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As ISTA's vice president of regulatory affairs quality and compliance Mr. Garrett works directly with the U.S. Food and Drug Administration (FDA) as well as regulatory authorities of various foreign ministries of health to steer ISTA's products along the path to commercialization. In this role Mr. Garrett oversees all of ISTA's regulatory activities and assures adequate compliance and product quality as it pertains to the company's pre-clinical and clinical research and manufacturing practices. Mr. Garrett has more than 25 years of professional experience in the field of regulatory affairs clinical development and quality. | 