The CME/CE objectives for IRB Advisor are to help physicians and nurses 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
Relias Learning designates this enduring material for a maximum of 1.5 AMA PRA Category 1 Credits™.
Physicians should claim only credit commensurate with the extent of their participation in the activity.
Relias Learning is accredited by the Accreditation Council for Continuing Medical Education (ACCME) to provide continuing medical education for physicians.
Author Melinda Young, Medical Writer Gary Evans, Editor Jill Drachenberg, Editor Dana Spector, Physician Editor Lindsay McNair, MD, MPH, MSBioethics, and Nurse Planner Kay Ball, RN, PhD, report no consultant, stockholder, speaker’s bureau, research, or other financial relationships with companies having ties to this field of study.