Suzanne Goodman is the Vice President of Regulatory and Quality at Anumana, bringing over 25 years of experience to the team and leveraging a bachelor’s degree in biomedical engineering from Duke University. She has supported a broad range of organizations (large and small medical device manufacturers, FDA, CROs, and consulting firms) with a wide range of medical devices and pharmaceutical development tools. She specializes in startup environments creating software-as-a-medical device (SaMD) and software-controlled electrical-mechanical devices.
Suzanne joined Anumana and nference in May 2022 with the goal of fully developing the Quality and Regulatory teams and Quality Management System to support design and development of world-class, globally-marketed medical devices.
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