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 MEDDEV Solutions, 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.
*Note: Limited live seats available.
Medical Device Executives
Regulatory Affairs Professionals and Management
Quality Professionals and Management
Clinical Affairs Professionals and Management
R&D Engineers and Management
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.
We are a team of Medical Device Professionals that provide expert knowledge and solutions to help your business.
We want to be the first choice for medical device companies seeking solutions. With our drive and focus on delivering value we aim to provide compliant solutions that are 'right first time'. Utilising our many years of experience across a wide range of companies and Notified Bodies we can achieve our tagline of Knowledge & value, delivered as standard.
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