Ti brings her understanding of Biomedical Engineering to the Regulatory Arena.
Ti has nearly 10 years of experience in medical device quality assurance and regulatory affairs. She began her career as one of six employees at medical device startup designing products for the radiologic and ophthalmic spaces. Since then, Ti has developed a proven track record of successful quality management system implementations, quality audits and regulatory submissions for Class II medical devices. She is passionate about improving patient outcomes, and her biomedical and ISO 13485:2016 auditor certifications allow her to help small and midsize companies bring safe and compliant products to market. Ti graduated from the University of Arizona with her B.S. in Biomedical Engineering with an emphasis in biomaterialsView Other Speakers