Denmark's Bavarian Nordic said on Monday the U.S. Food and Drug Administration has approved a freeze-dried formulation of its ...

The US Food and Drug Administration (FDA) has broadened the approval of Furoscix (furosemide injection) to treat edema in ...

When the FDA announced in January, before President Joe Biden's term ended, that it would ban a dye called red dye No. 3 in food and ingested drugs, the federal agency cited just one 1987 study on ...

The FDA conducts detailed safety assessments of all food contact materials, considering factors like chemical migration and ...

Pharmaceuticals generated fourth quarter 2024 net FUROSCIX ® revenue of $12.2 million, and full year 2024 revenue of ...

As the issue of independent review of the food industry’s GRAS declarations emerged, on another food safety issue Beyond ...

Approved in 1958, the Food Additive Amendment included a provision that enabled substances that are “generally recognized as safe” to be exempted from undergoing the FDA’s typical pre-market ...

Many Americans have started to question the quality of ingredients used within their food, some of which are banned in Europe.

Compound drugs are copies of U.S. Food and Drug Administration ... to patient than FDA-approved drugs because compounded drugs do not undergo FDA premarket review for safety, effectiveness ...

Director of Business Development for BioBond Adhesives, Inc. "Food safety is non-negotiable, and BioBond's technology gives us a cutting-edge advantage," said Luis Almeida, CEO of Nova Farms USA.

FDA and health officials said there is no evidence though that it is harmful, and food manufacturers said they need to be able to rely on ingredients generally recognized as safe. In the memo ...