Ashley V. Saba is an associate in Venable’s Washington, DC office. As a member of the firm’s Regulatory Practice, she advises clients on a variety of FDA and FTC regulatory matters, including advertising practices, manufacturing compliance, safety issues, labeling compliance, and other enforcement matters.
Her practice covers medical devices, food, cosmetic products, dietary supplements, pharmaceuticals, generic and over-the-counter drugs, and other consumer products and services.
Prior to joining Venable, Ashley worked in the Office of Compliance, Center for Drug Evaluation and Research (CDER) at the FDA. While at CDER, she provided regulatory counsel support on policy initiatives, rulemakings, legislative proposals, and enforcement actions.
Her compliance work in particular focused on good clinical practice, post-market safety reporting, Risk Evaluation and Mitigation Strategies, and other post-marketing requirements. Before joining CDER, Ashley served as a regulatory counsel in FDA’s Office of Compliance and Enforcement, Center for Tobacco Products.
Experience : Regulatory Counsel, U.S. Food and Drug Administration
J.D. cum laude University of Maryland School of Law 2011