IRB Advisor (Vol. 21, No. 7) – July 1, 2021

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.