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Electronic Code of Federal Regulations

e-CFR data is current as of December 5, 2019

Title 21Chapter ISubchapter F


TITLE 21—Food and Drugs

CHAPTER I—FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED)

SUBCHAPTER F—BIOLOGICS

rule
PartTable of
Contents
Headings
rule
600
600.2 to 600.90
BIOLOGICAL PRODUCTS: GENERAL
601
601.2 to 601.95
LICENSING
606
606.3 to 606.171
CURRENT GOOD MANUFACTURING PRACTICE FOR BLOOD AND BLOOD COMPONENTS
607
607.1 to 607.80
ESTABLISHMENT REGISTRATION AND PRODUCT LISTING FOR MANUFACTURERS OF HUMAN BLOOD AND BLOOD PRODUCTS AND LICENSED DEVICES
610
610.1 to 610.68
GENERAL BIOLOGICAL PRODUCTS STANDARDS
630
630.1 to 630.40
REQUIREMENTS FOR BLOOD AND BLOOD COMPONENTS INTENDED FOR TRANSFUSION OR FOR FURTHER MANUFACTURING USE
640
640.1 to 640.130
ADDITIONAL STANDARDS FOR HUMAN BLOOD AND BLOOD PRODUCTS
660
660.1 to 660.55
ADDITIONAL STANDARDS FOR DIAGNOSTIC SUBSTANCES FOR LABORATORY TESTS
680
680.1 to 680.3
ADDITIONAL STANDARDS FOR MISCELLANEOUS PRODUCTS
rule

SUBCHAPTER G—COSMETICS

700
700.3 to 700.35
GENERAL
701
701.1 to 701.30
COSMETIC LABELING
710
710.1 to 710.9
VOLUNTARY REGISTRATION OF COSMETIC PRODUCT ESTABLISHMENTS
720
720.1 to 720.9
VOLUNTARY FILING OF COSMETIC PRODUCT INGREDIENT COMPOSITION STATEMENTS
740
740.1 to 740.19
COSMETIC PRODUCT WARNING STATEMENTS
741-799
[RESERVED]

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