Full course description
This course will describe the informed consent process and answer the following questions: What is informed consent? Why is informed consent important? Who is involved in the process? Where and when does informed consent take place? And finally, how should the process be conducted? Additional topics to be discussed include electronic consent, short form consent, and the re-consent process.
Date: Tuesday, December 1, 2026
Time: 9:30 – 11:00 am
Location: Virtual Seminar. Enroll, return to the course website to obtain the zoom link. This class will be held LIVE on the date above.
Attend the 2-hr class, complete the quiz and evaluation to receive a certificate.
Clinical Research Professional Competency Domain: Clinical Trials Operations (GCPs)