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Best Practice Roundtable: Consent Document Simplification is a Course

Best Practice Roundtable: Consent Document Simplification

Self-paced

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Full course description

This is a Special Event, and does NOT count toward a Certificate of Achievement.

THIS LISTING IS THE TBA SESSION OF THIS EVENT.

To be notified when a session of this event is scheduled, or if you cannot attend the already scheduled session, please enroll in this course.


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.

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