The second edition of the International Comparative Legal Guide: Drug & Medical Device Litigation, co-authored by Alan E. Rothman, Daniel A. Spira, Anna-Shari Melin, and Sidley alumna Teri H. Peeples is now available. The chapter entitled, “Challenges for ex-U.S. Entities Confronting the U.S. Regulatory and Tort Labyrinth” covers personal jurisdiction over ex-U.S. entities, other preliminary forum-related considerations, discovery outside of the U.S., critical and dispositive motions, trial, and appeal, enforcement of judgments, and regulatory implications for litigation. This full chapter from the international guide can be viewed below, along with a separate U.S. chapter by the same co-authors featuring a Q&A on regulatory framework, manufacturing, transactions, advertising, promotion and sales, data privacy, clinical trials and compassionate use programs, product recalls, and litigation and dispute resolutions.
International Comparative Legal Guide: Drug & Medical Device Litigation 2021
April 23, 2021
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