Under the U. S. Department of Health and Human Services (HHS) and U. S. Food and Drug Administration (FDA) regulations, what is the Institutional Review Board (IRB) charged with

The Institutional Review Board is charged with the protection of the subjects used for clinical trials and also to ensure the protocols followed are legal and monitor the research protocols.

Explanation:

The United States Department of Health and Human Resources and the Food and Drug Administration charged the Institutional Review Board with the work of making sure the subjects used for clinical trials are taken care of, and all policies and regulations are followed as per governmental protocols. The IRB is a body charged with the protection of the subjects and reviewing the protocols followed.

This involves making sure that the subjects are given protection regarding their rights, welfare, and privacy. At the same time, it is also required to ensure the protocols followed are legal and binding, and to approve, disapprove, or even modify any changes needed accordingly.

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explanation:

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