Open Government Portal
The following is a list of health product advisories, type I drug recalls and summaries of completed safety reviews published …
The following is a list of health product advisories, type I drug recalls and summaries of completed safety reviews published …
The following is a list of health product advisories, type I drug recalls and summaries of completed safety reviews published …
The following is a list of health product advisories, type I drug recalls and summaries of completed safety reviews published …
In Canada, many different organizations and individuals play a role in communicating risks associated with health products.
Despite the strong foundation of Canada’s existing Regulations, more can be done to improve the safety and effectiveness of medical …
This guidance document is to help holders of Canadian authorizations for medical devices understand and comply with the regulatory requirements …
Requirements for manufacturers and importers for collecting medical device safety information and provide notification to Health Canada. A monitoring process …
Medical device licence holders and importers of Class II to IV devices must notify Health Canada when there’s a serious …
Information needed for a submission to comply with the Regulations, licence holders and/or importers of Class II to IV medical …