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UAB Procedure
Some sponsors restrict the total number of applications submitted per institution, school, and/or discipline. When the sponsor's program guidelines stipulate a limit, an internal review process may be necessary to determine the applicant(s) or proposal(s) to represent UAB.
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
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.
UAB Procedure
This procedure outlines the responsibilities of the investigator and OIRB for facilitated review of industry-sponsored research by Western IRB.
UAB Procedure
This procedure outlines the responsibilities of the investigator, IRB, and OIRB for maintaining the privacy of research subjects.
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.