Working narrowly is what lets us move quickly.
Every device category carries its own engineering constraints, evidence expectations and regulatory scrutiny.
These are the categories where our engineering, clinical and regulatory experience compounds, and where we can shorten the distance between a concept and a cleared product.
Device categories
Three categories, three evidence regimes.
Diagnostic devices
Devices whose output is an input to a clinical decision. Signal quality, reference-standard agreement and behaviour under degraded conditions carry the burden of proof.
Diagnostic devicesTherapeutic devices
Active devices that act on a patient. Energy delivery, dosing accuracy, fault detection and safe failure states sit at the centre of the design.
Therapeutic devicesDrug delivery
Delivery devices and combination products, where the device determines whether the dose arrives as intended.
Drug deliveryClinical domains
Clinical domains we work in.
Alongside the device categories, three clinical areas where our team has built devices, run studies and carried submissions.
Cardiology
Device development and clinical evidence strategy for cardiovascular monitoring, diagnostics and connected cardiac technologies.
Device families
Ambulatory ECG patches, resting ECG systems, connected cardiac monitors.
Neurology
Development and clinical research support for neurological monitoring, assessment and data-driven care.
Device families
EEG acquisition hardware, nerve conduction systems, movement quantification wearables.
Hypertension
Device engineering, validation and clinical research for blood pressure monitoring and hypertension management technologies.
Device families
Oscillometric monitors, cuffless wearables, home telemonitoring hubs.
Placeholder figure, to be replaced with verified data before launch.
Next step
Working in one of these areas?
Tell us the device category and the clinical setting. We will tell you what the programme looks like from here.