For IRB Members

Use these documents to guide your assigned committee reviews. If you require assistance, contact the assigned IRB analyst listed on the short agenda or email the general inbox.

• Reviewer guide

• Presenting a review summary
• Primary reviewer note-taking guide
• Common IRB acronyms
• Motion prompter

The IRB analyst will notify the primary reviewer if a checklist is required. Download and complete the assigned checklist and attach the completed version to the reviewer checklist form in OneAegis:

• HRP-415 – Waiver or alteration of the consent process
• HRP-418 – Research involving pregnant women
• HRP-419 – Research involving non-viable neonates
• HRP-420 – Research involving neonates of uncertain viability
• HRP-421 – Research involving children
• HRP-424 – Non-significant risk device
• HRP-425 – Waiver of the consent process for planned emergency research
• HRP-427 – Waiver or alteration of HIPAA authorization
• HRP-440 – Drugs and biologics
• HRP-441 – Devices

The following worksheets are used to guide your review, as applicable. All initial submissions and continuing reviews must meet the criteria for approval outlined in HRP-314. These documents do not need to be retained:

• HRP-311 – Criteria for approval and additional considerations
• HRP-314 – Criteria for approval for HUD
• Attachment D – ICF elements internal worksheet