This policy describes documentation requirements for the OIRB (Office of the IRB).

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

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

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, OIRB, and Pharmacy to ensure handling of investigational or unlicensed test articles meets organization standards relating to pharmacy, inventory control, and documentation.

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

This procedure outlines responsibilities for the Investigator, OIRB and IRB for the identification and communication of Human Subjects research to Non-UAB-Affiliated performance sites.

This procedure outlines responsibilities of the investigator, IRB and OIRB for review of decisionally impaired adults involved in human subjects research including assent