Workshop: Consenting a Subject to a Research Study
Sponsor(s): Duke Office of Clinical Research (DOCR)
This course presents information about best practices for consenting a subject to a research study. The course allows participants to observe and participate in consenting scenarios to reinforce skills.Completion of the Informed Consent course is a pre-requisite for this course. You can register for the course in the Duke LMS.
Type: RESEARCH
Contact: Duke Office of Clinical Research