EU – Mandate M/565 COMMISSION IMPLEMENTING DECISION C(2020) 2532 of 15.5.2020 on a standardisation request to the CEN and the CENELEC in support of Regulation (EU) 2017/745 and Regulation (EU) 2017/746
Published in European Commission, In Vitro Diagnostic Medical Device Regulation IVDR, Medical Device Regulation MDR, Standardisation Request and Standards
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