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

by Office of the Federal Register (Cfr) (Created by)

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