Current Good Manufacturing Practices (cGMP) For Blood and Blood Components

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The page below is a sample from the LabCE course Current Good Manufacturing Practices for Transfusion Services. Access the complete course and earn ASCLS P.A.C.E.-approved continuing education credits by subscribing online.

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Current Good Manufacturing Practices (cGMP) For Blood and Blood Components

Part 606 of CFR Title 21 includes the specific cGMP requirements for blood and blood components. In this part, you will find sections that discuss labeling of blood components, compatibility testing, and deviation reporting, among other cGMP requirements specific to blood and blood components.