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UAB Policy on Case Reports - IRB POL043
This policy differentiates case reports from human subjects research.
Procedure for the Informed Consent Process and Documentation of Informed Consent - IRB PRO113
This procedure outlines the responsibilities of the Investigator, OIRB and IRB regarding the informed consent process and documentation of informed consent.
UAB Expectations for Research Sponsors - IRB POL005
This policy outlines the requirements for formulating contracts with sponsors of proposed research.
UAB Policy on Quality Assurance and Quality Improvement for the Human Research Protection Program - IRB POL034
This policy requires the implenmentation of a quality assurance and quality improvement program to monitor compliance with federal regulations and improve the Human Research Protection Program processes
Procedure for Identifying and Managing Investigator and Institutional Conflicts of Interest - IRB PRO123
This procedure outlines the responsibilities of the Investigator, IRB, and OIRB for handling Investigator and Institutional Conflicts of Interest.
Procedure for Suspension or Termination of IRB-Approved Research and Administrative Hold - IRB PRO140
This procedure outlines the responsibilities of the investigator, OIRB and IRB with regard to suspension or termination of IRB-Approved research and administrative hold.
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 Communication Among IRBs - IRB PRO118
This procedure lists responsibilities of the investigator, ORIB and IRB for communication among IRBs.
UAB Policy on Reporting to Institutional Officials and Regulatory Agencies- IRB POL024
This policy describes the IRB's obligation to report certain determinations to UAB officials, regulatory and other federal regulatory agencies, and sponsors.
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
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