CFR 21, Parts 600 to 799, Food and Drugs, April 01, 2017 (Volume 7 of 9) - Paperback

Code of Federal Regulations Title 21, Volume 7, April 1, 2017 contains regulations governing Food and Drugs and may also be referenced as:

- Code of Federal Regulations Title 21, Volume 7, April 1, 2017
- CFR Title 21
- CFR 21, Food and Drugs
- CFR 21, Parts 600 to 799, Food and Drugs

This volume contains Parts 600 to 799:

- Part 600; BIOLOGICAL PRODUCTS: GENERAL
- Part 601; LICENSING
- Part 606; CURRENT GOOD MANUFACTURING PRACTICE FOR BLOOD AND BLOOD COMPONENTS
- Part 607; ESTABLISHMENT REGISTRATION AND PRODUCT LISTING FOR MANUFACTURERS OF HUMAN BLOOD AND BLOOD PRODUCTS AND LICENSED DEVICES
- Part 610; GENERAL BIOLOGICAL PRODUCTS STANDARDS
- Part 630; REQUIREMENTS FOR BLOOD AND BLOOD COMPONENTS INTENDED FOR TRANSFUSION OR FOR FURTHER MANUFACTURING USE
- Part 640; ADDITIONAL STANDARDS FOR HUMAN BLOOD AND BLOOD PRODUCTS
- Part 660; ADDITIONAL STANDARDS FOR DIAGNOSTIC SUBSTANCES FOR LABORATORY TESTS
- Part 680; ADDITIONAL STANDARDS FOR MISCELLANEOUS PRODUCTS
- Part 700; GENERAL
- Part 701; COSMETIC LABELING
- Part 710; VOLUNTARY REGISTRATION OF COSMETIC PRODUCT ESTABLISHMENTS
- Part 720; VOLUNTARY FILING OF COSMETIC PRODUCT INGREDIENT COMPOSITION STATEMENTS
- Part 740; COSMETIC PRODUCT WARNING STATEMENTS
- Parts 741-799; Reserved