This policy differentiates case reports from human subjects research.

This procedure outlines the responsibilities of the Investigator, OIRB and IRB regarding the informed consent process and documentation of informed consent.

This policy outlines the requirements for formulating contracts with sponsors of proposed research.

This policy requires the implenmentation of a quality assurance and quality improvement program to monitor compliance with federal regulations and improve the Human Research Protection Program processes

This procedure outlines the responsibilities of the Investigator, IRB, and OIRB for handling Investigator and Institutional Conflicts of Interest.

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

This procedure lists responsibilities of the investigator, ORIB and IRB for communication among IRBs.

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.