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MedNet EC-REP helps non-UK manufacturers to gain easy and fast access to the British markets England, Scottland and Wales. As your UK Responsible Person we provide regulatory represenation in the UK and helping you to bring your Medical Devices, In Vitro Diagnostics or Cosmetics on the market.
Following Brexit, the British Medical Device market is regulated by the UK MDR 2002. This regulation defines the access of non-British products to the British market. Non-British manufacturers are forced to comply to that regulation and appoint a UK Responsible Person (UK RP) based in the UK. Situated in Great Britain, MedNet as your UK Responsible Person is aware of local regulations and the latest changes to support you with quick market access by registering your Medical Devices on the British MHRA (Medicines and Healthcare Regulatory Agency) database.
DetailsSince Brexit, the UK MDR 2002 regulates the British market for In Vitro Diagnostics. To comply, the regulation forces non-British manufacturers to appoint an UK Responsible Person as their representative in Britain. As your UK RP, Mednet acts as the first contact person for local authoriies and is aware of all the current regulations and transitional rules in the UK. Furthermore we offer registration services to place your IVD products in the British Medicines and Healthcare products Regulatory Agency (MHRA) database.
When selling Cosmetics in England, Scotland and Wales, the product must comply with the local UK Cosmetics Products Regulation. Non-British manufacturers are forced to appoint a Responsible Person who is situated in the UK and registers your Cosmetics in the GB Cosmetics Notification Portal of the Office for Product Safety and Standards (OPSS). MedNet as your UK Responsible Person is your partner who provides you with a quick registration to ensure a short time to market. Furthermore we guide you the way through the UK regulation landscape and update you on the latest changes in local requirements.
DetailsWith our experts situated in Great Britain, we offer the necessary services for your products. With over 25 years of experience and an interdisciplinary team, we possess a profound understanding of the relevant regulations to provide you with comprehensive support.
We carry out fast and straightforward registrations in all EU member states, as well as in Great Britain and Switzerland.
We offer full service and a fast turn around for Free Sales Certificates. Including legalizations for almost every Country in the world if required.
Place all your regulatory needs into our hand:
Our intercultural team of PhD biologists and Medical Engineers will take care of your concerns - with one single point of contact and no matter which country you want to distribute into next.
