Federal Register

Code of Federal Regulations (CFR)

CFR TITLE 21

List of Subjects revised as of April 1, 2015.

21 CFR Part 1_General enforcement regulations.
Cosmetics
Drugs
Exports
Food labeling
Imports
Labeling
Reporting and recordkeeping requirements
21 CFR Part 2_General administrative rulings and decisions.
Administrative practice and procedure
Cosmetics
Drugs
Foods
21 CFR Part 3_Product jurisdiction.
Administrative practice and procedure
Biologics
Drugs
Medical devices
21 CFR Part 4_Regulation of combination products.
Biologics
Drugs
Human cells and tissue-based products
Medical devices
21 CFR Part 5_Organization.
Authority delegations (Government agencies)
Imports
Organization and functions (Government agencies)
21 CFR Part 7_Enforcement policy.
Administrative practice and procedure
Consumer protection
Reporting and recordkeeping requirements
21 CFR Part 10_Administrative practices and procedures.
Administrative practice and procedure
News media
21 CFR Part 11_Electronic records; electronic signatures.
Computer technology
Reporting and recordkeeping requirements
21 CFR Part 12_Formal evidentiary public hearing.
Administrative practice and procedure
21 CFR Part 13_Public hearing before a public board of inquiry.
Administrative practice and procedure
21 CFR Part 14_Public hearing before a public advisory committee.
Administrative practice and procedure
Advisory committees
Color additives
Drugs
Radiation protection
21 CFR Part 15_Public hearing before the Commissioner.
Administrative practice and procedure
21 CFR Part 16_Regulatory hearing before the Food and Drug Administration.
Administrative practice and procedure
21 CFR Part 17_Civil money penalties hearings.
Administrative practice and procedure
Penalties
21 CFR Part 19_Standards of conduct and conflicts of interest.
Conflict of interests
21 CFR Part 20_Public information.
Confidential business information
Courts
Freedom of information
Government employees
21 CFR Part 21_Protection of privacy.
Privacy
21 CFR Part 25_Environmental impact considerations.
Environmental impact statements
Foreign relations
Reporting and recordkeeping requirements
21 CFR Part 26_Mutual recognition of pharmaceutical good manufacturing practice reports, medical device quality system audit reports, and certain medical device product evaluation reports: United States and the European Community.
Animal
Animal drugs
Biologics
Drugs
Exports
Imports
21 CFR Part 50_Protection of human subjects.
Human research subjects
Prisoners
Reporting and recordkeeping requirements
Safety
21 CFR Part 54_Financial disclosure by clinical investigators.
Biologics
Drugs
Medical devices
Reporting and recordkeeping requirements
21 CFR Part 56_Institutional review boards.
Human research subjects
Reporting and recordkeeping requirements
Safety
21 CFR Part 58_Good laboratory practice for nonclinical laboratory studies.
Laboratories
Reporting and recordkeeping requirements
21 CFR Part 60_Patent term restoration.
Administrative practice and procedure
Drugs
Food additives
Inventions and patents
Medical devices
Reporting and recordkeeping requirements
21 CFR Part 70_Color additives.
Color additives
Cosmetics
Drugs
Labeling
Packaging and containers
21 CFR Part 71_Color additive petitions.
Administrative practice and procedure
Color additives
Confidential business information
Cosmetics
Drugs
Reporting and recordkeeping requirements
21 CFR Part 73_Listing of color additives exempt from certification.
Color additives
Cosmetics
Drugs
Medical devices
21 CFR Part 74_Listing of color additives subject to certification.
Color additives
Cosmetics
Drugs
21 CFR Part 80_Color additive certification.
Color additives
Cosmetics
Drugs
Reporting and recordkeeping requirements
21 CFR Part 81_General specifications and general restrictions for provisional color additives for use in foods, drugs, and cosmetics.
Color additives
Cosmetics
Drugs
21 CFR Part 82_Listing of certified provisionally listed colors and specifications.
Color additives
Cosmetics
Drugs
21 CFR Part 99_Dissemination of information on unapproved/new uses for marketed drugs, biologics, and devices.
Administrative practice and procedure
Biologics
Drugs
Medical devices
Reporting and recordkeeping requirements
21 CFR Part 100_General.
Administrative practice and procedure
Food labeling
Food packaging
Foods
Intergovernmental relations
21 CFR Part 101_Food labeling.
Food labeling
Nutrition
Reporting and recordkeeping requirements
21 CFR Part 102_Common or usual name for nonstandardized foods.
Beverages
Food grades and standards
Food labeling
Frozen foods
Oils and fats
Onions
Potatoes
Seafood
21 CFR Part 104_Nutritional quality guidelines for foods.
Food grades and standards
Frozen foods
Nutrition
21 CFR Part 105_Foods for special dietary use.
Dietary foods
Food grades and standards
Food labeling
Infants and children
21 CFR Part 106_Infant formula quality control procedures.
Food grades and standards
Infants and children
Nutrition
Reporting and recordkeeping requirements
21 CFR Part 107_Infant formula.
Food labeling
Infants and children
Nutrition
Reporting and recordkeeping requirements
Signs and symbols
21 CFR Part 108_Emergency permit control.
Administrative practice and procedure
Foods
Reporting and recordkeeping requirements
21 CFR Part 109_Unavoidable contaminants in food for human consumption and food-packaging material.
Food packaging
Foods
Polychlorinated biphenyls (PCB's)
21 CFR Part 110_Current good manufacturing practice in manufacturing, packing, or holding human food.
Food packaging
Foods
21 CFR Part 111_Current good manufacturing practice in manufacturing, packaging, labeling, or holding operations for dietary supplements.
Dietary foods
Drugs
Foods
Packaging and containers
21 CFR Part 113_Thermally processed low-acid foods packaged in hermetically sealed containers.
Food packaging
Foods
Reporting and recordkeeping requirements
21 CFR Part 114_Acidified foods.
Food packaging
Foods
Reporting and recordkeeping requirements
21 CFR Part 115_Shell eggs.
Eggs and egg products
Foods
21 CFR Part 118_Production, storage, and transportation of shell eggs.
Eggs and egg products
Food grades and standards
Reporting and recordkeeping requirements
21 CFR Part 119_Dietary supplements that present a significant or unreasonable risk.
Dietary foods
Food additives
Foods
21 CFR Part 120_Hazard Analysis and Critical Control Point (HACCP) systems.
Foods
Fruit juices
Imports
Reporting and recordkeeping requirements
Vegetable juices
21 CFR Part 123_Fish and fishery products.
Fish
Fisheries
Food grades and standards
Imports
Reporting and recordkeeping requirements
Seafood
21 CFR Part 129_Processing and bottling of bottled drinking water.
Beverages
Bottled water
Food packaging
Reporting and recordkeeping requirements
21 CFR Part 130_Food standards: General.
Food additives
Food grades and standards
21 CFR Part 131_Milk and cream.
Cream
Food grades and standards
Milk
Yogurt
21 CFR Part 133_Cheeses and related cheese products.
Cheese
Food grades and standards
Food labeling
21 CFR Part 135_Frozen desserts.
Food grades and standards
Food labeling
Frozen foods
Ice cream
21 CFR Part 136_Bakery products.
Bakery products
Food grades and standards
21 CFR Part 137_Cereal flours and related products.
Cereals (food)
Food grades and standards
21 CFR Part 139_Macaroni and noodle products.
Food grades and standards
21 CFR Part 145_Canned fruits.
Food grades and standards
Fruits
21 CFR Part 146_Canned fruit juices.
Food grades and standards
Fruit juices
21 CFR Part 150_Fruit butters, jellies, preserves, and related products.
Food grades and standards
Fruits
21 CFR Part 152_Fruit pies.
Bakery products
Food grades and standards
Frozen foods
Fruits
21 CFR Part 155_Canned vegetables.
Food grades and standards
Vegetables
21 CFR Part 156_Vegetable juices.
Food grades and standards
Vegetable juices
21 CFR Part 158_Frozen vegetables.
Food grades and standards
Frozen foods
Vegetables
21 CFR Part 160_Eggs and egg products.
Eggs and egg products
Food grades and standards
21 CFR Part 161_Fish and shellfish.
Food grades and standards
Frozen foods
Seafood
21 CFR Part 163_Cacao products.
Cacao products
Food grades and standards
21 CFR Part 164_Tree nut and peanut products.
Food grades and standards
Nuts
21 CFR Part 164_Tree nut and peanut products.
Peanuts
21 CFR Part 165_Beverages.
Beverages
Bottled water
Food grades and standards
21 CFR Part 166_Margarine.
Food grades and standards
Food labeling
Margarine
21 CFR Part 168_Sweeteners and table sirups.
Food grades and standards
Sugar
21 CFR Part 169_Food dressings and flavorings.
Food grades and standards
Oils and fats
Spices and flavorings
21 CFR Part 170_Food additives.
Administrative practice and procedure
Food additives
Reporting and recordkeeping requirements
21 CFR Part 171_Food additive petitions.
Administrative practice and procedure
Food additives
21 CFR Part 172_Food additives permitted for direct addition to food for human consumption.
Food additives
Reporting and recordkeeping requirements
21 CFR Part 173_Secondary direct food additives permitted in food for human consumption.
Food additives
21 CFR Part 174_Indirect food additives: General.
Food additives
Food packaging
21 CFR Part 175_Indirect food additives: Adhesives and components of coatings.
Adhesives
Food additives
Food packaging
21 CFR Part 176_Indirect food additives: Paper and paperboard components.
Food additives
Food packaging
21 CFR Part 177_Indirect food additives: Polymers.
Food additives
Food packaging
21 CFR Part 178_Indirect food additives: Adjuvants, production aids, and sanitizers.
Food additives
Food packaging
21 CFR Part 179_Irradiation in the production, processing and handling of food.
Food additives
Food labeling
Food packaging
Radiation protection
Reporting and recordkeeping requirements
Signs and symbols
21 CFR Part 180_Food additives permitted in food on an interim basis or in contact with food pending additional study.
Food additives
21 CFR Part 181_Prior-sanctioned food ingredients.
Food additives
Food packaging
21 CFR Part 182_Substances generally recognized as safe.
Food additives
Food packaging
Spices and flavorings
21 CFR Part 184_Direct food substances affirmed as generally recognized as safe._
Food additives
21 CFR Part 186_Indirect food substances affirmed as generally recognized as safe.
Food additives
Food packaging
21 CFR Part 189_Substances prohibited from use in human food.
Food additives
Food packaging
21 CFR Part 190_Dietary supplements.
Food additives
Reporting and recordkeeping requirements
21 CFR Part 200_General.
Drugs
Prescription drugs
21 CFR Part 201_Labeling.
Drugs
Labeling
Reporting and recordkeeping requirements
21 CFR Part 202_Prescription drug advertising.
Advertising
Prescription drugs
21 CFR Part 203_Prescription drug marketing.
Labeling
Prescription drugs
Reporting and recordkeeping requirements
Warehouses
21 CFR Part 205_Guidelines for State licensing of wholesale prescription drug distributors.
Intergovernmental relations
Prescription drugs
Reporting and recordkeeping requirements
Security measures
Warehouses
21 CFR Part 206_Imprinting of solid oral dosage form drug products for human use.
Drugs
21 CFR Part 207_Registration of producers of drugs and listing of drugs in commercial distribution.
Drugs
Reporting and recordkeeping requirements
21 CFR Part 208_Medication guides for prescription products.
Labeling
Prescription drugs
Reporting and recordkeeping requirements
21 CFR Part 209_Requirements for authorized dispensers and pharmacies to distribute a side effects statement.
Drugs
Prescription drugs
21 CFR Part 210_Current good manufacturing practice in manufacturing, processing, packing, or holding of drugs: General.
Drugs
Packaging and containers
21 CFR Part 211_Current good manufacturing practice for finished pharmaceuticals.
Drugs
Labeling
Laboratories
Packaging and containers
Prescription drugs
Reporting and recordkeeping requirements
Warehouses
21 CFR Part 212_Current good manufacturing practice for positron emission tomography drugs.
Drugs
Labeling
Laboratories
Packaging and containers
Prescription drugs
Reporting and recordkeeping requirements
21 CFR Part 216_Pharmacy compounding.
Drugs
Prescription drugs
21 CFR Part 225_Current good manufacturing practice for medicated feeds.
Animal drugs
Animal feeds
Labeling
Packaging and containers
Reporting and recordkeeping requirements
21 CFR Part 226_Current good manufacturing practice for Type A medicated articles.
Animal drugs
Animal feeds
Labeling
Packaging and containers
Reporting and recordkeeping requirements
21 CFR Part 250_Special requirements for specific human drugs.
Drugs
21 CFR Part 290_Controlled drugs.
Drugs
Labeling
21 CFR Part 299_Drugs: official names and established names.
Drugs
21 CFR Part 300_General.
Drugs
Prescription drugs
21 CFR Part 310_New drugs.
Administrative practice and procedure
Drugs
Labeling
Medical devices
Medical devices
Reporting and recordkeeping requirements
21 CFR Part 312_Investigational new drug application.
Drugs
Exports
Imports
Investigations
Labeling
Medical research
Reporting and recordkeeping requirements
Safety
21 CFR Part 314_Applications for FDA approval to market a new drug.
Administrative practice and procedure
Confidential business information
Drugs
Reporting and recordkeeping requirements
21 CFR Part 315_Diagnostic radiopharmaceuticals.
Biologics
Drugs
21 CFR Part 316_Orphan drugs.
Administrative practice and procedure
Drugs
Investigations
Medical research
Reporting and recordkeeping requirements
21 CFR Part 320_Bioavailability and bioequivalence requirements.
Drugs
Reporting and recordkeeping requirements
21 CFR Part 328_Over-the-counter drug products intended for oral ingestion that contain alcohol.
Alcohol and alcoholic beverages
Labeling
Over-the-counter drugs
21 CFR Part 330_Over-the-counter (OTC) human drugs which are generally recognized as safe and effective and not misbranded.
Over-the-counter drugs
21 CFR Part 331_Antacid products for over-the-counter (OTC) human use.
Labeling
Over-the-counter drugs
21 CFR Part 332_Antiflatulent products for over-the-counter human use.
Labeling
Over-the-counter drugs
21 CFR Part 333_Topical antimicrobial drug products for over-the-counter human use.
Labeling
Over-the-counter drugs
21 CFR Part 335_Antidiarrheal drug products for over-the-counter human use.
Labeling
Over-the-counter drugs
21 CFR Part 336_Antiemetic drug products for over-the-counter human use.
Labeling
Over-the-counter drugs
21 CFR Part 338_Nighttime sleep-aid drug products for over-the-counter human use.
Labeling
Over-the-counter drugs
21 CFR Part 340_Stimulant drug products for over-the-counter human use.
Labeling
Over-the-counter drugs
21 CFR Part 341_Cold, cough, allergy, bronchodilator, and antiasthmatic drug products for over-the-counter human use.
Labeling
Over-the-counter drugs
21 CFR Part 343_Internal analgesic, antipyretic, and antirheumatic drug products for over-the-counter human use.
Labeling
Over-the-counter drugs
21 CFR Part 344_Topical otic drug products for over-the-counter human use.
Labeling
Over-the-counter drugs
21 CFR Part 346_Anorectal drug products for over-the-counter human use.
Labeling
Over-the-counter drugs
21 CFR Part 347_Skin protectant drug products for over-the-counter human use.
Labeling
Over-the-counter drugs
21 CFR Part 348_External analgesic drug products for over-the-counter human use.
Labeling
Over-the-counter drugs
21 CFR Part 349_Ophthalmic drug products for over-the-counter human use.
Labeling
Ophthalmic goods and services
Over-the-counter drugs
21 CFR Part 350_Antiperspirant drug products for over-the-counter human use.
Labeling
Over-the-counter drugs
21 CFR Part 352_Sunscreen drug products for over-the-counter human use.
Labeling
Over-the-counter drugs
21 CFR Part 355_Anticaries drug products for over-the-counter human use.
Labeling
Over-the-counter drugs
21 CFR Part 357_Miscellaneous internal drug products for over-the-counter human use.
Labeling
Over-the-counter drugs
Reporting and recordkeeping requirements
21 CFR Part 358_Miscellaneous external drug products for over-the-counter human use.
Labeling
Over-the-counter drugs
21 CFR Part 361_Prescription drugs for human use generally recognized as safe and effective and not misbranded: drugs used in research.
Medical research
Prescription drugs
Radiation protection
21 CFR Part 369_Interpretative statements re: warnings on drugs and devices for over-the-counter sale.
Labeling
Medical devices
Over-the-counter drugs
21 CFR Part 500_General.
Animal drugs
Animal feeds
Cancer
Labeling
Packaging and containers
Polychlorinated biphenyls (PCB's)
21 CFR Part 501_Animal food labeling.
Animal foods
Packaging and containers
Reporting and recordkeeping requirements
21 CFR Part 502_Common or usual names for nonstandardized animal foods.
Animal foods
Labeling
21 CFR Part 509_Unavoidable contaminants in animal food and food-packaging material.
Animal foods
Packaging and containers
Polychlorinated biphenyls (PCB's)
21 CFR Part 510_New animal drugs.
Administrative practice and procedure
Animal
Labeling
Reporting and recordkeeping requirements
21 CFR Part 511_New animal drugs for investigational use.
Animal drugs
Medical research
Reporting and recordkeeping requirements
21 CFR Part 514_New animal drug applications.
Administrative practice and procedure
Animal drugs
Confidential business information
Reporting and recordkeeping requirements
21 CFR Part 515_Medicated feed mill license.
Administrative practice and procedure
Animal drugs
Confidential business information
Reporting and recordkeeping requirements
21 CFR Part 516_New animal drugs for minor use and minor species.
Administrative practice and procedure
Animal drugs
Confidential business information
Reporting and recordkeeping requirements
21 CFR Part 520_Oral dosage form new animal drugs.
Animal drugs
21 CFR Part 522_Implantation or injectable dosage form new animal drugs.
Animal drugs
21 CFR Part 524_Ophthalmic and topical dosage form new animal drugs.
Animal drugs
21 CFR Part 526_Intramammary dosage forms.
Animal drugs
21 CFR Part 528_New animal drugs in genetically engineered animals.
Animal drugs
21 CFR Part 529_Certain other dosage form new animal drugs.
Animal drugs
21 CFR Part 530_Extralabel drug use in animals.
Administrative practice and procedure
Advertising
Animal drugs
Labeling
Reporting and recordkeeping requirements
21 CFR Part 556_Tolerances for residues of new animal drugs in food.
Animal drugs
Foods
21 CFR Part 558_New animal drugs for use in animal feeds.
Animal drugs
Animal feeds
21 CFR Part 570_Food additives.
Animal feeds
Animal foods
Food additives
21 CFR Part 571_Food additive petitions.
Administrative practice and procedure
Animal feeds
Animal foods
Food additives
21 CFR Part 573_Food additives permitted in feed and drinking water of animals.
Animal feeds
Food additives
21 CFR Part 579_Irradiation in the production, processing, and handling of animal feed and pet food.
Animal feeds
Animal foods
Radiation protection
21 CFR Part 582_Substances generally recognized as safe.
Animal feeds
Animal foods
Food additives
21 CFR Part 584_Food substances affirmed as generally recognized as safe in feed and drinking water of animals.
Animal feeds
Food additives
21 CFR Part 589_Substances prohibited from use in animal food or feed.
Animal feeds
Animal foods
Food additives
21 CFR Part 600_Biological products: General.
Biologics
Reporting and recordkeeping requirements
21 CFR Part 601_Licensing.
Administrative practice and procedure
Biologics
Confidential business information
21 CFR Part 606_Current good manufacturing practice for blood and blood components.
Blood
Labeling
Laboratories
Reporting and recordkeeping requirements
21 CFR Part 607_Establishment registration and product listing for manufacturers of human blood and blood products.
Blood
21 CFR Part 610_General biological products standards.
Biologics
Labeling
Reporting and recordkeeping requirements
21 CFR Part 630_General requirements for blood, blood components, and blood derivatives.
Blood
Reporting and recordkeeping requirements
21 CFR Part 640_Additional standards for human blood and blood products.
Blood
Labeling
Reporting and recordkeeping requirements
21 CFR Part 660_Additional standards for diagnostic substances for laboratory tests.
Biologics
Labeling
Reporting and recordkeeping requirements
21 CFR Part 680_Additional standards for miscellaneous products.
Biologics
Blood
Reporting and recordkeeping requirements
21 CFR Part 700_General.
Cosmetics
Packaging and containers
21 CFR Part 701_Cosmetic labeling.
Cosmetics
Labeling
Reporting and recordkeeping requirements
21 CFR Part 710_Voluntary registration of cosmetic product establishments.
Cosmetics
21 CFR Part 720_Voluntary filing of cosmetic product ingredient composition statements.
Confidential business information
Cosmetics
21 CFR Part 740_Cosmetic product warning statements.
Cosmetics
Labeling
21 CFR Part 800_General.
Administrative practice and procedure
Medical devices
Ophthalmic goods and services
Packaging and containers
Reporting and recordkeeping requirements
21 CFR Part 801_Labeling.
Labeling
Medical devices
Reporting and recordkeeping requirements
21 CFR Part 803_Medical device reporting.
Imports
Medical devices
Reporting and recordkeeping requirements
21 CFR Part 806_Medical devices; reports of corrections and removals.
Imports
Medical devices
Reporting and recordkeeping requirements
21 CFR Part 807_Establishment registration and device listing for manufacturers and initial importers of devices.
Confidential business information
Imports
Medical devices
Reporting and recordkeeping requirements
21 CFR Part 808_Exemptions from Federal preemption of State and local medical device requirements.
Intergovernmental relations
Medical devices
21 CFR Part 809_In vitro diagnostic products for human use.
Labeling
Medical devices
21 CFR Part 810_Medical device recall authority.
Administrative practice and procedure
Medical devices
Reporting and recordkeeping requirements
21 CFR Part 812_Investigational device exemptions.
Health records
Medical devices
Medical research
Reporting and recordkeeping requirements
21 CFR Part 814_Premarket approval of medical devices.
Administrative practice and procedure
Confidential business information
Medical devices
Medical research
Reporting and recordkeeping requirements
21 CFR Part 820_Quality system regulation.
Medical devices
Reporting and recordkeeping requirements
21 CFR Part 821_Medical device tracking requirements.
Imports
Medical devices
Reporting and recordkeeping requirements
21 CFR Part 822_Postmarket surveillance.
Medical devices
21 CFR Part 822_Postmarket surveillance.
Reporting and recordkeeping requirements
21 CFR Part 830_Unique device identification.
Administrative practice and procedure
Incorporation by reference
Labeling
Medical devices
Reporting and recordkeeping requirements
21 CFR Part 860_Medical device classification procedures.
Administrative practice and procedure
Medical devices
21 CFR Part 861_Procedures for performance standards development.
Administrative practice and procedure
Medical devices
Reporting and recordkeeping requirements
21 CFR Part 862_Clinical chemistry and clinical toxicology devices.
Medical devices
21 CFR Part 864_Hematology and pathology devices.
Blood
Medical devices
Packaging and containers
21 CFR Part 866_Immunology and microbiology devices.
Biologics
Laboratories
Medical devices
21 CFR Part 868_Anesthesiology devices.
Medical devices
21 CFR Part 870_Cardiovascular devices.
Medical devices
21 CFR Part 872_Dental devices.
Medical devices
21 CFR Part 874_Ear, nose, and throat devices.
Medical devices
21 CFR Part 876_Gastroenterology-urology devices.
Medical devices
21 CFR Part 878_General and plastic surgery devices.
Medical devices
21 CFR Part 880_General hospital and personal use devices.
Medical devices
21 CFR Part 882_Neurological devices.
Medical devices
21 CFR Part 884_Obstetrical and gynecological devices.
Medical devices
21 CFR Part 886_Ophthalmic devices.
Medical devices
Ophthalmic goods and services
21 CFR Part 888_Orthopedic devices.
Medical devices
21 CFR Part 890_Physical medicine devices.
Medical devices
21 CFR Part 892_Radiology devices.
Medical devices
Radiation protection
X-rays
21 CFR Part 895_Banned devices.
Administrative practice and procedure
Labeling
Medical devices
21 CFR Part 898_Performance standard for electrode lead wires and patient cables.
Administrative practice and procedure
Medical devices
21 CFR Part 900_Mammography.
Electronic funds transfer
Health facilities
Medical devices
Radiation protection
Reporting and recordkeeping requirements
X-rays
21 CFR Part 1000_General.
Electronic funds transfer
Radiation protection
Reporting and recordkeeping requirements
X-rays
21 CFR Part 1002_Records and reports.
Electronic funds transfer
Radiation protection
Reporting and recordkeeping requirements
21 CFR Part 1003_Notification of defects or failure to comply.
Administrative practice and procedure
Electronic funds transfer
Radiation protection
21 CFR Part 1004_Repurchase, repairs, or replacement of electronic products.
Electronic funds transfer
Radiation protection
21 CFR Part 1005_Importation of electronic products.
Administrative practice and procedure
Electronic funds transfer
Imports
Radiation protection
Surety bonds
21 CFR Part 1010_Performance standards for electronic products: General.
Administrative practice and procedure
Electronic funds transfer
Exports
Radiation protection
21 CFR Part 1020_Performance standards for ionizing radiation emitting products.
Electronic funds transfer
Medical devices
Radiation protection
Reporting and recordkeeping requirements
Television
X-rays
21 CFR Part 1030_Performance standards for microwave and radio frequency emitting products.
Electronic funds transfer
Microwave ovens
Radiation protection
21 CFR Part 1040_Performance standards for light-emitting products.
Electronic funds transfers
Labeling
Lasers
Medical devices
Radiation protection
Reporting and recordkeeping requirements
21 CFR Part 1050_Performance standards for sonic, infrasonic, and ultrasonic radiation-emitting products.
Electronic funds transfers
Medical devices
Radiation protection
21 CFR Part 1107_Establishment registration, product listing, and subsequent equivalence reports.
Tobacco
21 CFR Part 1140_Cigarettes and smokeless tobacco.
Advertising
Labeling
Smoking
Tobacco
21 CFR Part 1141_Cigarette package and advertising warnings.
Advertising
Labeling
Packaging and containers
Smoking
Tobacco
21 CFR Part 1210_Regulations under the Federal Import Milk Act.
Administrative practice and procedure
Imports
Milk
Public health
Reporting and recordkeeping requirements
21 CFR Part 1230_Regulations under the Federal Caustic Poison Act.
Administrative practice and procedure
Labeling
Packaging and containers
Poison prevention
21 CFR Part 1240_Control of communicable diseases.
Communicable diseases
Public health
Travel restrictions
Water supplies
21 CFR Part 1250_Interstate conveyance sanitation.
Air carriers
Foods
Maritime carriers
Motor carriers
Public health
Railroads
Water supplies
21 CFR Part 1270_Human tissue intended for transplantation.
Communicable diseases
HIV/AIDS
Reporting and recordkeeping requirements
21 CFR Part 1271_Human cells, tissues, and cellular and tissue-based products.
Biologics
Communicable diseases
Drugs
HIV/AIDS
Human cells and tissue-based products
Medical devices
Reporting and recordkeeping requirements
21 CFR Part 1300_Definitions.
Chemicals
traffic control
21 CFR Part 1301_Registration of manufacturers, distributors, and dispensers of controlled substances.
Administrative practice and procedure
Drug traffic control
Security measures
21 CFR Part 1302_Labeling and packaging requirements for controlled substances.
Drug traffic control
Exports
Imports
Labeling
Packaging and containers
21 CFR Part 1303_Quotas.
Administrative practice and procedure
Drug traffic control
21 CFR Part 1304_Records and reports of registrants.
Drug traffic control
Reporting and recordkeeping requirements
21 CFR Part 1305_Orders for Schedule I and II controlled substances.
Drug traffic control
Reporting and recordkeeping requirements
21 CFR Part 1306_Prescriptions.
Drug traffic control
Prescription drugs
21 CFR Part 1307_Miscellaneous.
Drug traffic control
21 CFR Part 1308_Schedules of controlled substances.
Administrative practice and procedure
Drug traffic control
Reporting and recordkeeping requirements
21 CFR Part 1309_Registration of manufacturers, distributors, importers and exporters and List I chemicals.
Administrative practice and procedure
Drug traffic control
Exports
Imports
Security measures
21 CFR Part 1310_Records and reports of listed chemicals and certain machines.
Drug traffic control
Exports
Imports
Reporting and recordkeeping requirements
21 CFR Part 1311_Requirements for electronic orders and prescriptions.
Administrative practice and procedure
Control substances
Drug traffic control
Prescription drugs
Reporting and recordkeeping requirements
21 CFR Part 1312_Importation and exportation of controlled substances.
Administrative practice and procedure
Drug traffic control
Exports
Imports
Reporting and recordkeeping requirements
21 CFR Part 1313_Importation and exportation of List I and List II chemicals.
Administrative practice and procedure
Drug traffic control
Exports
Imports
Reporting and recordkeeping requirements
21 CFR Part 1314_Retail sale of scheduled listed chemical products.
Drug traffic control
Reporting and recordkeeping requirements
21 CFR Part 1315_Importation and production quotas for ephedrine, pseudoephedrine, and phenylpropanolamine.
Administrative practice and procedure
Chemicals
Drug traffic control
Imports
Reporting and recordkeeping requirements
21 CFR Part 1316_Administrative functions, practices, and procedures.
Administrative practice and procedure
Authority delegations (Government agencies)
Drug traffic control
Research
Seizures and forfeitures
21 CFR Part 1321_DEA mailing addresses.
Administrative practice and procedure
21 CFR Part 1321_DEA mailing addresses.
Drug traffic control
Reporting and recordkeeping requirements
21 CFR Part 1401_Public availability of information.
Freedom of information
21 CFR Part 1402_Mandatory declassification review.
Classified information

Top of Page

Federal Register >

The U.S. National Archives and Records Administration
1-86-NARA-NARA or 1-866-272-6272

.