Evaluation and manufacture of blood components - Chapter 6

• 6.1: Scope of the guidelines
• 6.2: Setting and maintaining specifications
• 6.3: Component and process monitoring tests
• 6.4: Component processing
• 6.5: Component shelf life
• 6.6: Labelling
• 6.7: Component storage
• 6.8: Non-conforming components and biohazards
• 6.9: Component release
• 6.10: Release of components which do not conform to specified requirements
• 6.11: Transportation of blood components
• 6.12: Component recall and traceability
• 6.13: References