Facility by formulation
- CDMO
- Manufacturing process
- Injection plant
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Facility by formulation
- Injection [Lyophilization / Liquid ampoule]
PAutomation system, 100% IPC process, and RABVS (Restricted Access Barrier System) are configured according to the PIC/S 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, 500L
CAPA: 2㎥
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step. 02
Filling
CAPA: 18,000amp/h
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step. 03
Lyophilization
CAPA : Ice Capa 450Kg * 4대
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step. 04
Sealing
CAPA: 18,000amp/h
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step. 05
Foreign matters inspection
CAPA: 14,400amp/h
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step. 06
Labeling/Packing
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