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The Institutional Review Board (IRB) process is a critical component in the ethical oversight of research involving human subjects. It ensures the protection of participants by reviewing study protocols, informed consent forms, and the risk-benefit ratio of research activities. This guide provides an overview of the IRB process, including the roles and responsibilities of researchers, IRB members, and institutional leaders. By outlining best practices and essential tips for successful IRB submissions, researchers can navigate the complexities of the review process efficiently.
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