Your medical device is built, validated, and preparing for deployment in France. This pack performs a final compliance and usability audit across your technical documentation and user interface. The resulting report provides your development team with terminology realignment/corrections and targeted, implementation ready recommendations.

Audit of your device documentation and UI for complete accurate French translation:

• Labeling

• IFU

• Safety warnings

• Packaging

• Software UI (menus, alerts, error messages)

• On device text (if any)

• Training manuals (250 pages)

• Training videos (2 hrs)

Audit of your documentation and UI for GDPR aligned data handling.