Download or read book CFR 21, Parts 600 to 799, Food and Drugs, April 01, 2017 (Volume 7 of 9) written by Office of the Federal Register (Cfr) and published by Regulations Press. This book was released on 2017-09-19 with total page 212 pages. Available in PDF, EPUB and Kindle. Book excerpt: 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