FDA 21 CFR (Code of Federal Regulations)

FDA 21 CFR (Title 21 of the Code of Federal Regulations) is a set of rules and guidelines developed by the U.S. Food and Drug Administration to ensure the safety, efficacy, and quality of food, drugs, medical devices, and other health-related products. It provides detailed requirements for manufacturing, labeling, testing, and distributing these products to protect consumers and ensure regulations are followed. Essentially, it helps regulate the production and sale of products that impact public health, ensuring they meet consistent standards and are safe for use.