Supervisory Regulatory Health Project Manager
Food and Drug Administration
CDR Hong Vu is a Commisisoned Corps Officer and a Supervisory Regulatory Health Project Manager in the Division of Clinical Trials Quality within the Office of Medical Policy in FDA Center for Drug Evaluation and Research (CDER). She has over 13 years of experience in FDA with expertise in policy and guidance generation as well as new drug development. Prior to her current position, she was a Team Leader in the Division of Gastroenterology for Inborn Errors Products within the Office of New Drugs (OND) managing new drug applications for inborn errors of metabolism. She started her career in OND as a Regulatory Research Officer in the CDER Rare Diseases Program performing regulatory research and developing rare disease-specific training and education. She developed an interest in pharmaceutical regulation and policy development during her internship at the FDA while on a full scholarship training via the FDA/CDER Academic Collaboration Program with the University of Florida. She received her Master of Science with specialization in pharmacoepidemiology from the University of Florida and Pharm.D. from Palm Beach Atlantic University.
Disclosure(s): No financial relationships to disclose
Workplace Well-Being: An FDA Perspective
Friday, March 22, 2024
3:00 PM – 3:30 PM East Coast USA Time