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Medical Device

Risk standard could go too far

This article was originally published in Clinica

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Executive Summary

The European medical devices industry is concerned that an international draft standard under preparation for risk management of medical devices could be too broad in its application.

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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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