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To approve research under or, the ¶¶Òõ̽̽ convened IRB or designated reviewer using the expedited procedure must determine that the research satisfies all the requirements set forth in:

The criteria for review must be used to approve research for initial review, continuing review, and review of modifications.

In working with investigators, the IRB staff have noticed common areas that tend to delay progress when moving protocols throughout the IRB process.

We have outlined a list of questions for you to consider while working your way through the IRB submission process.

Federal and state regulations, institutional policy, and good clinical and research practices require investigators to maintain documents related to human subjects research.

Guidance was developed to assist researchers in organizing research-related documents.

Guidance will help you through some common obstacles researchers face going through the IRB Approval process.

A plain language medical dictionary simplifies medical terms for easier understanding, helping researchers communicate effectively with diverse audiences. It ensures research findings are clear, accessible, and inclusive, fostering informed decision-making and broader engagement.

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