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How the Past Influenced Human Research Protection Regulations Shirley J. Hicks Director, Division of Education and Development Office for Human Research.
Constance Lewin, M.D., M.P.H. Associate Director for Human Subject Protection Acting Branch Chief, Good Clinical Practice Branch 1 Division of Scientific.
Council for Responsible Nutrition Supplyside West, October 19, 2006 The Case for Mandatory Reporting of Adverse Events for Dietary Supplements Steve Mister.
Human Research Protection Program 101 March 19-20, 2007 Cincinnati, Ohio.
Exempt and Expedited Reviews What Requires IRB and R&D Approvals
