This episode dives into the FDA's monumental shift from the Quality System Regulation (21 CFR Part 820) to the new Quality Management System Regulation (QMSR). We break down the incorporation of ISO 13485:2016, the critical effective date of February 2, 2026, and the specific additions and changes manufacturers must be aware of. We cover the new terminology, the integration of other FDA regulations, and the significant impact on inspections and risk management. Key Questions: • What is the new Quality Management System Regulation (QMSR)? • When does the new QMSR become mandatory? • How does the new rule incorporate ISO 13485:2016? • Are the Device Master Record (DMR) and Design History File (DHF) still required? • What key FDA regulations are now explicitly linked to the quality system? • Why are the new rules for labeling and packaging controls so important? • Are management review and internal audit records now subject to FDA inspection? • How does this change impact manufacturers who are not yet ISO 13485 certified? Ready to turn these insights into your competitive edge? Pure Global’s regulatory experts guide MedTech companies through every step of 30+ markets worldwide. Explore how we can accelerate your market entry at https://pureglobal.com or email [email protected] for tailored support.