Health Canada has published draft guidance relating to its planned implementation in April of the International Medical Device Regulators Forum’s Table of Contents (ToC) formats for use in medical device and IVD marketing authorization applications.
The draft guidance incorporates content from the IMDRF ToC documents and regional guidance specific to the Canadian context.
Read the full article – start your free trial today!
Join thousands of industry professionals who rely on Medtech Insight for daily insights
- Start your 7-day free trial
- Explore trusted news, analysis, and insights
- Access comprehensive global coverage
- Enjoy instant access – no credit card required
Already a subscriber?