This episode provides a detailed overview of Mexico's mandatory Good Manufacturing Practices (GMP) standard, NOM-241-SSA1-2021. The host breaks down the key requirements for medical device manufacturers, including the implementation of a Quality Management System, risk management protocols, and alignment with ISO 13485. We discuss the standard's scope, its effective date, and the practical implications for companies seeking to enter or remain compliant in the Mexican market. Key Questions - What is NOM-241-SSA1-2021 and why is it critical for the Mexican market? - How does this standard impact the entire lifecycle of a medical device? - What are the core requirements of a compliant Quality Management System under NOM-241? - How does NOM-241 align with the international ISO 13485 standard? - Are you prepared for a GMP inspection by Mexican authorities? - What documentation is essential for demonstrating compliance? - When did this mandatory standard become fully effective? - Does this regulation affect foreign manufacturers importing into Mexico? 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 help you develop efficient regulatory strategies, compile technical dossiers, and act as your local representative in over 30 markets, including Mexico. Our technology-driven approach ensures you navigate complex standards like NOM-241 with confidence. For assistance with your market access needs, visit us at https://pureglobal.com, contact [email protected], or explore our FREE AI tools and database at https://pureglobal.ai.