Mike Preto

Mike Preto is a strategic leader in Regulatory Affairs for medical devices, with extensive experience in global regulatory compliance. They began their career at Intertek as a Safety Team Leader, overseeing engineering projects and supporting regulatory inspections. At GE Healthcare, they served as Regulatory Affairs Leader, successfully delivering multiple 510(k) submissions and leading product safety initiatives. Currently, as Regulatory Affairs Program Director at Philips, Mike formulates long-range regulatory strategies and directs compliance programs for a wide range of medical devices. They hold a Bachelor of Science in Electrical Engineering from Ohio University.