MDR-compliant IFU translations: five common pitfalls to avoid in 2025
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Understanding the critical role of MDR compliance in IFU translations The European Medical Device Regulation (MDR) is continuously transforming how medical device manufacturers approach compliance, and one area that often doesn’t get enough attention is the translation of Instructions for Use (IFUs). Accurate, MDR-compliant translations are more than just a regulatory requirement, they are essential […]