Library Search Results

 Library Search Results

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UAB Procedure
This procedure lists the responsibilities of the OIRB and IRB for handling complaints or inquiries regarding research.
UAB Procedure
This procedure indicates the responsibilities of the investigator, ORIB and IRB for ensuring confidentiality of health information and data. Included in this document are definitions of private information and protected health information.
UAB Procedure
This procedure lists responsibilities for IRB members, the IRB Chair, OIRB and consultants for the IRB use of consultants.
UAB Procedure
This procedure lists the responsibilities of the OIRB for organization of protocol files, which allows for tracking of all IRB actions relating to a specific protocol.
UAB Procedure
This procedure lists the responsibilities of the investigator, IRB and OIRB for conducting data and safety monitoring for Human Subjects research.
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, ORIB and IRB for communication among IRBs.
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 Procedure
This procedure lists responsibilities of the investigator, OIRB and IRB for carrying out the initial review using the expedited procedure.
UAB Procedure
This procedure lists the responsibilities of the investigator, IRB, OIRB, and Pharmacy to ensure handling of investigational or unlicensed test articles meets organization standards relating to pharmacy, inventory control, and documentation.