Device traceability and patient adherence
A traceability and adherence platform for a medical device maker, covering device tracking, inventory control, role-based access, and scheduled and instant notifications.
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Medical Devices & Diagnostics
Software and engineering for device makers
Traceability platforms, factory-floor vision and design support, built to the access, audit and documentation discipline the sector expects.
About Medical Devices & Diagnostics
Device and diagnostics makers are judged on the record their systems leave behind. Who scanned, who signed, who was notified, and whether any of it can be reconstructed later for someone who was not in the room. That record has to hold on the production floor and in the field at the same time.
Peak builds the software that carries it. Traceability and adherence platforms, factory-floor vision systems and the operations dashboards over them, with device CAD and detailing running alongside through the drawing office.
What we deliver
Digital Product Engineering
Product Development & SaaS
Product strategy and advisory, SaaS platform engineering, modernisation of what you already run, and the lifecycle support to keep it current after launch.
Digital Product Engineering
AI & Data Solutions
Data infrastructure, analytics and insight, machine learning and applied AI, built as part of a working platform rather than a standalone experiment.
Digital Product Engineering
Enterprise Software & Applications
Architecture, legacy revamp, workflow automation, systems integration, mobile enterprise tools and customer experience platforms, built and maintained end to end.
Core Plant Engineering
2D & 3D CAD Design and Detailing
3D modelling, 2D detail drawings, and paper-sketch-to-CAD conversion, delivered as revision-controlled packages a fabricator can work from directly.
How we work
Device and diagnostics work runs under the same review discipline as the rest of the practice. Role-based access from the first release, audit trails on the records that matter, and documentation written for the reviewer who comes after us. Regulatory language in a build is scoped to what the system actually does.
Builds start with the workflow rather than the feature list, who scans, who signs, who is notified, and what an auditor will want to see six months later. Most platform builds run as phased fixed price, and device CAD and detailing runs separately through the drawing office, with the documentation package matched to your quality system.
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