The video recording (available with captioning) and slices from the March 14 UR-HRPP Educational Forum have been posted to Blackboard.
During the session, OHSP’s Kelly Unsworth and Elizabeth Lyda presented ‘FDA vs. non-FDA Regulated Research: What’s the difference and why does it matter?‘. The presentation compared the scope of HHS and FDA regulations, broke down how to determine when research is subject to FDA regulation, and discussed how day-to-day operations are impacted when research is subject to FDA regulation.
To access materials, enroll in the ‘UR-HRPP Educational Materials’ course in Blackboard. Training acknowledgement documentation is available for those who review the recording.