Skip to content

RED 621 | Best Practice Roundtable: Consent Document Simplification

Dr. Ann Johnson, Director, Institutional Review Board (IRB), will facilitate a discussion and workshop on how to simplify consent documents for human subject research. Examples of simplified consent documents will be provided for review. Participants should bring their own consent documents for simplification, as the group will work together to streamline the documents for submission to the IRB.

Please bring one printed copy of your consent document for simplification, and a laptop if desired.

This speical event is only live :

  • To register for a live class, please click here.
Last Updated: 8/5/22