- Log into eCompliance.
- From the IRB dashboard, choose IRB forms under the Submission to IRB heading (middle column).
- Choose the appropriate IRB form.
- IRB application: For all local exempt, expedited and full-board projects.
- Initial reliance request form: For studies relying on an external IRB.
- Initial request for MU to be the IRB of record: Submitted when you require documentation for a sponsor study submission and/or you are requesting MU IRB to be the sIRB for a multisite protocol.
- Emergency use of a test article: Submitted for emergency use of an FDA-regulated test article.
- Humanitarian use device (HUD): Submitted for HUD requests only.
- Complete the application to the best of your ability. Upload support documentation to the attached files section. Access consent and protocol templates and review our Informed consent FAQ.
- The IRB application requires a two-step process for submission.
- Student applications require an adviser to be listed and will prompt an email approval. See our student researcher page for more information.
- All principal investigators (PIs) must complete the PI assurance form received via email after you hit submit.
- Submission receipts and additional requests will be sent by email.
It is necessary to continuously monitor your email.