Clinical Research
Expert clinical research services with a personal touch
We offer comprehensive clinical trial monitoring services in the UK and Hong Kong. Our highly experienced monitors specialise in overseeing Phase I–IV clinical studies across a wide range of therapeutic areas.
End-to-End Support for Your Study
✅ Study Start-Up & Regulatory Submissions
We handle site feasibility assessments, regulatory and ethics submissions, and site initiation visits. With extensive experience in Hong Kong and UK regulatory processes, we can prepare and submit your competent authority and ethics committee submission packages seamlessly.
✅ Site Monitoring & Compliance
We provide regular on-site and remote monitoring, ensuring Good Clinical Practice (GCP) compliance through source data verification, facility checks, drug supply management, and site file reviews. Our team ensures sites maintain high-quality data collection and adhere to protocol standards.
✅ Study Close-Out & Audit Preparation
From final site visits to archiving, we help ensure a smooth study close-out. Having prepared for audits, we know how to keep your study inspection-ready.
Strong Site Relationships & Patient Safety
We believe in fostering strong, collaborative relationships with site staff to ensure efficient study progress and recruitment. Most importantly, we prioritise patient safety throughout the study duration.
Contact us today and have a chat with one of our friendly team.
