Get in touch with us and let us know how we can help
Whether you have a specific regulatory question, want to discuss your device's compliance requirements, or would like to learn more about how EUMEDIQ can support your organisation, our team is available to help. Reach out using the form below or contact us directly at one of our offices.
OUR OFFICES
Regulatory expertise across the EU, UK, and Switzerland from three European offices
With offices in Zug, Hardt, and London, EUMEDIQ provides medical device manufacturers with direct local access to regulatory expertise across the European Union, United Kingdom, and Switzerland.
United Kingdom
EUMEDIQ Ltd.
View Profile
GB-London N4 3FU
View Profile
+ 44 20 4551 8648
View Profile
European Union
EUMEDIQ GmbH
View Profile
DE-78739 Hardt
View Profile
+ 49 69 5060 77220
View Profile
Switzerland
EUMEDIQ AG
View Profile
CH-6300 Zug
View Profile
+ 41 41 562 7086
View Profile
Report a medical device complaint or safety concern
EUMEDIQ is required to maintain a medical device complaint register as part of its Authorised Representative mandate.
Use this form to report a complaint or safety concern related to a medical device for which EUMEDIQ acts as Authorised Representative/Responsible Person.
Stay informed to stay compliant in MedTech
Subscribe to the EUMEDIQ newsletter for regular regulatory updates, compliance guidance, and expert analysis covering MDR, IVDR, cybersecurity obligations, and the latest developments affecting medical device manufacturers across global markets.