All forms must be submitted online via IRBNet.
Appendix A – Exempt Review
Appendix B – Expedited Review
Appendix C – Data Repositories
Appendix D – Deception
Appendix E – Devices
Appendix F – Drugs or Biologics
Appendix G – Genetic Testing
Appendix H – Storage of Biological Materials
Appendix I – Minors
Appendix J – Non-English Speaking Participants
Appendix K – Pregnant Women, Fetuses, Neonates
Appendix L – Prisoners
Appendix M1 – Waiver or Alteration of Consent Process
Appendix M2 – Waiver or Documentation of Consent Documentation
Appendix N – Waiver or Alteration of HIPAA Research Authorization
Appendix O – Research in International Settings
Appendix P – Radiation
Appendix Q – Adults with Decisional Impairments
Appendix R – Additional Personnel
Appendix S – Event Reporting
Appendix T – Change in the Number of Participants
Appendix U – Final Study Report
Appendix V – Unaffiliated Investigator
Appendix W – Faculty Student Assurance
Appendix X – Conflict of Interest in Human Subjects Research
Informed Consent Templates
Informed Consent Guidelines
Per the IRB 2014 Policy, the IRB is responsible for stamping all approved informed consent documents with the URI logo, project reference number, and approval/expiration information. When submitting an informed consent document, be sure to leave the bottom right corner of the document BLANK as this is the location where we upload our stamp.
When submitting a continuing review for your project, it is required that you submit:
— The most recently used consent document that has been signed and whited out so that all personal information is no longer visible.
— A new, clean copy of the consent document with the bottom right corner BLANK.
When submitting an amendment/modification for your project, it is required that you submit:
— The most recently used consent document where all new revisions have been highlighted.
— A new, clean copy of the revised consent document with the bottom right corner BLANK.