At by-invite-only Medtech Executive Roundtable, biggest names in medical device manufacturing traded ideas on the transition from MDD into MDR.
Highlights from SlatorCon Remote’s Medtech Panel, featuring localization buyers from Medtronic and Varian discussing MT, regulation driving translation demand, and more.
LSPs and translators hopeful of a demand boost from EU Medical Devices Regulation (EU MDR) must wait a little longer as coronavirus delays application.
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.
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 adds to uncertainty.
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