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

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