The core activity of EUMEDIQ is to provide services to manufacturers of medical devices, particularly in the areas of: Authorized Representative for medical devices in Switzerland, the United Kingdom and the European Union; Medical Device Consulting; Audits and certifications according to ISO 27001 (Information Security Management); Import and customs clearance for medical devices; and Computerized System Validation (CSV). The company supports manufacturers of medical devices in complying with regulatory requirements and in obtaining market authorization for their products in Europe.