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Procedure for Approving a Waiver or Alteration of the Consent Process and the Waiver of Consent Documentation - IRB PRO153
This procedure outlines the responsibilities of the investigator, OIRB and IRB for approving a waiver or alteration of the consent process and the waiver of consent documenation.
Procedure for Assurance of Compliance with Department of Health and Human Services Policy on Protection of Human Subjects - IRB PRO107
This procedure lists the responsibilities delegated to the Investigator, OIRB and IRB for ensuring that the university complies with DHHS policy on the protection of Human Subjects.
Procedure for Communicating Among IRBs - IRB PRO118
This procedure lists responsibilities of the investigator, ORIB and IRB for communication among IRBs.
Procedure for Complaints and Inquiries for Research Participants, Investigators, Research Staff, and the Community - IRB PRO111
This procedure lists the responsibilities of the OIRB and IRB for handling complaints or inquiries regarding research.
Procedure for Compliance Issues with Human Subjects Regulations or IRB Requirements or Determinations - IRB PRO128
This procedure outlines responsibilities for dealing with compliance issues with Human Subjects regulations or IRB requirements or determinations.
Procedure for Conducting and Evaluating Activities Designed to Educate the Public about Human Subjects Research - IRB PRO130
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.
Procedure for Confidentiality of Data; HIPAA Authorization and Waiver - IRB PRO112
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.
Procedure for Continuing Review of Research Approved by the Convened IRB - IRB PRO147
This procedure outlines the responsibilities of the investigator, OIRB and IRB for continuing review of research approved by the convened IRB.
Procedure for Continuing Review of Research by the Expedited Procedure - IRB PRO150
This procedure outlines the responsibilities of the investigator, OIRB and IRB for the continuing review of research by the expedited procedure.
Procedure for Data and Safety Monitoring for Human Subjects Research - IRB PRO116
This procedure lists the responsibilities of the investigator, IRB and OIRB for conducting data and safety monitoring for Human Subjects research.
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