Connected Health
Remote patient monitoring, medication adherence and care-home telemetry - for OEMs, integrators and healthcare operators.
IoT-WorkS builds connected-health devices and telemetry for OEMs, integrators and care operators: remote patient monitoring, medication adherence and room-level care-home sensing. Hardware, firmware, cloud and integration come from one engineering team rather than three suppliers.
Where we deploy
3 typical use casesRemote patient monitoring
Cellular + BLE bridges that move vital-signs data from home devices to clinician dashboards without asking patients to manage WiFi.
Care-home environmental + occupancy
Room-level temperature, humidity and movement telemetry in residential care settings - early warning for falls, infections and cold-room events.
Connected-device development
Full hardware + firmware + cloud build for OEMs commercialising new connected medical devices, including MHRA / CE submission support.
What does remote patient monitoring involve building?
Four layers, and most projects underestimate at least one. There is the device itself, its firmware and power budget, the connectivity path from a home with unpredictable networking, and the cloud side that has to receive, store and surface readings reliably. We build all four, which avoids the common failure where hardware, app and backend come from different suppliers and integration becomes the customer problem.
- Device hardware and enclosure designed for home rather than clinical use
- Firmware with realistic power budgets and over-the-air update support
- Connectivity that tolerates poor home broadband or uses cellular directly
- Cloud ingestion, storage and clinician-facing surfacing of readings
How does care-home telemetry support residents?
By making conditions visible without intruding. Room-level temperature, humidity and movement sensing gives early warning of the situations that escalate quietly - a room that has become dangerously cold, an unusual absence of movement, a resident whose night-time pattern has changed. It is environmental and presence data, not cameras, which is what makes it acceptable to residents and families.
What regulatory support do OEMs get?
Where a device is a medical device, we build the technical evidence a submission requires alongside the product: design documentation, traceability, verification results and the manufacturing detail an assessment asks for. Where a product is a wellness or environmental device, we say so plainly rather than encouraging a regulatory route it does not need. Getting that classification right early is what keeps a project from stalling.
MHRA Good Distribution Practice guidance (gov.uk)How is health-related data protected?
Most of what we collect is environmental and device telemetry rather than clinical records, which limits exposure by design. Where a deployment does handle patient-identifiable data, handling is aligned to the Data Security and Protection Toolkit standards the operator already reports against, hosting is UK-based by default, and data flows are documented for information-governance review before deployment rather than after.
NHS Data Security and Protection ToolkitEvery vertical runs on the same engines: AI Telemetry for sensor data, Engineering services for hardware + firmware + integration, the same platform for dashboards, alerts and compliance exports. The vertical changes the asset class and the regulatory frame; the stack underneath doesn't.
Frequently asked questions
- Do you build the device as well as the platform?
- Yes. Hardware, firmware, cloud and integration come from one team, which removes the integration gap that appears when device, app and backend are sourced from three separate suppliers.
- Is care-home monitoring camera based?
- No. It uses room-level temperature, humidity and movement sensing, so it gives early warning of cold rooms or changed night-time patterns without the intrusion that cameras bring.
- Can you support a medical device submission?
- We build the technical evidence a submission requires alongside the product, including design documentation, traceability and verification results, and we advise plainly when a product does not need a medical-device route.
- Where is the data hosted?
- UK hosting is the default, and data flows are documented for information-governance review before deployment rather than retrospectively.
- What if a patient has poor home broadband?
- The connectivity path is designed for it. Devices can use cellular directly or buffer and forward when a link returns, so readings are not lost when home networking is unreliable.
Tell us about your connected health project.
A local engineer will reply within one working day with a recommended sensor mix, gateway architecture and a rough deployment timeline.