Application Forms

• For new protocols, please go to our new electronic system, Cayuse IRB, and login with your Career Account and BoilerKey.

• Non-Exempt Consent Form Template for Participants
  • The sections and certain language in this template must be followed for non-exempt research. Use the information in this document to better understand what your study participants need to know to be fully informed regarding the risks and benefits of participating in your research.
• Exempt Research Study Information Sheet for Participants
  • This is for use with exempt studies only. If your study is determined to be non-exempt, you will need to use the Non-Exempt Consent Form Template for Participants above.
• Additional forms for special populations or sensitive data

Applications that were submitted or reviewed by IRB prior to August 19, 2019 will be considered “legacy protocols” and will only be converted for use within Cayuse on an as-needed basis (e.g., if study modifications are requested or protocol renewals are required).

• When Should I Report Study Problems to the IRB?
  • Provides researchers with a decision matrix in the event that an unanticipated adverse event occurs during the course of the study.
• Reporting Unanticipated Problem and/or Adverse Event
  • Used to report an unanticipated problem or adverse event to the IRB. If an unexpected event happens during the course of your research. Report it promptly in detail to the IRB.
• Research Closure
  • Informs IRB of project closure

Follow these steps to submit an incident report in Cayuse IRB.