Expert resources on translation and localization for the medical and pharmaceutical industries.
Clinical Documentation Translation Workflow
On 26 May 2021, EU Medical Device Regulation (MDR) replaced the EU’s current Medical Device Directives and while the medical devices manufacturers have largely ensured compliance with the new regulation, this change will have an impact on development of documentation related to the medical devices, translation and regulatory cycles in the EU.
In literally every survey that we have ever conducted among our clients from the pharmaceutical and medical devices industries, accurate terminology has always been singled out as the primary concern in translation for these sectors. In this article, we will take a closer look at the reasons for this and how the translation technologies can help us address this issue and ensure accuracy of terminology.
We are happy to announce that Ciklopea, in its capacity as one of the leading providers of advanced language solutions for the life sciences sector, will exhibit at the forthcoming DIA Europe 2021 (virtual) event.
Ciklopea
