Federal Register

Code of Federal Regulations (CFR)

CFR TITLE 21

List of Subjects revised as of January 1, 2016.

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 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 112_Standards for the growing, harvesting, packing, and holding of produce for human consumption.
Dietary foods
Food grades and standards
Foods
Fruits
Incorporation by reference
Packaging and containers
Reporting and recordkeeping requirements
Safety
Vegetables
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 117_Current good manufacturing practice, hazard analysis, and risk-based preventive controls for human food.
Food packaging
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
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 329_Nonprescription human drug products subject to section 760 of the Federal Food, Drug, and Cosmetic Act.
Alcohol and alcoholic beverages
Over-the-counter drugs
Reporting and recordkeeping requirements
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 507_Current good manufactring practice, hazard analysis, and risk-based preventive controls for food for animals.
Animal foods
Labeling
Packaging and containers
Reporting and recordkeeping requirements
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_Requirements for blood and blood components intended for transfusion of for further manufacturing use.
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
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 1150_User fees.
Fees
Tobacco products
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 1317_Disposal.
Drug traffic control
Security measures
21 CFR Part 1321_DEA mailing addresses.
Administrative practice and procedure
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

.