Clinical Monitoring

Trial monitoring is in the hands of our highly qualified CRAs.

Our CRAs are fully prepared and equipped for both on-site and off-site visits, and can offer a risk-based approach to monitoring visits if required. All site visits are undertaken in accordance with ICH GCP and Standard Operating Procedures requirements, monitoring plan, protocol and client expectations. Quality of data review and interaction with study sites are key, and support is 24/7.

Our CRAs provide:

  • site selection/qualification visits
  • site initiation visits
  • routine site monitoring visits
  • study close-out visits
  • tracking of the query resolution process
  • site management, including regular contacts with sites via phone, email etc