Our services
Across our full range of services, we optimise patient recruitment, lower screen failure rates and ensure successful follow up. Our services deliver success across all clinical trial stages.
Follow Us
Across our full range of services, we optimise patient recruitment, lower screen failure rates and ensure successful follow up. Our services deliver success across all clinical trial stages.
Rapid data insights to verify trial protocol feasibility
Rapid & customised feasibility assessments
Refine your protocol
Access to 20 million patient records
Comprehensive support and guidance
Integrating PPIE ensures studies are patient-centric, accessible and effective
Increase success by reducing dropout rates
Identify barriers to recruitment
Incorporating patient and HCP perspectives
Increase engagement and compliance
Meet regulatory requirements more efficiently
Optimise protocol development and unlock the full potential of EHR-enabled trials
Comprehensive trial planning
Medical Advisory Group consultancy
Refine trial design & maximise value
Decentralised study designs
Expert regulatory and compliance support
Highly experienced clinical trial delivery methods
Gold standard safety reporting
Operational excellence – smooth trial execution
Unparalleled network access
Specialist compliance support
Unmatched real-time data management, providing actionable insights
Secure data capture
Continuous quality verification
Actionable insights
Regulatory compliant datasets ready for submission
✓ Decentralised Clinical Trial (DCT)
✓ Real time remote safety monitoring
✓ Direct Data Capture (DDC)
✓ Electronic Data Capture (EDC)
✓ Individual Case Safety Report (ICSR)
✓ Trial Dataset Generation
✓ Real World Data & Evidence
✓ End to End Trial Support
✓ Protocol design
✓ Feasibility
✓ Patient identification & Recruitment
✓ Index Deprivation Tool
✓ Dataset Coverage – UK
✓ Proven Track Record
✓ Data Visualisations
