This procedure describes how human materials or data not involving human subjects may be classified as Not Human Subjects Research.

This procedure lists responsibilities of the investigator, IRB, OIRB, and sponsor for waiver to the informed consent process in research planned for emergency settings.

This procedure lists responsibilities of the investigator, OIRB and IRB for carrying out the initial review using the expedited procedure.

This procedure lists the responsibilities of the investigator, IRB and OIRB for conducting the initial review of proposed research at the convened IRB meetings.

This procedure outlines responsibilities for dealing with compliance issues with Human Subjects regulations or IRB requirements or determinations.

This procedure outlines the responsibilities of the investigator, OIRB and IRB for conducting and evaluating activities designed to educate the public about Human Subjects research.

This procedure outlines the responsibilities of the OIRB, CQIP Team, IRB Member, Research Community and the Institution for quality assurance and quality improvement for the Human Research Protection Program.

This document lists specific responsibilities of the investigator, OIRB and IRB for monitoring human subjects research

This procedure outlines the responsibilities of the investigator, IRB, OIRB for the review of modifications to previously approved research by the convened IRB.

This procedure outlines the responsibilities of the investigator, OIRB and IRB for the continuing review of research by the expedited procedure.