We are an internationally operating service provider – headquartered in Switzerland – comprising experts in tailored solutions within Regulatory Affairs and Medical Devices. We serve as an Authorised Representative and importer in Switzerland, the United Kingdom, and the European Union. Furthermore, we provide audit services according to information security management systems (ISMS) ISO 27001 and medical device quality management systems ISO 13485. Our consulting services encompass medical device compliance within the comprehensive product life cycle.  

Our goal: Accompanying medical device manufacturers – from idea to successful market launch. 

Our vision: Safety through digitalisation.

Today, we help companies to further expand their innovative edge and staying up to date.

EUMEDIQ

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