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Medical devices - Canada.ca

    https://www.canada.ca/en/health-canada/services/drugs-health-products/medical-devices.html
    The term Medical Devices, as defined in the Food and Drugs Act, covers a wide range of health or medical instruments used in the treatment, mitigation, diagnosis or prevention of a disease or abnormal physical condition. Additional …

Medical Devices Regulations ( SOR /98-282) - laws …

    https://laws-lois.justice.gc.ca/eng/regulations/SOR-98-282/
    Medical Devices Regulations. 1 - Interpretation; 2 - Application; 6 - Classification of Medical Devices; 8 - PART 1 - General. 8 - Application; 9 - …

Guidance documents – Medical devices - Canada.ca

    https://www.canada.ca/en/health-canada/services/drugs-health-products/medical-devices/application-information/guidance-documents.html
    Guidance documents have been prepared to assist in the interpretation of policies and governing statutes and regulations. They are intended to assist in preparing …

Canada - Medical Devices - International Trade …

    https://www.trade.gov/country-commercial-guides/canada-medical-devices
    The Canadian market presents opportunities for U.S. exporters of medical devices. Total imports of medical devices satisfy approximately seventy percent of …

Health Canada CMDR Medical Device Registration and Approval

    https://www.emergobyul.com/services/canadian-cmdr-consulting-health-canada-medical-device-registration
    Before you can market your medical device in Canada, you must comply with the Medical Device Single Audit Program (MDSAP), which includes compliance with the quality …

List of regulatory agencies and foreign jurisdictions

    https://www.canada.ca/en/health-canada/services/drugs-health-products/reports-publications/medeffect-canada/foreign-risk-notification-medical-devices-guidance/list.html
    Dec 23, 2020



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