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Europeans may begin to flex more legal muscle to back demands for labelling in their own languages

This article was originally published in Clinica

Executive Summary

European requirements for labelling medical devices are burdensome and expensive, but companies taking short-cuts could face even stiffer penalties. Speakers at the recent London ABHI/IBC conference on Understanding Medical Device Labelling and Packaging in Europe demonstrated how the sanctions for non-compliance could be much stricter than companies anticipate and could be enforced through a variety of channels.

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