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)