Title 21 presents regulations promulgated by the Food and Drug Administration, the Drug Enforcement Administration, and the Office of the National Drug Control Agency in the area of food and drugs. These regulations encompass food and drugs for human and animal use, biologics, cosmetics, medical devices, radiological health, and controlled substances. Additions and revisions to this section of the code are posted annually by April. Publication follows within six months.
“Code of Federal Regulations, Title 21: Food and Drugs” is the definitive source for the complete and current regulations governing food safety, drug approval, and medical device standards in the United States. Essential for professionals and researchers, this volume offers detailed insights into the rules and procedures administered by the U.S. Food and Drug Administration (FDA).
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