A series of panels convened by the Food and Drug Administration is raising concerns that the agency is skirting federal rules and promoting fringe views about antidepressants and other products.

Bill SB0073 will prohibit manufacturers from selling, distributing, or offering baby food that contains toxic heavy metals over the limits approved by the U.S. Food and Drug Administration.

The biotech, which cut jobs following the rejection in May of its Barth syndrome therapy, claimed it has addressed the agency’s concerns and now sees potential for a speedy review.

Families concerned about color additives in school lunches, at grocery stores and at fast-food counters can now reference a new Food and Drug Administration (FDA) website that […]

The U.S. Food and Drug Administration has approved Tonix Pharmaceuticals' drug to manage pain related to a type of chronic condition called fibromyalgia, the company said on Friday.

The FDA said in letters to five sunscreen makers that they are not authorized to market sunscreen sold in mousse or whipped form.

In a highly unusual move, a small biotech has disclosed a rejection letter from the FDA in hopes of rallying support for regulatory approval of an ultra-rare disease drug.

Lead is toxic to people of any age or health status and higher exposure levels can lead to neurological changes

The dessert dip was initially recalled by manufacturers in late July with its risk classification raising to a Class II Friday.