video1.0<iframe src="https://www.loom.com/embed/c87146ae3ace4713ad522a390bac2445" frameborder="0" width="1878" height="1408" webkitallowfullscreen mozallowfullscreen allowfullscreen></iframe>14081878Loomhttps://www.loom.com14081878https://cdn.loom.com/sessions/thumbnails/c87146ae3ace4713ad522a390bac2445-ce9568e176a7d026.gif523.286In this video, I walk you through the Compliance Intelligence MD-SAP framework, which helps manage regulatory requirements across multiple countries efficiently. MD-SAP stands for the Medical Device Single Audit Program, allowing a single audit to satisfy the quality management system requirements of various regulatory authorities, including the FDA, Health Canada, and others. I emphasize the importance of understanding applicability, as not all country-specific requirements will apply to your organization. If you do not operate in a country, you can opt out of those requirements to streamline your compliance efforts. I encourage you to assess your market presence and regulatory approvals to determine which requirements you can exclude.