Moria Zigman

Moria Zigman is a Regulatory Affairs Specialist at TytoCare, where they ensure compliance for multi-disciplinary medical device systems that integrate hardware and software. With over a decade of experience, Moria has facilitated global regulatory approvals, including FDA submissions and EU MDR documentation. Previously, Moria held various roles, including Senior Regulatory Affairs Officer at Keeler Ltd, and has expertise in navigating complex international regulations, technical documentation, and submission management. Moria earned a B.Sc. in Pharmaceutical Chemistry from Bar-Ilan University.