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239 Results

Resource Listings

Articles

10 Things You Need to Know about Life Sciences Patent Litigation in Canada

By Sheldon Hamilton, Principal, Smart & Biggar LLP, Barrister and Solicitor Patent and Trademark Agent, and Nancy Pei, Principal, Smart & Biggar LLP, Barrister and Solicitor Patent and Trademark Agent

Patented medicine regulations in Canada can be complex and the review process is fast-paced. In this Top Ten, in-house counsel will learn the essential points of how to prepare for the "Regulations" review. Editor's note: This article was updated to reflect recent developments; a prior version of this article was published on August 6, 2020.

Articles

Ten Considerations Regarding State Government Public Health Powers to Mandate COVID-19 Protective Measures and Vaccination in the United States

By Author: Grant C. Killoran, O'Neil, Cannon, Hollman, DeJong & Laing S.C., Milwaukee, Wisconsin

People around the world continue to grapple with the COVID-19 pandemic, the most extreme public health emergency in a century. This Top Ten discusses the public health law framework in the United States and summarizes some recent developments in the law arising from the COVID-19 pandemic.

Articles

Personalized Medicine FDA Scope Progress 2022

By Antoinette F. Konski

The Personalized Medicine Coalition (PMC) recently released its annual report on the progress of precision medicine as measured by precision medicine FDA approvals in 2022 (“Report”). As summarized in the Report, 2022 milestones include progress in diagnostics, therapeutics and new treatment modalities that are covered in this resource from Foley and Lardner LLP.

Articles

State Digital Health Funding 2023

By Louis Lehot

With the pandemic, there came a digital health explosion, with companies working swiftly to bring new technologies to light that would pave the way forward in telehealth and other critical areas. We saw an incredible interest in this space then, but what is the state of digital health now? This resource from Foley & Lardner LLP looks at data from public and private financing markets in the digital health space in 2022, and look forward to what to expect in 2023.

Articles

Health AI Frontier Innovation Health Care Sector

By Navid Fanaeian

With the health care industry under pressure to improve patient outcomes while controlling costs, artificial intelligence (AI) and machine learning (ML) are quickly becoming indispensable tools. These technologies show promise in supporting decision-making, enhancing the delivery of care, and personalizing medicine. This resource from Foley & Lardner explores opportunities for health care organizations deploying AI-based solutions.

Articles

Antitrust DOJ ACO Guidance Provider

By Kinal M. Patel, Alexis Finkelberg Bortniker, Diane Hazel

This resource provided by Foley & Lardner LLP covers the DOJ’s announcement on February 6th of their withdrawal of the 2011 Statement of Antitrust Enforcement Policy Regarding Accountable Care Organizations Participating in the Medicare Shared Savings Program (2011 ACO Statement) in addition to two other health care antitrust policy statements.

Articles

Retraining the Acquisition Model: How to Approach the Risks and Rewards of Deals With Artificial Intelligence Targets

By Natasha Allen, David W. Kantaros, Shabbi S. Khan, Avi B. Ginsberg, Graham P. MacEwan

In recent years, companies specializing in artificial intelligence (AI) technologies have been increasingly coveted acquisition targets. Foley & Lardner have provided insight into the AI field transforming our approaches to key issues. Accordingly, it is no surprise that AI has emerged as a prime sector for M&A activity. This guide helps breakdown how to approach risks and rewards in dealing with the rising importance of Artificial Intelligence.

Articles

DEA’s Proposed Rules on Telemedicine Controlled Substances Prescribing after the PHE Ends

By Nathaniel M. Lacktman, Foley & Lardner LLP

This guide provided by Foley & Lardner summarizes the key elements and requirements contained in the proposed rule. In addition it explains how it differs from the special telemedicine registration rule. Finally, it describes what stakeholders can do to make their voice heard, including by submitting comments to the proposed rule, during these next 30 days.