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Date: IRB Protocol No: SECTION 1: To be filled out by the Study Protocol Title: Study Protocol Number: Principal Investigator: Sponsor: Name of the study medicine/device: Subject I.D. (Site and Cerf
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What is IRB Protocol No: Form?

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The IRB protocol no. is a unique identifier assigned to each research protocol reviewed by an Institutional Review Board.
Researchers conducting human subjects research are required to file an IRB protocol no.
The IRB protocol no. is typically filled out by the principal investigator of the research study.
The purpose of the IRB protocol no. is to track and monitor the progress of research protocols involving human subjects.
The IRB protocol no. must include information about the study design, risks to participants, informed consent procedures, and how participant confidentiality will be maintained.
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