This policy explains UAB's commitment to its compliance with the DHHS Policy on Protection of Human Subjects.

This policy differentiates case reports from human subjects research.

This procedure describes the responsibilities of the IRB and OIRB for facilitating communication regarding complaints and inquiries for research participants, investigators, research staff and the community.

This policy describes the process of reporting, investigating and deciding upon non-compliance as it relates to Human Subjects Regulations.

This policy details the protection of human subjects in research and the guidelines established by the IRB to ensure confidentiality of data.

This policy details the process for reviewing and handling financial (or other) conflicts of interest surrounding the investigator of a proposed project.

This policy describes data monitoring plans which are required for all human subjects research involving greater than minimal risk. Details on plan content and submission are included in the document.

This policy states that consent may be obtained from an individual's legally authorized representative when that individual is unable to consent to participate in research for themselves. The document includes the definition of "legally authorized representative."

This policy defines child, parent and guardian and their associated requirements as research subjects.

This policy describes the IRB's process of determining human subjects research and research exempt from Federal Human Subjects Protection Regulations. This document lists what the IRB is authorized to determine and includes multiple definitions related to the review process for research involving human subjects.