Our experienced Clinical Research Associates (CRAs) work effectively with sites — on-site or remotely — to ensure the study protocol is followed, informed consent is correctly obtained, adverse events are reported, accurate records are maintained, and study drug or devices are accounted for.

Our monitoring services include traditional, full-service monitoring as well as risk-based approach. CTC has both office-based and regional CRAs.

Pathway to clinic


  • Monitoring visits including site initiation, routine monitoring visits, and close out
  • Risk-based monitoring
  • On-site and remote monitoring (centralized)
  • Monitoring plan
  • Site Management support to ensure site regulatory compliance and adherence to the clinical study protocol
  • Site training
  • Co-monitoring visits

We provide our customers with cost-effective advice, conduct and reporting of clinical trials.