According to federal regulations, the option that best describes when expedited review of a new, proposed study may be used by the IRB (Institutional Review Board) is when the research activities are within regulatory categories that have been designated as eligible and pose just a small risk.
The key role of the IRB is to ensure that suitable measures are made to protect the rights and welfare of those participating as research subjects both in advance and during periodic evaluation.
Thus, it is right to indicate that expedited review of a new, proposed study may be used by the IRB (Institutional Review Board) is when the research activities are within regulatory categories that have been designated as eligible and pose just a small risk.
Learn more abut the IRB at:
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