About Keke Feng
Keke Feng has over a decade of experience helping people harmed by pharmaceutical products and medical devices. She combines legal advocacy with practical knowledge of how drug companies operate.
Before focusing on patient cases, she worked in-house on drug licensing, compliance, manufacturing agreements, and product launch strategy in the United States and Asia-Pacific.
She later represented clients in federal litigation, including multidistrict litigation (MDL) and mass tort cases. Her work includes building evidence, coordinating experts, and handling negotiations.
Keke is fluent in English and Mandarin and focuses on clear communication so clients understand what is happening and what comes next.