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As a consequence of the review, authorization and oversight of COVID-19 drugs under the Regulations, manufacturers may benefit from intellectual …
The Interim Order (IO) expedites the authorization of Class I to IV medical devices used for COVID-19: sets out the …
Information about filtering facepiece respirators and their certification and testing process.
All Canadian-manufactured respirators must meet the minimum performance testing requirements.
For an IO submission, Health Canada requires a report on the results of the performance testing requirements that apply to …
Due to the urgent public health needs relating to COVID-19, we can issue a market authorization with conditions. This is …
At the time of authorization, no major safety concerns have been reported in the available data submitted to Health Canada. …
Information on the Moderna COVID-19 vaccine, including how it works, how it's given, possible side effects and vaccine safety after …
As part of the government’s broad response to the pandemic, Health Canada introduced a number of innovative and agile regulatory …
The guidance document concerning amendments to the Food and Drug Regulations for drugs for use in relation to COVID-19 indicates …