Our Mission is to establish a leading independent Conformity Assessment Body for medical devices to advance patient safety and care, as well as optimized patient outcomes, by complying to the MDR/IVDR and by adhering to key principles and standards of medical device vigilance, post market surveillance and device risk management.

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QMD Services

Florian Heffeter

This department ensures compliance with relevant regulations for medical devices and in vitro diagnostics while overseeing product certification and review processes.

Regulatory Affairs

This department oversees the planning, execution, and completion of projects, ensuring alignment with organizational goals.

QMD Services

Org chart

Teams

Regulatory Affairs

Project Management

Offices