21 CFR Subchapter F - SUBCHAPTER F—BIOLOGICS
- PART 600—BIOLOGICAL PRODUCTS: GENERAL (§§ 600.2 - 600.90)
- PART 601—LICENSING (§§ 601.2 - 601.95)
- PART 606—CURRENT GOOD MANUFACTURING PRACTICE FOR BLOOD AND BLOOD COMPONENTS (§§ 606.3 - 606.171)
- PART 607—ESTABLISHMENT REGISTRATION AND PRODUCT LISTING FOR MANUFACTURERS OF HUMAN BLOOD AND BLOOD PRODUCTS AND LICENSED DEVICES (§§ 607.1 - 607.80)
- PART 610—GENERAL BIOLOGICAL PRODUCTS STANDARDS (§§ 610.1 - 610.68)
- PART 630—REQUIREMENTS FOR BLOOD AND BLOOD COMPONENTS INTENDED FOR TRANSFUSION OR FOR FURTHER MANUFACTURING USE (§§ 630.1 - 630.40)
- PART 640—ADDITIONAL STANDARDS FOR HUMAN BLOOD AND BLOOD PRODUCTS (§§ 640.1 - 640.130)
- PART 660—ADDITIONAL STANDARDS FOR DIAGNOSTIC SUBSTANCES FOR LABORATORY TESTS (§§ 660.1 - 660.55)
- PART 680—ADDITIONAL STANDARDS FOR MISCELLANEOUS PRODUCTS (§§ 680.1 - 680.3)