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 describes documentation requirements for the OIRB (Office of the IRB).
UAB Policy Library Entry
This guidebook contains information on the IRB and its relevance to UAB Investigators. Specific instructions on training, the review process and approvals are included in the guidebook.
UAB Policy
This policy details the roles and responsibilities of IRB and the OIRB.
UAB Procedure
This procedure outlines responsibilities of the OIRB and IRB for IRB member selection for convened meeting.
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.