IRB Consent Form Templates

Are you conducting a human participant research project that requires enrollment of Cornell students on the first day of the Fall 2025 semester (August 25)? 
1. Submit your IRB protocol by July 28th to enable approval (or exemption) in time.
2. Include the relevant semester in your protocol title (i.e., "Fall 2025").
3. Make sure your protocol is well-prepared and complete: attach all documents, fully answer all questions clearly and consistently.
4. Respond swiftly to IRB reviewer comments.
5. Anticipate more time for studies requiring ancillary reviews (e.g., IBC, Radiation Safety).
6. As always, contact irbhp@cornell.edu with any questions.

A collection of informed consent, assent, and debriefing templates that can be used for your human participant research study.