The Informed Consent Process
Thursday, October 16, 2014
1:00 pm - 3:00 pm
Pat Bixby
https://vmw-lmsweb.duhs.duke.edu/SabaLogin/?/Main/goto/GuestOfferingDetails?offeringId=class000000000032237
Sponsor(s): Duke Office of Clinical Research (DOCR)
This course outlines the importance of the informed consent process in the protection of human subjects and identifies key regulatory elements that need to be in-place during the consent process. Register in the Duke LMS.
Type: RESEARCH
Contact: Duke Office of Clinical Research
