IRB: Ethics

Results: 397



#Item
31Clinical research ethics / Design of experiments / Drug safety / Institutional review board / Regulatory compliance / Common Rule / IRB / Clinical research coordinator

Microsoft Word - SOP - Department of Defense.doc

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Source URL: research.missouri.edu

Language: English - Date: 2015-07-01 12:42:00
32Medical ethics / Clinical research ethics / Human subject research / Design of experiments / Institutional review board / Consent / Informed consent

REQUEST FOR CHANGE IN CAMPUS IRB APPROVAL UNIVERSITY of MISSOURI - ROLLA (UMRIRB-2) Review Requested: Amendment ____ Revision ____ Addendum ____ Other ____ *This form is not intended to be used for continuing review purp

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Source URL: irb.mst.edu

Language: English - Date: 2014-01-22 05:22:59
33Clinical research / Design of experiments / Research ethics / Medical ethics / Public Responsibility in Medicine and Research / Human subject research / Clinical trial / Common Rule / Protocol

CHG-3 CHARGE TO THE ADMINISTRATIVE PANELS ON HUMAN SUBJECTS IN MEDICAL RESEARCH BY THE VICE PROVOST AND DEAN OF RESEARCH (IRB/SCRO) (August 2015)

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Source URL: researchcompliance.stanford.edu

Language: English - Date: 2016-04-12 01:21:54
34Research ethics / Medical ethics / Clinical research / Human subject research

Research Involving Private Information or Biological Specimens, 2005

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Source URL: www.irb.purdue.edu

Language: English - Date: 2014-06-04 09:40:57
35Autonomy / Medical ethics / Clinical research ethics / Consent / Tort law / Clinical research

Top  Ten  IRB  Application  Mistakes   1. Exempt  Applications   a. Description  of  Project:   i. In  lieu  of  six  separate  responses  to  the  Description  of

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Source URL: www.fmp.hawaii.edu

Language: English - Date: 2014-07-29 17:22:22
36Research ethics / Professional ethics / Medical ethics / Applied ethics / Clinical research / Ethics / Human subject research / Business ethics / Certified IRB Professional / Public Responsibility in Medicine and Research

Panel Discussion 2: Empowering Investigators for Ethical Health Research Certification for Ethics in Research Proficiency Hwei-Ling Lee, Ph.D., CIP

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Source URL: www.fercap-sidcer.org

Language: English - Date: 2010-02-19 02:38:08
37Clinical research ethics / Medical ethics / Human subject research / Clinical trials / Experimental psychology / Public Responsibility in Medicine and Research / Informed consent / Debriefing / Clinical research coordinator / Ethical research in social science

Top of Form Education Department IRB Application: Cover Page Applicants are responsible for reading the Belmont Report and the Education Department Thesis manual prior to completing this application. Print and complete t

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Source URL: wagner.edu

Language: English - Date: 2014-08-19 14:13:03
38Clinical research / Medical ethics / Principal investigator / Consent / Email

RTRN IRB AUTHORIZATION AGREEMENT (IAA) REQUEST FOR RELIANCE I. Lead Principal Investigator at the Reviewing Institution

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Source URL: www2.rtrn.net

Language: English - Date: 2016-01-04 16:02:46
39Clinical research ethics / Human subject research / Medical ethics / Design of experiments / Institutional review board / Regulatory compliance / Informed consent / IRB / Higher Education Research Institute / Clinical research coordinator

https://webirb.research.ucla.edu/WEBIRB/Doc/0/CE8URQKMVJT451LI624S35H462/fromString.html  

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Source URL: www.heri.ucla.edu

Language: English - Date: 2016-01-14 19:15:55
40Clinical research ethics / Institutional review board / Office for Human Research Protections / Grant / IRB / Protocol / Common Rule / Clinical research coordinator / Public Responsibility in Medicine and Research

Microsoft Word - SOP - Reporting Requirements.doc

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Source URL: research.missouri.edu

Language: English
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