Canada's medical device market is a significant opportunity, but navigating its regulatory framework, the CMDR (SOR/98-282), is essential for market entry. This episode provides a comprehensive overview of the Canadian Medical Devices Regulations, from its risk-based classification system to licensing, quality management, and post-market surveillance obligations for manufacturers and importers. • What are the four risk classes for medical devices in Canada? • What is the difference between a Medical Device Licence (MDL) and a Medical Device Establishment Licence (MDEL)? • Which device classes require an MDL before being sold in Canada? • What is the mandatory Quality Management System standard for Class II, III, and IV devices? • How does the Medical Device Single Audit Program (MDSAP) fit into Canadian compliance? • What are the bilingual labelling requirements for devices sold to the public? • Who is responsible for mandatory incident reporting? • What are the key post-market surveillance activities required under the CMDR? 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.