A spokesperson told The Independent that the FDA is actively working to ensure continuity of operations during the reorganization period and remains committed to ensuring critical programs and ...

The Food and Drug Administration (FDA) is coming under fire for not publicizing its own report into an E. coli outbreak last year that spread across 15 states and infected 89 people, one of whom died.

Despite the severity of the outbreak, the Food and Drug Administration (FDA) never made a public announcement. According to an internal report, the investigation was closed quietly in February ...

Well-known baby product maker Gerber Products Company issued a recall reminder in tandem with the Food and Drug Administration (FDA) on April 18 after affected products were still seen on store ...

Languages: English. The Food and Drug Administration (FDA) has classified both of the two Tony's Chocolonely chocolate bars that were part a nationwide recall as a Class II health hazard after ...

The Food and Drug Administration (FDA) has approved a prefilled syringe formulation of Vyvgart ® Hytrulo (efgartigimod alfa and hyaluronidase-qvfc) that allows patients to self-inject the medication.

The Food and Drug Administration (FDA) announced Thursday it plans to phase out animal testing requirements for biological products and drugs, instead moving toward alternative testing models such ...

The Food and Drug Administration (FDA) has cleared diabetes-management firm DexCom's (DXCM) new continuous glucose monitoring (CGM) system. The San Diego, Calif.-based firm said Thursday that its ...

To get FDA approval, scientists must be able to demonstrate that a new drug or treatment is safe and effective. And currently, before they can test a new therapy in humans, they must show proof ...

U.S. Food and Drug Administration approvals of life-changing, high-risk medical devices reportedly slowed to a 10-year low for the January to March period, as recent layoffs have reportedly had ...

Layoffs at the Food and Drug Administration are expected to reduce the FDA's workforce by 20%. Susan Mayne, former director of the Center for Food Safety and Applied Nutrition at the FDA ...

Minnesota is home to hundreds of medical device companies that can't sell new technologies or produce revenue without FDA review. A federal official did not answer questions about the cause of the ...