Solutions

Connected point-of-care devices, from reader to result

Point-of-care analysers, readers and rapid tests have to deliver a trustworthy result in minutes, wherever they are used — a GP practice, a pharmacy, an ambulance. Extra Horizon provides the certified backend around your device: fleet management, secure updates, role-based access and diagnostic algorithms running in your own cloud cluster.

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Point-of-care analysers in a GP practice, a pharmacy and an ambulance sending results through a private Extra Horizon cluster to the physician, the patient and the quality team

At the point of care

The assay was the hard part. The rest shouldn't be.

Point-of-care devices deliver a result in minutes, wherever care happens. Making that result trustworthy, connected and compliant takes a backend most diagnostics teams would rather not build themselves.

A result has to leave the device

A result that stays on the instrument never reaches the physician, the patient or the surveillance report. Every test needs a secure, traceable path to the people who act on it.

Devices everywhere, managed nowhere

Analysers sit in practices, pharmacies and ambulances, run by staff who never bought them. Firmware, calibration and connectivity have to be managed remotely, across the whole fleet.

IVDR raises the bar

IVDR brings most in vitro diagnostics under notified body review. The software, cybersecurity and data handling around your assay now need evidence of their own.

Proven at the point of care

From rapid tests to the ambulance

ABCDx
In Vitro Diagnostics

LVOCheck identifies large vessel occlusion stroke directly in the ambulance, within 10 minutes. Extra Horizon powers the LVOCheck Digital Platform — the AI analysis and data management behind the device in the field.

Read the ABCDx case →
ams AG
In Vitro Diagnostics

A spectral sensor reads lateral flow tests in around 15 minutes, without lab infrastructure. Extra Horizon delivers each result securely to the patient's smartphone within seconds, on a backend built to handle up to millions of results concurrently.

Read the ams AG case →

Built for regulated diagnostics

Evidence for the software around your assay

Your notified body will review the connected part of your device as closely as the assay. Build it on a platform that arrives with the evidence already in place.

IVDR technical documentation

The software and cybersecurity section of your technical file covers infrastructure you don't control. A qualified supplier with inheritable evidence closes that gap.

Cybersecurity

IEC 81001-5-1 and MDCG cybersecurity guidance expect patchable devices, access control and vulnerability management — exactly what the platform services above are built around.

Health data protection

Test results are special-category data under GDPR. A dedicated deployment in the region you choose, with scoped access, keeps them where they belong.

All platform regulations & certifications →

Let's talk about your point-of-care device!

Get in touch, explain what you want to build, or have us help you build, and we'll get back to you ASAP! →