In this episode of MedTech Global Insights, we dissect the audit criteria of the Medical Device Single Audit Program (MDSAP), focusing on the specific requirements detailed in the influential AU P0002.008 audit model. We explore how this single audit program, crucial for market access in the US, Canada, Australia, Brazil, and Japan, has evolved and what it demands from your Quality Management System. We move beyond theory to discuss the practical implications of recent updates. We cover the increased scrutiny on manufacturer-sponsor agreements for Australian market entry and the critical importance of a "closed-loop" system that integrates post-market feedback directly into your risk management files. This episode is essential for any MedTech professional involved in quality, regulatory affairs, and global strategy. **Key Takeaways:** * What are the seven core chapters that structure every MDSAP audit? * How did the AU P0002.008 update change the audit focus for devices entering Australia? * Why is simply collecting post-market feedback no longer enough to satisfy MDSAP auditors? * What specific evidence do you need to present to demonstrate a closed-loop risk management process? * How can a deficiency in your purchasing process lead to a major non-conformance in design and development? * What are the most common pitfalls companies face when preparing for their first MDSAP audit? * How does the MDSAP model integrate ISO 13485 with specific country requirements from the FDA, TGA, and other bodies? To learn more about navigating global regulatory challenges, contact us at [email protected] or visit https://pureglobal.com/.