About me
Linda C. Akunne is a Chief, Project Management Staff in the Division of Regulatory Operations for Infection Diseases in CDER's Office of New Drugs. In this role, Linda provides technical direction, oversight, and leadership to the DROID staff on the drug review process for antiviral products from pre-clinical to withdrawal from market. Prior to joining the FDA, Linda was a Research Associate at the Forum for Collaborative Research, where she worked on several infectious disease research projects and initiatives. She received her graduate training in health policy from the George Washington University School of Public Health and Health Services and her B.S. in Biobehavioral Health at the Pennsylvania State University.
