The European Commission has published a draft implementing regulation which would allow instructions for use in electronic format (eIFU) for all medical devices intended for exclusive use by healthcare professionals.
It is inviting feedback on the text, which will be published on its website, with the comment period due to...
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?