UK Responsible Person (UKRP) representation service for medical devices and IVDs seeking market authorization in the United Kingdom. Ensures regulatory compliance with UK MDR requirements and facilitates in-country representation for non-UK established manufacturers.
Manufactured by
MDSS USA LLC
Chicago, IL, United States
With over 30 years of experience, MDSS is a leading Authorized Representative and Regulatory Consulting organization, headquartered in Germany with offices in the United States, the United Kingdom, Switzerland, and Australia. Our services include: European Authorized Representative (EC REP) UK Responsible Person (UKRP) Swiss Authorized Representative (CH-REP) U.S. Agent Australian Sponsor Other services (e.g. Free Sales Certificates, GDPR, GPSR, Representative for Clinical Investigations, Vigilance, …) In addition to providing In-Country Representation services — helping streamline global market access through a single, reliable partner, so you can focus on your core business and innovation — we offer regulatory strategy consulting for medical devices and IVDs, support with pre-submissions and marketing authorization applications to the FDA , and assistance with EU MDR and EU IVDR compliance. Why MDSS? 30+ years of regulatory expertise Same trusted address for 20+ years Personalized support and tailored approach that sets MDSS apart from other regulatory service providers Collaborative network of offices spanning from the USA to Australia – single verification that grants access to three key markets: the EU, the UK, and Switzerland Independent services that protect your intellectual property Full control of your technical product files—no need to share with local importers or distributors MDSS is a member of the European Association of Authorized Representatives ( EAAR ), the UK Responsible Person Association ( UKRPA ), Swiss Medtech and the Medical Technology Association of Australia ( MTAA ).
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Obelis Group S.A. · Belgium
UK Responsible Person designation and regulatory compliance service for medical devices and in vitro diagnostics entering the UK market. Ensures manufacturers meet UK MDR and IVDR post-Brexit requirements, including technical file preparation, quality management oversight, and regulatory submissions.
MedNet EC-REP GmbH · Germany
Regulatory representation service enabling medical device manufacturers to market products in the UK under the Medical Devices Regulations. The service manages post-market surveillance, technical documentation, and compliance obligations for Class I through Class III devices, allowing manufacturers to distribute products without establishing a UK legal entity.
EUCEREP B.V. · Netherlands
UK Responsible Person regulatory representation service enabling non-EU medical device manufacturers to achieve compliant market access in the UK. Encompasses MHRA registration, technical documentation support, Quality Management System establishment, and ongoing regulatory compliance guidance.
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