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Webinar: Safe, Smart, Seamless: Navigating HMI Hurdles in Lab Equipment

This webinar is part of a two-part series that explores how medical Human–Machine Interfaces (HMIs) are designed in regulated healthcare, whether on lab equipment or IT systems. It examines technical and operational pressures like regulatory requirements, workflow issues, hardware limits, integration needs, and long device lifecycles, showing how these influence medical software development.

In this first webinar, Qt Group's experts discussed how manufacturers reduced training time from days to hours, achieved maximal code reuse across hardware platforms, and generated FDA-ready traceability documentation as a byproduct of development. There was also a live walkthrough of our OxyScan demo showcasing guided workflows, multi-user access, reporting, and multilingual support.