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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

dma@hmlirb.com

 

cc Penelope A. Lantz, Esq., General Counsel

plantz@hmlus.com