The following guideline can be ordered through the address listed in the "Source/Publisher"-category. In cases in which you can order through the Internet we have established a hyperlink.

21 CFR Part 606 Current Good Manufacturing Practice for Blood and Blood Components


US Federal Register

Document Type:
Code of Federal Regulations
US GMP Requirements for manufacturers of blood and blood components

Go back

GMP Conferences by Topics

Cookies help us in providing our services. By using our services, you agree that we use cookies. Further information