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Code of Federal Regulations, Title 21 Food and Drugs 170-199, Revised as of April 1, 2022

Code of Federal Regulations, Title 21 Food and Drugs 170-199, Revised as of April 1, 2022

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  • More about Code of Federal Regulations, Title 21 Food and Drugs 170-199, Revised as of April 1, 2022

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

Format: Paperback / softback
Length: 1 pages
Publication date: 31 May 2023
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. Once published, the regulations take effect within six months.

Title 21 plays a crucial role in ensuring the safety, effectiveness, and security of food and drugs in the United States. It provides a framework for regulating the manufacture, distribution, and marketing of these products, as well as for monitoring and enforcing compliance with applicable laws and regulations.

The regulations encompass a diverse range of topics, including the approval and regulation of new drugs and medical devices, the safety of food and food ingredients, the prevention of drug abuse and addiction, and the regulation of controlled substances.

To ensure the effectiveness of Title 21, the FDA, DEA, and ONDCP work closely with other federal agencies, such as the Centers for Disease Control and Prevention (CDC) and the Environmental Protection Agency (EPA), as well as with industry stakeholders and public health organizations.

In conclusion, Title 21 is a critical component of the U.S. food and drug regulatory system. It provides a comprehensive framework for ensuring the safety and effectiveness of food and drugs, and for protecting the public health and well-being of individuals and communities.

Weight: 853g
Dimension: 228 x 154 x 33 (mm)
ISBN-13: 9781636711898

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