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Clinical Study Monitoring & CRA Services

Risk-based, on-site and remote monitoring delivered by experienced CRAs. TCR Solutions ensures data integrity, patient safety and GCP compliance throughout the lifecycle of your trial.

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What we deliver

  • Risk-based monitoring (RBM) plans
  • On-site, remote and centralised monitoring
  • Source data verification and source data review
  • Investigator and site staff training
  • Monitoring visit reports and follow-up letters

Why it matters

  • Early detection of data and protocol deviations
  • ICH E6 R3 aligned, risk-proportional oversight
  • Reduced cost via centralised and remote monitoring

FAQs

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.

European CRO for US companies

Start the conversation

If you are considering clinical trial support as part of your development strategy, TCR Solutions would be pleased to discuss how our services could support your programme.

Contact usinfo@tcr-solutions.com