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

Tags

Topics

Categories