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Procedure for Initial Review of Proposed Research at the Convened IRB Meetings - IRB PRO122
This procedure lists the responsibilities of the investigator, IRB and OIRB for conducting the initial review of proposed research at the convened IRB meetings.
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 Quality Assurance and Quality Improvement for the Human Research Protection Program - IRB PRO134
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.
Procedure for Quality Assurance (Monitoring of Human Subjects Research) - IRB PRO102
This document lists specific responsibilities of the investigator, OIRB and IRB for monitoring human subjects research
UAB Policy on Determination of Human Subject Research on Cell Lines - IRB POL042
This policy outlines UAB's approach to determining whether use of commercially available cell lines is defined as human subjects research.
Procedure for Determination of Exemption from Human Subjects - IRB PRO105
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.
Procedure for Policy Development and Communication for the Human Research Protection Program - IRB PRO110
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.
Procedure for Not Human Subjects Research Designation - IRB PRO117
This procedure describes how human materials or data not involving human subjects may be classified as Not Human Subjects Research.
Procedure for Waiver to Informed Consent Process in Research Planned for Emergency Settings - IRB PRO119
This procedure lists responsibilities of the investigator, IRB, OIRB, and sponsor for waiver to the informed consent process in research planned for emergency settings.
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