Medical Device Translations: Using Translation Memory for MDR and IVDR Compliance
Achieving accurate and consistent translations has always been essential in the global medical device industry. However, it is now even more crucial in light of the Medical Devices Regulation (EU) 2017/745 (MDR) and In Vitro Diagnostic Medical Devices Regulation (EU) 2017/746 (IVDR). To ensure translation consistency while meeting the requirements of MDR and IVDR, translation …
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