Facility by formulation
- CDMO
- Manufacturing process
- Injection plant
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Facility by formulation
- Injection [Lyophilization / Liquid vial]
Automation system, 100% IPC process, and RABVS (Restricted Access Barrier System) are configured according to the PICS Guidelines for GMP in Pharmaceuticals. Automation lines are established from the manufacturing process to the finished packaging process, with tracking management made possible through serial number management.
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step. 01
Cleaning / sterilization / preparation
CAPA : 150L, 300L, 500L
- Load cell (METTLER TOLEDO, CAS)
- CIP/SIP
- Automatic transfer system
CAPA : 12,000V/h
- 15Ø, 22Ø, 24Ø, 26Ø, 30Ø, 33.5Ø, 42Ø, 50Ø
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step. 02
Filling
CAPA : 12,000V/h
- 15Ø, 22Ø, 24Ø, 26Ø, 30Ø, 33.5Ø, 42Ø, 50Ø
- 100% IPC
- CIP / SIP
- High-volume vial filling (- 100mL)
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step. 03
Lyophilization
CAPA: Ice Capa 450Kg * 4 EA
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step. 04
Sealing
CAPA : 12,000V/h
- 15Ø, 22Ø, 24Ø, 26Ø, 30Ø, 33.5Ø, 42Ø, 50Ø
- 20mm, 32mm
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step. 05
Foreign matters inspection
CAPA : 6,000V/h
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step. 06
Labeling
CAPA : 6,000V/h
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step. 07
Weight selection
CAPA : 6,000Case/h
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step. 08
2D barcode process
CAPA : 6,000Case/h
