The IRB review process typically involves several steps:
Submission: Researchers submit their study protocols, consent forms, and other relevant documents to the IRB. Initial Review: The IRB reviews the submission for completeness and assigns it to a primary reviewer. Full Board Review: For studies with more than minimal risk, the full IRB board reviews the protocol in a meeting. Decision: The IRB can approve, require modifications, or disapprove the study. Ongoing Monitoring: Approved studies are subject to periodic review and monitoring by the IRB.
