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The FDA has just 89 inspectors for its bioresearch monitoring program. Experts say the Food and Drug Administration’s oversight of clinical trials for new vaccines and drugs is “grossly ...
The United States Food and Drug Administration (FDA or US FDA) is a federal agency of the Department of Health and Human Services.The FDA is responsible for protecting and promoting public health through the control and supervision of food safety, tobacco products, caffeine products, dietary supplements, prescription and over-the-counter pharmaceutical drugs (medications), vaccines ...
The FDA began enforcing its new powers against drug manufacturers who could not substantiate the efficacy claims made for their drugs, and the United States Court of Appeals for the Ninth Circuit ruling in Alberty Food Products Co. v. United States (1950) found that drug manufacturers could not evade the "false therapeutic claims" provision of ...
The history of early food regulation in the United States started with the 1906 Pure Food and Drug Act, when the United States federal government began to intervene in the food and drug businesses. When that bill proved ineffective, the administration of President Franklin D. Roosevelt revised it into the Federal Food, Drug and Cosmetic Act of ...
The regulation finalized Monday by the Food and Drug Administration will gradually phase in oversight of new tests developed by laboratories, a multibillion-dollar industry that regulators say ...
What Is the FDA? The FDA – that’s the U.S. Food and Drug Administration – is part of the federal government. Its mission is to make sure that foods, medicines, and other products important ...
To amend the Federal Food, Drug, and Cosmetic Act with respect to the safety of the food supply. The Food Safety Modernization Act ( FSMA) was signed into law by President Barack Obama on January 4, 2011. The FSMA has given the Food and Drug Administration (FDA) new authority to regulate the way foods are grown, harvested and processed.
The FDA might consider requiring manufacturers to notify or register with the agency before marketing a product and providing a copy of the label, the report recommended.
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