WHEN: October 17, 2024 | 12:00 - 1:00PM

Join the HRPP and IRB Office for a webinar where attendees will learn about reportable events, including protocol deviations and unanticipated problems, why these events must be tracked and reported to the IRB; and when/how to report these events to the IRB. 

WHO SHOULD ATTEND?

1. Principal Investigators and key study personnel engaged in conducting human subjects research. 
2. Study coordinators and regulatory staff who support human subjects research.
3. Individuals who are new to research as well as individuals who can benefit from a reminder of the reporting requirements.