Gloria Nyankima, PhD, is a Senior Policy Analyst with expertise in the regulation of medical devices and digital health policy. Previously, they served as a Lead Reviewer at the U.S. Food and Drug Administration (FDA) and have five years of experience in enhancing FDA’s digital health initiatives. Gloria's educational background includes a PhD in Bioengineering and Biomedical Engineering from North Carolina State University, where they conducted significant research on ultrasound technologies. Currently, they lead efforts in policy development and implementation, ensuring safe and effective medical products for patients.
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