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RESEARCH & ETHICS
In order to conduct an ad hoc IRB review and approval, we will need the following information:
2. An 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, or the World Health Organization websites.
4. 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.
Please submit all your IRB application materials via email to:
Dr. D. Michael Anderson, IRB Chair
cc Penelope A. Lantz, Esq., General Counsel
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