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Appendix G Form 5CENTRA HEALTH Institutional Review Board PROTECTED HEALTH INFORMATION: WAIVER OF AUTHORIZATION Version 4, 19DEC2017Use this form if you need to access and use only the minimum amount
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The IRB modification form is a document used to request changes to an approved research study by the Institutional Review Board (IRB).
Researchers conducting studies that have been approved by the IRB are required to file an IRB modification form if any changes to the study are proposed.
To fill out an IRB modification form, researchers must provide detailed information about the proposed changes to the study, justification for the changes, and any potential risks or benefits.
The purpose of the IRB modification form is to ensure that any changes to an approved research study are properly reviewed and approved by the IRB to protect the rights and welfare of research participants.
The IRB modification form must include details about the proposed changes, rationale for the changes, any potential risks to participants, and any modifications to the informed consent process.
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