The commissioner of the Food and Drug Administration on Wednesday described as "woefully inadequate" the budget from Congress devoted to FDA regulation of dietary supplement products.
Four former FDA officials, including several who worked on dietary supplement issues, discuss the myriad impacts of a government shutdown on the Food and Drug Administration.
As the Council for Responsible Nutrition celebrates its 50th anniversary, NutraIngredients-USA caught up with Steve Mister, CRN President and CEO, to hear about the association’s history, its commitment to its founding values, and how it is gearing up for the challenges of the next 10 years.
The National Institutes of Health kicked off its annual Office of Dietary Supplements Seminar Series this week with a presentation by Dr. Cara Welch on how the Food and Drug Administration (FDA) regulates the dietary supplement marketplace.
On Aug. 14, 2023, U.S. Food and Drug Administration (FDA or the Agency) Commissioner Robert Califf provided an update on changes to the Agency’s dietary supplement program, under the proposed human foods program redesign. In January 2023, the FDA announced it would transform the current organizational structure of the food programs into one unified Human Foods Program (HFP).