On 25 October 2019, the European Commission’s Medical Device Coordination Group (MDCG) released a document outlining future guidance on the Medical Device Regulation (MDR) and In Vitro Diagnostic Medical Device Regulation (IVDR). The document indicated that much of the guidance would be endorsed later in 2019 or in 2020. Read the original coverage through the source below.
MDR and IVDR: Commission announces guidance development
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