Title 21 of the Code of Federal Regulations

Main article: Code of Federal Regulations

US code governing food and drugs

Title 21 is the portion of the Code of Federal Regulations that governs food and drugs within the United States for the Food and Drug Administration (FDA), the Drug Enforcement Administration (DEA), and the Office of National Drug Control Policy (ONDCP).[1]

It is divided into three chapters:

* Chapter I — Food and Drug Administration
* Chapter II — Drug Enforcement Administration
* Chapter III — Office of National Drug Control Policy

## Chapter I

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Most of the Chapter I regulations are based on the Federal Food, Drug, and Cosmetic Act.

Notable sections:

* 11 — electronic records and electronic signature related
* 50 Protection of human subjects in clinical trials
* 54 Financial disclosure by clinical investigators [2]
* 56 Institutional review boards that oversee clinical trials
* 58 Good laboratory practices (GLP) for nonclinical studies

The 100 series are regulations pertaining to food:

* 101, especially 101.9 — Nutrition facts label related
* (c)(2)(ii) — Requirement to include trans fat values
* (c)(8)(iv) — Vitamin and mineral values
* 106-107 requirements for infant formula
* 110 et seq. cGMPs for food products
* 111 et seq. cGMPs for dietary supplements
* 170 food additives
* 190 dietary supplements

The 200 and 300 series are regulations pertaining to pharmaceuticals :

* 202-203 Drug advertising and marketing
* 210 et seq. cGMPs for pharmaceuticals
* 310 et seq. Requirements for new drugs
* 328 et seq. Specific requirements for over-the-counter (OTC) drugs.

The 500 series are regulations for animal feeds and animal medications:

* 510 et seq. New animal drugs
* 556 Tolerances for residues of drugs in food animals

The 600 series covers biological products (e.g. vaccines, blood):

* 601 Licensing under section 351 of the Public Health Service Act
* 606 et seq. cGMPs for human blood and blood products

The 700 series includes the limited regulations on cosmetics:

* 701 Labeling requirements

The 800 series are for medical devices:

* 803 Medical device reporting
* 814 Premarket approval of medical devices [3]
* 820 et seq. Quality system regulations (analogous to cGMP, but structured like ISO) [4]
* 860 et seq. Listing of specific approved devices and how they are classified

The 900 series covers mammography quality requirements enforced by CDRH.

The 1000 series covers radiation-emitting device (e.g. cell phones, lasers, x-ray generators); requirements enforced by the Center for Devices and Radiological Health. It also talks about the FDA citizen petition.

The 1100 series includes updated rules deeming items that statutorily come under the definition of "tobacco product" to be subject to the Federal Food, Drug, and Cosmetic Act as amended by the Tobacco Control Act. The items affected include E-cigarettes, Hookah tobacco, and pipe tobacco.[5]

The 1200 series consists of rules primarily based in laws other than the Food, Drug, and Cosmetic Act:

* 1240 Rules promulgated under 361 of the Public Health Service Act on interstate control of communicable disease, such as:
* Requirements for pasteurization of milk
* Interstate shipment of turtles as pets.
* Interstate shipment of African rodents that may carry monkeypox.
* Sanitation on interstate conveyances (i.e. airplanes and ships)
* 1271 Requirements for human cells, tissues, and cellular and tissue-based products (i.e. the cGTPs).

## Chapter II

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Notable sections:

* 1308 — Schedules of controlled substances
* 1308.03(a) — Administrative Controlled Substances Code Number
* 1308.11 — List of Schedule I drugs
* 1308.12 — List of Schedule II drugs
* 1308.13 — List of Schedule III drugs
* 1308.14 — List of Schedule IV drugs
* 1308.15 — List of Schedule V drugs

## See also

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* Title 21 of the United States Code \- Food and Drugs
* EudraLex (medicinal products in the European Union)

## References

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1. ^ "CFR Title 21". US FDA. Retrieved February 10, 2014.
2. ^ Food and Drug Administration (2008). "Subchapter A — General: Financial Disclosure by Clinical Investigators". Archived from the original on October 3, 2002. Retrieved 9 April 2009.
3. ^ Food and Drug Administration (2008). "Subchapter H — Medical Devices: Part 814 Premarket Approval of Medical Devices". Retrieved 9 April 2009.
4. ^ Food and Drug Administration (2008). "Subchapter H — Medical Devices: Part 820 Quality System Regulation". Retrieved 9 April 2009.
5. ^ "Extending Authorities to All Tobacco Products, Including E-Cigarettes, Cigars, and Hookah". FDA.gov. United States Food and Drug Administration. Archived from the original on August 15, 2015. Retrieved 11 May 2016.

## External links

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* Title 21 of the Code of Federal Regulations (current "Electronic CFR")

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Food and Drug Administration of the United States

Divisions|

* Center for Biologics Evaluation and Research
* Center for Devices and Radiological Health
* Center for Drug Evaluation and Research
* Center for Food Safety and Applied Nutrition
* Center for Tobacco Products
* Center for Veterinary Medicine
* National Center for Toxicological Research
* Office of Criminal Investigations
* Office of Global Regulatory Operations and Policy

Major acts|

* Family Smoking Prevention and Tobacco Control Act
* Modernization Act of 1997
* Federal Food, Drug, and Cosmetic Act
* Food Safety Modernization Act
* Prescription Drug User Fee Act
* Pure Food and Drug Act

Title 21 regulations and rules|

| Administrative law|

Title 21 of the Code of Federal Regulations (CFR)

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Federal journal|

Federal Register (FR)

Federal law|

Title 21 of the United States Code (U.S.C.)

Commissioners|

* Harvey W. Wiley
* Carl L. Alsberg
* Charles A. Browne
* Walter G. Campbell
* Paul B. Dunbar
* Charles W. Crawford
* George P. Larrick
* James L. Goddard
* Herbert L. Ley
* Charles C. Edwards
* Alexander M. Schmidt
* Donald Kennedy
* Jere E. Goyan
* Arthur H. Hayes Jr.
* Frank E. Young
* David A. Kessler
* Jane E. Henney
* Mark McClellan
* Lester Crawford
* Andrew von Eschenbach
* Margaret Hamburg
* Robert Califf
* Scott Gottlieb
* Stephen Hahn
* Robert Califf
* Sara Brenner

Society and culture|

* Criticism of the Food and Drug Administration
* FDA Most Wanted Fugitives
* History of the Food and Drug Administration
* Regulation of food and dietary supplements by the U.S. Food and Drug Administration

* Commissioner of Food and Drugs

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United States Department of Health and Human Services

* Headquarters: Hubert H. Humphrey Building

* Robert F. Kennedy Jr., Secretary of Health and Human Services
* Vacant, Deputy Secretary of Health and Human Services

Secretariat staff offices|

* Office of the Secretary of Health and Human Services
* Office of the Deputy Secretary of Health and Human Services
* Office of Inspector General
* Office of the National Coordinator for Health Information Technology

Public Health Service|

* Office of the Assistant Secretary for Health
* Office of the Surgeon General
* Public Health Service Commissioned Corps
* Agency for Healthcare Research and Quality
* Centers for Disease Control and Prevention
* Agency for Toxic Substances and Disease Registry
* National Center for Injury Prevention and Control
* National Center for Health Statistics
* National Institute for Occupational Safety and Health
* Food and Drug Administration
* Health Resources and Services Administration
* Indian Health Service
* National Institutes of Health
* Substance Abuse and Mental Health Services Administration
* Center for Behavioral Health Statistics and Quality

Human services agencies|

* Administration for Children and Families (Administration for Native Americans, Office of Refugee Resettlement)
* Administration for a Healthy America
* Administration for Community Living
* Administration on Aging
* Centers for Medicare & Medicaid Services

Programs|

* Child Welfare Information Gateway
* National Toxicology Program

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