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Author: Peter Argondizzo

Medical Device Translation Requirements

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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How to Write Localized Content

Developing a marketing plan to stand out from the competition can be challenging in the crowded online business landscape. When it comes to international growth, whether you’re just starting out as a brand new company or have an established brand identity, customers need to connect with your content during all stages of their content journey….

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