Human Research Protection Office and IRBs

Frequently Used Services

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Protocol and Consent Form Resources

IRB reviews, creating and submitting a protocol, Consent Form templates and suggested language

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Maintain IRB Approval

All changes to the research protocol must be submitted for prospective IRB approval unless a change needs to be implemented immediately to remove or minimize an imminent harm to subjects.

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Human Subjects Protection Training Program

As a prerequisite for IRB approval, all human subjects researchers must complete CITI Human Subjects Protection and HIPAA Privacy training

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Information for Research Participants

Find information about participating in research at the University

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Human Research Policy Guide

Policy overviews and guidelines relevant to human research. In addition, the Clinical Research Handbook provides a comprehensive overview of all policies and guidelines for clinical research at the University.

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Human Subjects Research Regulations

Listing of federal and state human subjects research regulations and guidance 

Recent Announcements