Webcast: How to Plan for EU MDR 2020

The new European Union Medical Device Regulation (EU MDR) comes into effect May 2020. Device manufacturers will need to make substantial changes throughout the product life cycle. That includes clinical trials through to gathering and reporting of post-market surveillance data.

Listen to this webcast and hear Sparta Systems and Axendia discuss how these changes will have an impact on sustainable, positive disruption by identifying possible challenges, areas of interest and steps to prepare for the upcoming regulations.

Highlights include:
  • Key changes in the regulations
  • Tools needed to build a strategic plan
  • Impact on your QMS

Watch it Now

We will never sell, distribute or reveal your email address to anyone. Privacy Policy

What People are Saying

How to Embed a Tweet

  1. Click on the (...) icon at the bottom of the tweet you wish to embed
  2. Click "Embed Tweet"
  3. Copy the selected text
  4. Paste the copied code into one of the Tweet boxes above