Column - EU MDR: Ensuring Labeling Compliance - MedTech Intelligence

Retrieved on: 2023-10-25 23:51:28

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Regulation of medical devices

Regulation (EU) 2017/745

Regulation (EU) 2017/746

Unique Device Identification

Medical device

MDR

CE marking

Packaging and labeling

Design controls

Single Use Medical Device Reprocessing

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Column - EU MDR: Ensuring Labeling Compliance - MedTech Intelligence. View article details on HISWAI: https://medtechintelligence.com/column/eu-mdr-ensuring-labeling-compliance/

Excerpt

It aims to move the industry towards a more patient-centered approach to regulation, and will enhance patient and user safety. EU MDR involves the ...

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