Our Services

EU MDR

The Regulation (EU) 2017/745 on Medical Devices.

EU IVDR

The Regulation (EU) 2017/746 on In-Vitro Diagnostic Devices.

Specific Topics

Cross-cutting and global subjects.

Interested in our services?

Contact AKRA TEAM for support, hands on implementation services and personalized training by experts with key competencies in the areas listed above.

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