Our Experience:
We Know The
European Market.

Based on our long-term experience and specialists, we are in the position to accelerate the health market access of your device! Seminars in health care, on the medical device law and the health aid directories complement our service palette. Think of EUROM as "your" external department for issues about regulatory affairs.

Capitalise on our extensive competence!

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We provide support with getting listed in the technical aid index and extensive CE-certification maintenance services, in addition to introducing quality management systems.

Profit from our knowledge.

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According to the Council Directive 93/42/EEC concerning medical devices non-European manufactures have to have an authorised representative.

EUROM - your authorised representative.

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We specialize in registration and licensing but understand that each submission is unique. Our expertise is knowing what is right for each client and employ optimized methods.

Consulting, development, coordination.

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Eurom Service Ltd