Our Services
Clinical Study Monitoring & CRA Services
Risk-based, on-site and remote monitoring delivered by experienced CRAs ensuring data integrity and GCP compliance.
Study Monitoring
What We Deliver
TCR Solutions ensures data integrity, patient safety and GCP compliance throughout the lifecycle of your trial.
We develop risk-based monitoring (RBM) plans and deliver on-site, remote and centralised monitoring.
Our CRAs carry out source data verification and review, investigator and site staff training, monitoring visit reports and follow-up letters — building genuine relationships with site teams to identify and resolve issues quickly.
The Value
Why It Matters
Effective monitoring means early detection of data and protocol deviations, ICH E6 R3 aligned risk-proportional oversight, and reduced cost through centralised and remote monitoring approaches.
Our CRAs are trusted by site teams, leading to better data quality and fewer queries.
FAQs
Frequently Asked Questions
Do you offer remote monitoring? Yes — we deliver hybrid monitoring strategies combining on-site, remote and centralised approaches.
Are your CRAs GCP trained? All TCR CRAs are ICH GCP certified with active therapeutic-area experience.