This episode demystifies the Medical Device Single Audit Program (MDSAP), a framework allowing a single audit to satisfy the regulatory requirements of five different countries. We explore its history, the participating authorities, the benefits for manufacturers—including reduced audit fatigue and faster market access—and how the program streamlines global compliance. • What is the Medical Device Single Audit Program (MDSAP)? • Which five major global markets can you access with a single audit? • How does MDSAP reduce audit fatigue and save resources for manufacturers? • What makes MDSAP a mandatory requirement for selling medical devices in Canada? • How can one audit report substitute for a routine FDA inspection? • What is the role of an Auditing Organization (AO) in the MDSAP process? • Which international body initiated the MDSAP program in 2012? 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.