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EU MDR: What will it mean for Medical Device Manufacturers?

August 14, 2019 by medtechufacewqaz  

In this video, AssurX presents information explaining EU MDR, which will be in effect May 26, 2020, and how the new European Union Medical Device Regulations will affect the Medical Device Manufacturing industry, as well as Medical Device Suppliers, moving forward. 


For further information please visit: 

"EU MDR Rules Could Impact Medical Device Business Strategies" - https://www.assurx.com/eu-mdr-rules-could-impact-business-strategies/

To request a live demo today, visit https://www.assurx.com/demo-request/



With decades of expertise built into our quality management and regulatory compliance software, the AssurX Quality Management Software Platform helps companies maintain quality and compliance standards, streamline workflow and better manage any enterprise. Our configurable software and understanding of users’ needs produce a unique system that easily adapts as a customer’s business evolves. AssurX is an ideal partner for regulated companies looking for better operational control and efficiency while staying compliant. To learn more, visit www.assurx.com.


For more information about how AssurX can aid your medical device manufacturing organization's quality and compliance management efforts, please visit https://www.assurx.com/medical-device-manufacturing/