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Articles by Julianna Dzwierzynski
'Made in America' claims face scrutiny under executive order
+2 Julianna Dzwierzynski,Jack Wenikand 2 more At a Glance Executive Order 14392 prioritizes Federal Trade Commission enforcement actions. Online marketplaces may face new compliance rules. Qualified claims offer a safer path for compliance. On March 13, 2026, President Trump signed Executive Order 14392, titled Ensuring Truthful Advertising of Products Claiming to Be Made in America, which broadly targets false or misleading country-of-origin claims across industries.
Is Your Product Ready to Be Listed? What the Dietary Supplement Listing Act of 2026 Means for Your Business
The Dietary Supplement Listing Act of 2026 (H.R. 8370, 119th Congress) (the “Act”), introduced in the U.S. House of Representatives on April 20, 2026, has the potential to significantly impact the dietary supplement industry. The Act proposes to amend the Federal Food, Drug, and Cosmetic Act (“FDCA”), via a new Section 403D, and create the first mandatory FDA product-listing regime for dietary supplements.
New York’s Food Safety and Chemical Disclosure Act: A State-Level Overhaul of GRAS Regulation
New York’s Food Safety and Chemical Disclosure Act: A State-Level Overhaul of GRAS Regulation Wednesday, April 29, 2026 New York has passed sweeping food additive legislation that, if signed by the Governor, will fundamentally reshape how food manufacturers and suppliers operate in the state.
DOJ Creates National Fraud Enforcement Division: What It Means for Fraud Enforcement in America
Takeaways Several areas of federal criminal prosecution, including health care fraud, have been pulled under the umbrella of the new National Fraud Enforcement Division (“NFED”) of the Department of Justice (“DOJ”), with the stated goal of “rapidly and substantially” increasing resources and creating a robust litigating division.
Closer Look at H.R. 7291: What the “GRAS Oversight and Transparency Act” Could Mean for Dietary Supplements
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Closer Look at H.R. 7291: What the “GRAS Oversight and Transparency Act” Could Mean for Dietary Supplements | JD Supra
On January 30, 2026, Representative Michael Lawler introduced H.R. 7291, the “GRAS Oversight and Transparency Act.” H.R. 7291 is the latest congressional effort to address longstanding concerns about the federal regulatory framework governing “generally recognized as safe” (“GRAS”) designations for food-related substances.
A Closer Look at H.R. 7291: What the “GRAS Oversight and Transparency Act” Could Mean for Dietary Supplements
On January 30, 2026, Representative Michael Lawler introduced H.R. 7291, the “GRAS Oversight and Transparency Act.” H.R. 7291 is the latest congressional effort to address longstanding concerns about the federal regulatory framework governing “generally recognized as safe” (“GRAS”) designations for food-related substances.
Legislative Push for FDA Preemptive Authority Over Dietary Supplement Regulation | JD Supra
A newly introduced House Bill, H.R. 7366, titled the Dietary Supplement Regulatory Uniformity Act, would amend the Federal Food, Drug, and Cosmetic Act (“FDCA”) to expressly clarify and affirm the Food and Drug Administration’s (“FDA”) preemptive authority over dietary supplement regulation.
HHS Recommends Re-Classification of Marijuana as a Schedule III Controlled Substance – A Bellwether for the Future of Cannabis-ness | JD Supra
On August 30, an official at the United States Department of Health and Human Services (HHS) released one of the most significant announcements made at the federal level concerning marijuana reclassification.
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