Library Search Results

 Library Search Results

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UAB Procedure
This procedure outlines responsibilities for dealing with compliance issues with Human Subjects regulations or IRB requirements or determinations.
UAB Procedure
This procedure outlines responsibilities of the investigator, OIRB and IRB for observation of the informed consent process in ongoing research.
UAB Procedure
This procedure outlines the responsibilities of the investigator, OIRB and IRB for conducting and evaluating activities designed to educate the public about Human Subjects research.
UAB Procedure
This procedure outlines the responsibilities of the investigator, ORIB, and IRB to facilitate questions and concerns as part of the Informed Consent process.
UAB Procedure
This procedure outlines responsibilities for the investigator, OIRB and IRB for review when pregnant women, fetuses and neonates are involved as participants in research.
UAB Procedure
This procedure outlines responsibilities for the investigator, OIRB and IRB for review when prisoners are involved as participants in research.
UAB Procedure
This procedure outlines the responsibilities of the OIRB, CQIP Team, IRB Member, Research Community and the Institution for quality assurance and quality improvement for the Human Research Protection Program.
UAB Procedure
This procedure outlines the responsibilities of the investigator, OIRB and IRB for the use of repositories of human tissues and databanks for research.
UAB Procedure
This procedure outlines the responsibilities of the OIRB and the IRB for documentation of research undergoing initial or continuing review by the expedited procedure.
UAB Procedure
This procedure outlines the responsibilities for the investigator, institution and IRB to determine that necessary resources are available for care and safety of human research participants.