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Page 21 of the IRB is used only for internal purposes by the Institutional Review Board.
Researchers and institutions conducting research involving human subjects are required to fill out and maintain page 21 of the IRB.
Page 21 of the IRB is typically filled out by the principal investigator of the research study with information relevant to the study's ethics review.
The purpose of page 21 of the IRB is to document certain aspects of the ethics review process and protocols for conducting research involving human subjects.
Information such as study protocols, risks and benefits to participants, informed consent procedures, and any conflicts of interest must be reported on page 21 of the IRB.
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