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FRANCE UP CLOSE: Can you sell your CE-marked device in French overseas territories?

This article was originally published in Clinica

Executive Summary

You have CE marked your medical device or in vitro diagnostic product, and produced the labelling in French. But are these steps then sufficient to allow you to market your products throughout the French territories that lie outside France and indeed outside Europe? In the first instalment of Clinica’s new series focused on issues specific to Europe’s second largest medtech market, Alexandre Regniault* and Damien Bertier* explain the legalities of selling your product in French overseas territories and aim to provide some practical answers

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