Code of Federal Regulations (alpha)

CFR /  Title 21  /  Part 606: Current Good Manufacturing Practice For Blood And Blood Components

Section No. Description
Section 606.3 Personnel
Section 606.20 Facilities
Section 606.40 Equipment
Section 606.60 Supplies and reagents
Section 606.65 Standard operating procedures
Section 606.100 Plateletpheresis, leukapheresis, and plasmapheresis
Section 606.110 Labeling, general requirements
Section 606.120 Container label
Section 606.121 Circular of information
Section 606.122 Laboratory controls
Section 606.140 Compatibility testing
Section 606.151 Records
Section 606.160 Distribution and receipt; procedures and records
Section 606.165 Adverse reaction file
Section 606.170 Reporting of product deviations by licensed manufacturers, unlicensed registered blood establishments, and transfusion services
Section 606.171 Definitions