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Procedure for Observation of the Informed Consent Process in Ongoing Research - IRB PRO129
This procedure outlines responsibilities of the investigator, OIRB and IRB for observation of the informed consent process in ongoing research.
Procedure for Participants to Communicate Questions and Concerns to Investigators and the IRB as Part of Informed Consent Process - IRB PRO131
This procedure outlines the responsibilities of the investigator, ORIB, and IRB to facilitate questions and concerns as part of the Informed Consent process.
Procedure for Waiver to Informed Consent Process in Research Planned for Emergency Settings - IRB PRO119
This procedure lists responsibilities of the investigator, IRB, OIRB, and sponsor for waiver to the informed consent process in research planned for emergency settings.
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.
UAB Policy on Elements of Informed Consent, the Informed Consent Process, and Documentation of Informed Consent - IRB POL013
This policy provides instructions for informed consent. Researchers seeking to utilize human subjects must obtain informed consent in accordance with all applicable federal regulations.
UAB Policy on Inclusion of a Procedure for Participants to Communicate Questions and Concerns to Investigators and the IRB as Part of Informed Consent Process - IRB POL031
This policy describes the inclusion of a procedure for participants to voice questions and concerns to the Investigator or the IRB as part of the Informed Consent Process.
UAB Policy on Waiver of Informed Consent Requirements in Research Planned for Emergency Settings - IRB POL019
This policy defines the circumstances under which research may be conducted without the requirement of informed consent.
UAB Policy on Waiver, Alterations, and Exceptions to Informed Consent; Waiver of Documentation of Informed Consent - IRB POL036
This policy describes the exceptions to beginning human subjects research without informed consent. Links to corresponding procedures are included within the document.
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