CROLLL - Monitoring
  • Crolll


With our team of long-term experienced clinical monitors and in close cooperation with investigational sites and data management we cover all parts of monitoring nationwide.

    Pre-trial monitoring

  • Recruitment of investigational sites / Review of sites for qualification
  • Conduct of pre-trial visits
  • Development of the monitoring plan
  • Project specific training of clinical monitors

    Periodic monitoring

  • On site monitoring
  • Co-monitoring
  • Continuous support of sites between monitoring visits
  • Close-out visits at investigational sites