Library Search Results

 Library Search Results

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UAB Policy
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
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
This policy outlines UAB's approach to determining whether use of commercially available cell lines is defined as human subjects research.
UAB Policy
This policy details the process for reviewing and handling financial (or other) conflicts of interest surrounding the investigator of a proposed project.
UAB Policy
This policy establishes UAB’s program for the protection of human subjects and describes the ethical standards and institutional commitments applicable to the conduct of human subjects research at UAB.
UAB Policy
This policy describes documentation requirements for the OIRB (Office of the IRB).
UAB Policy
This policy details the requirements for reviews of UAB research involving humans.
UAB Policy
This policy details the definitions of unanticipated problems involving risks to subjects in UAB research, and outlines the procedures to be followed should such a problem arise.
UAB Policy
This policy explains UAB's commitment to its compliance with the DHHS Policy on Protection of Human Subjects.
UAB Policy
This policy details the additional safeguards that must be used when conducting research that involves children.