What is the scope of the FDA’s authority in regulating the pharmaceutical industry?

The Food and Drug Administration (FDA) is the organization in charge of regulating the pharmaceutical industry on a national level. In Florida, the FDA has authority over drugs and devices, including those used for veterinary purposes, as well as supplements and over-the-counter (OTC) drugs. The FDA’s authority over the pharmaceutical industry covers a wide range of activities. The agency has the power to develop safety and efficacy standards for drugs sold in the US, ensure that medications are correctly labeled and meet quality standards, monitor clinical trials of new drugs, inspect manufacturing facilities, and take legal action against those who violate federal regulations. The FDA also has the power to require pharmaceutical companies to provide additional safety information as well as additional tests to ensure product safety. The FDA is also responsible for approving new drugs and devices before they can be marketed to the public. The agency reviews applications for new drugs and medical devices, makes sure they are safe and effective for their intended uses, and monitors the marketing of those drugs and medical devices. All of this is done so that people can have confidence in the medications they buy. The FDA also works to reduce drug shortages in Florida and nationwide by closely monitoring drug production and supply. The FDA works with manufacturers to ensure a steady supply of medications and makes sure drugs are stored and labeled accurately. By regulating the pharmaceutical industry, the FDA helps ensure that people in Florida and across the country have access to safe and effective medications.

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What is the scope of the FDA’s authority in regulating the pharmaceutical industry?

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