Library Search Results

 Library Search Results

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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 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. This policy also serves as POL001 for UAB's Human Research Protection Program.
UAB Policy
This policy describes the recruitment regulations and requirements for research involving human subjects at UAB. Corresponding policies and procedures are linked within the document.
UAB Policy
This policy describes the process by which the IRB determines if risks are minimized for particpants in a proposed project. Review process and relevant definitions are included in the document.
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 describes the IRB's process of determining human subjects research and research exempt from Federal Human Subjects Protection Regulations. This document lists what the IRB is authorized to determine and includes multiple definitions related to the review process for research involving human subjects.
UAB Policy
This policy describes the process of reporting, investigating and deciding upon non-compliance as it relates to Human Subjects Regulations.
UAB Policy
This policy describes the circumstances underwhich expedited review of Human Subjects research is granted by the IRB.
UAB Policy
All human subjects research must be reviewed by a convened meeting of the IRB unless the research qualifies for review under expedited or exempt categories. This document includes defines a convened IRB as well as the process for reviewing a project.
UAB Policy
This policy describes data monitoring plans which are required for all human subjects research involving greater than minimal risk. Details on plan content and submission are included in the document.