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5347a8c8-cae8-4f82-b108-c12f5ffbf010
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NetForum Committee Code
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Elevate ID
12542

Pharmacy Benefit Managers (“PBMs”) are no longer just an insurance concern—they are central players in how drugs are priced, accessed, and reimbursed across the healthcare system. As states rapidly expand licensing, registration, and operational requirements for PBMs, attorneys across healthcare disciplines are increasingly encountering PBM-related issues in provider contracts, reimbursement disputes, compliance obligations, and transactional strategy.  In this presentation, Jennifer Osborn, an insurance regulatory partner at Polsinelli PC—a national Am Law 100 firm with a leading healthcare practice—provides a practical overview of the evolving PBM regulatory landscape, including new licensing regimes, transparency mandates, and patient protection rules. The session also explores how these changes are reshaping risk and opportunity for providers, pharmacies, pharmaceutical and medical device companies, and plan sponsors.

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 Health Law Network Community

Join us for a focused review of the most significant healthcare regulatory developments impacting in-house counsel over the past year. This webinar will cover key agency guidance, enforcement trends, rulemaking, and notable court decisions affecting life sciences and healthcare organizations.

Designed specifically for in-house legal teams, the session will highlight practical implications, emerging compliance risks, and strategic considerations to help you advise your business and plan for the year ahead.

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 Health Law Network Community


Co-sponsored with the Women in the House Network

Join us for an intimate fireside chat with Tejal Vakharia, Senior Vice President & General Counsel at Veradigm, a seasoned in-house leader operating at the intersection of healthcare, data, and technology. Tejal will share candid insights on navigating regulatory complexity, advising executives, managing risk in moments of crisis, and building credibility as the role of in-house counsel continues to expand. This conversation is designed to resonate with both new and experienced in-house lawyers, offering practical takeaways, career perspective, and a real-world look at what it means to be a strategic legal leader today. Come for the insights. Stay for the perspective. Leave with clarity.

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 Health Law Network Community


This session offers a clear, general‑audience roadmap to FDA enforcement and response strategy—using clinical trial fraud as the practical lens to understand risk, regulator expectations, and what works when the government comes knocking. Led by former U.S. Attorney Michael F. Easley Jr. and former FDA Office of Chief Counsel/DOJ Consumer Protection Branch leader Clint Narver, we will translate current FDA/DOJ priorities into action‑ready guidance for legal, compliance, and regulatory leaders. We will unpack recent actions and policies, highlight red flags that trigger inspections, 483s, subpoenas, and CIDs, map who does what across FDA, DOJ, and HHS‑OIG, and show how cases escalate into misbrandingFalse Claims Act, and related theories. We will also how to respond when an inquiry becomes a multi‑agency investigation. Attendees will leave with practical playbooks and strategies that resonate with enforcement authorities.

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 Health Law Network Community

Alexandra Shalom, Madeline Knight, and Kate Pamperin (Foley & Lardner LLP)
11 pages

This article breaks down the evolution of the Hospital Price Transparency Rule. This resource highlights new compliance obligations and offers insights into emerging enforcement trends that hospitals should be tracking closely.

Resource Details
Interest Area: Health Law
Region: United States
Jason Mehta & Samantha Gerencir (Foley & Lardner LLP)

It’s not every day your company gets a letter from the government demanding documents, data, and sworn answers under tight deadlines.

Your response, thus, must be swift, strategic, and legally sound. Here’s a practical guide to navigating Civil Investigative Demands.

Resource Details
Region: Global, United States
Foley & Lardner LLP
4 pages

As Trump seeks to raise U.S. tariffs (which currently tend to be among the lowest worldwide), manufacturers, distributors, retailers, and other companies that frequently import (“importers”) must determine the best strategy to deal with the resulting uncertainties.

This article discusses 6 steps to manage tariff risks in a trade war.

Resource Details
Region: Global, United States
Foley & Lardner LLP
19 pages

The focus on tariffs by the Trump administration presents significant risks for frequent importers. This in-depth white paper discusses strategies for managing risks during a trade war.

Resource Details
Region: Global, United States
Pamela L. Johnston, Lisa M. Noller, Lori Rubin Garber, and Ryan J. Lowry (Foley & Lardner LLP)
3 pages

US Attorney General Pam Bondi has renewed the prior Trump administration’s prohibition on the use of sub-regulatory guidance, potentially altering the landscape for False Claims Act cases pursued during the second Trump administration.

Resource Details
Interest Area: Health Law, Government
Region: United States
Foley & Lardner LLP
5 pages

The provision of patient assistance, including transportation and other free or discounted items and services to patients by health care providers and suppliers implicate certain fraud and abuse laws.

These law include the prohibition on beneficiary inducements under the federal Civil Monetary Penalties (“CMP”) Law and the federal Anti-Kickback Statute (“AKS”).

This article provides a summary of the CMP Law and AKS and certain exceptions under those laws.

Resource Details
Interest Area: Health Law
Region: United States
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