Rina Lev, PhD

Dr. Rina Lev is a scientific regulatory and clinical affairs consultant with over twenty years of experience in the medical device industry. During this time, Rina has led multidisciplinary projects in the clinical, regulatory, and QA field that included among others, preparation of clinical and regulatory strategies (IL, EU, US, China), clinical evaluation reports (EU), management of clinical trials activities worldwide, risk management activities, biological safety assessment and quality system management (quality planning, CAPA). Rina has a broad scientific background, she holds a M.Sc., in Clinical Biochemistry from Tel Aviv University and a Ph.D. in Clinical Neurophysiology from the Faculty of Medicine from the Technion, where she published her scientific work.

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