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The agency responsible for evaluating safety to persons and the risk-to-benefit ratio of biomedical research is the Institutional Review Board (IRB). IRBs review research proposals to ensure that ethical standards are upheld, protecting the rights and welfare of participants. They assess potential risks and benefits, ensuring that research complies with regulatory guidelines. In some cases, federal agencies like the Food and Drug Administration (FDA) also play a role in overseeing the safety of biomedical research involving drugs and medical devices.

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2w ago

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