The Office of Responsible Research Practices and the Center for Clinical and Translational Science are offering an introductory workshop about the IRB submission process. The session will:
- Provide an overview of informed consent alteration and waivers
- Provide regulatory definitions and discuss case examples
- Discuss Buck-IRB navigation
- Review best practices and available resources
While the session will be tailored to medical researchers, anyone preparing IRB submissions is welcome.
The workshop will be held on Tuesday, June 20, from 8 a.m. to 9 a.m. in the Clinical Skills Education and Assessment Center, Room 620, 6th Floor Prior Health Sciences Library, 376 West Tenth Avenue.
Contact: 614-688-8641 or email@example.com