EU Delays New Medical Device Translation Requirements
LSPs and translators hopeful of a demand boost from EU Medical Devices Regulation (EU MDR) must wait a little longer as coronavirus delays application. Continue reading
Tag: EU MDR
Deadline 2020: What LSPs Need to Know About the EU’s New Medical Device Regulation
Europe’s new medical device regulation requires that labeling, packaging, and other content be translated into the official language of each EU country where the device will be sold. Continue reading
Medical Device Manufacturers Brace for Regulatory Overhaul, Brexit Fallout
The EU is expected to enact a sweeping overhaul of its regulatory framework for medical devices in early 2017, which includes changes to requirements for multilingual documentation. Brexit also... Continue reading
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