Mid-size manufacturing companies face challenges in complying with international regulations and standards. As these companies expand their operations and reach new markets, the need for accurate and reliable translation services becomes increasingly vital. This...
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...
In the global e-commerce landscape, translating product descriptions is critical for communicating effectively with customers in their native language is a game-changer. One of the most critical aspects of this communication is the translation of product descriptions....
What exactly is the EU MDR? The European Union’s Medical Device Regulation (EU MDR) was a significant update to the regulatory framework for medical devices in the EU, replacing the Medical Devices Directive (MDD) and the Active Implantable Medical Devices...
