eBook: EU MDR and IVDR Language Guidance

Have questions about the language requirements in the European Union’s Medical Device Regulation (MDR) and In Vitro Diagnostic medical Device Regulation (IVDR)? These regulations mark notably more stringent requirements and a full life cycle emphasis that impacts how medical device manufacturers approach life sciences translation services and life sciences localization. Read our eBook to understand how to plan your regulatory translations and medical device translation projects, to meet every EU MDR and IVDR deadline and requirement.

Whether you’re a manufacturer or other economic operator, you’ll benefit from this comprehensive industry guidance on regulatory translations. You’ll get a systematic review of all Articles of the MDR and IVDR with focus on language and language outcomes. We also offer guidance on how you can benefit from AI and Large Language Models under a life cycle language strategy.