Nada joined Experien Group in 2017 after working 12 years at FDA’s Center for Devices & Radiological Health (CDRH). Since 2010, she was a CDRH Senior Science Health Advisor, serving as an expert consultant in the Center Director’s office. Nada combines her deep institutional knowledge with innovative approaches to help companies successfully communicate product information to FDA throughout the total product life cycle. Leveraging her years of reviewer experience and broad FDA exposure, she develops actionable premarket strategies to guide programs through successful submission. While at FDA, Nada led postmarket investigations and she applies this knowledge to help companies effectively manage postmarket requirements. Nada holds an MS in Biomaterials & a BE in Biomedical Materials Science & Engineering from Queen Mary College, Univ of London. She earned her MPH from Johns Hopkins Bloomberg School of Public Health and holds certifications from the American Society for Quality (ASQ).