MDR team leader at Eurofins | Li-Med RA & QA Experts - Petah Tikva, Center District, Israel
Since 2007 Li-Med has been working with both domestic and internationalcustomers to formulate and execute successful regulatory activities and qualityassurance, exclusively serving the medical device industry. Our dedicatedexperts are focused on producing the most meaningful, comprehensive, andsubmission-ready compilation of non-clinical data, to ensure compliance withregulation and approval for marketing and clinical trials. As global regulatoryrequirements keep evolving, our experts are fully updated in all changes and arein constant contact with notified bodies representatives and competent authoritiesto pave the appropriate path to market success. On top of that we support ourclients in their endeavors to provide evidence that meets regulatory standardsby liaising with several prominent laboratories.Expertise