European Authorized Representative (EU-REP) service providing regulatory compliance and market access support for medical devices, IVDs, cosmetics, and PPE across EU, UK, and Switzerland. Enables manufacturers to meet MDR 2017/745, IVDR 2017/746, and GPSR requirements for all device classes.
Manufactured by
MedNet EC-REP GmbH
Münster, Germany
With many years of experience and a highly qualified team, MedNet EC-REP offers all services for the pan-European marketing authorization of your products: the European Authorized Representative (EC-REP), the UK Responsible Person (UK RP) and the Swiss Authorized Representative (CH-REP). We specialize in medical devices, in vitro diagnostics (IVD), personal protective equipment (PPE), clinical investigations and performance studies, and application for certificates of free sale (FSC).
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MDSS USA LLC · United States
European Authorized Representative and regulatory compliance service for medical devices and IVDs. Provides in-country representation across EU, UK, Switzerland, USA, and Australia to ensure manufacturers meet MDR, IVDR, AI Act, and GDPR requirements.
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EU Authorised Representative service enabling medical device manufacturers and importers to demonstrate regulatory compliance with EU MDR/IVDR requirements. Provides expert guidance on EU, UK, US, and Swiss regulatory pathways for medical devices, in vitro diagnostics, and cosmetic products. Facilitates market access and post-market surveillance documentation.
Metecon GmbH · Germany
Regulatory representation services for medical devices and IVDs under MDR, IVDR, and related frameworks. EC-REP, CH-REP, and PRRC designation support enables market access and compliance across EU and international jurisdictions. Expert guidance on regulatory strategy, documentation, and post-market obligations.
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