Notice: Guidance Document – Requirements in the Recognition Process for Medical Device Single Audit Program (MDSAP) Auditing Organizations
Description
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.
Resources
| Name |
Format |
Description |
Link |
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21 |
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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 |
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21 |
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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 |