20/10/2026
The EU expanded the scope for electronic instructions for use for medical devices intended for professional users in 2025. That brings a practical translation question into view: which version will someone find when they need it?
A translated instruction may be linked from a product page, a QR code or a distributor portal. When the source changes, each route needs to lead to the appropriate language version for the device concerned.
It helps to plan language selection, revision identifiers and access to earlier instructions alongside the translation workflow. Those decisions are much harder to untangle after several versions have been published.
For teams working with electronic instructions, where does version control become most complicated?