Clinical Monitoring

You can trust trial monitoring in the hands of our highly-qualified CRAs.

Our CRAs are always prepared and equipped for both on-site and off-site visits and can offer risk-based approaches to monitoring visits, when needed. All site visits are undertaken in accordance with ICH GCP procedure, study protocol, monitoring plans, and client expectations. Quality data review and constant interaction with study sites are paramount, and support is 24/7.

Our CRAs provide:

  • site initiation visits
  • routine site monitoring visits
  • site management – including regular site contact via phone, email, etc.
  • tracking of query resolution process
  • site support during database lock process
  • study close-out visits