References in periodicals archive ?
Dispute: The U S Food and Drug Administration (FDA) does not test cosmetic ingredients except for color additives before they reach the public That's because the law requires that only colors be approved Manufacturers of cosmetics are responsible for ensuring that their products and ingredients are safe before they market them After a cosmetic product hits the stores, however, if the FDA finds that it is not safe for consumers, it can take steps to have the product removed
Draft Guidance for Industry on Food and Drug Administration Staff; Hospital Bed System Dimensional Guidance to Reduce Entrapment; Availability.
Food and Drug Administration Children & Tobacco Checker Data Reports, National Summary Results for September 1997 - February 2000, Updated February 2, 2000.
And though a nonprescription form of the allergy drug ultimately depends on the Food and Drug Administration, Thousand Oaks-based WellPoint is advocating its approval.
The company has extensive modern manufacturing facilities and laboratories in Melbourne and is licensed by the Australian Therapeutic Goods Administration (TGA) and the United States Food and Drug Administration (FDA) for production of active pharmaceutical ingredients.
For more information contact the Food and Drug Administration at 1-888-INFOFDA or go to http://vm.
In another example, Shelby says that, following the CERHR's phthalate reviews, the Food and Drug Administration issued guidance pointing out potential harm to newborns and infants undergoing medical treatments using medical devices containing DEHP.
China's State Drug Administration (SDA) has awarded Pharmagenesis Inc.
Food and Drug Administration (FDA) is to foster the development of vaccines, drugs and diagnostic products, safeguards of the food supply, and other measures needed to respond to bioterrorist threats.
High fat is defined by the Food and Drug Administration as more than 20 percent of the daily value for fat.
Food and Drug Administration (FDA) has approved trimetrexate glucuronate for the treatment of moderate to severe Pneumocystis carinii pneumonia (PCP), a potentially fatal infection that often strikes people with AIDS.
Food and Drug Administration (FDA) has granted orphan drug designation to Defibrotide for the prevention of hepatic veno-occlusive disease (VOD) in the U.