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.