Submit the study protocol to an institutional review board (IRB) or ethics committee for review and approval, addressing any concerns they raise.

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The process of obtaining approvals for medical and health clinical research involves two primary steps: securing approval from an institutional review board or ethics committee, and developing informed consent forms for potential participants.

Steps of Writing Medical And Health Clinical Research: Obtain Approvals

Develop informed consent forms that clearly explain the study's purpose, procedures, risks, and benefits to potential participants.

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