UAB encourages the procurement and licensing of patents for inventions in the interest of the public, the inventor, and the university.

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 with regard to suspension or termination of IRB-Approved research and administrative hold.

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 policy describes the IRB's obligation to report certain determinations to UAB officials, regulatory and other federal regulatory agencies, and sponsors.