IRB Overview
Sponsor(s): Duke Office of Clinical Research (DOCR)
This course offers an overview of the DUHS IRB review process and requirements, federal regulations, and Duke policies pertaining to research involving human subjects. The course highlights tools available to study teams on the IRB web site; presents an example of an eIRB submission; and provides strategies for working efficiently with the IRB are discussed. Register for this course in the Duke LMS.
Type: RESEARCH
Contact: Duke Office of Clinical Research