Notice: New regulations strengthening the post-market surveillance and risk management of medical devices in Canada (English, HTML)
View metadata and access the original English HTML file: Notice: New regulations strengthening the post-market surveillance and risk management of medical devices in Canada.
- Format
- HTML
- Access
- file-only
- Publisher-reported update
- 2022-10-21
Health Canada is making regulatory changes to the Medical Devices Regulations to strengthen the lifecycle approach to the regulation of medical devices by increasing post-market surveillance authorities.
Data overview
- Formats
- HTML
- File languages
- English
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