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Clinical Monitoring

Smarter monitoring. Stronger partnerships.

At ICON, we’re redefining clinical monitoring to meet the demands of today’s complex trials.

Data integrity and quality

Accurate, complete, and consistent data collection, minimising errors and discrepancies

Patient safety

Assessing participant safety and well-being and promptly addressing adverse events and safety concerns

Protocol adherence

Ensuring your trial is conducted in alignment with the study protocol and in accordance with defined procedures and eligibility criteria

Regulatory compliance

Ensuring compliance with regulatory requirements and guidelines, including GCP standards

Timely reporting

Facilitating timely and accurate reporting of trial progress, data, and safety information

Flexible and agile monitoring solutions to meet the needs of your organisation

Our agile, tech-enabled model combines high-performing CRAs, real-time data, and integrated systems to deliver faster, more predictable, and inspection-ready studies.
 

Whether you need tactical oversight or a fully holistic approach, our flexible monitoring models adapt to your trial’s risk profile, site needs, and patient pathways. CRAs are engaged early, trained continuously, and equipped with mobile tools to drive quality, not just compliance.

With ICON, you gain:

  • Strategic CRA support that strengthens site relationships and accelerates activation
  • Clear visibility into site performance, risk signals, and operational metrics
  • Integrated technology that streamlines documentation, reduces admin burden, and improves audit readiness
  • Data-driven insights to guide smarter decisions and continuous improvement

From study start-up to close-out, ICON’s monitoring solutions are built to reduce complexity, enhance oversight, and keep your trial on track, every step of the way.
 

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