Institutional Review Board

The Institutional Review Board (IRB) is an administrative body established to protect the rights and welfare of human research subjects recruited to participate in research activities conducted under the auspices of the institution with which it is affiliated.

The IRB is charged with the responsibility of reviewing, prior to its initiation, all research (whether funded or not) involving human participants. The IRB is concerned with protecting the welfare, rights, and privacy of human subjects. The IRB has the authority to approve, disapprove, monitor, and require modifications in all research activities that fall within its jurisdiction as specified by both the federal regulations and institutional policy.

Regulatory Update

Regulatory Update: January 19, 2019

Do I Need IRB Approval?

If you are unsure if you need IRB approval for your study, please review the Decision Guide and information provided by the Division of Research and Innovation and Dept of Health and Human Services. Discover if you need IRB approval here.

Board Members and Meetings

The Institutional Review Board is chaired by Dr. James Whelan. All applications for review are submitted through Cayuse. Meet the IRB Members and view the schedule

Submit for Human Research Review 

If you are using human subjects, you need to apply for review by the IRB through Cayuse. Details on the application process are found at the link below. Information on training for IRB application is also found at the link. Submit a Human Subjects Research Protocol

Human Subjects Data Sharing Agreement

Data sharing agreements are required when human subject data is shared by another party with the PI. The process for establishing a shared data agreement is human subject data.

Training