UF Continuing Medical Education & Department of Obstetrics & Gynecology Continuing Medical Education Series
This event has ended.
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Date and time
Description
Title Overview of the Institutional Review Board (IRB-0)
Presented by R. Peter Iafrate, Pharm.D. Chairman, Health Center IRB-01 University of Florida
Presentation will be in lecutre format with Q&A following.
Educational Objectives
Upon completion of this presentation, participants will be able to:
To be able to state what local, state, and Federal regulations exist that govern human experimentation and what oversight is required in human subject's research. To define what is considered human subjects research. To be aware of the confidentiality issues surrounding human subjects research. To be able to discuss the process of Informed Consent. To differentiate the role of the Principal Investigator. To list ways to avoid regulatory compliance issues. To be better prepared to submit an IRB application to IRB-01.