Mary Dadone, Ph.D.

Has nearly 30 years of global medical device regulatory and quality experience with a proven track record in bringing new products to market and building certified quality systems for organizations. She has worked both in-company and as a consultant to a wide range of medical device companies — innovative start-ups to well-established Fortune 500 corporations. Her expertise encompasses not only regulatory affairs and quality assurance but also biostatistics, technical training, and program management. Dr. Dadone holds a PhD in biological sciences from the University of New Mexico. Additionally, she was a post-doctoral fellow and a research faculty member at the University of Utah School of Medicine.

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