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Results from your Search are visible below. You may further refine your search using the Refine Your Results links below, right. Clicking on one of the refinement items will return a subset of your original search. To return to your original results, simply choose the "Any [term] link at the top of each section. You may also sort your results, either by Relevance/Ranking (default result), Title, or Date Modified.
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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 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.
UAB Policy on Use of and Investigation with Drugs, Biologics, Devices, or Test Articles under FDA Regulations - IRB POL021
Clinical investigations involving human subjects and drugs, biologics, devices or test articles are subject to review. In order to comply with federal regulations, the IRB will determine what types of applications and exemptions (when applicable) are required for the study. This document describes various types of studies and instructions for submission and compliance.
UAB Policy on Minimizing Risks to Subjects - IRB POL027
This policy describes the process by which the IRB determines if risks are minimized for participants in a proposed project. Review process and relevant definitions are included in the document.
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 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.
Procedure for Communication Among IRBs - IRB PRO118
This procedure lists responsibilities of the investigator, ORIB and IRB for communication among IRBs.
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
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.
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