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Institutional Review Board Modification Application A Modification Application must be completed if major or substantive changes are required for a project after IRB approval has been granted. Such
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How to fill out institutional review board modification
How to fill out institutional review board modification
01
Fill out the required modification form provided by the Institutional Review Board (IRB).
02
Clearly state the changes you are requesting in the modification form.
03
Provide detailed justification for why the modifications are necessary.
04
Include any supporting documentation or evidence to support your request.
05
Submit the completed modification form and any additional materials to the IRB for review.
Who needs institutional review board modification?
01
Researchers conducting studies involving human subjects.
02
Institutions or organizations conducting research that is subject to IRB oversight.
03
Anyone making changes to an approved research protocol that was previously reviewed by the IRB.
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What is institutional review board modification?
An institutional review board modification refers to any changes made to an approved research protocol or study by the IRB.
Who is required to file institutional review board modification?
Researchers or institutions conducting research studies that have been approved by the IRB are required to file for modifications.
How to fill out institutional review board modification?
To fill out an IRB modification, researchers must submit a request detailing the changes being made, rationale for the changes, any potential risks or benefits, and any revised study documents.
What is the purpose of institutional review board modification?
The purpose of an IRB modification is to ensure that any changes to a research study are ethical, compliant with regulations, and do not pose additional risks to participants.
What information must be reported on institutional review board modification?
Researchers must report detailed information about the changes being made, rationale for the changes, any potential risks or benefits, and any updated study documents.
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