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 requires relevant administrators and employees of UAB and UABHSF to ensure that clinical services associated with research studies are billed appropriately and in compliance with relevant laws, regulations, and contractual obligations.
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 clarifies rights and benefits (individual and institutional) associated with ownership of copyrights and intellectual property.
UAB Policy
This policy details guidelines regarding underage individuals (minors) in University of Alabama at Birmingham (UAB) research laboratories or facilities.
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
All laboratories and related support areas in all UAB buildings, facilities, and spaces shall be labeled with the name and after hours telephone number of the principal investigator and two alternates.
UAB Policy
This policy describes documentation requirements for the OIRB (Office of the IRB).