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Kelly S. Crawford, Riker Danzig co-chair and head of the Firm’s Products Liability and Mass Tort Practice Group, will be speaking at the New Jersey State Bar Association's Product Liability Forum on December 3, 2026 at the New Jersey Law Center in New Brunswick, NJ. She will participate in two back-to-back panels beginning at 12:55 P.M. On the Medical Devices panel, she and her fellow panelist will examine FDA approval and 510(k) clearance, manufacturing and design defects, and failure-to-warn claims, including issues surrounding physician training, sales representative advice, and explant preservation. At 1:30 P.M., she will join the Pharmaceutical Drugs panel, which will address labeling and failure-to-warn, federal preemption, the learned intermediary doctrine, and the admissibility of expert testimony post-Accutane.
For more information and to register, click here.
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