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: medical device
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
RWS Spends Big on 82.5m Acquisition of LUZ
One of the most attractive pure-play, life sciences players changes hands as RWS bolsters position in fast-growing vertical. Price tag in line with 2015 acquisition of CTi. 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
Impact of China’s New Medical Device Directives on Translation
Will the latest China Food and Drug Administration medical device requirements and clinical trial exemptions impact dossier translation volumes? Two experts weigh in Continue reading
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How US Medical Device Exporters Localize to Succeed in China
Two barriers to entry face US medical device companies that want in to China, and the Chinese government has begun to close loopholes; a look at opportunities and expert insights on the medical... Continue reading
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