CROS NT can support Sponsors with clinical monitoring needs through our international panel of clinical monitors allowing us to select the most appropriately qualified CRA rather than assigning a less suitable in-house CRA who happens to be available.

They consistently work to the quality standards our clients expect by providing support, encouragement and motivation of clinical sites (hospital-based/GP-based/academic sites/Phase I site) and clinical personnel to ensure patients are identified, screened and recruited to clinical trials as efficiently as possible.

clinical monitoringClinical Monitoring Services

  • Site qualification visits
  • Site initiation visits
  • Site interim monitoring visits
  • Site close-out visits
  • Data collection/query resolution
  • Investigator Site File review and product reconciliation
  • Safety reporting (AEs & SAEs)
  • Pharmacy & Laboratory monitoring/reconciliation