What is an IRB or Institutional Review Board?
An IRB is a diverse group of scientific and non-scientific individuals who conduct the initial and ongoing review of clinical research studies in order to ensure the protection of the rights and welfare of human subjects participating in those trials. The Code of Federal Regulations Title 21, Parts 50 and 56 and Title 45 CFR Part 46 governs the composition and conduct of IRBs.
Related Questions
- Our organization requires review of all research projects by our Institutional Review Board (IRB). Do we need to secure final IRB approval for the proposal process?
- When should an Institutional Review Board (IRB) or institution request a "407" review for research involving children as subjects?
- Do I need to complete Institutional Review Board, IRB, training for the DNP program?
