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Initial supplies of authorized COVID-19 vaccines are not expected to be sufficient to offer vaccination to all Canadians in …
Medical devices that are eligible for importation and sale under the interim order (IO) are known as “designated” devices. They …
Once a device is placed on the list, establishments must notify Health Canada at least 5 calendar days before the …
Information about a medical device must be available and in a form that is accessible to users, to ensure it …
List of terms used in the guidance document.
This guidance document is intended to help importers, distributors, manufacturers and other establishments meet their regulatory requirements.
During the COVID-19 pandemic, Health Canada is working closely with domestic and international partners to anticipate and meet Canadians' …
These measures expedite the regulatory review of COVID-19 health products without compromising safety, efficacy and quality standards.
During the COVID-19 pandemic, we continue to take a risk-based approach to inspections.
Appearance of Minister of Employment, Workforce Development and Disability Inclusion - Standing Committee on Human Resources, Skills and Social Development …