Code of Federal Regulations, Title 21 Food and Drugs 600-799, Revised as of April 1, 2021

Title 21 of the Code of Federal Regulations governs food and drugs, including human and animal use, biologics, cosmetics, medical devices, radiology, and controlled substances. Updates are published annually by April, with publication following within six months.

Format: Paperback / softback
Length: 210 pages
Publication date: 30 April 2022
Publisher: Rowman & Littlefield

Title 21 is a comprehensive set of regulations established by the Food and Drug Administration (FDA), the Drug Enforcement Administration (DEA), and the Office of the National Drug Control Agency (ONDCP). These regulations cover a wide range of food and drug-related areas, including human and animal use, biologics, cosmetics, medical devices, radiological health, and controlled substances. The regulations are updated and revised on an annual basis, with the latest additions and revisions being published by April. Following this publication, the regulations take effect within six months.

Title 21 is a crucial regulatory framework that ensures the safety, effectiveness, and security of various food and drug products. It encompasses a wide array of products, including prescription medications, over-the-counter drugs, dietary supplements, foods, and cosmetics. The regulations are designed to protect consumers from harm and ensure that the products they use are safe and reliable.

The FDA is responsible for regulating food and drugs, including the approval of new products, monitoring for safety concerns, and enforcing regulations. The DEA is responsible for enforcing drug laws and regulations, including the control and regulation of drugs such as marijuana, heroin, and cocaine. The ONDCP is responsible for coordinating national drug control policies and programs, including drug prevention, education, and research.

Title 21 includes a variety of regulations and guidelines that apply to different types of products. For example, the Food and Drug Administration regulates food products, including meats, vegetables, and fruits, to ensure that they are safe, wholesome, and properly labeled. The FDA also oversees the manufacturing and distribution of food and drug products, including prescription medications and over-the-counter drugs.

The Drug Enforcement Administration is responsible for enforcing drug laws and regulations, including the control and regulation of drugs such as marijuana, heroin, and cocaine. The DEA also oversees the manufacturing and distribution of drugs, including prescription medications and over-the-counter drugs.

The Office of the National Drug Control Agency is responsible for coordinating national drug control policies and programs, including drug prevention, education, and research. The ONDCP also oversees the distribution of drugs, including prescription medications and over-the-counter drugs, to ensure that they are distributed safely and effectively.

In addition to these regulatory agencies, Title 21 also includes a variety of laws and regulations that apply to specific industries, such as the pharmaceutical industry and the food industry. These laws and regulations are designed to ensure that the products produced by these industries are safe and effective for consumers.

Overall, Title 21 is a critical component of the U.S. food and drug regulatory system. It ensures that consumers have access to safe and effective products and that the industries that produce these products are held to high standards of safety and quality.

Weight: 286g
Dimension: 219 x 154 x 11 (mm)
ISBN-13: 9781636718392