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Medical Device Registration in Mexico

This article was originally published in RAJ Devices

Executive Summary

Evangeline Loh describes the regulatory process for marketing medical devices in Mexico and highlights some new rules affecting importers.

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The Chinese State Food and Drug Administration (SFDA) has revised its rules on the advertising of medical devices. Here, Evangeline Loh, vice-president of regulatory affairs at the international consultancy, Emergo Group, tells Clinica readers how to apply for permission to advertise a product, what to include in the applications and the timelines for expecting an approval.

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