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Pharmaceutical and medical device manufacturers encounter numerous risks which, if not handled properly, could lead to litigation. Risks include the challenges of properly marketing products, complying with numerous regulations and emerging adverse events. Mass tort litigation, and challenges based on the False Claims Act and the Antikickback Statute among others, pose perpetual risks along with handling the erosion of time tested defenses such as the learned intermediary doctrine. With an ever-shifting tide, it is important to stay current on these topics. Register now to learn from top attorneys whose focus is watching for and defending against these risks.
Who Should Attend
What You Will Learn
Samuel J. Abate, Jr. is a partner in Pepper Hamilton’s New York office. Mr. Abate focuses his practice in civil litigation, with an emphasis on the defense of pharmaceutical and medical device companies in complex litigation involving marketed products and medical devices. He also advises clients on issues relating to electronic discovery.
Mark C. Hegarty is a partner in the firm’s Kansas City office. His practice is focused on nationwide complex litigation, including the defense of pharmaceutical and medical device manufacturers. Mr. Hegarty has spoken on numerous occasions regarding various litigation topics, including at DRI’s Drug and Medical Device’s Annual Seminar.
Allison M. Brown is a partner in Weil, Gotshal & Manges’ Princeton office. Ms. Brown has extensive experience in complex litigation, including commercial, environmental, pharmaceutical product liability, and mass tort actions. She also served as trial counsel in a high-profile antitrust case to block a multi-billion dollar merger between two companies.
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