IRB APPLICATION MATERIALS
IN ORDER TO CONDUCT AN AD HOC IRB REVIEW & APPROVAL, WE WILL NEED THE FOLLOWING INFORMATION:
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.
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.