The In Vitro Diagnostic Regulation (IVDR) is a new set of regulations introduced by the European Union (EU) to ensure the safety and performance of in vitro diagnostic medical devices (IVDs). These devices, which include everything from pregnancy tests to blood...
For a life sciences company choosing a translation provider, does the size of the agency matter? Absolutely! There are several reasons why a life sciences company might prefer to work with a smaller, mid-size translation company like TrueLanguage over larger...
Navigating MDR & IVDR Compliance: Streamlining Localization with TrueLanguage For medical device manufacturers, it is crucial to understand and comply with the Medical Device Regulation (MDR) and In Vitro Diagnostic Regulation IVDR for your products. These...
In the era of digital globalization, e-commerce businesses are increasingly looking to expand their reach beyond domestic borders. However, to truly resonate with international customers, it’s not enough to simply translate your website into different languages....
The Global Harmonization Task Force (GHTF) does not directly affect translation companies since its primary focus is on regulatory harmonization and standardization of medical device regulations. However, the work and initiatives of the GHTF indirectly impact...
