Alicia has extensive experience litigating and prosecuting biologics, biotechnology, bioinformatics and pharmaceutical patents. She has a B.S. in Biology and Chemistry, and an M.S. in Biomedical Sciences. Alicia has published original papers in Science, Nature, Cell and the Proceedings of the National Academia of Sciences.
Information contained in the Venable BiologicsHQ database relates to FDA-approved drug products listed in the CDER Purple Book or on the FDA website (www.fda.gov). Information relating to FDA licensed products, FDA-approved indications, and aBLA and 505(b)(2) applications is obtained from public sources including the U.S. FDA website (www.fda.gov). Information relating to litigations is given only for cases active from January 31, 2010 onward. Information relating to foreign biosimilar / biologics follow-on products approved in Australia, Canada, the E.U., Japan and South Korea is from public sources. Statistics graphics are compiled from information contained in the Venable BiologicsHQ database.
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