Food and Drug Administration
Peter J. Yang, PhD is the De Novo Program Lead in the Office of Regulatory Programs in the Office of Product Evaluation and Quality (OPEQ) in the Center for Devices and Radiological Health (CDRH). Dr. Yang facilitates regulatory oversight and consistency and provides programmatic support for De Novo classification requests across the Center. He joined CDRH in 2014 as a biomedical engineer and reviewer in the Plastic and Reconstructive Surgery Devices Branch 2 in the Division of Surgical Devices. Peter received his bachelor’s degree in bioengineering from Rice University and his Ph.D. in bioengineering from Georgia Tech.
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Monday, September 12, 2022
3:30 PM – 4:30 PM MST