Mexico
In general terms, tariff codes are a series of numbers to identify products for international trade purposes. These codes are standardized worldwide by the Harmonized
In our Classification and Grouping Ultimate Guide, we have explained how to classify and group medical devices according to the 23 rules detailed in the
Introduction As we have detailed in our previous article, Apostille and Legalization are common procedures to authenticate legal documents in the Medical Device Industry.
In Mexico, activities related with medical devices such as advertising, manufacturing, importation, exportation, storage, disposal and others are strictly regulated by COFEPRIS. In this article,
Last April the 4th 2025, the Ministry of Health in Mexico released the official update of the Good Manufacturing Practice (GMP) Norm for Medical Devices
Introduction The Mexican Pharmacopoeia (FEUM) is an independent organization dedicated to advice the Mexican Ministry of Health. It is also in charge to elaborate
