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More than a Quality Management System: Tools for the entire MedTech Lifecycle.

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Featured Capabilities:

Document Management Training Management CAPA Management Audit Management Product Development

Experience the #1 QMS software for medical device companies first-hand. Click through an interactive demo.

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Accelerate development with integrated design control and risk software.

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Featured Capabilities:

Design Controls Risk Management Risk Intelligence

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Data collection and management designed for MedTech clinical trials.

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Featured Capabilities:

Electronic Data Capture (EDC) Electronic Case Report Forms (eCRF) Electronic Patient Reported Outcomes (ePRO) Ad-Hoc Data Collection (Cases) Post-Market Surveys Product Add-Ons

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FREE ON-DEMAND WEBINAR

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

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.

Watch the webinar
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...
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

Hosted by

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Presenter: RICHARD TULLY

Director, CompliantMD
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Moderator: Nick Tippmann

VP of Marketing, Greenlight Guru

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About Greenlight Guru

Greenlight Guru is the only Medical Device Success Platform (MDSP) for companies to bring new products to market faster while simplifying regulatory compliance and reducing risk. Being the only industry specific, cloud-based software, Greenlight Guru is easier to implement, easier to use and designed to fit all medical device needs to enable innovative, safe and effective, True Quality medical devices. Visit our homepage to learn more.

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