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...
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...
Manufacturing and Engineering Translation Start a Dialogue Manufacturing and Engineering Expertise Manufacturing and engineering translations play a crucial role in bridging the language gap in the globalized world of industry and technology. As companies expand their...
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...
