Ethan Naylor is a Vice President of Regulatory Affairs at MCRA, an IQVIA business, responsible for developing regulatory strategies for medical device submissions and compliance. With over thirteen years of experience in medical device regulation and a strong background in biomedical engineering, they previously held leadership roles at the FDA, managing teams and reviewing complex spinal device submissions. Ethan's diverse experience spans clinical, pharmaceutical, and academic settings, marked by significant contributions to research and product launches in the orthopedic space. They hold a Master's degree in Biomedical Engineering from The Johns Hopkins University School of Medicine and a Bachelor’s degree in Biochemistry from Indiana Wesleyan University.
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