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The Top 10 Most Significant Changes Introduced by the New EU MDR (And How to Avoid the Common Mistakes)

Watch the Free Webinar

As most of you have likely heard, the EU's new Medical Device Regulations (MDR) went into effect earlier this year replacing the old MDD and setting in motion a three-year countdown for manufacturers to comply to continue selling in the European market. 

You also likely have a lot of questions about what do these changes mean, how can you begin preparing, how will they affect your company, what are their greatest implications, etc.?

Join us for the free, 90 minute webinar presented by our guest Richard Tully, Director at CompliantMD, where he will be sharing with you the top 10 most significant changes introduced by the new EU MDR and how you can avoid the most common mistakes when implementing.


Specifically you will learn:

  • How much will the new Medical Device Regulation cost?
  • Why did it need to happen and what is the new structure? 
  • What additional activities does a manufacturer have to carry out? 
  • What are the top 10 most significant changes? 
  • What is EUDAMED and how has its role changed? 
  • And much more...

*Note: Limited live seats available.

Who should attend?

  • Medical Device Executives

  • CAPA Managers or anyone who participates in your company's CAPA Board
  • Regulatory Affairs Professionals and Management

  • Quality Professionals and Management

  • Clinical Affairs Professionals and Management 

  • R&D Engineers and Management








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Greenlight Guru


About greenlight guru

Greenlight Guru is a modern quality management software platform used by medical device companies in over 25 countries to bring new products to market faster while simplifying regulatory compliance and reducing risk. Being the only industry specific, cloud-based eQMS, Greenlight Guru is easier to implement, easier to use and simply fits medical device processes out of the box allowing companies to innovate faster and be more efficient. Visit our homepage to learn more.