Eurofins Medical Device Testing France provides medical device consuilting and testing services.

With over 40 years of expertise, Eurofins Medical Device Services offers comprehensive solutions across the entire medical device lifecycle. Through our global network of regulatory and toxicology experts, laboratories, and sterile packaging sites in Europe, North America, and Asia Pacific, we help manufacturers achieve compliance and market readiness.

Our Medical Device Consulting Business Unit supports manufacturers in meeting regulatory requirements, implementing quality management systems and preparing for audits. From product approval to MDR and ISO compliance to post-market activities, we reliably guide you through all regulatory processes.

Our Medical Device Testing Business Unit performs testing in accordance with international standards, including biocompatibility, chemical characterisation, sterility and packaging validation tests to ensure the safety and compliance of your products.