Where We Fit
dabl in Clinical Trials
We provide compliant, extended services for the collection, automated validation and completeness of blood pressure data in clinical trials
Patients measuring at home, at clinics, across time zones
Strict guidelines from bodies like ESH and FDA that shape how data must be collected and reported
Protocol-defined windows that are easy to miss and hard to adjudicate
Artefacts are common; distinguishing noise from signal requires domain expertise
Multiple readings per visit, multiple visits per patient, across hundreds of sites and studies
BP data can generate a disproportionate volume of data queries
Device calibration, training gaps, and site variability all introduce risk
A well-documented bias that can distort your primary endpoint
… but at dabl – It’s What We Do
Protocol Based Customisation
Standardisation Throughout Decentralised Trials
We work closely with your study team to configure the dabl system to your unique protocol requirements. We advise on blood pressure measurement schedules, validation rules and device provision during clinical trials protocol design.
In decentralised and multiregional trials, dabl’s system upholds compliance according to local regulations while maintaining a unified, consistent dataset.
De-Risking your Clinical Trial
Less Data Queries and Faster Data Locks
dabl automates blood pressure data capture across multiregional and decentralised trials – automatically validating measurements upon capture, and flagging errors, outliers, and data completeness across locations.
dabl ensures the completeness and validity of BP data before it enters your EDC, reducing data queries and monitoring burdens.
Specialists in the Management & Measurement of BP Data
Built for Trial Success
Our team knows that clinical trials’ success lies in patient retention, protocol design, fast site activation and compliance. Our technology coupled with our team’s high-quality communication and support, enable the foundation for success in your trial.
See Our StoryAdvantages of dabl in Clinical Trials
High Data Completeness by Design
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Automated data capture and real-time validation reduce errors and support local regulations and protocol design, ensuring data is accurate before EDC submission.
Audit-Ready From Day One
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Every action, change, and data point is automatically logged with a full audit trail — recording the who, what, when, and why — keeping your study inspection-ready throughout.
Standardised Across Sites & Sponsors
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Centralised blood pressure data collection across multiple sites, regions, and sponsors — using validated Home, Office, and ABPM devices — ensures consistency at every level of your trial.
Faster Database Locks
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Real-time validation means errors are caught at the point of capture, not at data review. Fewer queries, reduced site burden, and cleaner data mean your database lock happens on time.
Protocol-Tailored Configuration
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Timing windows, blinding rules, role-based permissions, and EDC export formats are all configured to your exact protocol — with dabl's team supporting setup from study start-up.
Blood Pressure Specialists
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With over 25 years of experience in clinical and cardiovascular trials, dabl brings specialist knowledge that generic eClinical platforms cannot replicate — purpose-built for blood pressure endpoints.
