Clinical Research Regulatory & Ethics (CRRE)
CRRE makes sure there are adherence to the study protocols, Good Clinical Practice (GCPs), Federal Regulations, and research standard operating procedures; ensures the integrity of the scientific data; and determines that the rights and welfare of human research subjects are being or have been adequately protected. CRRE consults with the directors, managers, investigators, and research coordinators on study findings and ensures that corrective action plans are implemented. The staff is comprised of monitors whom have a vast knowledge of State, Federal and International laws and guidelines, which govern clinical research and know where and whom to go to for guidance and direction, e.g. Research Compliance.