FDA Expert Panels
FDA Expert Panels are roundtable discussions with independent panels of scientific experts that will review the latest scientific evidence, evaluate potential health risks, explore safer alternatives, and individual experts may offer their recommendations for regulatory action. This initiative is part of the FDA’s broader efforts to apply rigorous, evidence-based standards to ingredient safety and modernize regulatory oversight, thoroughly considering evolving science and consumer health.
The public and media will be invited to attend and listen to each event and the sessions will be livestreamed.
Upcoming Events
Below is a list of upcoming events. If you have questions, please email publicengagement@fda.hhs.gov.
Date: Monday, October 6, 2025
Time: 10 a.m. - noon
Location: FDA White Oak Campus, 10903 New Hampshire Ave., Bldg. 31, Great Room Section A, Silver Spring, MD 20993-0002. There will be limited seating for the public.
Registration: Registration is only required for in-person listen-in attendance. Space is limited. Please plan to arrive at least 30 minutes prior to the start time to be checked in. The public will also have the option to view through a live webcast on the FDA YouTube Channel.
Click here for more information about this event.
Previous Events
- FDA Expert Panel on Selective Serotonin Reuptake Inhibitors (SSRIs) and Pregnancy
- FDA Expert Panel on Menopause and Hormone Replacement Therapy for Women
- FDA Expert Panel on Infant Formula
- FDA Expert Panel on Talc