mdi Europa GmbH acts as European Authorized Representative for a wide range of companies – from start-ups to established corporations throughout the world. Need assistance complying with US FDA, European or other global medical device regulations? mdi Europa is your single source for helping you access the largest and fastest growing medical device markets worldwide. mdi Europa was created in 2000 to provide high quality regulatory affairs services. Our customers are manufacturers, importers, exporters and distributors of medical devices and in vitro diagnostics world-wide. Our high quality compliance solutions, as confirmed by our ISO 9001:2008 certification, include classification, identification of EU standards, technical Documentation compilation and review, EU Authorized Representative, product registration to national EU Authorities, Labeling Compliance, Free Sales Certificates, market research, translation services, and more. Imprint http://mdi-europa.com/imprint Privacy Policy http://mdi-europa.com/privacy-policy