A TGA-regulated medical device portal

Clinics use it to manage their scanners, review results and run their own users. Behind it sits an API that handles device communication, scan processing, document generation and notifications, and under both sits infrastructure we own and operate. The same people built every layer, so nothing was handed across a boundary where the reasoning got lost.

Because the software is part of a regulated device, the evidence matters as much as the code. It is built to IEC 62304: documentation versioned with the code and true at every commit, tests that stand as evidence rather than reassurance, and a change history that will survive an audit years from now.

There are no screenshots here, and there will not be. Aptium can be named; what is on its screens cannot be shown.

This is software work. See how software works