Building Translation Workflows for Medical Device Documentation: A Developer's Guide to MDR Compliance

Working on medical device software or documentation management systems? You'll inevitably face the challenge of managing multilingual content that meets strict regulatory requirements. The EU's Medical Device Regulation (MDR) doesn't just require translations—it demands terminological precision that can make or break a product's market approval.

After working with several MedTech companies on their documentation pipelines, I've learned that the technical challenges go far beyond just calling a translation API.…