This Device Advice: e-Learning tool is intended to educate stakeholders on the
premarket regulatory requirements for medical devices in Canada. Designed as an interactive learning platform, it covers a range of topics, including risk classification, licensing and labelling requirements, required submission documents, licence application types, licence amendments, and management of applications.
This tool is recommended for various medical device stakeholders, including manufacturers, importers, distributors, consultants, healthcare groups and academia.
