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FOR IRB USE ONLY APPROVED BY: IRB01 IRB ID #: 201612723 APPROVAL DATE: 06×06/19 EXPIRATION DATE: 09×17/19INFORMED CONSENT DOCUMENT Project Title:Nicotinamide ringside (NR) in Paclitaxelinduced Peripheral
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What is for irb use only?
For IRB use only refers to information that is meant to be accessed and used by the Institutional Review Board (IRB) for review and approval purposes.
Who is required to file for irb use only?
Researchers conducting studies involving human subjects are required to file for IRB use only.
How to fill out for irb use only?
To fill out for IRB use only, researchers need to provide detailed information about the study, including protocols, procedures, and any risks involved for human subjects.
What is the purpose of for irb use only?
The purpose of for IRB use only is to ensure that the study involving human subjects complies with ethical standards and regulations set by the IRB.
What information must be reported on for irb use only?
Information such as study protocols, procedures, risks and benefits, informed consent forms, and any data collected from human subjects must be reported on for IRB use only.
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