Lisa Pray is the Director of Regulatory Affairs at Philips, where they currently manage regulatory strategies for ultrasound products. They have held various positions in regulatory and clinical affairs at companies such as Nonin Medical, Inc., Candela Medical, and Merz North America. In their earlier career, Lisa gained experience as an Engineering Intern at Terumo Cardiovascular and served as a Sr. Human Research Review Analyst at The University of New Mexico Health Sciences Center. Lisa continues to pursue a BA in Public Affairs at Michigan State University.
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