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Medical Device

Draft US bill on foreign inspections circulated

This article was originally published in Clinica

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Executive Summary

A draft bill laying out requirements for country-of-origin labelling of medical devices and inspections of medical device plants is being circulated among Democratic members of the US House of Representatives.

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This copy is for your personal, non-commercial use. For high-quality copies or electronic reprints for distribution to colleagues or customers, please call +44 (0) 20 3377 3183

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