JESSIKA TUAZON is an Associate in the Health Care and Life Sciences practice, in the Los Angeles office of Epstein Becker Green. Her practice focuses on drug and device, food, and life sciences law.
Ms. Tuazon’s experience includes:
Counseling clients on compliance and regulatory issues involving over-the-counter and homeopathic drugs, devices for human and veterinary use, food products, dietary supplements, and cosmetics
Preparing medical device premarket submissions, including identifying predicate devices, developing intended uses and claims, and ensuring compliance with U.S. Food and Drug Administration (FDA) guidance and requirements
Providing clients risk-based assessments of viable marketing pathways based on their business strategies and marketing priorities, as well as the product’s regulatory classification, intended uses, claims, and technology
Advising clients on issues pertaining to premarket clearance and approval for products regulated by FDA, as well as the associated risks and implications on business operations, product development, labeling, and advertising
Articles in the National Law Review database by Jessika Tuazon