Law360, New York (May 23, 2012, 4:00 PM EDT) -- Areta L. Kupchyk is a partner in Nixon Peabody LLP's Washington, D.C., office who provides counsel to clients on the U.S. Food and Drug Administration regulation of drug, medical device, biotechnology and biologic products. She is the leader of the firm's FDA regulatory practice.
Q: What is the most challenging case you have worked on and what made it challenging?
A: Shortly after I started practicing in the FDA’s Office of the Chief Counsel in 1993, I was assigned a case against a drug manufacturer for...
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