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EU MDR

19 01, 2021

Addressing the EU MDR and IVDR Certification Bottleneck
Addressing the EU MDR and IVDR Certification Bottleneck

Addressing the EU MDR and IVDR Certification Bottleneck

By AssurX Blog|2021-01-19T07:00:36+00:00January 19th, 2021|EU MDR, Medical Device Industry, Quality Management, Regulatory Compliance Management|

With the May 26, 2021 implementation deadline looming for the new EU Medical Dev [...]

11 01, 2021

EU MDR Compliance Check-in: Challenges and Action Items
EU MDR Compliance Check-in: Challenges and Action Items

EU MDR Compliance Check-in: Challenges and Action Items

By AssurX Blog|2021-01-11T07:36:20+00:00January 11th, 2021|EU MDR, Medical Device Industry, Quality Management, Regulatory Compliance Management|

The new EU Medical Device Regulation (MDR) goes into effect in less than six mon [...]

25 06, 2019

EU MDR Rules Could Impact Medical Device Business Strategies
EU MDR Rules Could Impact Medical Device Business Strategies

EU MDR Rules Could Impact Medical Device Business Strategies

By AssurX Blog|2019-06-25T09:38:18+00:00June 25th, 2019|FDA Regulated Industries, Medical Device Industry, Quality Management, Regulatory Compliance Management|

Changes in the European Union (EU) MDR and IVDR standards could force business c [...]