Chapter I-i 6. CHAPTER I—FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED)

• PART 600 [§ 600.2 - § 600.90] - PART 600—BIOLOGICAL PRODUCTS: GENERAL
• PART 601 [§ 601.2 - § 601.95] - PART 601—LICENSING
• PART 606 [§ 606.3 - § 606.171] - PART 606—CURRENT GOOD MANUFACTURING PRACTICE FOR BLOOD AND BLOOD COMPONENTS
• PART 607 [§ 607.1 - § 607.80] - PART 607—ESTABLISHMENT REGISTRATION AND PRODUCT LISTING FOR MANUFACTURERS OF HUMAN BLOOD AND BLOOD PRODUCTS AND LICENSED DEVICES
• PART 610 [§ 610.1 - § 610.68] - PART 610—GENERAL BIOLOGICAL PRODUCTS STANDARDS
• PART 630 [§ 630.1 - § 630.40] - PART 630—REQUIREMENTS FOR BLOOD AND BLOOD COMPONENTS INTENDED FOR TRANSFUSION OR FOR FURTHER MANUFACTURING USE
• PART 640 [§ 640.1 - § 640.130] - PART 640—ADDITIONAL STANDARDS FOR HUMAN BLOOD AND BLOOD PRODUCTS
• PART 660 [§ 660.1 - § 660.55] - PART 660—ADDITIONAL STANDARDS FOR DIAGNOSTIC SUBSTANCES FOR LABORATORY TESTS
• PART 680 [§ 680.1 - § 680.3] - PART 680—ADDITIONAL STANDARDS FOR MISCELLANEOUS PRODUCTS
• PART 700 [§ 700.3 - § 700.35] - PART 700—GENERAL
• PART 701 [§ 701.1 - § 701.30] - PART 701—COSMETIC LABELING
• PART 710 [§ 710.1 - § 710.9] - PART 710—VOLUNTARY REGISTRATION OF COSMETIC PRODUCT ESTABLISHMENTS
• PART 720 [§ 720.1 - § 720.9] - PART 720—VOLUNTARY FILING OF COSMETIC PRODUCT INGREDIENT COMPOSITION STATEMENTS
• PART 740 [§ 740.1 - § 740.19] - PART 740—COSMETIC PRODUCT WARNING STATEMENTS
• PART 741–799 - PARTS 741–799 [RESERVED]