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 ...Read more

Clinical Affairs

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

Lifecycle Processes

Medical devices and in-vitro diagnostics are subject to strict process requirements. We know the details... ... Read more

Health Software

The importance of software in medical technology is increasing rapidly....

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