Kellie Ann Moore, Esq, is a practical business savvy attorney with over 19 years of experience providing legal counsel to pharmaceutical, biologic and medical device organizations for compliant conduct in conformance with FDA and international regulations.
Moore thrives on helping organizations strategically (and contractually) drive their FDA-regulated products and R&D services forward. By mapping contractual relationships and identifying regulatory risk mitigation strategies proactively, Moore utilizes her unique role as an FDA-Regulatory lawyer to expedite product lifecycle events and the achievement of corporate goals.
After Graduating from University of Southern California in 1992, Moore began her regulatory career developing Biologics at AMGEN. Later, she earned her Juris Doctor Degree from Loyola Law School. Better known to USC’s students as “Professor Moore,” she has been teaching MPTX 516, “Medical Products and the Law” for the USC Regulatory Science Program since 2001. Professor Moore currently performs legal, regulatory and contract consulting services for a range of pharmaceutical and medical device clients. BioMedLegal@gmail.com