Overview

The Clinical Trials Office assists investigators, scholars, and staff in the conduct of clinical research by providing education in regulatory and clinical research administration, help with study recruitment, and a vast array of static and interactive resources to guide investigational teams through the myriad of local, state, and federal requirements. By supporting investigators with IRB and FDA applications, research budgeting and billing, and cost analysis, the CTSC facilitates efficient compliant clinical research at UC Davis. Additionally, the group provides investigators with access to a highly trained staff of clinical research coordinators who are experienced and trained in the complex clinical research environment and can help monitor, mentor, and foster quality assurance through all phases of a clinical research protocol.

Services We Offer

  • Clinical trial consultation
  • Study management
  • IRB application
  • FDA application (IND/IDE)
  • Clinicaltrials.gov
  • Monitoring and quality assurance
  • Coverage analysis