Regulatory Affairs

We inform you continuously and always up-to-date about the most important topics from all areas of medical technology.

The approvals of medical technology products for first-time market introduction are subject to special approval procedures. The heterogeneous international procedures and regulatory requirements are continuously changing and becoming more and more extensive. We provide you with ongoing and always up-to-date information on the most important topics from all areas of medical technology.

Regulatory Affairs

The approval of medical devices is complex and often confusing. We clarify ...

Clinical Affairs

Medical devices require numerous verifications and assessments. What we know about this ...

Quality-management

Medical devices are subject to strict quality assurance requirements. We know the details ...

Development Excellence

Product development in medical technology is subject to its own laws. We bring light into the dark ...

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