Elizabeth Richards

Practice Areas

Advises clients in all facets of U.S. Food and Drug Administration (FDA) oversight and regulation. Regularly counsels clients in the pharmaceutical, medical device, digital health, food, dietary supplement, cosmetic, and other biotechnology industries in navigating regulatory, compliance, transactional, and legislative matters. Also counsels clients on matters involving regulation by the Drug Enforcement Administration (DEA).

Career

She currently serves as a member of the Food and Drug Law Institute’s Medical Products Committee and Digital Health Planning Committee and is an inaugural member of her firm’s Digital Health Steering Committee.

Ms. Richards regularly writes and speaks on technical FDA regulatory and enforcement matters.

Professional Memberships

Member, District of Columbia Bar, Maryland Bar

Personal

JD, Georgetown University Law Center, 2008 cum laude, MPH, Johns Hopkins Bloomberg School of Public Health, 2008 AB, Georgetown University, 2004 summa cum laude