1. Cleaning Validation
CIP (Clean in Place)
COP (Clean out of Place)
Manual Cleaning
2. Sterilization
SIP (Steam in Place)
EtO (Ethylene Oxide)
Dry Heat
Steam Autoclave
VHP (Vapor of Hydrogen Peroxide)
Filtration
3. Depyrogenation
4. Lyophilization
5. Mixing Validation
6. Process Capabilities Studies
7. Performance Analyses
8. Scrap Reduction Program