Workshop Consenting a Subject to a Research Study
Thursday, September 04, 2014
8:30 am - 11:30 am
Pat Bixby
Sponsor(s): Duke Office of Clinical Research (DOCR)
This course presents information about best practices for consenting a subject to a research study, allows participants to observe consenting scenarios and participate in consenting scenarios to reinforce skills. Completion of the DOCR Informed Consent course is a pre-requisite for this course.
Type: RESEARCH
Contact: Duke Office of Clinical Research
