What statute created the FDA?

Pure Food and Drugs Act
Though FDA can trace its origins back to the creation of the Agricultural Division in the Patent Office in 1848, its origins as a federal consumer protection agency began with the passage of the 1906 Pure Food and Drugs Act.

What is Republic No 3720?

Food, Drug and Cosmetic Act (Republic Act No. 3720). An Act to ensure the safety and purity of food, drugs and cosmetics being made available to the public by creating the Food and Drug Administration which shall administer and enforce the laws pertaining thereto.

Is the FDA a statute?

The Federal Food, Drug, and Cosmetic Act (FD&C Act) is a federal law enacted by Congress. It and other federal laws establish the legal framework within which FDA operates. The FD&C Act can be found in the United States Code, which contains all general and permanent U.S. laws, beginning at 21 U.S.C.

What is the act that gives authority to the FDA?

As a regulatory agency under the Department of Health, the Food and Drug Administration, created under Republic Act No. 3720, series of 1963, as amended by Executive Order 175, series of 1987, otherwise known as the “Food, Drugs and Devices, and Cosmetics Act”, and subsequently Republic Act No.

What caused the FDA to be created?

The United States Food and Drug Administration (FDA) was first created to enforce the Pure Food and Drug Act of 1906. In this capacity, the FDA is charged with protecting the health of the US public, to ensure the quality of its food, medicine, and cosmetics.

When did FDA approval begin?

1906
Although it was not known by its present name until 1930, FDA’s modern regulatory functions began with the passage of the 1906 Pure Food and Drugs Act, a law a quarter-century in the making that prohibited interstate commerce in adulterated and misbranded food and drugs.

What is RA 9711 all about?

This Act aims to protect and promote the right to health of the Filipino people and to establish and maintain an effective health products regulatory system. This Act created the Food and Drug Administration in the Department of Health to replace the Bureau of Food and Drugs.

Is the FDA regulated by the government?

The federal regulation of food, drugs, cosmetics, biologics, medical products and tobacco is legally mandated by acts of the United States Congress.

What is the RA 9711?

9711). Country. Legislation. This Act aims to protect and promote the right to health of the Filipino people and to establish and maintain an effective health products regulatory system.

Who approved RA 9711?

Begun and held in Metro Manila, on Monday, the twenty-eight day of July, two thousand eight. Be it enacted by the Senate and House of Representatives of the Philippines in Congress assembled: SECTION 1.