Medical device CE marking

MDCG 2021-23 Guidance on certification activities – MDR-IVDR


On August 20, the European Union published MDCG 2021-23 – Guidance for notified bodies, distributors and importers on certification activities in accordance with Article 16(4) of Regulation (EU) 2017/745 and Regulation (EU) 2017/746.

The document can be downloaded in our library

Source: European Commission