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The top documents tagged [continuing review of]
HISTORY OF INFORMED CONSENT –Human subjects research has a checkered past –Nazi experiments 1935-1945 –“Extensive, willfully harmful experimentation” –Nuremberg
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Ethical committee-role, Principal Investigator
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SOP Melody Lin, Ph.D. Deputy Director, Office for Human Research Protections Director, International Activities
[email protected]
Santiago, Chile August
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Continuing Review Presented by: Karen Jeans, PhD, CCRN, CIP Program Analyst, COACH
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OHRP Electronic Access E-mail:
[email protected]
Web Site:
216 views
Continuing Review VA Requirements Kevin L. Nellis, M.S., M.T. (A.S.C.P.) Program Analyst Program for Research Integrity Development and Education (PRIDE)
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Common Audit Findings UTHSC Institutional Review Board (IRB)
220 views
Research: Intramural and Extramural Jacquelyn Goldberg, JD CIRB Review Board Administrator Clinical Investigations Branch, CTEP Division of Cancer Treatment
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Integrating a Federated Healthcare Data Query Platform With Electronic IRB Information Systems Shan He IPHIE 2010
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The NCI Central IRB Initiative Jacquelyn L. Goldberg, J.D. VA IRB Chair Training April 8, 2004
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Continuing Review
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RESEARCH COMPLIANCE AUDITING
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