May 16, 2022 | Basic page
AMDF Resources
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| Guidelines for inspection of manufacturing site(s) for assessment of the quality management system of medical devices based on ISO 13485:2016 - English | French | Guidelines for registration of medical devices establishments - English | French | |||
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| Guidelines on import and export of medical devices including in-vitro diagnostic medical devices - English | French | Guidelines on regulatory requirements for issuance of market authorization of medical devices including in-vitro diagnostic medical devices - English | French |
