Office of Responsible Research Practices
The Ohio State University


Troubleshooting Informed Consent

Posted: May 9, 2019

The Office of Responsible Research Practices and the Center for Clinical and Translational Science are offering an educational session on common informed consent screening and IRB review findings, and consent issues that arise during ongoing research projects. The presentation will:

  • Identify common submission screening questions
  • Examine IRB-required modifications related to the consent process
  • Discuss common post-approval monitoring findings
  • Discuss case examples
  • Review best practices and available resources

While the session will be tailored to medical researchers, anyone preparing IRB submissions is welcome. The presentation will be held on Wednesday, June 5 from 8 to 9:30 a.m. in the Biomedical Research Tower, Room 115, 460 West Twelfth Avenue.

Registration requested.

Live streaming available upon request. Please do not register if you plan to attend via live stream. CME credit is available only for in-person attendance. Contact Sandra Meadows at 614-688-8641 or
The Ohio State University Center for Continuing Medical Education designates this RSS (Regularly Scheduled Series) for a maximum of 1.5 AMA PRA Category 1 Credit(s)™. Physicians should claim only the credit commensurate with the extent of their participation in the activity.


Category : Educational Offerings / IRB / ORRP