Code of Federal Regulations > Title 21 > Chapter I - FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED)

U.S. Code of Federal Regulations

Regulations most recently checked for updates: Mar 30, 2023

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]