The worldwide medical device market is a multi-billion dollar industry and provides ample opportunities for companies with a global strategy. Translations.Health helps medical device manufactuers localize a variety of in-vitro diagnostics and other medical devices between English and Spanish, English and Chinese, English and German, and many other languages. We have the linguistic resources, subject matter expertise, and language technologies to deliver accurate medical device translation services with efficiency and scale. As healthcare infrastructure expands globally (especially in emerging markets), medical device demand will continue to increase in an ever growing number of new hospitals and surgical facilities around the world. Translations.Health provides quality translation and localization services in emerging languages such as Vietnamese, Thai, Burmese, Indonesian and many African languages to bridge the language gap while allowing medical device companies to stay compliant with local regulatory requirements.

Translations.Health has one of the largest teams of professional medical technology translators in over 100 languages. We help the medical device industry translate all major categories and types of devices, including diagnostic imaging systems, orthopedic devices, IVD (in-vitro devices), cardiovascular devices, minimally invasive surgical (MIS) devices, dental equipment, ophthalmic devices, and more. Our services range from documentation translation (user manuals, IFUs, compliance documents, patents), software localization (UI string translation, online help translation, localization testing), elearning localization, and video translation. We have streamlined the medical device localization workflow onto the cloud, allowing our clients to receive the most efficient translation solutions they need to stay ahead of the completion in global markets.

Quality multilingual communication is now a mandatory requirement for medical device manufacturers marketing products on international markets to ensure patient safety and regulatory compliance. The European Union’s Medical Device Regulation (MDR) that officially went into effect on May 26, 2020 is designed for this exact purpose. MDR along with the upcoming EU In Vitro Devices Regulation (EU IVDR) make it mandatory for medical device manufacturers to produce user documentation such as instruction manuals and device labels in the target EU country language the devices are marketed. The European Union has 24 official languages, making the translation effort a major undertaking in order to obtain the CE mark and achieve EU regulatory compliance. The good news translating your medical device documents with quality for the EU market doesn’t have to break the bank. You’ve spent time and money developing your medical devices and the last thing you want is to work with an average translation company to localize your technical content with mediocre quality and excessively high price. This is why you need Translations.Health. We deliver professional medical device translations in all European languages with the best ROI.