Research Compliance Office

Human Research Protection Program (HRPP)

Collaborative IRB Training Initiative (CITI)

Required Course in the Protection of Human Research Subjects

• CITI instruction page - Basic CITI Course and Refresher Course
• Step-by-step Registration Instructions
• CITI Login/Registration

Institutional Review Board Office (IRB)

• Consent Form Checklist for IRB Members
• IRB Submission Deadlines and Meeting Dates
• Contact the Administrator
• Research Compliance Office Staff

Ethical and Regulatory Links

• The Belmont Report
• US DHHS Office for Human Research Protections (OHRP)
• Food and Drug Administration

Institutional Review Board (IRB) Submission and Forms

To submit a new research study, please use the electronic submission system, iRIS.
You must have an account to access iRIS. Contact Monica Silcott to set up an account.

Special Forms

Emergency Use Notification Form

Consent Template for Emergency Use

Review Preparatory to Research Form

Continuing Review Forms for ongoing studies NOT in iRIS

Internal Adverse Event Report

External Adverse Event Report

Request for Change in Key Personnel

Protocol Deviations/Violations Submission Form

Monitor/Auditor Report Submission Form

Continuing Review Report

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