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

Notice: Guidance Document – Requirements in the Recognition Process for Medical Device Single Audit Program (MDSAP) Auditing Organizations 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. 2023-12-02 Health Canada open-ouvert@tbs-sct.gc.ca Health and Safetynoticeguidance documentrequirementsrecognition processmedical-device single-audit programMDSAPauditing organizationsmedical-device stakeholders Notice: Guidance Document – Requirements in the Recognition Process for Medical Device Single Audit Program (MDSAP) Auditing OrganizationsHTML https://www.canada.ca/en/health-canada/services/drugs-health-products/medical-devices/activities/announcements/notice-guidance-document-requirements-recognition-process-mdsap-auditing-organizations.html Notice: Guidance Document – Requirements in the Recognition Process for Medical Device Single Audit Program (MDSAP) Auditing OrganizationsHTML https://www.canada.ca/fr/sante-canada/services/medicaments-produits-sante/instruments-medicaux/activites/annonces/avis-ligne-directrice-exigences-processus-reconnaissance-organismes-daudit-paumm.html

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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