Food And Drug Act Of 1906 Essay

The US Food and Drug Administration is a federal organization that safeguards the public's health by guaranteeing the efficacy, security, and safety of human and veterinary medications, biological products, and medical devices, as well as the security of our country's food supply and cosmetics.Due to the 1906 Pure Food and Drugs Act's approval and the need to safeguard consumers, the Food and Drug Administration was established. President Theodore Roosevelt approved the Pure Food and Drugs Act in 1906, making it illegal for misbranded and contaminated foods, drinks, and drugs to be traded across state lines. The structure of the Food and Drug Administration is made up of the Office of the Commissioner and four directorates that are in charge of the agency's core responsibilities, including

The Pure Food and Drug Act of 1906, which we have already discussed, was the primary reason the Food and Drug Administration (FDA) was established. This law was created because many people relocated to cities to work in factories and other urban jobs, and because there was little to no workplace or product safety, pre-made goods were required because city dwellers could not produce them themselves. The Food and Drug Administration is responsible for a wide range of duties, including dietary supplements, bottled water, food additives, infant formulas, prescription drugs, non prescription drugs, vaccines for humans, blood and blood products, cellular and gene therapy products, tissue and tissue products, allergenics, heart pacemakers, dental devices, surgical implants and prosthetics, x-ray equipment, ultrasonic therapy equipment, color additives found in makeup and other personal care products, skin moisturizers and cleansers, nail polish and perfume, livestock feeds, pet foods, veterinary drugs and devices, cigarettes, e-cigarettes, and