Director of Clinical Regulatory & Quality

Lisa uses her 17 years of regulatory experience to assist BRIGHT clients in the development and execution of thoughtful, creative, and efficient regulatory strategies and market authorization applications. She has worked at small and large medical device companies with urology, cardiovascular, and biologic products regulated under all classifications and worldwide regulations and guidance. She approaches the nuances of the ever-evolving regulatory atmosphere with patience, keen attention to detail, and a direct communication style. Lisa earned her Bachelor of Science degree in biomedical engineering from Marquette University in Milwaukee, WI, and maintains her Regulatory Affairs Certification (RAC) credentials. Outside of work, Lisa enjoys biking, yoga, traveling, and reading. Additionally, she and her husband tackle home and garden projects and keep their three energetic boys engaged in various sport, science, and outdoor activities. They also enjoy a good family movie night.