Code of Federal Regulations (CFR)
CFR TITLE 21
List of Subjects revised as of January 1, 2004.
- 21 CFR Part 1
- Cosmetics
- Drugs
- Exports
- Food labeling
- Imports
- Labeling
- Reporting and recordkeeping requirements
- 21 CFR Part 2
- Administrative practice and procedure
- Cosmetics
- Drugs
- Foods
- 21 CFR Part 3
- Administrative practice and procedure
- Biologics
- Drugs
- Medical devices
- 21 CFR Part 5
- Authority delegations (Government agencies)
- Imports
- Organization and functions (Government agencies)
- 21 CFR Part 7
- Administrative practice and procedure
- Consumer protection
- Reporting and recordkeeping requirements
- 21 CFR Part 10
- Administrative practice and procedure
- News media
- 21 CFR Part 11
- Administrative practice and procedure
- Computer technology
- Reporting and recordkeeping requirements
- 21 CFR Part 12
- Administrative practice and procedure
- 21 CFR Part 13
- Administrative practice and procedure
- 21 CFR Part 14
- Administrative practice and procedure
- Advisory committees
- Color additives
- Drugs
- Radiation protection
- 21 CFR Part 15
- Administrative practice and procedure
- 21 CFR Part 16
- Administrative practice and procedure
- 21 CFR Part 17
- Administrative practice and procedure
- Penalties
- 21 CFR Part 19
- Conflict of interests
- 21 CFR Part 20
- Confidential business information
- Courts
- Freedom of information
- Government employees
- 21 CFR Part 21
- Privacy
- 21 CFR Part 25
- Environmental impact statements
- Foreign relations
- Reporting and recordkeeping requirements
- 21 CFR Part 26
- Animal drugs
- Biologics
- Drugs
- Exports
- Imports
- 21 CFR Part 50
- Human research subjects
- Prisoners
- Reporting and recordkeeping requirements
- Safety
- 21 CFR Part 54
- Biologics
- Drugs
- Medical devices
- Reporting and recordkeeping requirements
- 21 CFR Part 56
- Human research subjects
- Reporting and recordkeeping requirements
- Safety
- 21 CFR Part 58
- Laboratories
- Reporting and recordkeeping requirements
- 21 CFR Part 60
- Administrative practice and procedure
- Drugs
- Food additives
- Inventions and patents
- Medical devices
- Reporting and recordkeeping requirements
- 21 CFR Part 70
- Color additives
- Cosmetics
- Drugs
- Labeling
- Packaging and containers
- 21 CFR Part 71
- Administrative practice and procedure
- Color additives
- Confidential business information
- Cosmetics
- Drugs
- Reporting and recordkeeping requirements
- 21 CFR Part 73
- Color additives
- Cosmetics
- Drugs
- Medical devices
- 21 CFR Part 74
- Color additives
- Cosmetics
- Drugs
- 21 CFR Part 80
- Color additives
- Cosmetics
- Drugs
- Reporting and recordkeeping requirements
- 21 CFR Part 81
- Color additives
- Cosmetics
- Drugs
- 21 CFR Part 82
- Color additives
- Cosmetics
- Drugs
- 21 CFR Part 99
- Administrative practice and procedure
- Biologics
- Drugs
- Medical devices
- Reporting and recordkeeping requirements
- 21 CFR Part 100
- Administrative practice and procedure
- Food labeling
- Food packaging
- Foods
- Intergovernmental relations
- 21 CFR Part 101
- Food labeling
- Nutrition
- Reporting and recordkeeping requirements
- 21 CFR Part 102
- Beverages
- Food grades and standards
- Food labeling
- Frozen foods
- Oils and fats
- Onions
- Potatoes
- Seafood
- 21 CFR Part 104
- Food grades and standards
- Frozen foods
- Nutrition
- 21 CFR Part 105
- Dietary foods
- Food grades and standards
- Food labeling
- Infants and children
- 21 CFR Part 106
- Food grades and standards
- Infants and children
- Nutrition
- Reporting and recordkeeping requirements
- 21 CFR Part 107
- Food labeling
- Infants and children
- Nutrition
- Reporting and recordkeeping requirements
- Signs and symbols
- 21 CFR Part 108
- Administrative practice and procedure
- Foods
- Reporting and recordkeeping requirements
- 21 CFR Part 109
- Food packaging
- Foods
- Polychlorinated biphenyls (PCB's)
- 21 CFR Part 110
- Food packaging
- Foods
- 21 CFR Part 113
- Food packaging
- Foods
- Reporting and recordkeeping requirements
- 21 CFR Part 114
- Food packaging
- Foods
- Reporting and recordkeeping requirements
- 21 CFR Part 115
- Eggs and egg products
- Foods
- 21 CFR Part 119
- Dietary foods
- Food additives
- Foods
- 21 CFR Part 120
- Foods
- Fruit juices
- Imports
- Reporting and recordkeeping requirements
- Vegetable juices
- 21 CFR Part 129
- Beverages
- Bottled water
- Food packaging
- Reporting and recordkeeping requirements
- 21 CFR Part 130
- Food additives
- Food grades and standards
- 21 CFR Part 131
- Cream
- Food grades and standards
- Milk
- Yogurt
- 21 CFR Part 133
- Cheese
- Food grades and standards
- Food labeling
- 21 CFR Part 135
- Food grades and standards
- Food labeling
- Frozen foods
- Ice cream
- 21 CFR Part 136
- Bakery products
- Food grades and standards
- 21 CFR Part 137
- Cereals (food)
- Food grades and standards
- 21 CFR Part 139
- Food grades and standards
- 21 CFR Part 145
- Food grades and standards
- Fruits
- 21 CFR Part 146
- Food grades and standards
- Fruit juices
- 21 CFR Part 150
- Food grades and standards
- Fruits
- 21 CFR Part 152
- Bakery products
- Food grades and standards
- Frozen foods
- Fruits
- 21 CFR Part 155
- Food grades and standards
- Vegetables
- 21 CFR Part 156
- Food grades and standards
- Vegetable juices
- 21 CFR Part 158
- Food grades and standards
- Frozen foods
- Vegetables
- 21 CFR Part 160
- Eggs and egg products
- Food grades and standards
- 21 CFR Part 161
- Food grades and standards
- Frozen foods
- Seafood
- 21 CFR Part 163
- Cacao products
- Food grades and standards
- 21 CFR Part 164
- Food grades and standards
- Nuts
- Peanuts
- 21 CFR Part 165
- Beverages
- Bottled water
- Food grades and standards
- 21 CFR Part 166
- Food grades and standards
- Food labeling
- Margarine
- 21 CFR Part 168
- Food grades and standards
- Sugar
- 21 CFR Part 169
- Food grades and standards
- Oils and fats
- Spices and flavorings
- 21 CFR Part 170
- Administrative practice and procedure
- Food additives
- Reporting and recordkeeping requirements
- 21 CFR Part 171
- Administrative practice and procedure
- Food additives
- 21 CFR Part 172
- Food additives
- Reporting and recordkeeping requirements
- 21 CFR Part 173
- Food additives
- 21 CFR Part 174
- Food additives
- Food packaging
- 21 CFR Part 175
- Adhesives
- Food additives
- Food packaging
- 21 CFR Part 176
- Food additives
- Food packaging
- 21 CFR Part 177
- Food additives
- Food packaging
- 21 CFR Part 178
- Food additives
- Food packaging
- 21 CFR Part 179
- Food additives
- Food labeling
- Food packaging
- Radiation protection
- Reporting and recordkeeping requirements
- Signs and symbols
- 21 CFR Part 180
- Food additives
- 21 CFR Part 181
- Food additives
- Food packaging
- 21 CFR Part 182
- Food additives
- Food packaging
- Spices and flavorings
- 21 CFR Part 184
- Food additives
- 21 CFR Part 186
- Food additives
- Food packaging
- 21 CFR Part 189
- Food additives
- Food packaging
- 21 CFR Part 190
- Food additives
- Reporting and recordkeeping requirements
- 21 CFR Part 200
- Drugs
- Prescription drugs
- 21 CFR Part 201
- Drugs
- Labeling
- Reporting and recordkeeping requirements
- 21 CFR Part 202
- Advertising
- Prescription drugs
- 21 CFR Part 203
- Labeling
- Prescription drugs
- Reporting and recordkeeping requirements
- Warehouses
- 21 CFR Part 205
- Intergovernmental relations
- Prescription drugs
- Reporting and recordkeeping requirements
- Security measures
- Warehouses
- 21 CFR Part 206
- Drugs
- 21 CFR Part 207
- Drugs
- Reporting and recordkeeping requirements
- 21 CFR Part 208
- Labeling
- Prescription drugs
- Reporting and recordkeeping requirements
- 21 CFR Part 210
- Drugs
- Packaging and containers
- 21 CFR Part 211
- Drugs
- Labeling
- Laboratories
- Packaging and containers
- Prescription drugs
- Reporting and recordkeeping requirements
- Warehouses
- 21 CFR Part 216
- Drugs
- Prescription drugs
- 21 CFR Part 225
- Animal drugs
- Animal feeds
- Labeling
- Packaging and containers
- Reporting and recordkeeping requirements
- 21 CFR Part 226
- Animal drugs
- Animal feeds
- Labeling
- Packaging and containers
- Reporting and recordkeeping requirements
- 21 CFR Part 250
- Drugs
- 21 CFR Part 290
- Drugs
- Labeling
- 21 CFR Part 299
- Drugs
- 21 CFR Part 300
- Drugs
- Prescription drugs
- 21 CFR Part 310
- Administrative practice and procedure
- Drugs
- Labeling
- Medical devices
- Reporting and recordkeeping requirements
- 21 CFR Part 312
- Drugs
- Exports
- Imports
- Investigations
- Labeling
- Medical research
- Reporting and recordkeeping requirements
- Safety
- 21 CFR Part 314
- Administrative practice and procedure
- Confidential business information
- Drugs
- Reporting and recordkeeping requirements
- 21 CFR Part 315
- Biologics
- Drugs
- 21 CFR Part 316
- Administrative practice and procedure
- Drugs
- Reporting and recordkeeping requirements
- 21 CFR Part 320
- Drugs
- Reporting and recordkeeping requirements
- 21 CFR Part 328
- Alcohol and alcoholic beverages
- Labeling
- Over-the-counter drugs
- 21 CFR Part 330
- Over-the-counter drugs
- 21 CFR Part 331
- Labeling
- Over-the-counter drugs
- 21 CFR Part 332
- Labeling
- Over-the-counter drugs
- 21 CFR Part 333
- Labeling
- Over-the-counter drugs
- 21 CFR Part 335
- Labeling
- Over-the-counter drugs
- 21 CFR Part 336
- Labeling
- Over-the-counter drugs
- 21 CFR Part 338
- Labeling
- Over-the-counter drugs
- 21 CFR Part 340
- Labeling
- Over-the-counter drugs
- 21 CFR Part 341
- Labeling
- Over-the-counter drugs
- 21 CFR Part 343
- Labeling
- Over-the-counter drugs
- 21 CFR Part 344
- Labeling
- Over-the-counter drugs
- 21 CFR Part 346
- Labeling
- Over-the-counter drugs
- 21 CFR Part 347
- Labeling
- Over-the-counter drugs
- 21 CFR Part 348
- Labeling
- Over-the-counter drugs
- 21 CFR Part 349
- Labeling
- Ophthalmic goods and services
- Over-the-counter drugs
- 21 CFR Part 350
- Labeling
- Over-the-counter drugs
- 21 CFR Part 352
- Labeling
- Over-the-counter drugs
- 21 CFR Part 355
- Labeling
- Over-the-counter drugs
- 21 CFR Part 357
- Labeling
- Over-the-counter drugs
- Reporting and recordkeeping requirements
- 21 CFR Part 358
- Labeling
- Over-the-counter drugs
- 21 CFR Part 361
- Medical research
- Prescription drugs
- Radiation protection
- 21 CFR Part 369
- Labeling
- Medical devices
- Over-the-counter drugs
- 21 CFR Part 429
- Administrative practice and procedure
- Drugs
- Labeling
- Packaging and containers
- Reporting and recordkeeping requirements
- 21 CFR Part 500
- Animal drugs
- Animal feeds
- Cancer
- Labeling
- Packaging and containers
- Polychlorinated biphenyls (PCB's)
- 21 CFR Part 501
- Animal foods
- Labeling
- Packaging and containers
- Reporting and recordkeeping requirements
- 21 CFR Part 502
- Animal foods
- Labeling
- 21 CFR Part 509
- Animal foods
- Packaging and containers
- Polychlorinated biphenyls (PCB's)
- 21 CFR Part 510
- Administrative practice and procedure
- Animal drugs
- Labeling
- Reporting and recordkeeping requirements
- 21 CFR Part 511
- Animal drugs
- Medical research
- Reporting and recordkeeping requirements
- 21 CFR Part 514
- Administrative practice and procedure
- Animal drugs
- Confidential business information
- Reporting and recordkeeping requirements
- 21 CFR Part 515
- Administrative practice and procedure
- Animal drugs
- Confidential business information
- Reporting and recordkeeping requirements
- 21 CFR Part 520
- Animal drugs
- 21 CFR Part 522
- Animal drugs
- 21 CFR Part 524
- Animal drugs
- 21 CFR Part 526
- Animal drugs
- 21 CFR Part 529
- Animal drugs
- 21 CFR Part 530
- Administrative practice and procedure
- Advertising
- Animal drugs
- Labeling
- Reporting and recordkeeping requirements
- 21 CFR Part 556
- Animal drugs
- Foods
- 21 CFR Part 558
- Animal drugs
- Animal feeds
- 21 CFR Part 570
- Animal feeds
- Animal foods
- Food additives
- 21 CFR Part 571
- Administrative practice and procedure
- Animal feeds
- Animal foods
- Food additives
- 21 CFR Part 573
- Animal feeds
- Food additives
- 21 CFR Part 579
- Animal feeds
- Animal foods
- Radiation protection
- 21 CFR Part 582
- Animal feeds
- Animal foods
- Food additives
- 21 CFR Part 584
- Animal feeds
- Food additives
- 21 CFR Part 589
- Animal feeds
- Animal foods
- Food additives
- 21 CFR Part 600
- Biologics
- Reporting and recordkeeping requirements
- 21 CFR Part 601
- Administrative practice and procedure
- Biologics
- Confidential business information
- 21 CFR Part 606
- Blood
- Labeling
- Laboratories
- Reporting and recordkeeping requirements
- 21 CFR Part 607
- Blood
- 21 CFR Part 610
- Biologics
- Labeling
- Reporting and recordkeeping requirements
- 21 CFR Part 630
- Blood
- Reporting and recordkeeping requirements
- 21 CFR Part 640
- Blood
- Labeling
- Reporting and recordkeeping requirements
- 21 CFR Part 660
- Biologics
- Labeling
- Reporting and recordkeeping requirements
- 21 CFR Part 680
- Biologics
- Blood
- Reporting and recordkeeping requirements
- 21 CFR Part 700
- Cosmetics
- Packaging and containers
- 21 CFR Part 701
- Cosmetics
- Labeling
- Reporting and recordkeeping requirements
- 21 CFR Part 710
- Cosmetics
- 21 CFR Part 720
- Confidential business information
- Cosmetics
- 21 CFR Part 740
- Cosmetics
- Labeling
- 21 CFR Part 800
- Administrative practice and procedure
- Medical devices
- Ophthalmic goods and services
- Packaging and containers
- Reporting and recordkeeping requirements
- 21 CFR Part 801
- Labeling
- Medical devices
- Reporting and recordkeeping requirements
- 21 CFR Part 803
- Imports
- Medical devices
- Reporting and recordkeeping requirements
- 21 CFR Part 806
- Imports
- Medical devices
- Reporting and recordkeeping requirements
- 21 CFR Part 807
- Confidential business information
- Imports
- Medical devices
- Reporting and recordkeeping requirements
- 21 CFR Part 808
- Intergovernmental relations
- Medical devices
- 21 CFR Part 809
- Labeling
- Medical devices
- 21 CFR Part 810
- Administrative practice and procedure
- Medical devices
- Reporting and recordkeeping requirements
- 21 CFR Part 812
- Health records
- Medical devices
- Medical research
- Reporting and recordkeeping requirements
- 21 CFR Part 814
- Administrative practice and procedure
- Confidential business information
- Medical devices
- Medical research
- Reporting and recordkeeping requirements
- 21 CFR Part 820
- Medical devices
- Reporting and recordkeeping requirements
- 21 CFR Part 821
- Imports
- Medical devices
- Reporting and recordkeeping requirements
- 21 CFR Part 822
- Medical devices
- Reporting and recordkeeping requirements
- 21 CFR Part 860
- Administrative practice and procedure
- Medical devices
- 21 CFR Part 861
- Administrative practice and procedure
- Medical devices
- Reporting and recordkeeping requirements
- 21 CFR Part 862
- Medical devices
- 21 CFR Part 864
- Blood
- Medical devices
- Packaging and containers
- 21 CFR Part 866
- Biologics
- Laboratories
- Medical devices
- 21 CFR Part 868
- Medical devices
- 21 CFR Part 870
- Medical devices
- 21 CFR Part 872
- Medical devices
- 21 CFR Part 874
- Medical devices
- 21 CFR Part 876
- Medical devices
- 21 CFR Part 878
- Medical devices
- 21 CFR Part 880
- Medical devices
- 21 CFR Part 882
- Medical devices
- 21 CFR Part 884
- Medical devices
- 21 CFR Part 886
- Medical devices
- Ophthalmic goods and services
- 21 CFR Part 888
- Medical devices
- 21 CFR Part 890
- Medical devices
- 21 CFR Part 892
- Medical devices
- Radiation protection
- X-rays
- 21 CFR Part 895
- Administrative practice and procedure
- Labeling
- Medical devices
- 21 CFR Part 898
- Administrative practice and procedure
- Medical devices
- 21 CFR Part 900
- Electronic products
- Health facilities
- Medical devices
- Radiation protection
- Reporting and recordkeeping requirements
- X-rays
- 21 CFR Part 1000
- Electronic products
- Radiation protection
- Reporting and recordkeeping requirements
- X-rays
- 21 CFR Part 1002
- Electronic products
- Radiation protection
- Reporting and recordkeeping requirements
- 21 CFR Part 1003
- Administrative practice and procedure
- Electronic products
- Radiation protection
- 21 CFR Part 1004
- Electronic products
- Radiation protection
- 21 CFR Part 1005
- Administrative practice and procedure
- Electronic products
- Imports
- Radiation protection
- Surety bonds
- 21 CFR Part 1010
- Administrative practice and procedure
- Electronic products
- Exports
- Radiation protection
- 21 CFR Part 1020
- Electronic products
- Medical devices
- Radiation protection
- Reporting and recordkeeping requirements
- Television
- X-rays
- 21 CFR Part 1030
- Electronic products
- Microwave ovens
- Radiation protection
- 21 CFR Part 1040
- Electronic products
- Labeling
- Lasers
- Medical devices
- Radiation protection
- Reporting and recordkeeping requirements
- 21 CFR Part 1050
- Electronic products
- Medical devices
- Radiation protection
- 21 CFR Part 1210
- Administrative practice and procedure
- Imports
- Milk
- Public health
- Reporting and recordkeeping requirements
- 21 CFR Part 1220
- Administrative practice and procedure
- Customs duties and inspection
- Imports
- Public health
- Tea
- 21 CFR Part
- Administrative practice and procedure
- Imports
- Labeling
- Packaging and containers
- Poison prevention
- 21 CFR Part 1240
- Communicable diseases
- Public health
- Travel restrictions
- Water supply
- 21 CFR Part 1250
- Air carriers
- Foods
- Maritime carriers
- Motor carriers
- Public health
- Railroads
- Water supply
- 21 CFR Part 1270
- Communicable diseases
- HIV/AIDS
- Reporting and recordkeeping requirements
- 21 CFR Part 1271
- Biologics
- Drugs
- Human cells and tissue-based products
- Medical devices
- Reporting and recordkeeping requirements
- 21 CFR Part 1300
- Chemicals
- Drug traffic control
- 21 CFR Part 1301
- Administrative practice and procedure
- Drug traffic control
- Security measures
- 21 CFR Part 1302
- Drug traffic control
- Exports
- Imports
- Labeling
- Packaging and containers
- 21 CFR Part 1303
- Administrative practice and procedure
- Drug traffic control
- 21 CFR Part 1304
- Drug traffic control
- Reporting and recordkeeping requirements
- 21 CFR Part 1305
- Drug traffic control
- 21 CFR Part 1306
- Drug traffic control
- Prescription drugs
- 21 CFR Part 1307
- Drug traffic control
- 21 CFR Part 1308
- Administrative practice and procedure
- Drug traffic control
- Reporting and recordkeeping requirements
- 21 CFR Part 1309
- Administrative practice and procedure
- Drug traffic control
- Exports
- Imports
- Security measures
- 21 CFR Part 1310
- Drug traffic control
- Exports
- Imports
- Reporting and recordkeeping requirements
- 21 CFR Part 1312
- Administrative practice and procedure
- Drug traffic control
- Exports
- Imports
- Reporting and recordkeeping requirements
- 21 CFR Part 1313
- Administrative practice and procedure
- Drug traffic control
- Exports
- Imports
- Reporting and recordkeeping requirements
- 21 CFR Part 1316
- Administrative practice and procedure
- Authority delegations (Government agencies)
- Drug traffic control
- Research
- Seizures and forfeitures
- 21 CFR Part 1401
- Freedom of information
- 21 CFR Part 1402
- Classified information
- 21 CFR Part 1403
- Accounting
- Grant programs
- Indians
- Intergovernmental relations
- Reporting and recordkeeping requirements
- 21 CFR Part 1404
- Administrative practice and procedure
- Grant programs
- Loan programs
- Reporting and recordkeeping requirements
- 21 CFR Part 1405
- Administrative practice and procedure
- Drug abuse
- Grant programs
- Loan programs
- Reporting and recordkeeping requirements
