On June 11, 2025, the US Food and Drug Administration (FDA) released educational materials to broaden dietary supplement manufacturers’ ...

On April 22, 2025, the US Food and Drug Administration (FDA) and the US Department of Health and Human Services (HHS) announced a plan to phase ...

A meeting Wednesday at the Food and Drug Administration about fluoride supplements became, at one point, a contentious ...

Explore the FDA’s 2025 Human Foods Program Guidance Agenda and what it means for US food and beverage businesses. Key ...

The Boston-based digital pathology firm's updated US Food and Drug Administration clearance will help it to quickly validate its software with new hardware combinations.

FDA issues warning letters to distributors of food, dietary supplements and unapproved drugs that contain ...

Unlike drugs, dietary supplements are not pre-approved by the Food and Drug Administration (FDA) for safety or efficacy before they ... Pharmacopeia (USP), or ConsumerLab. For personalized guidance, ...

The FDA has published its proposed agenda for 2025 guidance, including new topics such as food colorings. Topics on the agenda are a priority for the Food ...

FDA issues warning letters about botulism risk in canned desserts and illegal drug claims in supplements By News Desk on June 30, 2025 ...

U.S. Food and Drug Administration FDA issues draft guidance related to the transfer of 510 (k) Premarket Notification Clearance for medical-device clearance ...

Here’s your chance to discuss the U.S. Food and Drug Administration (FDA) possibly pulling fluoride supplements for children from the market.

FDA Official Says FDA Plans to Issue Guidance as Normal Despite “10-1 Executive Order” by: Food and Drug Law at Keller and Heckman ...