Metecon Blog: Regulatory updates for medical devices and IVDs

Stay up to date on regulatory compliance with our regular blog posts!

We explain the current events and classify them for you: Quality Management, Technical Documentation, Clinical Affairs, Regulatory Affairs as well as Software und Digitization: Browse through our articles or use the search or filter function below to quickly retrieve the content of interest to you.

Our expert's helpful tips and best practices on documentation, market access, and market monitoring will help you implement MDR, IVDR and other regulations for your medical devices and in vitro diagnostics (IVD).

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Regulatory History: Blog Archive

You can find older posts in our blog archive. Please make sure that this content is up to date before using it; we are happy to help.