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...
Medical device translations are a critical aspect of the healthcare industry. They ensure that important information related to the use, maintenance, and safety of medical devices is available to users in different languages. However, medical device translations are...
The medical device industry is highly regulated and demands precise and accurate translations to ensure patient safety and compliance with regulatory requirements. To reach a wider audience, medical device companies with global operations must translate their...
Clinical trials are the backbone of medical advancement, paving the way for groundbreaking treatments and therapies to reach patients worldwide. However, the success of these trials hinges on effective communication across multiple languages and cultures. Ensuring...
As 2024 draws to a close, it’s time to reflect on a transformative year for the translation and transcreation industry. Globalization continues to drive demand for multilingual communication, while advances in technology and shifting consumer expectations have...
