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Life Sciences Co-Chair Discusses Drug & Medical Device Good Manufacturing Practices on Food and Drug Law Institute Panel

Ropes & Gray partner Gregory Levine (Washington, D.C.), co-chair of the firm’s life sciences practice, discussed drug and medical device good manufacturing practices at the Food and Drug Law Institute’s Enforcement, Litigation & Compliance conference on Dec. 9 in Washington, D.C. Mr. Levine addressed trends in recent regulatory agency warning letters and investigations along with device and pharmaceutical quality metrics programs. 

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