Code of Federal Regulations, Title 21, Food and Drugs, Pt. 600-799, Revised as of April 1, 2017

The Code of Federal Regulations is a codification of the general and permanent rules published in the Federal Register by the Executive departments and agencies of the United States Federal Government. This print ISBN is the official U.S. Federal Government edition.
 Title 21 CFR, Parts 600-799, includes rules, regulations, procedures and administrative procedures associated with the Food and Drug Administration and Department of Health and Human Services (biologics), biological products: general, current good manufacturing practice for blood and blood components, establishment registration and product listing for manufacturers of human blood and blood products and licensed devices, cosmetics, cosmetic labeling, cosmetic warning statements, and more...

Related products:
USAMRID's Medical Management of Biological Casualties Handbook is available here: https://bookstore.gpo.gov/products/usamriids-medical-management-biological-casualties-handbook

New Drug Application: Biologic Licensing Application, Archival Copy (Blue Polyethylene Folder) is available here: https://bookstore.gpo.gov/products/new-drug-application-biologic-licensing-application-archival-copy-blue-polyethylene-folder
Military Quantitative Physiology: Problems and Concepts in Military Operational Medicine is available here: https://bookstore.gpo.gov/products/military-quantitative-physiology-problems-and-concepts-military-operational-medicine --NOTE: NO further discount-- already significantly reduced -available while print copies last