APPLICATION & FORMS
1. REQUEST ETHICS APPROVAL OF RESEARCH PROTOCOL
To briefly describe your study plan, including rational, objectives, design, methodology, data collection instruments, and most importantly, written protocols for the protection of human subjects. NEW for 2021!
2. EXPEDITED IRB REVIEW CHECKLIST
To determine if you need an Expedited or Full IRB review.
3. INFORMED CONSENT SAMPLE
If you need help with this, please see our Informed Consent page, or the US Department of Health and Human Services website.
4. REQUEST AN EXEMPTION
Complete the Request for Exemption from Ongoing IRB Review
5. REQUEST A RENEWAL
Complete this annual IRB Renewal Request Form
6. REQUEST A CHANGE IN PROTOCOL
Complete this Change in Protocol Form
7. REQUEST A STUDY CLOSURE
8. REPORT AN ADVERSE EVENT
Complete this Adverse Event Reporting Form
9. RESEARCH INVOLVING PRISONERS
Complete this Research Involving Prisoners Form
PLEASE SUBMIT ALL YOUR IRB APPLICATION MATERIALS VIA EMAIL TO:
Dr. D. Michael Anderson, IRB Chair
cc Penelope A. Lantz, Esq., General Counsel