Gina Q. is a Regulatory Affairs Manager and Clinical Operations Lead at Philips, where they focus on clinical compliance and regulatory development for medical devices. They hold a Master’s Degree in Bioengineering and Biomedical Engineering from The University of Texas at Dallas and a Master's degree in Polymer Science from the University of Massachusetts Lowell. Gina is regulatory affairs certified and possesses extensive knowledge in European regulations, risk management, and clinical research related to medical implants.
Location
Dallas, United States
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