The full answer
Device software has two halves: the regulated firmware or embedded component, which your device team or manufacturer usually owns, and the connected software around it, which is what we build. That includes apps that pair over Bluetooth, services that ingest readings, dashboards for clinicians and carers, and integrations with EHR systems through standards such as HL7 FHIR.
Where your product falls under medical device regulation, we work to the rigour those frameworks expect from software: documented requirements, risk analysis, traceability from requirement to test, version control, controlled releases and defect records. We produce the technical documentation your regulatory team needs for its submission, and we are clear that certification and classification remain your responsibility with your notified body or regulator.
Wearable health apps follow the same discipline with consumer expectations on top: quick pairing, battery-aware syncing, offline capture, clear charts, and integrations with Apple Health and Google Health Connect. Our Binimise smart city platform shows how we ingest and monitor data from thousands of connected devices and turn it into alerts operators act on.
AI is applied to signal processing and triage: detecting patterns in readings, prioritising alerts for clinicians and summarising trends for patients, always evaluated with test sets and with a clinician responsible for decisions. Hosting is placed in your required region, with encryption, role-based access and penetration testing before launch. Discovery maps your device class, data flows and regulatory pathway before we scope.