University at Buffalo (UB)
We will review the basics of Good Clinical Practice (GCP) and the recent updates that impact practice in an increasingly electronic environment. We 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.
This workshop series is free and open to all students, fellows, faculty, and staff at UB and the Buffalo Translational Consortium.
Catherine Sedota
Email: cmp9@buffalo.edu
Phone: 7168449282