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