EUMEDIQ is an internationally operating service provider – headquartered in Switzerland – comprising experts in tailored solutions within Regulatory and Medical Device consulting. We serve as Authorised Representatives and Importers in Switzerland, the United Kingdom, and the European Union. Our expertise encompasses advising on the development, manufacturing, and distribution of Medical Devices with specialization in digitalization, software, IT security, CSV, and data protection. Additionally, we provide audit services according to Information Security Management System ISO 27001 and Medical Device Quality management systems ISO 13485. The goal: Helping Medical Device manufacturers to make important products available on the market as quick and as easy as possible. The vision: Being a pragmatic partner in the MedTech industry, supporting manufacturers in a highly complex environment to improve and enable the lives of patients with their products. Today, we help companies to further expand their innovative edge and provide the fastest possible information in the event of Regulatory changes.
