Human Research Protection Office and IRBs

Frequently Used Services

IRB reviews, creating and submitting a protocol and RASCAL submissions

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.

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

Find information about participating in research at the University

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.

Listing of federal and state human subjects research regulations

Recent Announcements