MDR and IVDR Resources

A collection of informational resources on the European MDR and IVDR regulations for medical devices and in vitro diagnostic medical devices.

This section brings together introductory guides, useful references and links to official sources. It is designed to help navigate the main topics of the European regulatory framework.

The resources are organised by topic and intended for quick consultation.

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Quick access from your smartphone

If you often consult these guides from your smartphone, you can add this page to your device’s Home Screen.

This allows you to access the MDR and IVDR resource collection quickly, as if it were a direct shortcut to an app.

Usually, you can open the page in your browser, tap Share and select Add to Home Screen. The wording may vary depending on the device and browser used.

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Why this section exists

This page was created to collect evergreen content organised by topic and easy to consult.

It is not a chronological blog, but an introductory regulatory library dedicated to the main topics related to MDR and IVDR.

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Informational note

The resources in this section are provided for informational purposes only and do not constitute regulatory, legal, technical or professional advice.

The content is based on publicly available sources and, where appropriate, refers to official texts, European Commission pages and updated institutional documentation.

In this section, the images are for illustrative purposes only and may have been generated or edited with the support of artificial intelligence tools.

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