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Latest / Medical Device Global Market Access

Navigating Canada's MedTech Market: A Guide to the CMDR

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…

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