VP Quality, Regulatory and Clinical Affairs
Gerry Tal is an expert with more than 20 years of experience in the field of research and design, quality, clinical and regulatory affairs of medical devices. Mr. Tal has been involved in and managed all aspects of medical devices R&D, including engineering, product design and manufacturing, documentation, quality control, budget, personnel recruitment, compliance and regulations. Mr. Tal completed his Bachelor of Science at the Technion Israel Institute of Technology and has an MBA in Marketing from Tel Aviv University. Mr. Tal is also a certified CRA and completed an ISO:13485 auditor’s course at the Standards Institution of Israel.