Eurofins Li-Med has been working with both domestic and international customers to formulate and execute successful regulatory activities and quality assurance, exclusively serving the medical device industry. Our dedicated experts are focused on producing the most meaningful, comprehensive, and submission-ready compilation of non-clinical data, to ensure compliance with regulation and approval for marketing and clinical trials. As global regulatory requirements keep evolving, our experts are fully updated in all changes and are in constant contact with notified bodies representatives and competent authorities to pave the appropriate path to market success. On top of that we support our clients in their endeavors to provide evidence that meets regulatory standards by liaising with several prominent laboratories. Expertise