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Best Practices to Leverage EU MDR QMS Requirements to Drive Process Optimization, Product Innovation, and Enhanced Patient Outcomes

The European Union’s Medical Device Regulations (EU MDR), governing the production and distribution of medical devices in the European Union, has been in effect since 26 May 2021, three years after the revisions were announced. It replaces the EU’s Medical Device Directive (93/42/EEC) and the EU’s Directive on active implantable medical devices (90/385/EEC). These regulations […]

The post Best Practices to Leverage EU MDR QMS Requirements to Drive Process Optimization, Product Innovation, and Enhanced Patient Outcomes appeared first on ComplianceQuest: AI-powered PLM, QMS, EHS & SRM Platform.

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Best Practices to Leverage EU MDR QMS Requirements to Drive Process Optimization, Product Innovation, and Enhanced Patient Outcomes

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