What is the MDR? In basic terms, the MDR defines what regulations must be followed to sell a medical device in the European Union. Many of the regulations focus on quality assurance and medical device translation requirements. You can find the complete text on the EU website: “Regulation (EU) 2017/745 of the European Parliament and…
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In a globalized world, website translation is becoming an increasingly important part of business strategy. Our latest ebook will show you exactly why.
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