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FDA Proposes Reorg; Industry Reacts to Impact on Dietary Supplements - Whole Foods Magazine
The U.S. Food and Drug Administration (FDA) recently provided an update on its proposal to create a unified Human Foods Program (HFP). This reorganization includes a new model for the Office of Regulatory Affairs (ORA).
FDA Provides Update on Reagan-Udall Tobacco Panel - Convenience Store Decisions
The administration summarized its progress and next steps following the evaluation from the expert panel regarding the FDA's tobacco program.
FDA proposes relocation of Office of Dietary Supplement Programs, industry reacts - Food Navigator USA
The dietary supplement industry is expressing concern over a proposed update to a Food and Drug Administration (FDA) reorganization that would relocate the current Office of Dietary Supplement Programs (ODSP) to a new office under its “Risk Management Functions”.
FDA takes steps to decrease barriers for overdose reversal agents with Dr. Marta Sokolowska - Q&A with FDA Podcast
Welcome to another episode of our podcast series, “Q&A with FDA”, from the FDA’s Division of Drug Information, where we answer some of the most frequently asked questions that we’ve received. In a previous episode, we discussed FDA’s Overdose Prevention Framework with Dr.
US FDA’s Office Of Regulatory Affairs To Focus On Investigations, Inspections And Imports - Pink Sheet
ORA to shed more responsibilities as the FDA focuses the likely-to-be renamed field organization more on inspections while revamping the agency's Human Food Program.