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EU Regulations for MDR and IVDR

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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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What does the EU Regulations for MDR and IVDR template show?

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.

Is the EU Regulations for MDR and IVDR template free to use?

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Yes, every element is fully editable. Icons, labels, colors, arrows, shapes and layout can all be changed to match your preferences or needs using BioRender's drag-and-drop editor. You can add or remove elements to fully customize your use case.

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What is EU Regulations for MDR and IVDR used for / who typically uses this template?

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