EU MDR and IVDR: Uncovering Hidden Cost Savings While Complying with Device Traceability and UDI Requirements

This white paper will outline the significant challenges medical device companies may have as they comply with the European Union Medical Device Regulation (MDR) and In Vitro Diagnostic Regulation (IVDR). It will also explore the device traceability portion of the MDR and IVDR and uncover lessons learned from the United States Food and Drug Administration (FDA) Unique Device Identification (UDI) regulation. Finally, it will provide a list of actionable steps that medical device manufacturers can take to ensure device traceability compliance, and how they can reduce operational costs along the way. 

White paper - EU MDR and IVDR

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