IRB Advisor (Vol. 18, No. 11) – November 1, 2018

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.