IRB Advisor (Vol. 21, No. 5) – May 1, 2021

Learning Objectives
Upon completion of this educational activity, participants should be able to:
1. establish clinical trial programs using accepted ethical principles for human subject protection;
2. apply the mandated regulatory safeguards for patient recruitment, follow-up and reporting of findings for human subject research;
3. comply with the necessary educational requirements regarding informed consent and human subject research.