Scrip is part of Informa PLC

This site is operated by a business or businesses owned by Informa PLC and all copyright resides with them. Informa PLC’s registered office is 5 Howick Place, London SW1P 1WG. Registered in England and Wales. Number 8860726.

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

Printed By


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






Ask The Analyst

Please Note: Click here for more information on the Ask the Analyst service.

Your question has been successfully sent to the email address below and we will get back as soon as possible. my@email.address.

All fields are required.

Please make sure all fields are completed.

Please make sure you have filled out all fields

Please make sure you have filled out all fields

Please enter a valid e-mail address

Please enter a valid Phone Number

Ask your question to our analysts