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Ӱ̳ / Research / Research Compliance / IRB / IRB FORMS & TEMPLATES

IRB Application for Human Participant Research

  • NEW version for Spring 2025.
  • Use this form to submit a new human subject research protocol to the IRB.
  • This is a Microsoft Word form that CAN be used and shared in Google Drive!
  • Contact the IRB Office if you have any problems with this form.

Download Here:IRB Application Form 8.0

IRB Revision Request Form (new version coming soon!)

  • Used to request a change to a previously approved or exempted IRB protocol.
  • This is a Microsoft Word form with fillable fields.
  • DO NOT use it as a Google Doc or in a Google Drive

Download Here: IRB Revision Request Form 4.0

IRB Continuation RequestForm (new version coming soon!)

  • Used to extend the approval period for an IRB protocol
  • Continuing Review is not always required for minimal-risk IRB protocols. Refer to the Notice of Approval document for the approval expiration date of your protocol.
  • Must be submitted 4-5 weeks BEFORE the approval expiration date
  • If an approved protocol expires, research must CEASE IMMEDIATELY

Download Here: IRB Continuation Request Form 6.0

Individual Investigator Agreement (IIA)

  • Researchers who are external to Ӱ̳ must submit this form with their completed IRB Application for Human Subject Research.
  • Please see the IRB Administrator for specific instructions.

Download Here: Ӱ̳ Individual Investigator Agreement

Ӱ̳ Informed Consent/Assent Documents

First: Review