Office of Responsible Research Practices
The Ohio State University


Electronic Informed Consent: Processes, Platforms, and Participants

Posted: March 17, 2019

The Office of Responsible Research Practices and the Center for Clinical and Translational Science are offering an educational session on electronic informed consent that is consistent with legally valid signature requirements. Speakers from the Office of the Chief Information Officer (OCIO), Office of Research Information Systems, Department of Biomedical Informatics, and the Clinical Trials Management Office will:

  • Provide an update regarding OCIO approval of eSignature methods and IRB submission requirements
  • Highlight two available Ohio State electronic consent platforms, REDCap and Signet
  • Discuss how to conduct informed consent using the available platforms
  • Review available resources and guidance

The workshop will be held on Wednesday, April 17 from 8 to 9:30 a.m. in the Ross Heart Hospital, Room H1213, 452 West 10th 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