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UAB Procedure
This procedure details the responsibilities of the investigator, OIRB, IRB and the institution for reviewing and signing of independent investigator agreements.
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 the responsibilities of the Investigator, OIRB and IRB regarding the informed consent process and documentation of informed consent.
UAB Procedure
This procedure describes how investigators may request documentation from the OIRB that the research involving the use of human cell lines in vitro or in research animals does/did not require IRB review and approval.
UAB Procedure
This procedure describes the responsibilities of the OIRB and the IRB in relation to maintaining the IRB member roster and quorum.
UAB Procedure
This procedure describes mandatory training for individuals who supervise or are involved in research with human subjects. Links to corresponding policies and other documents are included.
UAB Procedure
This procedure lists the responsibilities of investigators, OIRB and IRB for ensuring that all investigators are qualified to perform their role (s) in conducting research.
UAB Procedure
This procedure details the requirements for the composition of IRBs and IRB staff members.
UAB Procedure
This procedure documents the requirements for determining an exemption from Human Subjects research regulations, including the responsibilities of the Investigator, OIRB and IRB. An attachment that details federal criteria for determining exemption is also included in the document.
UAB Procedure
This procedure delegates responsibilities of the Investigator, OIRB and IRB for ensuring prompt reporting of unanticipated problems encountered in research.