This episode provides a detailed overview of Mexico's medical device regulations, focusing on the Reglamento de Insumos para la Salud. We explore the role of the regulatory authority, COFEPRIS, the risk-based device classification system, and the available registration pathways, including the Standard and Equivalency routes. The host also covers the crucial updates from the 5th edition of the Mexican Pharmacopoeia's supplement, which became effective in July 2023. - What is the primary regulation for medical devices in Mexico? - How does COFEPRIS classify medical devices based on risk? - What is the difference between the Standard and Equivalency registration routes? - Which foreign approvals can be used to expedite registration in Mexico? - What key changes were introduced in the July 2023 regulatory update? - What are the documentation and language requirements for a submission? - Why is a Mexico Registration Holder (MRH) necessary for foreign manufacturers? - What is the role of the NOM-241 standard in Mexico's QMS requirements? Pure Global offers end-to-end regulatory consulting solutions for MedTech and IVD companies, combining local expertise with advanced AI to streamline global market access. We act as your local representative in over 30 markets, including Mexico, developing efficient regulatory strategies and using AI to compile and submit technical dossiers. Our services ensure your products meet all local standards for a faster path to market. Contact us at [email protected], visit our website at https://pureglobal.com, or explore our free AI tools and database at https://pureglobal.ai to learn how we can accelerate your global expansion.