Monitoring Gesetzessammlung

Gesetze und Verordnungen USA alphabetisch

A B C D E F G H I J
K L M N O P Q R S T
U V W X Y Z
0 1 2 3 4 5 6 7 8 9
PART 60—PATENT TERM RESTORATION
21 CFR Part 60
PART 600—BIOLOGICAL PRODUCTS: GENERAL
21 CFR Part 600
PART 601—LICENSING
21 CFR Part 601
PART 606—CURRENT GOOD MANUFACTURING PRACTICE FOR BLOOD AND BLOOD COMPONENTS
21 CFR Part 606
PART 607—ESTABLISHMENT REGISTRATION AND PRODUCT LISTING FOR MANUFACTURERS OF HUMAN BLOOD AND BLOOD PRODUCTS AND LICENSED DEVICES
21 CFR Part 607
PART 610—GENERAL BIOLOGICAL PRODUCTS STANDARDS
21 CFR Part 610
PART 630—REQUIREMENTS FOR BLOOD AND BLOOD COMPONENTS INTENDED FOR TRANSFUSION OR FOR FURTHER MANUFACTURING USE
21 CFR Part 630
PART 640—ADDITIONAL STANDARDS FOR HUMAN BLOOD AND BLOOD PRODUCTS
21 CFR Part 640
PART 660—ADDITIONAL STANDARDS FOR DIAGNOSTIC SUBSTANCES FOR LABORATORY TESTS
21 CFR Part 660
PART 680—ADDITIONAL STANDARDS FOR MISCELLANEOUS PRODUCTS
21 CFR Part 680
PART 7—ENFORCEMENT POLICY
21 CFR Part 7
PART 70—COLOR ADDITIVES
21 CFR Part 70
PART 700—GENERAL
21 CFR Part 700
PART 701—COSMETIC LABELING
21 CFR Part 701
PART 71—COLOR ADDITIVE PETITIONS
21 CFR Part 71
PART 710—VOLUNTARY REGISTRATION OF COSMETIC PRODUCT ESTABLISHMENTS
21 CFR Part 710
PART 720—VOLUNTARY FILING OF COSMETIC PRODUCT INGREDIENT COMPOSITION STATEMENTS
21 CFR Part 720
PART 73—LISTING OF COLOR ADDITIVES EXEMPT FROM CERTIFICATION
21 CFR Part 73
PART 74—LISTING OF COLOR ADDITIVES SUBJECT TO CERTIFICATION
21 CFR Part 74
PART 740—COSMETIC PRODUCT WARNING STATEMENTS
21 CFR Part 740
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