Monitoring Service

Ensuring the quality and regulatory compliance of clinical studies

Experience: Our team is experienced in SDV of study Phases I, II, III for healthy volunteer, patient and Japanese bridging studies for multiple therapeutic areas.

Risk-Based Monitoring:
Our monitoring approach incorporates risk-based strategies, allowing for targeted monitoring activities and efficient resource allocation.

Certified CRAs:
Our in-house team of Certified Clinical Research Associates (CRAs) ensures high-quality monitoring services and adherence to regulatory requirements.

Eligibility Source Data Verification (SDV) Prior to Randomisation:
We emphasise the importance of pre-dose eligibility verification through comprehensive SDV, minimising protocol deviations and ensuring data integrity and patient safety.

Clinical Compliance

Efficiently upholding the highest clinical trial standards

Contact the Richmond Data Science Team today