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Jessica Greenbaum is counsel in King & Spalding’s Washington, D.C. office and a member of the firm’s FDA and Life Sciences practice.
Prior to joining King & Spalding, Jessica served as a Regulatory Counsel in FDA’s Office of Therapeutic Biologics and Biosimilars. In that position, Jessica developed and implemented regulatory policy related to biosimilars and other therapeutic biological products, including with respect to combination products, biosimilar labeling, reference product exclusivity, the Purple Book, and the review and approval of biologics license applications. Previously, Jessica was an Associate Chief Counsel in FDA’s Office of the Chief Counsel, where her portfolio included issues related to drugs (both originator and follow-on) and tobacco products. Before joining FDA, Jessica was a litigator at Gibson, Dunn & Crutcher LLP handling patent litigation disputes relating to pharmaceutical and biotechnology products.
J.D., New York University School of Law
B.S., Brown University
District of Columbia
New York
September 15, 2023
Approval Regs Must Change To Keep Up With Biologics Tech
September 15, 2023
Approval Regs Must Change To Keep Up With Biologics Tech
J.D., New York University School of Law
B.S., Brown University
District of Columbia
New York