Library Search Results

 Library Search Results

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UAB Procedure
This procedure lists responsibilities of the investigator, IRB, OIRB, and sponsor for waiver to the informed consent process in research planned for emergency settings.
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 document lists specific responsibilities of the investigator, OIRB and IRB for monitoring human subjects research
UAB Procedure
This procedure documents the requirements for determining an exemption from Human Subjects research regulations, including the responsibilities of the Investigator, OIRB and IRB. An attachment that details federal criteria for determining exemption is also included in the document.
UAB Policy
This policy outlines UAB's approach to determining whether use of commercially available cell lines is defined as human subjects research.
UAB Procedure
This procedure outlines the responsibilities of the investigator, OIRB and IRB for continuing review of research approved by the convened IRB.
UAB Procedure
This procedure outlines the responsibilities of the investigator, IRB, OIRB for the review of modifications to previously approved research by the convened IRB.
UAB Procedure
This procedure outlines the responsibilities of the investigator, OIRB and IRB for the continuing review of research by the expedited procedure.
UAB Procedure
This procedure lists responsibilities of the investigator, OIRB and IRB for carrying out the initial review using the expedited procedure.
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.