Notice: Guidance Document – Requirements in the Recognition Process for Medical Device Single Audit Program (MDSAP) Auditing Organizations (French, HTML)

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HTML
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file-only
Publisher-reported update
2023-12-02

This guidance document provides medical device stakeholders with information on the requirements that the Therapeutics Products Directorate will use in recognizing Auditing Organizations under the MDSAP.

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HTML
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French
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