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On Oct. 30, President Joe Biden signed the Executive Order on the Safe, Secure, and Trustworthy Development and Use of Artificial Intelligence, an initiative designed to position the United States...

A recent court case in the Eastern District of New York is a great example of "another bite at the apple" of patent subject matter eligibility.

The pharmaceutical industry is approaching one of the most consequential inflection points in its modern history. By 2027, patent expirations on a wave of blockbuster drugs will expose approximately $150 billion in annual revenue to generic and biosimilar competition — a reckoning that is already reshaping how companies build, defend, and monetize their intellectual property.

Sen. Thom Tillis, Chair of the Senate Judiciary Subcommittee on Intellectual Property for the 119th Congress, said that one of his top priorities is to advance the Patent Eligibility Restoration Act (PERA)...

The U.S. Department of Homeland Security (DHS) announced the addition of 37 companies based in the People's Republic of China (PRC)...

On July 30, 2025, the U.S. Department of the Treasury's Office of Foreign Assets Control (OFAC) designated Brazilian Supreme Court Justice Alexandre de Moraes as a Specially Designated National...

On June 16, 2025, the White House published an Executive Order (EO) containing the general terms of the United States-United Kingdom Economic Prosperity Deal.

In the January episode of the Seventh Circuit Roundup podcast, Kian Hudson and Mark Crandley examine two decisions— Farhan v. 2715 NMA LLC and Martin v. Goldsmith — that address issues familiar to many litigators...

We have previously written about decisions requiring a manufacturer to warn about dangers in other manufacturers’ products. See 9/6/12 Toxic Tort Alert – Supreme Court Expands Manufacturer’s Duty to Warn.

In a recent decision that could alter how plaintiffs present expert witness testimony in state court toxic tort claims, the Georgia Court of Appeals in Sterigenics US LLC v. Mutz, No. A25A1377, 2025...

Any comments should be submitted to the Georgia DOR prior to the hearing on Nov. 3 at 10 a.m.

Last June, the National Labor Relations Board formally proposed to amend its procedures for resolving disputes about union representation in a Notice of Proposed Rulemaking (NPRM), commonly known as the "quickie" election rule because it would shorten the amount of time between the filing of a representation petition and the election.

On Nov. 9, 2010, the EEOC published its final regulations under Title II of the Genetic Information Nondiscrimination Act of 2008 (GINA) – 18 months after the EEOC published its proposed regulations for public comment.

Despite the protection that Bostock v. Clayton County provides transgender employees, many may not feel protected. Why, you might ask? Since Bostock was decided...

The National Labor Relations Board (NLRB) issued two 3-1 decisions revisiting two decertification issues. These decisions, UGL-UNICCO Service Co., 357 NLRB No. 76 (Aug. 26, 2011), and Lamons Gasket Co., 357 NLRB No. 72 (Aug. 26, 2011).

The FDA recently issued a draft guidance titled, "Refused to Accept Policy for 510(k)s." In addition to explanation of the new policy, the draft guidance includes three checklists – one each for traditional, abbreviated, and special 510(k)s – for use by FDA staff in determining whether to accept a 510(k) for filing.

The FDA recently notified Congress of its intention to regulate laboratory developed tests as medical devices and accompanied the notice with two draft guidance documents on the topic.

During the last four years, real estate lenders collecting defaulted commercial loans from financially distressed borrowers have often sought court appointment of receivers with the power to sell mortgaged real estate free and clear of liens and redemption rights in states that recognize redemption rights, including Michigan.