EUMEDIQ brings regulatory clarity to international MedTech manufacturers at every stage of the device lifecycle.
Legal representation across the EU, UK, and Switzerland under MDR, IVDR, UKCA, and Swissmedic frameworks.
Regulatory strategy, documentation, clinical evaluation, and post-market surveillance across the full device lifecycle.
Certified lead auditors for management systems in the MedTech industry to ISO 13485, MDSAP and ISO 27001.
Swiss importer services under MedDO and IvDO, including swissdamed registration and Swissmedic coordination.
Validation and verification support for computerised systems and software-driven devices, aligned with GAMP 5 and MDR.
Knowledge
Regulatory clarity begins here
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