Update: Join us on Zoom today at 5PM (GMT +8)

Link: https://us02web.zoom.us/j/83369815906?pwd=n0esjdYdC0HYtJ1Ia2BntJRcexqq9d.1

Passcode: 967309

 

Join Qualtech's Webinar on 2025 Updates & Forecast for European Medical Device Regulations

This February, Qualtech is hosting a one-hour webinar that delves into the latest updates of the European Medical Device Regulation (MDR). We believe this event will be a valuable resource for your medical device compliance in Europe.

You'll gain crucial insights on:

  • Extended MDR transition: Ongoing for legacy devices, with full compliance required for new products
  • Mandatory reporting of supply chain disruptions
  • EUDAMED implementation: Critical modules go live, requiring business preparation
  • Artificial intelligence medical device regulations
  • MDR system evaluation: Commission's assessment will shape future improvements
  • UK medical device regulatory update: New post-market rules and upcoming pre-market reforms
  • EU-Switzerland mutual recognition

 

Webinar details:

Secure your spot for our webinar and interact with our exclusive professional speaker.

We look forward to seeing you there!

If you have any questions, feel free to contact us at globalra@qualtechs.com.

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