VP Regulatory and Clinical Affairs
Gerry Tal is an expert with over 20 years of experience in the fields of research and development, quality, clinical and regulatory affairs of medical devices. Mr. Tal has been involved in and managed all aspects of the Research and Development of medical devices, including engineering, product design and manufacturing, documentation, quality control, budget, personnel recruitment, compliance and regulations.
Since 2012 Mr. Tal has been a consultant for medical devices and in-vitro diagnostics companies for QA, RA and product development. He has led external audits and the implementation of corrective actions, prepared regulatory submissions for the CE, FDA, Israel MOH, Health Canada, performed internal audits and supplier audits and much more.
Mr. Tal completed his Bachelor of Science at the Technion (Israel Institute of Technology) with honors and has an MBA in Marketing from Tel Aviv University. Mr. Tal is also a certified Clinical Research Associate (CRA) and completed an ISO:13485 auditor’s course at the Standards Institution of Israel.