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Pharmaceuticals & Biologics

Overview

By bringing innovative products to market, pharmaceutical companies help people live longer, higher-quality lives — and our attorneys and other professionals are dedicated to facilitating that progress. Our professionals include former in-house counsel and senior executives for some of the world’s largest pharmaceutical companies, as well as an interdisciplinary team of experienced attorneys and professionals who provide regulatory, transactional, litigation, intellectual property, and government affairs services tailored to the pharmaceutical industry. We help clients tackle business and financing pressures, regulatory scrutiny, and litigation threats on a national and international scale. We have steered global pharma companies through multibillion-dollar transactions and helped international drug manufacturers accelerate drug development through creative joint ventures. Our IP attorneys work to patent your inventions in countries around the globe; shield your brands through trademark policing and anti-counterfeiting strategies; and negotiate commercial, licensing, and other strategic agreements — freeing you to focus on product development and innovation. We serve as outside general counsel for regulatory compliance matters and support on all interactions with the Food and Drug Administration and other regulatory parties, including inspections, investigations, and enforcement. And when disputes occur, our trial lawyers are there to handle any issue. Whether enforcing your rights or defending against alleged wrongdoing, including in product liability litigation, our team of skilled trial attorneys is ready to represent you in high-stakes, bet-the-company litigation every day.

Insights & Events

Latest

Updates May 2026

HHS Office of Inspector General Declares That Fair-Market-Value Transactions Can Be Kickbacks

FAQ 17 Was Added on April 23, 2026
3 min read
News May 2026

Faegre Drinker Represents Teva Pharmaceutical in its Agreement to Acquire Emalex Biosciences

2 min read
Updates April 2026

FDA-Related Legislative and Regulatory Proposals and Funding Change the President's FY27 Budget

Between a Doorstop and a Starting Gun
121 min read
Published Articles April 2026

Expert Witness Practice in U.S. Drug and Medical Device Litigation

International Comparative Legal Guide – Drug & Medical Device Litigation 2026
1 min read
News April 2026

Wayne Mason Inducted as Fellow to the International Academy of Trial Lawyers

1 min read
Updates April 2026

The Intel Report: Quarterly National Security Briefing

Key Regulatory Developments and Enforcement Actions Affect National Security Priorities, Risks, and Opportunities across Sectors
14 min read
Updates March 2026

FDA Finalizes Rule Requiring 12-Digit National Drug Code (NDC)

Two Little Digits, One Very Big Operational Headache
4 min read
Updates February 2026

FDA Publishes Long-Awaited Draft Guidance on “Plausible Mechanism Framework” to Spur the Development of New Individualized Medicines

Anticipated Deadline for Comments Is April 27, 2026
7 min read
Speaking Engagement Recap May 16, 2025

AI Policy and the New Administration: Implications for FDA-Regulated Industries

2025 FDLI Annual Conference
1 min read
Speaking Engagement Recap November 20, 2024

Managed Care, Enforcement and Compliance

Healthcare Enforcement Compliance Conference
1 min read
Insights
Updates May 2026

HHS Office of Inspector General Declares That Fair-Market-Value Transactions Can Be Kickbacks

FAQ 17 Was Added on April 23, 2026
3 min read
Updates April 2026

FDA-Related Legislative and Regulatory Proposals and Funding Change the President's FY27 Budget

Between a Doorstop and a Starting Gun
121 min read
Published Articles April 2026

Expert Witness Practice in U.S. Drug and Medical Device Litigation

International Comparative Legal Guide – Drug & Medical Device Litigation 2026
1 min read
Updates April 2026

The Intel Report: Quarterly National Security Briefing

Key Regulatory Developments and Enforcement Actions Affect National Security Priorities, Risks, and Opportunities across Sectors
14 min read
Updates March 2026

FDA Finalizes Rule Requiring 12-Digit National Drug Code (NDC)

Two Little Digits, One Very Big Operational Headache
4 min read
Updates February 2026

FDA Publishes Long-Awaited Draft Guidance on “Plausible Mechanism Framework” to Spur the Development of New Individualized Medicines

Anticipated Deadline for Comments Is April 27, 2026
7 min read
Updates December 2025

Significant Drug & Device Developments of 2025

Drug & Device Companies Need to Be Vigilant and Nimble in Adapting to These Shifts
17 min read
Updates November 2025

Potential Challenges to State AI Laws; Senate Hearing on AI; and More Developments

Artificial Intelligence Briefing
6 min read
Updates November 2025

SCOTUS Weighs Trump Administration’s Tariff Authority Under IEEPA; Pharma and Device AI; and More

Biopharma & Medical Devices Briefing
7 min read
Updates October 2025

FDA Launches Dashboard to Provide Access to Real-Time Adverse Event Data for Cosmetics

How Users Might Get the Most Out of This Version
3 min read

Meet The Team

Meet The Full Pharmaceuticals & Biologics Team