Library Search Results

 Library Search Results

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UAB Procedure
This procedure outlines the responsibilities of the Investigator, OIRB and IRB regarding the informed consent process and documentation of informed consent.
UAB Policy
This policy outlines UAB's approach to determining whether use of commercially available cell lines is defined as human subjects research.
UAB Policy
This policy details the process for reviewing and handling financial (or other) conflicts of interest surrounding the investigator of a proposed project.
UAB Policy
This policy establishes UAB’s program for the protection of human subjects and describes the ethical standards and institutional commitments applicable to the conduct of human subjects research at UAB.
UAB Policy
This policy describes documentation requirements for the OIRB (Office of the IRB).
UAB Procedure
This procedure outlines the responsibilities of the OIRB and IRB for formation and assignment of IRB member primary review teams for initial or continuing review or review of modifications to research at convened IRB meetings.
UAB Procedure
This procedure outlines the responsibilities of the OIRB for timing of document distribution for meetings.
UAB Procedure
This procedure outlines the responsibilities of the OIRB and the IRB for documentation of convened IRB proceedings.
UAB Procedure
This procedure outlines the responsibilities of the investigator, OIRB and IRB for facilitated review of research for NCI pediatric central IRB-approved research protocols.