FDA (Food and Drug Administration) certification is a certificate of food or drug quality issued by the Food and Drug Administration of the U.S. government. Due to its scientific and rigorous nature, this certification has become a world-recognized standard. Drugs that have obtained FDA certification can be sold not only in the United States, but also in most countries and regions in the world. FDA is the abbreviation of the U.S. Food and Drug Administration. It is an international medical review authority authorized by the U.S. Congress, i.e. the federal government, and is the highest law enforcement agency specializing in food and drug management.
The FDA is a government health control and monitoring agency composed of doctors, lawyers, microbiologists, pharmacologists, chemists and statisticians, etc., dedicated to protecting, promoting and improving the health of the nation. Food, drugs, cosmetics and medical devices certified by the FDA are guaranteed to be safe and effective for the human body. In the United States and nearly 100 other countries, only materials, devices and technologies approved by the FDA can be used in commercial clinical applications.