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 a crucial legal resource for professionals in the food and drug industries, legal experts, and regulatory agencies. This volume contains the detailed regulations issued by the U.S. Food and Drug Administration (FDA) and other authorities overseeing the safety, efficacy, and labeling of food, drugs, cosmetics, and medical devices.
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