Medical monitoring

At DICE, we provide end-to-end medical monitoring, from study start-up through to completion. Our approach combines consistency, scientific rigor and hands-on involvement, ensuring that safety data is continuously assessed, risks are identified early and findings are aligned with study objectives and regulatory requirements.

Medical support during study start-up and execution

Ongoing medical input to support study design, initiation and execution, ensuring alignment with clinical and regulatory requirements.

Medical review of clinical data

Continuous review of clinical data to identify safety signals, inconsistencies and potential risks at an early stage.

Coding review

Medical oversight of coding to ensure accurate and consistent classification of adverse events and medical terminology.

Medical coherence review

Assessment of consistency across data sources, ensuring alignment between clinical narratives and datasets.

DSMB preparation and support

Preparation of documentation and support for Data Safety Monitoring Boards, ensuring clear and accurate safety reporting.

Common challenges we help to prevent

• Delayed identification of safety signals
• Inconsistencies between clinical data and narratives
• Misclassification of adverse events
• Misalignment with regulatory safety expectations

The result

You get consistent and reliable medical monitoring that strengthens patient safety, study integrity and regulatory confidence.

How we work

We take a proactive and structured approach, with continuous oversight, direct communication and careful documentation. This allows for timely decision-making and effective risk management throughout your study.