Library Search Results

 Library Search Results

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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 Procedure
This procedure lists the responsibilities delegated to the investigators, OIRB and IRB, and Institutional Official to ensure proper maintenance, development and use of IRB policies.
UAB Procedure
This procedure describes how human materials or data not involving human subjects may be classified as Not Human Subjects Research.
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 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 with regard to suspension or termination of IRB-Approved research and administrative hold.
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.