IRB Advisor (Vol. 18, No. 7) – July 1, 2018

Learning Objectives

Upon completion of this educational activity, participants should be able to:

  • establish clinical trial programs using accepted ethical principles for human subject protection;
  • apply the mandated regulatory safeguards for patient recruitment, follow-up and reporting of findings for human subject research;
  • comply with the necessary educational requirements regarding informed consent and human subject research.