How to Plan for EU MDR 2020

 Wednesday, Sep 19th

 9:00am EDT
 200pm BST / 3:00pm CEST

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.  

Join Sparta Systems and Axendia as they 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

Register Today

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Tom Middleton

Solutions Architect

Sparta Systems

Tom has a passion for helping people ensure management system quality and robust compliance through value-added, process-driven programs. His experience includes standards and regulations for the automotive, life sciences, medical devices and consumer product verticals, including ISO 9001, ISO 13485, ISO 14000, FDA 21 CFR 820, Japanese Pharmaceutical Affairs Law (JPAL), Canadian Medical Devices Conformity Assessment System (CMDCAS), EU Medical Device Directive (MDD), and the Brazilian ANVISA standards.

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