The eSTAR pilot: Notice to industry
Industry notice regarding the electronic submission and reporting pilot between Health Canada and FDA. Supports cross-border regulatory harmonization and efficiency.
🔖 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 ↗