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Gerry Tal Quality and Regulation

Gerry Tal

VP Quality, Regulatory and Clinical Affairs

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Gerry Tal is an expert with more than 20 years of experience in the 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 his MBA in marketing at Tel Aviv University. Mr. Tal is also a certified CRA and completed ISO:13485 auditor’s course at the Israel Institute of Standards.

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