Simha Martine Sibony is a highly experienced professional in regulatory affairs and quality assurance within the medical device sector, currently serving as the Owner and Global RA/QA Consultant at GMRE since July 2020. In addition to co-founding M.M.A.Tech Ltd. in 2000, Simha has played a pivotal role in developing MP-1™, a biocompatible polyimide biomaterial for various orthopedic implants, showcasing superior mechanical properties and biocompatibility. Previously, Simha held positions such as Global RA/QA Director at Noris Medical and Senior Regulatory Affairs Consultant at Emergo, providing extensive consulting services across multiple regulatory frameworks including FDA, CE, and ISO standards. Academic background includes a Master of Science in Biomedical Engineering and a Bachelor of Science in Chemical Engineering from the Technion - Israel Institute of Technology, alongside specialized training in EU MDR implementation.
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