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Multilingual Medical Device Recommendations: Fundamentals For Translation

Selling medical devices globally requires complying with the requirements, including translations, set by regulatory bodies in each country or region.

In our new guide, “Multilingual Medical Device Recommendations: Fundamentals For Translation,” you will learn:

  • Regulatory and go-to-market requirements for translation
  • Translation tools that make the process more efficient
  • How to find the right language service provider for your medical device linguistic needs; such as, quality procedures and ISO certifications
  • How to prepare to work with your language service provider including, establishing process and needs up front and providing general and project specific information

Ensure your go-to-market plans meet all regulatory requirements including translation and discover how to best find and establish a relationship with a language service provider. Download our complementary guide using the form below to get started: