If you work on software or tooling for medical device manufacturers, you've probably run into IVDR (Regulation (EU) 2017/746) somewhere in a requirements doc. It's the regulation governing in vitro diagnostic devices in the EU, and it has a language requirement that's easy to underestimate until you're the one building the system that has to manage it: every Member State can require its own official language for labels, instructions for use (IFU), and technical documentation. The M21Global ar...