Title 21

Volume 7 CHAPTER I

Chapter I - Food And Drug Administration, Department Of Health And Human Services (continued)

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

21:7.0.1.1SUBCHAP F
SUBCHAPTER F - BIOLOGICS
21:7.0.1.1.1PART 600
   PART 600 - BIOLOGICAL PRODUCTS: GENERAL
21:7.0.1.1.2PART 601
   PART 601 - LICENSING
21:7.0.1.1.3PART 606
   PART 606 - CURRENT GOOD MANUFACTURING PRACTICE FOR BLOOD AND BLOOD COMPONENTS
21:7.0.1.1.4PART 607
   PART 607 - ESTABLISHMENT REGISTRATION AND PRODUCT LISTING FOR MANUFACTURERS OF HUMAN BLOOD AND BLOOD PRODUCTS AND LICENSED DEVICES
21:7.0.1.1.5PART 610
   PART 610 - GENERAL BIOLOGICAL PRODUCTS STANDARDS
21:7.0.1.1.6PART 630
   PART 630 - REQUIREMENTS FOR BLOOD AND BLOOD COMPONENTS INTENDED FOR TRANSFUSION OR FOR FURTHER MANUFACTURING USE
21:7.0.1.1.7PART 640
   PART 640 - ADDITIONAL STANDARDS FOR HUMAN BLOOD AND BLOOD PRODUCTS
21:7.0.1.1.8PART 660
   PART 660 - ADDITIONAL STANDARDS FOR DIAGNOSTIC SUBSTANCES FOR LABORATORY TESTS
21:7.0.1.1.9PART 680
   PART 680 - ADDITIONAL STANDARDS FOR MISCELLANEOUS PRODUCTS
21:7.0.1.2SUBCHAP G
SUBCHAPTER G - COSMETICS
21:7.0.1.2.10PART 700
   PART 700 - GENERAL
21:7.0.1.2.11PART 701
   PART 701 - COSMETIC LABELING
21:7.0.1.2.12PART 710
   PART 710 - VOLUNTARY REGISTRATION OF COSMETIC PRODUCT ESTABLISHMENTS
21:7.0.1.2.13PART 720
   PART 720 - VOLUNTARY FILING OF COSMETIC PRODUCT INGREDIENT COMPOSITION STATEMENTS
21:7.0.1.2.14PART 740
   PART 740 - COSMETIC PRODUCT WARNING STATEMENTS
21:7.0.1.2.15PART 741-799
   PARTS 741-799 [RESERVED]