An internal process has been created to manage requests for data from the RDR. In order for a Department of Anesthesiology researcher to gain access to data from the RDR, the researcher must first follow department protocol and vet their research question through the Director of Clinical Research. Once approved, the researcher must develop a scientific protocol and submit it for review to the Clinical Study Evaluation Committee (CSEC) and the Institutional Review Board (IRB). Once approval is gained from these governing bodies, the governance committee in the Department of Anesthesiology will review study documents and approve the transfer of data. Questions related to this process should be sent to CPO staff or the Clinical Research Team.