Healthcare & Clinical Diagnostics

Connected devices, measurement systems, and compliant software built for dependable clinical and healthcare use.

We build connected medical and diagnostic hardware, and the secure software behind it, for clinical and laboratory settings where reliability and traceability are non-negotiable. Our work spans measurement instruments, embedded devices and data platforms with LIMS-grade APIs and encrypted exchange, including a hospital blood-sample system that ingests analyser results, decrypts on receipt and re-encrypts for storage with full patient-to-operator traceability. We develop with regulatory pathways such as ISO 13485 and IEC 62304 in mind, so what we prototype can be carried through to a compliant product.

Core Capabilities

Connected devices, measurement systems and compliant software for dependable clinical and healthcare use.

How it works

Discovery & feasibility

We scope the clinical need, the users and the intended use, and map the regulatory pathway early. Feasibility studies de-risk the hard engineering and compliance questions before significant budget is committed.

Design & prototype

Electronics, sensing, firmware and secure data software are designed in parallel and proven on real hardware early, so performance and reliability are validated against your requirements rather than assumed.

Verification & compliance

We verify the design against its specification and the relevant standards — from EMC and electrical safety to medical pathways such as ISO 13485 and IEC 62304 — with documentation that supports a route to a compliant product.

Production & deployment

A supported handover into manufacture, qualifying suppliers and staying involved through first builds, so the device reaches clinical or laboratory use reliably and at the right cost.

For Clinical & Lab Teams

Connected medical and diagnostic hardware, and the secure software behind it, for settings where reliability and traceability are non-negotiable.

For MedTech & Procurement

A single specialist team that designs, verifies and productionises the device — with regulatory pathways considered from the start.