Christine Michel Lentz
Associate @DLA Piper
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WORK HISTORY
Associate @DLA Piper
San Diego, CA, US
Practice focused on FDA regulatory compliance, counseling clients that develop and commercialize FDA-regulated products, including drugs, biologics, medical devices, diagnostics, and digital health. Experience navigating complex requirements at the intersection of FDA law, including issues that impact products and services regulated by FTC, DEA, CMS, USDA, TTB, CPSC, and state licensing authorities.
EDUCATION
SKEMA Business School
Master’s Degree, MS, Management - International Sales & Marketing
University of San Diego School of Law
Doctor of Law - JD, Concentrations in Business & Corporate Law and in IP & Technology Law
University of California, Davis
B.S., A.B., Cell Biology, French
SKILLS
ABOUT CHRISTINE MICHEL LENTZ
As an Associate in DLA Piper\'s FDA Regulatory Practice, I provide strategic business and regulatory advice to medical product companies, including pharma, biologics, diagnostics, medical devices, and wellness apps, on complex issues related to clinical research, manufacturing, advertising and promotion, post-market safety, and compliance. I also serve as a resource for DLA colleagues in other practices by responding to questions on regulatory issues that arise in the course of our clients\' business operations, as well as in transactions and disputes involving products and services regulated by various federal and state licensing authorities. Prior to practicing law, I worked for a preclinical contract research organization (CRO) in France where I was responsible for advertising and promotion of our molecular analysis services and software product, as well as drafting and negotiating project agreements for international clients. I also spent several years in the patent and intellectual property research and analytics space, supporting research-based organizations in IP and regulatory operations and strategy.
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