All IRB submissions must include consent form(s) and/or a parental permission and assent form (if subjects are under 18 years of age), and be signed by all parties involved (primary investigator, co-PIs, and faculty adviser, if applicable). Submissions must include copies of current (within 3 years) CITI certificates for all such parties (investigators and faculty adviser).
•Please read all relevant policies and procedures before submitting a protocol. Because forms are frequently updated, always download the most recent documents from the website when submitting to the IRB.
•The following documents are read-only Word documents, so please download and save a copy in order to fill out the submission form and proper appendices (if relevant) correctly.
•After reviewing the checklist and FAQ sheet for exempt reviews, if you believe your study qualifies as exempt, please submit an Application for Exemption from IRB Review. Applications meeting the criteria for exemption typically take 2-3 business days to process (unless the study must be elevated to a higher review level).
Application for Exemption
Social-Behavioral Protocol Submission Form
Biomedical Protocol Submission Form
Informed Consent Documents
For consistency and for ensuring all required parts are present in the informed consent form, we encourage you to use our sample templates below. However, you may submit an alternate consent form, or alter the templates below to fit the needs of your particular research study.
Standard, written informed consent template (Adults)
Assent template for minors
Parental Permission template
Appendix A: Alteration or Waiver of Consent
Appendix B: Research with Minors
Appendix C: Research with Prisoners
Appendix D: Research with Pregnant Women
Appendix E: Research Involving Adults with Decisional Impairments
Appendix F: Use of Deception
Appendix G: International Research
Modification Request Form
Continuing Review / Downgrade to Exempt Form