Are you ready for Brexit impacts? Do you have a Brexit contingency plan? You may need either an EU/EC European authorized representative based in EU-27 countries or a UK Authorised Representative based in UK, or may need both EU & UK representatives, depending on different brexit scenarios. Register/Notify your MD-Medical Devices & IVD-In Vitro Diagnostic Medical Devices with MHRA in UK & other EEA (EU/EFTA) authorities by world-leading consultancy- Wellkang team based in both UK (England) & EU-27 (Ireland). Wellkang team can help you under all Brexit scenarios! Click here to get FREE Guide Now! Wellkang Group also offer CE marking Compliance Consulting service, as well as European Authorized Representative service for the following products: Are you ready for Brexit? Wellkang can help under all Brexit scenarios! Machinery under new Machinery Directive 2006/42/ec Personal Protective Equipment (PPE) Low Voltage Electrical Equipment (LVD) Products covered by directive of Electromagnetic Compatibility (EMC) Toys under Toy Safety Directives (TSD) 88/378/eec & 2009/48/ec WEEE registration compliance and solutions Cosmetic Products Other Products Let Wellkang be your professional CE Marking authorized representative! Our service varies greatly from case to case, from product to product. Please click here now for a quotation. Click here to view our Auth Rep fee list.   Why do you need a representative in Europe? Why must the manufactures of medical devices appoint a EU Authorized Representative? Why is the Authorized Representative different from the importer/distributor ? Why choose Wellkang? How can Wellkang help you? For more information, please visit our Questions and Answers section.  | Home | About Us | Contact Us | Copyright & Disclaimer | Privacy | Log-in | Order Now |