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A medical device is any instrument or component used to treat, diagnose or prevent a human disease or abnormal physical condition. Page about what medical device problems are and how to report them.

Health Canada information related to adverse reaction reporting of drugs and health products on the Canadian market

This report, which is tabled under section 20 of the Service Fees Act and section 4.2.8 of the Directive on Charging and Special Financial Authorities, contains information about the fees that Health Canada had the authority to charge in the 2022-23 fiscal year.

Under IO No. 2, manufacturers and importers must report shortages of specified medical devices (including their components, accessories or parts) of critical medical devices to Health Canada. This new interim order outlines the mandatory reporting requirements.

Health Canada has published the highlights report since 2019. The report gives information about what Health Canada is doing to help people make healthier food choices. Recent editions include information about choosing nutritious food and making food safe.

This report, which is tabled under section 20 of the Service Fees Act and section 4.2.8 of the Directive on Charging and Special Financial Authorities, contains information about the fees that Health Canada had the authority to charge in the 2021-22 fiscal year.

A report on departmental regulatory transparency initiatives for 2017-18