Cfr 21, Parts 600 to 799, Food and Drugs, April 01, 2016 (Volume 7 of 9)

Code of Federal Regulations Title 21, Volume 7, April 1, 2016 contains regulations governing Food and Drugs and may also be referenced as:

- Code of Federal Regulations Title 21, Volume 7, April 1, 2016

- 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

- 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