IVDR and MDR Regulations

The European Commission has published many artefacts relating to EUDAMED and the Medical Device and the In-Vitro Regulations (MDR/IVDR). The links to the regulations are below, these links are to the searchable texts and the pdf documents.
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EUDAMED, IVDR, and MDR

EC Regulations

PublicationSearchable HTMLPDF
Medical Device Regulation MDR (EU) 2017/745 ConsolidatedEuropean Medical Device Regulation (MDR) EUDAMED ConsolidatedLink
Medical Device Regulation MDR (EU) 2017/745European Medical Device Regulation (MDR) EUDAMEDLink
Medical Device Regulation MDR (EU) 2017/745 CorrigendumEuropean Medical Device Regulation (MDR) Corrigendum EUDAMEDLink
Medical Device Regulation MDR (EU) 2017/745 Corrigendum IIEuropean Medical Device Regulation (MDR) Corrigendum EUDAMEDLink
In Vitro Diagnostic Medical Devices Regulations IVDR (EU) 2017/746European In Vitro Device Regulation (IVDR) EUDAMEDLink
In Vitro Diagnostic Medical Devices Regulations IVDR (EU) 2017/746 CorrigendumEuropean In Vitro Device Regulation (IVDR) Corrigendum EUDAMEDLink
In Vitro Diagnostic Medical Devices Regulations IVDR (EU) 2017/746 Corrigendum IIEuropean In Vitro Device Regulation (IVDR) Corrigendum EUDAMEDLink

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