Optimizing and localizing IFUs for MDR and IVDR compliance
Facing a growing need to shorten in-country review cycles and update and translate large volumes of instructions for use (IFUs) to ensure compliance with the EU Medical Device Regulation (MDR) and faster time to market, this client needed a new way of working.
Learn how RWS improved and harmonized the client’s IFU translation and publishing workflows to deliver consistent quality, faster time to market and lower localization costs for 20+ languages. The results include:
- 50% shorter in-country review cycle
- 15% translation savings through translation memory centralization
- Improved MDR compliance and audit readiness