Significant Drug & Device Developments of 2025

As we welcome the new year, it is time to reflect on some of the most significant legal developments in the drug and device space in 2025.

1. Navigating a New Skepticism in Science

Not long ago, the average American likely could not name the U.S. secretary of health and human services. Yet, following this year’s change in administration and major shakeup in the regulatory landscape, skepticism in science has become the elephant in the room for anyone working in the drug and device sphere. Practitioners should start thinking about how to present scientific evidence to juries in 2026 as the old norms may no longer apply.

Read the full article on the Faegre Drinker website.

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About the Author: Jim Frederick

With a sophisticated background leading litigation, Jim Frederick defends innovative life sciences companies in pharmaceutical and medical device product liability, mass tort and consumer fraud lawsuits. Jim also represents clients in commercial litigation and appellate matters. A former Assistant U.S. Attorney in the District of Maryland, Jim wields his background investigating and prosecuting civil and criminal fraud cases to inform his defense strategy for clients.

About the Author: Caroline "Cari" Wadman

Caroline provides counsel on product regulatory compliance and is focused on defending companies in complex product liability and mass tort litigation.

About the Author: Erica Abshez Moran

Erica Abshez Moran helps clients prevent, defend, manage and resolve product liability litigation. Erica has been involved in all stages of litigation, including bringing multiple cases to trial. Her experience includes case evaluation and client counseling, drafting pleadings and motions, managing pre-trial discovery, negotiating with opposing counsel, trial preparation, and second-chairing arbitrations.