Nada Hanafi

Nada advises the company on regulatory strategy and assists the CEO as she prepares for FDA submissions. She also serves as Senior Vice President of Regulatory Strategy at Veranex where she oversees the regulatory team by supporting clients with setting strategic direction, evidence pipeline, and all aspects of design, development, commercial distribution of devices, and postmarket compliance to ensure products remain safe and effective while on the market. A results-oriented executive with over 20 years of experience advising CEOs and Founders in the MedTech and life-sciences industry. Hanafi spent over 12.5 years at FDA’s Center for Devices and Radiological Health (CDRH) working on a range of products from breast implants to neurological devices, and co-founded the CDRH Health of Women Program. Nada holds an MSc. in Biomaterials and a BEng in Biomedical Materials Science & Engineering from Queen Mary College, University of London. She earned an MPH from Johns Hopkins Bloomberg School of Public Health. Nada is a Certified Quality Improvement Associate and a Certified Quality Auditor from the American Society for Quality.