Lisa Pray possesses extensive experience in regulatory affairs and clinical management within the medical device and healthcare industries. Notably, Lisa has held key positions such as Sr. Manager of Regulatory, Clinical and Design Assurance at Nonin Medical, Inc., and Director of Regulatory Affairs at both Candela Medical and currently at Philips. Previous roles include regulatory positions at Merz North America and Terumo Cardiovascular, as well as a senior analyst position in human research review at The University of New Mexico Health Sciences Center. Lisa Pray holds a Bachelor of Arts degree from Michigan State University, specifically from the James Madison College of Public Affairs.
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