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.
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.
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.
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.
Will the latest China Food and Drug Administration medical device requirements and clinical trial exemptions impact dossier translation volumes? Two experts weigh in
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 device market in the world's most populous nation.
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