Ayse holds a M.S. in Biomedical Engineering from the University of Florida and has over four years of experience in the medical device and regulatory industries. Ayse began her career in medical device development and quality control developing 21 CFR 820 and ISO 13485 compliant quality systems, performing internal quality audits, responding to FDA objections, and developing medical devices. Her expertise and passion for quality management systems are an invaluable asset to the team.