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Medical device directives revision: variations in national laws

This article was originally published in Clinica

Executive Summary

How successful have the EU member states been in implementing the revision of the medical device directives into national law? And has this been done in harmonised way? Alexandre Regniault, partner at the Paris office of law firm Simmons & Simmons, and colleagues* report on variations that have resulted from deviations from the original directives and their impact

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