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French Regulator Makes Medical Device Surveillance A Priority As Work Expands

This article was originally published in Clinica

Executive Summary

The French regulatory agency for healthcare products, ANSM, is reinforcing its market surveillance systems for medical devices with the future EU medical device regulation in mind. It also acknowledges the European Commission’s appeal for better cooperation between EU authorities in the area of market surveillance and says that it wishes to optimize the role it plays in this regard.

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