Event Reporting in Human Subjects Research

Start date
End date
Biomedical Research Tower, Room 115
Event Content

The Office of Responsible Research Practices and the Center for Clinical and Translational Science are offering a workshop on human subjects research event reporting. The session will:

  • Provide an overview of the event reporting policy
  • Differentiate between investigator, sponsor, and IRB reporting requirements
  • Provide definitions and discuss case examples
  • Review best practices and available resources

While the session will be tailored to medical researchers, anyone preparing IRB submissions is welcome.