Health Canada's Action Plan on Medical Devices
Three-part strategy to strengthen medical device regulation in Canada: improve how devices reach market, strengthen monitoring of devices in use, and provide Canadians with better information about medical devices. Includes initiatives such as publishing Regulatory Decision Summaries for Class III and IV devices.
🔖 Status: in-development
This reform is part of Health Canada's ongoing programme to modernise and strengthen the Canada medical device regulatory framework. Monitor the official source for updates on timelines, consultation opportunities, and implementation guidance. Where relevant, begin assessing potential impacts on your existing registrations, technical documentation, and compliance timelines so your organisation is prepared when the reform takes effect.
View official source ↗