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BioRender Template
EU Regulations for MDR and IVDR
Description
This template compares the transition timelines for four EU medical device regulations, showing when the Medical Device Directive and In Vitro Diagnostic Directive certificates remain valid alongside the phase-in of the Medical Device Regulation and In Vitro Diagnostic Regulation from 2020 through 2028. Key milestones are marked, including regulation enactment in May 2020, MDR fully applying in May 2023, and IVDR fully applying in May 2025.
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