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. Continue reading
Xplanation
Navigating Europe’s regulatory landscape is no easy task for manufacturers looking to market their products across the continent’s multilingual single market. Translations are linked to product liability and lacking a language strategy can result in spiralling costs. Continue reading
This information will never be shared with third parties. No Spam.