LaVonne Lang, DrPH

Senior Director, Regulatory Affairs

LaVonne Lang, DrPH, serves as a senior strategist, providing a full range of regulatory services to pharmaceutical and biotechnology clients, including cradle-to-grave strategic planning, managing submission and liaison activities with the FDA, and helping clients prepare for health authority meetings.

With 18 years of experience in pharmaceutical development, including 12 years in positions of increasing responsibility in regulatory strategy at Parke-Davis and Pfizer, Dr. Lang has assisted in the development of more than 20 product candidates in varying stages of development ranging from exploratory to post-marketing line extensions, including successful NDA submissions.

The Regulatory Lead for gene transfer products with Parke-Davis and dermatologic drugs at Pfizer, she also has therapeutic expertise in cardiovascular and inflammation.

A licensed registered nurse, Dr. Lang holds an MPH in Environmental and Industrial Health (subspecialty: Toxicology) and a Doctorate in Public Health Policy from the University of Michigan.

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