Summary:
- This article provides frequently asked questions (FAQs) about Institutional Review Boards (IRBs), which are responsible for reviewing and approving research studies involving human subjects to ensure their safety and ethical conduct.
- The FAQs cover topics such as the purpose and responsibilities of IRBs, the composition and operations of IRBs, the review process for research studies, and the requirements for informed consent from research participants.
- The article aims to help researchers, study participants, and the general public understand the role and function of IRBs in the oversight of human subject research, which is critical for protecting the rights and well-being of research participants.