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Last month, we wrote about the toxic chemicals legislation bouncing between the Vermont House and Senate.

President Trump has nominated Karen Sessions to serve a seven-year term as Commissioner of the Consumer Product Safety Commission (CPSC), marking the latest step in reconstituting the agency following unprecedented...

17 months since it's last issuance of a Withhold Release Order U.S. Customs and Border Protection revives its enforcement mechanism to target a Chinese importer and its affiliates operating ...

A recent Kelley Drye client advisory summarizes important new draft model state legislation that embodies an expansive approach to the regulation of per- and polyfluoroalkyl substances (PFAS) in consumer products.

With the 2014 holiday season fast approaching, businesses should not lose sight of what the Proposition 65 "bounty hunter" plaintiffs’ lawyers are eagerly awaiting.

Wiley's Environmental and FDA Regulatory practices launch a new joint podcast examining the intersection of environmental policy, scientific innovation, and FDA-regulated industries.

In January 2019, in conjunction with Version 1.0 of its Working Model for the Software Precertification Program,

In the October 8, 2015, Federal Register, FDA proposed to rename pediatric hospital beds as pediatric medical cribs and establish special controls for these devices.

On January 28, 2015, a group of Democratic senators and representatives introduced the "Safe Food Act of 2015," a bill largely aimed at creating a new Food Safety Administration that would absorb and consolidate the food safety functions currently split between FDA and USDA—a reorganization plan mirroring the proposal outlined in President Obama's budget.

This week Formycon AG ("Formycon") announced positive preliminary efficacy and safety data from the VESPUCCI Phase III clinical trial for FYB202, Formycon's biosimilar version of STELARA (ustekinumab).

Michael Brown and Lisa Baird from our Life Sciences Health Industry Team will be presenting an hour-long AdvaMed Medical Technology Learning Institute webinar on "Top 10 Product Liability Issues" on July 20 at 1 p.m. ET.

The spring of 2015 is shaping up to be a busy time in the field of food and nutrition.

On Oct. 10, 2006, the Department of Justice announced a settlement with Oracle Corporation (“Oracle”) for $98.5 million to settle allegations that PeopleSoft Inc. (“PeopleSoft”) overcharged federal buyers under the General Service Administration’s (“GSA’s”) Multiple Award Schedule (“MAS”) program.

The Sixth Circuit affirmed summary judgment for J.M. Smucker Company in a dispute over how many insurance retained limits applied to thousands of claims from a 2022 peanut-butter salmonella recall. ACE American Insurance argued each claimant's exposure was a separate occurrence, potentially requiring Smucker to satisfy up to $112.5 million in retained limits, while Smucker contended the contamination constituted a single occurrence under Ohio law's cause test.

Earlier this week in the Opioid MDL, Judge Polster denied the defendant pharmacies' motion for certification of an interlocutory appeal.

A California jury awarded $6 million in damages to a woman who alleged childhood social media use caused severe mental health issues, marking one of the first verdicts holding major tech companies financially...

The accident involving Asiana Airlines Flight 214 led to the filing of lawsuits against Asiana Airlines in various federal district courts, which were subsequently consolidated as an MDL in the Northern District of California.

Businesses need to start thinking about this and making preparations now.