This workshop reviews the basics of Good Clinical Practice (GCP) and the recent updates that impact practice in an increasingly electronic environment. It will highlight the responsibilities the Sponsor/Clinical Research Office (CRO), Institutional Review Board (IRB), independent ethics committees and study staff have in conducting GCP compliant research with a focus on investigator responsibilities.
The session will include multiple case studies that every researcher has or will run into, and what to do to remain GCP compliant.
Catherine Sedota
Email: cmp9@buffalo.edu
Phone: 716-844-9282
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