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This meeting is for internal users only.
IRBMED Course: Reporting Requirements for Human Subject's Research: Adverse Events, ORIOs, and Unanticipated Problems (Level I)
This course will identify what constitutes an Adverse Event, ORIO, and Unanticipated Problem and review the requirements of reporting such events to the IRB in eResearch. This session will also include a discussion on when it may be appropriate to use a study specific AE reporting plan instead of the U-M standard time table for reporting adverse events to the IRB.

Sep 29, 2020 10:00 AM in Eastern Time (US and Canada)

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