Major effort needed to remove illegal vaping products, review finds - The Washington Post

An independent review of the Food and Drug Administration’s tobacco regulators described them as overwhelmed, reactive and fatigued by an oppressive workload involving e-cigarettes and called for a major effort, by several parts of the Biden administration, to remove millions of illegal vaping products from the market.

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Expert Panel Submits Operational Evaluation of FDA’s Tobacco Program to Commissioner

(December 19, 2022) The Independent Expert Panel for Tobacco today submitted its recommendations to Commissioner Robert Califf at the U.S. Food and Drug Administration. The Operational Evaluation of Certain Components of FDA’s Tobacco Program was facilitated by the Reagan-Udall Foundation at the Commissioner’s request. 

Report Recommends Overhaul Of FDA Food Program, Separate Food Agency - Inside Health Policy

FDA and Congress need to overhaul the agency’s food program, including by making structural changes, such as establishing a separate food-focused agency under HHS, and appointing an overarching head of the food program to remedy issues with work culture and lack of a clear mission, a panel of experts from the Reagan-Udall Foundation wrote in an FDA-commissioned report released this week. 

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Reagan-Udall Foundation for the FDA Launches Real-World Data Initiative to Address Disparities

(December 15, 2022) The Reagan-Udall Foundation for the FDA (FDA Foundation) is launching the Real-world Accelerator to Improve the Standard of collection and curation of race and Ethnicity data in health care (RAISE). The initiative, funded by the Food and Drug Administration’s Office of Minority Health and Health Equity (OMHHE), focuses on understanding, aligning, and disseminating best practices to improve real-world reporting, collection, curation, and integration of race and ethnicity data. 

FDA’s food safety failings flagged in independent report as agency reviews internal systems and budget limitations - Food Industry Today

In scrutiny of the US Food and Drug Administration’s (FDA) Human Food Program, an independent expert panel is arguing that the agency “lacks the resources and authority to do what is expected to do – ensure the safety and availability of food on the market.” 

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