LanguageWire Hosts Medtech Roundtable on Scaling Marketing in the Age of MDR
At by-invite-only Medtech Executive Roundtable, biggest names in medical device manufacturing traded ideas on the transition from MDD into MDR.
SlatorCon Zurich is now SOLD OUT — See you on October 4th!
EU MDR
Medtech Localization Buyers on Tech, Regulations, and Translation Demand
Highlights from SlatorCon Remote’s Medtech Panel, featuring localization buyers from Medtronic and Varian discussing MT, regulation driving translation demand, and more.
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.
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.
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 adds to uncertainty.
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