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Secretary's Advisory Committee on Human Research Protections (SACHRP)
SACHRP March 13 – 14, 2006 Meeting Presentations
March 13, 2006 – Presentations
Status Summary of SACHRP
By: Bernard A. Schwetz, D.V.M., Ph.D. Subpart A Subcommittee (SAS)Update
By: Felix Gye, Pharm.D, M.B.A., CIP, and Daniel K. Nelson, M.S., CIP Models of IRB Review Workshop Update
By: Ernest Prentice, Ph.D., and Bernard A. Schwetz, D.V.M., Ph.D.
March 14, 2006 - Presentations
9th Report for SACHRP Consideration Clarifying 45 CFR Subpart D Definitions
By: Celia B. Fisher, Ph.D., and Susan Z. Kornetsky, M.P.H. International Research Ethics: An Overview
By: Robert Levine, M.D. Status of Research Ethics Training Internationally
By: Melody Lin, Ph.D. FDA and International Clinical Trials
By: David Lepay, M.D., Ph.D. Pharmaceutical Industry International Clinical Research
By: Jean-Louis Saillot, M.D. IRB Capacity Building in Resource-limited Settings NIAID Approaches
By: Maureen Power, RN, MPH International Bioethics Education & Career Development Program Review
By: Barbara Sina, Ph.D.
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