End-to-End Enablement for Digital Health Technologies in Clinical Trials
Partner with qointa for Confidence in Compliance
With Device360™, you’re not just buying a service — you’re gaining a global compliance partner. We help you reduce risk, accelerate timelines, and protect the integrity of your trial data.
Device360: Your End-to-End Compliance Solution for Digital Health Technologies
Device360™ is qointa’s modular platform purpose-built to support the selection, validation, integration, training, and oversight of Digital Health Technologies in regulated clinical trials.
Whether you’re using connected devices for decentralized trials or implementing SaMD tools for primary endpoints, Device360™ ensures regulatory-grade readiness from Day 1.
What Device360 Enables
Rapid DHT classification and regulatory documentation
Fit-for-purpose validation and usability assessments
Real-time compliance dashboards and audit preparedness
Device traceability across geographies
The Risk of Doing Nothing
Using unvalidated, misclassified, or poorly documented devices can lead to:
Invalidated endpoints
Ethics board or customs delays
Patient safety risks
Regulatory inspection failures
With Device360, You Get
Faster trial startup
Reduced regulatory burden
Global inspection readiness
Confidence in every device deployed
Device360 transforms DHT risk into regulated readiness.
Click on each product for more info: