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.

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

Complete this Study Closure Form

8. REPORT AN ADVERSE EVENT

Complete this Adverse Event Reporting Form

9. RESEARCH INVOLVING PRISONERS

Complete this Research Involving Prisoners Form