Clinical Trials
Blood Pressure Data Services
Explore Our Services
Tailored for Your Clinical Trial
Built Around Your Protocol.
Every trial is different. That’s why we work closely with your clinical study team to tailor the system to your protocol's needs, from device setup to data and reports. Your study will get to know your dedicated dabl team over the course of the trial.
• Personalised study configuration
• Protocol-specific measurement schedules
• Device provision and training support
Transparent Logistics System
Validated Device Provision & Supply
dabl provides a full supply chain service, delivering regionally approved Home, Office, and ABPM devices with complete transparency throughout the shipping process.
All devices are calibrated prior to deployment, with certificates issued as part of the handover process. Recalibration is available at any point during the study lifecycle, ensuring every measurement is taken on a device that is validated, traceable, and fit for purpose.
Submission Ready Data
Complete Data That Drives Decisions
dabl’s data layer sits between the device and the EDC, transforming raw blood pressure readings into complete, structured, validated datasets.
Device data is normalised, quality-checked, and ensues full traceability from source to export. Your study’s BP data is readily exportable in CSV+ to your EDC, formatted to your specific requirements.
Compliant and Fully Auditable
Ready for Regulatory Scrutiny
The dabl system de-risks complex blood pressure data with consistent, compliant delivery from study setup through export. We maintain automated, time-stamped, audit trails with secure, role-based access controls.
Our platform is developed and operated in alignment with EU Annex 11 and FDA 21 CFR Part 11 requirements, ensuring electronic records and signatures meet the highest standards for data integrity, security, and traceability in regulated clinical environments. This provides sponsors and CROs with confidence that all data handling processes are inspection-ready and globally compliant.
Global Support from your Dedicated Study Team
Support When You Need It.
Clinical trials don’t stop and neither do we. Our dedicated support team is available to ensure everything runs smoothly. In our experience, this maximises User Experience, minimises downtime & resolves queries fast.
• Technical and operational assistance
• Proactive monitoring and troubleshooting
• Comprehensive user guides and training
• Bespoke user training for your protocol
