Institutional Review Board reviews the research that involves the use of human participants. This is carried out under FDA regulations. This is a group that is formally designated to monitor and review biomedical research that involves human subjects. They have been given the authority to approve, modify or disapprove the research.
There are three major levels of review of human subjects. The first is the full board review is greater than the minimal research and includes minimal research of the risk. The second is the expedited review under which some research may be approved without having the meeting of the IRB. The last is the limited or exempt review where IRB approval is required only for limited matters. These matters must be clearly specified.
Institutional Research Board must review all projects that meet the definition of research including humans. This should be carried out before any data collection by the researcher.
1. Learn more about the Institutional Review Board here:
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2. Learn more about the exempt review here:
https://brainly.com/question/7883590
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