Webcast: Food and Drug Administration Developments: Key Updates and Compliance
Webcasts | October 22, 2025
Join our lawyers for a recorded in-depth discussion of recent developments at the U.S. Food and Drug Administration, including the FDA’s crackdown on direct-to-consumer drug advertising and the impact of the Make America Healthy Again initiative, and their implications for the food, drug, device, and cosmetics industries. Our panel of attorneys provide practical insights and strategies for navigating emerging FDA policy, as well as regulatory and enforcement trends.
MCLE CREDIT INFORMATION:
This program has been approved for credit in accordance with the requirements of the New York State Continuing Legal Education Board for a maximum of 1.5 credit hours, of which 1.5 credit hours may be applied toward the areas of professional practice requirement. This course is approved for transitional/non-transitional credit.
Gibson, Dunn & Crutcher LLP certifies that this activity has been approved for MCLE credit by the State Bar of California in the amount of 1.5 hours.
Gibson, Dunn & Crutcher LLP is authorized by the Solicitors Regulation Authority to provide in-house CPD training. This program is approved for CPD credit in the amount of 1.5 hours. Regulated by the Solicitors Regulation Authority (Number 324652).
Neither the Connecticut Judicial Branch nor the Commission on Minimum Continuing Legal Education approve or accredit CLE providers or activities. It is the opinion of this provider that this activity qualifies for up to 1.5 hours toward your annual CLE requirement in Connecticut, including 0 hour(s) of ethics/professionalism.
Application for approval is pending with the Colorado, Illinois, Texas, Virginia, and Washington State Bars.
PANELISTS:
Jonathan Phillips is a partner in Gibson Dunn’s Washington, D.C. office and co-chairs the firm’s FDA & Health Care Practice. His practice centers on FDA and health care enforcement, compliance, and litigation — including False Claims Act, Anti-Kickback, and regulatory defense work for pharmaceutical, medical device, and health-services clients. Prior to joining Gibson Dunn Jonathan served as a Trial Attorney in the Civil Division, Fraud Section of the U.S. Department of Justice where his work included handling a variety of health care enforcement cases.
Gustav Eyler is a partner in Gibson Dunn’s Washington, D.C. office and co-chairs the firm’s FDA & Health Care and Consumer Protection Practice Groups. Leveraging years of experience as Director of the U.S. DOJ Consumer Protection Branch — where he led enforcement actions involving drugs, medical devices, food, deceptive marketing, and public health statutes — he defends clients in government investigations and counsels on the design and implementation of compliance programs.
Katlin McKelvie is a partner in Gibson Dunn’s Washington, D.C. office and co-chairs the firm’s FDA & Health Care Practice. With over twenty years of experience in food and drug law, including as Deputy General Counsel at the Department of Health and Human Services (HHS), senior staff on the Senate HELP Committee, and various roles at FDA, she advises clients on regulatory, enforcement, legislative, and compliance strategies across FDA-regulated product categories.
John Partridge is a partner in Gibson Dunn’s Washington, D.C. office and co-chairs the firm’s FDA & Health Care Practice. He specializes in white-collar defense, government and internal investigations, and complex litigation for life sciences and health care clients and brings deep experience defending corporations in enforcement actions under the False Claims Act, Anti-Kickback Statute, FCPA, and the Federal Food, Drug, and Cosmetic Act.
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