Library Search Results

 Library Search Results

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UAB Procedure
This procedure outlines the responsibilities of the Investigator, OIRB and IRB regarding the informed consent process and documentation of informed consent.
UAB Procedure
UAB sub-recipient agreements (third-party agreements) must be in compliance with all applicable laws, regulations, and terms and conditions included in UAB’s prime award(s). Certain procedures have been established to ensure proper monitoring of these agreements.
UAB Procedure
This procedure outlines responsibilities of the OIRB and IRB for IRB member selection for convened meeting.
UAB Procedure
This procedure outlines the responsibilities of the OIRB and IRB for formation and assignment of IRB member primary review teams for initial or continuing review or review of modifications to research at convened IRB meetings.
UAB Procedure
This procedure outlines the responsibilities of the OIRB for timing of document distribution for meetings.
UAB Procedure
This procedure outlines the responsibilities of the OIRB and the IRB for documentation of convened IRB proceedings.
UAB Procedure
This procedure outlines the responsibilities of the investigator, OIRB and IRB for facilitated review of research for NCI pediatric central IRB-approved research protocols.
UAB Procedure
This procedure outlines the responsibilities of the investigator, OIRB and IRB for emergency use of FDA-Regulated test articles. This document also includes basic elements and disclosures included in informed consent for emergency use of test articles.
UAB Procedure
This procedure outlines the responsibilities of the investigator, OIRB and IRB for identification and communication of human subjects research to UAB-affiliated performance sites.
UAB Procedure
This procedure outlines the responsibilities of the investigator, OIRB and IRB for approving a waiver or alteration of the consent process and the waiver of consent documenation.