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.

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Champ Valeur
Dernière modification avril 17, 2026, 21:57 (TU)
Créé le avril 17, 2026, 21:57 (TU)
criticality_level []
geographic_scope []
open_canada_collection publication
open_canada_date_published 2018-11-07 00:00:00
open_canada_keywords {"fr": ["avis", "document d'orientation", "exigences", "processus de reconnaissance", "programme d'audit unique des dispositifs médicaux", "MDSAP", "organismes d'audit", "parties prenantes du secteur des dispositifs médicaux"], "en": ["notice", "guidance document", "requirements", "recognition process", "medical-device single-audit program", "MDSAP", "auditing organizations", "medical-device stakeholders"]}
open_canada_subject ["health_and_safety"]
sensitivity_level unrestricted
title_fr Avis : Ligne Directrice – Exigences du processus de reconnaissance pour les Organismes d’audit du Programme d’audit unique pour le matériel médical (PAUMM)
update_frequency as_needed