Applications for medical devices under the Interim Order for use in relation to COVID-19 - Guidance document

Guidance documents are administrative instruments not having force of law and, as such, allow for flexibility in approach. This guidance document is intended to provide guidance to manufacturers and importers to organize and submit an application in a timely manner for the sale or importation of medical devices that are manufactured, sold or represented for use in relation to COVID-19.

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Dernière modification avril 17, 2026, 17:24 (TU)
Créé le avril 17, 2026, 17:24 (TU)
criticality_level []
geographic_scope []
open_canada_collection publication
open_canada_date_published 2020-04-02 00:00:00
open_canada_keywords {"fr": ["Demandes relatives aux instruments médicaux", "arrêté d’urgence", "instruments médicaux déstinés à être utilisés à l'égard de la COVID-19", "autorité réglementaire étrangère", "Médicaments annonces."], "en": ["Applications for medical devices", "Interim Order", "COVID-19 related Medical devices", "foreign regulatory authority", "Drug product announcements."]}
open_canada_subject ["health_and_safety"]
sensitivity_level unrestricted
title_fr Demandes relatives aux instruments médicaux visés par l’arrêté d’urgence pour leur utilisation à l’égard de la COVID-19 - Ligne directrice
update_frequency as_needed