Tony Championsmith
Regulatory Affairs
Tony Championsmith has over 25 years of experience working within the biotechnology pharmaceutical industry. He has 17 plus years in Regulatory Affairs working with major companies such as Dendreon, Genentech, Chiron, SmithKline, and Cell Genesys. His regulatory experience encompasses early and late stage drug development strategies, promotional and advertising, due-diligence, and major regulatory filings. While Director of Regulatory Affairs at Dendreon, he was successful in filing an electronic Biologics License Application for a cancer immunotherapy drug, Provenge. In addition, other regulatory submissions include products such as conjugate vaccines, recombinant proteins, monoclonal antibodies, and gene therapy products. Tony holds a BS in Biochemistry from the University of California Riverside.
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