IRB Submission Form - Mississippi State Department of Health 2025

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Under FDA regulations, an Institutional Review Board is group that has been formally designated to review and monitor biomedical research involving human subjects.
Institutional Review Board (IRB) The primary purpose of the IRB is to protect the rights and welfare of human subjects involved in research activities being conducted under its authority.
There is an IRB at every health care facility that does clinical research, and every trial is reviewed by an IRB before the trial begins. Also called Institutional Review Board.
The IRB will provide the investigator and the institution with written notification of decisions to approve or disapprove research and of modifications required to secure IRB approval of the research activity; the written notification must include reasons for the decision and give the investigator an opportunity to
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