Daniel Nelson, Director, Office of Human Research Ethics, University of North Carolina at Chapel Hill
Cynthia Hahn, VP, Clinical Research and Regulatory Affairs, North Shore-LIJ Health System
*The views and opinions expressed in this video are those of the speaker and do not necessarily reflect the official policy or position of CTTI.
Webinar Objective
To share experiences from two research institutions about implementation of a central IRB model for multi-center clinical trials
Webinar Agenda
Results from a randomized, controlled trial of central versus local IRB review
The institutional policy resulting from study results and a summary of conclusions that can be applied more broadly
The continuing role of the institution in research compliance
Examples from a research institution that serves as a central IRB and relies on commercial, academic, and federal external IRBs for multi-center clinical trials