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 describes the IRB's obligation to report certain determinations to UAB officials, regulatory and other federal regulatory agencies, and sponsors.
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 underscores the ethical principles for responsible conduct by which all UAB faculty, employees, and trainees must abide in the performance, recording, and reporting of research and scholarly activities. It also sets forth the procedures to be followed in the case of suspected research misconduct, from preliminary assessment through final outcome of an investigation.
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 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.