Ruth K. Miller, JD PDA

Ruth K. Miller is the Director of Regulatory Affairs for PDA. She manages the activities of PDA’s Regulatory and Quality Advisory Board, leading the team in shaping regulatory and policy documents globally. She is PDA’s primary point of communication with regulatory and policy bodies around the world.

Before joining PDA, Ruth served in legal and regulatory roles covering the entire scope of the pharmaceutical supply chain. She was the Senior Director of Regulatory Affairs for a drug wholesaler trade association, working to impact U.S. federal and state regulations relating to the safe movement of pharmaceuticals, foods, and medical devices. She also has served as a regulatory and administrative law attorney in the U.S. Drug Enforcement Administration (DEA) Office of Chief Counsel; as Senior Counsel for the U.S. Pharmacopeia; and as an Associate in the food and drug practice of Covington & Burling, LLP, in the law firm’s Washington and London offices.

Ruth holds a BA from The College of William and Mary in Virginia and a JD magna cum laude from the Boston University School of Law, where she was Executive Editor of the American Journal of Law and Medicine.