Argos Multilingual
3 min. read
Get Ready for What’s Next: The IVDR Challenge
New EU medical device regulations are approaching fast – what role will translation and localization play in making them viable? Manufacturers of medical devices for the EU market will soon have more requirements to comply with as part of the European Medical Device Regulation (MDR) for general medical devices and the In-Vitro Diagnostics Regulation (IVDR) […]
