Translation services play a crucial role in helping mid-size manufacturers comply with international regulations and standards. They break down language barriers, facilitate effective communication, ensure product safety, navigate cultural nuances, and streamline global operations, enabling manufacturers to expand their reach and navigate the complexities of international business.
In this article we explore emerging trends and technologies in the e-learning industry, with a focus on the evolution of translation and localization.
The Americans with Disabilities Act (ADA) and European Accessibility Act (EAA) in the European Union have been enacted to ensure equal access to digital content, including e-learning and translation platforms. This article explores the potential ramifications of these acts on both industries.
It’s crucial to ensure that our e-learning platforms are inclusive and accessible to all, regardless of language, location, or disability. This is where the strategic roles of translation, localization, and adherence to accessibility guidelines come into play.
In Vitro Diagnostic Regulation in the EU will have a profound impact on the translation industry. This article summarizes those changes and the importance of picking a translation provider with experience and expertise in this area.
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.
The Global Harmonization Task Force. What is it, and how does it affect translation companies working on medical device translations? This article explores the GHTF’s initiatives and why translation companies need to be aware of them.
The EU MDR has several implications for the medical device translation industry. This article covers key points, the recent updates, and how they affect U.S. based translation companies.