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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 help you comply with the European legal requirements and establish constructive relationships with Competent Authorities, Notified Bodies, hospital networks, the European Commission, and industry associations.

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

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