What is the role of the FDA in the regulation of pharmaceuticals?

The Food and Drug Administration (FDA) is a federal agency that regulates pharmaceuticals (prescription and over-the-counter medicines) in the United States, including the state of Mississippi. The FDA is responsible for ensuring that these drugs are safe and effective before they are marketed. The FDA also regulates the manufacturing process for these drugs to ensure they meet quality standards. The FDA reviews drug companies’ applications for new or modified drugs to make sure they meet the requirements for safety, quality, and effectiveness. It also inspects manufacturing facilities and investigates any reports of adverse events related to drug use. The FDA also evaluates the labels and advertising of drugs to make sure they are not misleading. The FDA also works with state and local authorities to ensure that pharmaceuticals are safely and properly used. It reviews reports of possible violations of pharmaceutical regulations and takes enforcement action when necessary. In Mississippi, the Mississippi State Board of Pharmacy works in partnership with the FDA to ensure that the laws and regulations governing the sale, distribution, and use of pharmaceuticals are followed. This includes reviewing applications for new pharmacy licenses, setting minimum standards for the practice of pharmacy, and inspecting pharmacies to make sure they meet those standards.

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What is the role of the FDA in the regulation of pharmaceuticals?

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