Medical devices for COVID-19: Conducting a clinical trial

Manufacturers of medical devices intended to treat COVID-19 can choose between 2 different processes to apply for a trial authorization: process for investigational testing outlined in the Medical Devices Regulations or process outlined in the new interim order for clinical trials for medical devices and drugs related to COVID-19.

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Last Updated April 17, 2026, 21:45 (UTC)
Created April 17, 2026, 21:45 (UTC)
criticality_level []
geographic_scope []
open_canada_collection publication
open_canada_date_published 2021-05-03 00:00:00
open_canada_keywords {"fr": ["COVID-19", "pandémie", "essais cliniques", "médicaments", "instruments médicaux", "demande d'autorisation d'essai", "Règlement sur les instruments médicaux", "arrêté provisoire pour essais cliniques liés à COVID-19"], "en": ["COVID-19", "pandemic", "clinical trials", "drugs", "medical devices", "apply for a trial authorization", "Medical Devices Regulations", "interim order for clinical trials related to COVID-19"]}
open_canada_subject ["health_and_safety"]
sensitivity_level unrestricted
title_fr Instruments médicaux contre la COVID-19 : Tenue d’essais cliniques
update_frequency as_needed