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Meditrial is a professional European Authorized Representative organization serving Medical Device and In-Vitro Diagnostic manufacturers in accordance with the European Medical Device Directives.

Meditrial is pleased to put at your disposal our support and recognized reputation in Europe as a leading supplier of regulatory, CE marking and clinical services.

We operate according to the European Commission guideline MEDDEV 2.5/10.

Why Meditrial

Meditrial is certified for regulatory services, clinical trials, data management, and medical training courses.

ISO 9001:2008 Certificate

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