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FDA’s Office of Patient Affairs hosts Patient Listening Sessions. These sessions are a resource for the medical product Centers to engage with patients and their advocates. Patient Listening Sessions are one of many ways the…
The Reagan-Udall Foundation, the group tasked with reviewing the FDA’s food safety and tobacco programs, opened up a public portal for anonymous feedback on the FDA’s food safety program on Monday.
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For the past several months, the U.S. Food and Drug Administration has been working around the clock with our U.S. government partners, including the U.S. Department of Health and Human Services and the U.S. Department of Agriculture, to expand consumer…
The Reagan-Udall Foundation is looking to collect perspectives and experiences on the Food and Drug Administration’s human foods program through a new “Stakeholder Portal.”
The Reagan-Udall Foundation’s independent expert panel has been charged with…
The Reagan-Udall Foundation opened a Stakeholder Portal on September 16, 2022, to collect perspectives and experiences with the U.S. Food and Drug Administration’s (FDA's) human foods program. In addition, the Foundation announced a public…
The FDA has launched an initiative warning about over-the-counter skin lightening products after receiving reports of side effects.
The agency's Skin Facts! Initiative, announced last week, is aimed at promoting safe use of skin care products,…
The Reagan-Udall Foundation has announced five members of an independent expert panel who will conduct an operational evaluation of the Food and Drug Administration’s human foods program. Dr. Jane Henney, former FDA Commissioner, was named as chair of…
In 2021, a record number of Americans – more than 107,000 – died from drug overdoses. While the loss of human life alone is staggering, we know that the effects of the drug overdose crisis are even broader, including enormous individual and societal…
In June, long-simmering criticism of the way the U.S. Food and Drug Administration is handling premarket tobacco product applications (PMTAs) culminated in a public uproar. “The whole regulatory process is becoming surreal now,” wrote Clive Bates, an…
Work is poised to get underway on a somewhat rare internal review by the U.S. Food and Drug Administration (FDA) that could impact how the agency processes new tobacco products and enforces the sale of them by retailers.
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