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IRB PROTOCOL MODIFICATION REQUEST Change of Principal or Principal Investigator 11.01.13For study personnel changes OTHER than PI or COPY use the Modification request to add or delete key personnelPrincipal
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How to fill out institutional review board modification

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How to fill out institutional review board modification

01
Start by accessing the institutional review board (IRB) website or portal.
02
Login to your IRB account using your credentials.
03
Locate the section for modification requests or amendments.
04
Click on the 'New Modification' or 'Submit Amendment' button.
05
Fill out the required fields, such as study title, principal investigator information, and study protocol number.
06
Provide a detailed description of the modification you are requesting.
07
Include any supporting documents or additional information that may be necessary for the IRB to review your request.
08
Review all the information you entered and make sure it is accurate and complete.
09
Click on the 'Submit' or 'Send' button to send your modification request to the IRB.
10
Wait for the IRB to review your request and provide any feedback or further instructions.

Who needs institutional review board modification?

01
Researchers conducting human subjects research that is already approved by the IRB may need to submit an institutional review board modification if they want to make any changes to the study protocol, data collection procedures, consent forms, or any other aspect of their research that was previously approved by the IRB.

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An institutional review board (IRB) modification refers to changes or amendments to a previously approved research study that must be reviewed and approved by the IRB to ensure the continued protection of human subjects.
Researchers or institutions conducting studies involving human subjects must file an IRB modification if they wish to change aspects of their approved research.
To fill out an IRB modification, researchers typically need to complete a specific form provided by the IRB, detailing the proposed changes, their justification, and any potential impacts on participant safety or study integrity.
The purpose of an IRB modification is to ensure that any changes made to a research study do not compromise participant safety, ethical considerations, or the integrity of the research.
Information that must be reported includes a description of the changes, rationale for the modifications, potential risks or benefits, changes to data collection methods, and updated consent forms if applicable.
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