approval Date: 00Approval Date: [removed]190500For IRB Use Only 00For IRB Use Only Add to Reading List Source URL: research.unt.edu Language: English - Date: 2014-08-22 14:54:42 Medicine Medical ethics Design of experiments Pharmacology Drug safety Institutional review board National Institutes of Health Human subject research Informed consent Clinical research Research Ethics
182	HawkIRB Training Sessions The Institutional Review Board (IRB) offers a two-part training series on how to complete forms in HawkIRB, the electronic IRB application system. How to Complete a HawkIRB New Project Applicati Add to Reading List Source URL: hso.research.uiowa.edu Language: English - Date: 2014-08-20 14:53:20 Institutional review board Pharmacology Ethics Applied ethics Scientific method Clinical research Design of experiments Drug safety
183	Chadron State College Institutional Review Board IRB Full Board Review Application Form Submit one original copy with signatures and one digital copy, with signatures, IRB Administrative Chair—allow at least four w Add to Reading List Source URL: www.csc.edu Language: English - Date: 2012-11-09 22:46:27 Medical ethics Applied ethics Research ethics Design of experiments Pharmacology Institutional review board Informed consent Human subject research Psychology Clinical research Ethics Research
184	Chadron State College Institutional Review Board Request for Administratively-Reviewed Exempt Certification Submit one complete copy to IRB Administrative Chair – allow at least two weeks for review Research Project T Add to Reading List Source URL: www.csc.edu Language: English - Date: 2012-11-09 22:46:18 Medical ethics Research Research ethics Design of experiments Pharmacology Institutional review board Informed consent Human subject research Clinical research coordinator Clinical research Ethics Applied ethics
185	INDIANA UNIVERSITY EAST INSTITUTIONAL REVIEW BOARD (IRB) REVIEW NONCOMPLIANCE REPORTING FORM This form should only be used to report observed or apparent noncompliance. Noncompliance is defined as any action or activit Add to Reading List Source URL: www.iue.edu Language: English - Date: 2009-03-10 14:52:47 Drug safety Institutional review board Ethics Scientific method Research Clinical research Design of experiments Pharmacology
186	WSU IRB Policies and Procedures October 22, 2013 Version Office of Research Assurances (ORA) and Add to Reading List Source URL: www.irb.wsu.edu Language: English - Date: 2013-12-19 16:13:50 Science Pharmacology Drug safety Medical ethics Design of experiments Institutional review board Investigational New Drug Public Responsibility in Medicine and Research Belmont Report Clinical research Research Medicine
187	INDIANA UNIVERSITY EAST INSTITUTIONAL REVIEW BOARD (IRB) REVIEW DOCUMENTATION OF REVIEW AND APPROVAL (DRA) IRB STUDY NUMBER:______________________________ (IRB Office will assign) Add to Reading List Source URL: www.iue.edu Language: English - Date: 2010-10-29 14:00:41 Science Scientific method Design of experiments Pharmacology Drug safety Institutional review board Informed consent Clinical research coordinator Clinical trial Clinical research Research Medical ethics
188	University of California Los Angeles[removed]Kinross Avenue, Suite 211 Los Angeles, CA[removed]http://ohrpp.research.ucla.edu GC-IRB: ([removed]M-IRB: ([removed] Add to Reading List Source URL: www.heri.ucla.edu Language: English - Date: 2014-04-07 18:22:00 Science Medicine Design of experiments Pharmacology Drug safety Institutional review board Informed consent Treaty Clinical research coordinator Clinical research Research Medical ethics
189	[removed]4191000247650Approval Date: 00Approval Date: [removed]190500For IRB Use Only 00For IRB Use Only Add to Reading List Source URL: research.unt.edu Language: English - Date: 2014-08-22 14:45:56 Medicine Medical ethics Design of experiments Pharmacology Drug safety Institutional review board Human subject research National Institutes of Health Informed consent Clinical research Research Ethics
190	Iowa State University Institutional Review Board (IRB) - Request to Run Background Checks (this form is used for individuals involved in IRB research projects only) Title of Research Project: Principal Investigator (PI): Add to Reading List Source URL: www.riskmanagement.iastate.edu Language: English - Date: 2014-02-05 14:41:22 Institutional review board Pharmacology Ethics Applied ethics Scientific method Clinical research Design of experiments Drug safety

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