About

Dr. Mirit Dekel-Dahan has over 12 years of experience in the field of medical device technology. Her experience encompasses a broad range of technologies, therapies, and indications. Dr. Mirit Dekel-Dahan gained local and global expertise in the development and management of clinical projects at all stages- from idea, proof of concept to post marketing. From her Post-doctoral fellow in Neurobiology as an electrophysiologist at the prestigious Weizmann Institute of Science, to work in the pharmaceutical industry with Teva, Dr. Dekel-Dahan progressed to hold senior regulatory and clinical management positions at leading innovative medical device start-up companies. Ultimately founding her own company, CSC, as a provider of regulatory and clinical strategic planning and product development services for the medical device industry. Today Mirit is recognized as an expert in clinical development of medical devices and their representation to the regulatory authorities as well as a BSI certified ISO 13485 Lead Auditor. Mirit`s career is at the focal point of science, technology, regulation, and healthcare. Her unique scientific, technical, data background and training makes her the perfect candidate to help companies with cutting-edge technologies navigate and optimize their regulatory approval process within different markets and for diverse end users. Mirit focuses on regulation of innovative products in treatment and diagnostics in many fields – CNS, oncology, neuropsychology, cardiology and biologics. Mirit also has substantial experience characterizing and analyzing medical big-data and has been at the forefront of several of the most recent approvals of innovative AI based medical devices.