IRB APPLICATION MATERIALS
IN ORDER TO CONDUCT AN AD HOC IRB REVIEW & APPROVAL, WE WILL NEED THE FOLLOWING INFORMATION:
1. AN HML EXPEDITED IRB REVIEW CHECKLIST
To determine if you need an Expedited or Full IRB review.
2. HML REQUEST FOR IRB APPROVAL OF RESEARCH PROTOCOL
Document, from your study’s research design, to briefly describe your study plan, including rational, objectives, design, methodology, and most importantly, written protocols for the protection of human subjects.
3. COPIES OF ALL INFORMED CONSENT FORMS
If you need help with this, please see our Informed Consent page, or the US Department of Health and Human Services website.
4. SURVEY OR OTHER QUESTIONS
We would also like to see your survey or other questions and your subject recruitment plan, and any other parts of your research plan that are relevant to human subject protections and IRB approval.
5. REQUEST AN EXEMPTION
Complete the Request for Exemption from Ongoing IRB Review
PLEASE SUBMIT ALL YOUR IRB APPLICATION MATERIALS VIA EMAIL TO:
Dr. D. Michael Anderson, IRB Chair
cc Penelope A. Lantz, Esq., General Counsel
