Hina M. Pinto currently serves as an Acting Team Lead in the Regulations, Policy and Guidance Staff in the Office of Product Evaluation and Quality (OPEQ) at FDA’s Center for Devices and Radiological Health (CDRH).  In this role, Hina is involved in a range of regulatory and scientific issues and decisions in OPEQ, including development and implementation of product-specific and cross-cutting policies for device regulation. Most recently, Hina has been involved in the review and policy oversight for numerous emergency use authorizations of medical devices during the COVID-19 pandemic.

Hina Pinto received her B.S. in Applied Science (Biomedical Materials Science Track) from the University of North Carolina-Chapel Hill and M.S.E. in Biomedical Engineering from Tulane University. Join us for a conversation with Hina to learn about her path and current role at the FDA.

This event is sponsored by Honors Carolina. Register on the Go Anywhere Platform.