Understanding The Role Of The FDA

The Food and Drug Administration (FDA) is the government agency responsible for regulating and monitoring most foods, drugs, medical devices, and cosmetics. The FDA was founded in 1927 and was originally created through a reorganization of the Bureau of Chemistry.

You may browse this site if you want to check FDA orange book.

Over the years the FDA has lost and gained regulatory power over our country’s products. The Food, Drug, and Cosmetics Act of 1938 expands the range of products that the agency is responsible for controlling.

A number of changes have been made to FD&C laws over the years that have allowed advertising agencies to develop better ways to organize our products and reduce the time it takes to “approve” products for consumption.

1. Examine newly developed food, medical and cosmetic products for health and safety risks. This includes approving safe products and rejecting products that do not meet state safety standards.

2. Withdrawal of orders for products that are placed on the market but not safe for consumers.

Although the Food and Drug Administration protects Americans from dangerous products, it has often been surrounded by controversy over the years.

FDA approval ensures that consumer products are safe for consumption. The Food and Drug Administration requires thorough testing of new products to ensure product safety and quality.