The CC Office of Protocol Services provides centralized support services for clinical research related to the regulatory requirements for the protection of human subjects research and the Institutional Review Board (IRB) protocol submission requirements. In addition, OPS maintains a data repository containing protocols for the NIH Intramural Research Program (IRP) that populates data to the Clinical Center Search the Studies website, Library of Medicine ClinicalTrials.gov website and protocol consent/assent documents websites.

Kim Mitchell, RHIA, CIM
mitchellkjj@cc.nih.gov
301.435.2401