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Did you know anything about FDA?

Did you know anything about FDA?


The U.S Food and Drug Administration (FDA) is a government agency established in 1906 with the passage of the Federal Food and Drugs Act.1

The U.S Food and Drug Administration (FDA) is a government agency established in 1906 with the passage of the Federal Food and Drugs Act.1 The agency is separated into divisions that oversee a majority of the organization's obligations involving food, drugs, cosmetics, animal food, dietary supplements, medical devices, biological goods, and blood products.

FDA Mission 

The Food and Drug Administration is responsible for protecting the public health by ensuring the safety, efficacy, and security of human and veterinary drugs, biological products, and medical devices; and by ensuring the safety of nation's food supply, cosmetics, and products that emit radiation.

FDA also has responsibility for regulating the manufacturing, marketing, and distribution of tobacco products to protect the public health and to reduce tobacco use by minors.

FDA is responsible for advancing the public health by helping to speed innovations that make medical products more effective, safer, and more affordable and by helping the public get the accurate, science-based information they need to use medical products and foods to maintain and improve their health.

Ways FDA Approvals Influence Industry and the Market 

Companies that are focused on the development and sale of new drugs can be left without key products to drive their revenue if their products fail to receive approvals. The influence the FDA wields regarding drug testing can affect the stock market. The release of test data might be seen by investors as a measure for future growth for companies that manufacture and market drugs.

The FDA is responsible for inspecting and reviewing production facilities that make items that are regulated by the agency. This includes but is not limited to vaccine and drug manufacturers, blood banks, food processing facilities, dairy farms, animal feed processors, and compounding pharmacies.

Imported regulated products must also be inspected by the FDA when they arrive at the border of the country. The agency publishes announcements of product recalls in collaboration with companies and local partners.

The agency conducts preapproval inspections for companies that applied to market new products. Inspections may be launched “for cause” if there is an issue reported at a facility. Such recalls can be the result of undeclared ingredients in the contents, which can pose risks for consumers with allergies. The contamination of products or the failure to handle the product according to safety parameters can also be the cause for recalls. 

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