Please read all relevant policies and procedures before submitting a protocol.
- To reduce paper consumption, we accept electronic submissions only. Send all materials as attachments to email@example.com.
- Always download the most recent forms from this site.
- Separate all individual parts (informed consent, appendices, flyers, recruitment scripts) into individual, clearly labeled files (with PI last name,nature of form, date) Use PDF or Word -- NO JPGs. Example: Smith.Informed Consent.Aug.2016
- Review and sign the application checklist to ensure you have provided all required elements for a complete protocol submission.
NOTE: We now have one submission form for all expedited/full board, social-behavioral or biomedical protocols. Be sure to visit our website and always download forms from our links. If you submit an old form, we will ask you to resubmit with the new one.
- IRB Exped or Full Protocol Application Form
- Application for Exemption from IRB Review
- (Review the checklist and FAQ sheet for more information.)
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.
- Sample Informed Consent Form.1.13(Adults)
- Sample Minor Assent Form.4.22
- Sample Parental Permission Form.6.26.13
- 3b.Appendix B.Research with Minors Request FORM
- 4b.Appendix C.Research with Prisoners Request FORM
- 5.Appendix D.Research with Pregnant Women.Neonates Request FORM(1)
- 6.Appendix E.Research Involving Adults with Decitional Impairments FORM
- 7.Appendix F.Use of Deception Request FORM
- 8b.Appendix G.International Research FORM