mdr

EU Commission Proposes Codes for Medical Devices Under MDR/IVDR

The Commission of the European Union (EU) has issued a detailed list of proposed codes to be used by EU Notified Bodies in the categorization and assessment of medical devices under the EU’s Medical Device Regulation (Regulation (EU) 2017/745, also known as the MDR) and the In Vitro Diagnostic Device Regulation (Regulation (EU) 2017/746, also known as the IVDR).

The EU’s MDR and IVDR Achieve Final Approval

The wait is nearly over for the official publication of the European Union’s (EU)...

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