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When you’re dealing with the translation of IFUs, regulatory documentation, or digital interfaces, the quality of the outcome hinges on one thing: the quality of your brief. Yet, many organisations, particularly those entering the world of medical translation, overlook the importance of a comprehensive brief. A strong brief does more than just keep your project […]
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Comprendiendo el papel crucial de la conformidad MDR en las traducciones de IFU El Reglamento Europeo de Dispositivos Médicos (MDR) sigue transformando la manera en que los fabricantes abordan la conformidad, y un aspecto que a menudo recibe poca atención es la traducción de las Instrucciones de Uso (IFU). Las traducciones precisas y conformes al […]
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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 […]
