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CDMO

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The largest CDMO in Korea

Manufacturing process

Facility by formulation

  • Lyophilized Injection

We are fully equipped with the automation line following the PIC/S Guidelines for GMP in Pharmaceuticals, from the manufacturing process to the finished packaging process, with tracking management made possible through serial number management.

  • step. 01

    Cleaning / sterilization / preparation

    CAPA : 650L
    • Low-temperature cooling function (up to 3℃)
    • Load cell (METTLER TOLEDO, MAX: 550Kg)
    • CIP / SIP available
    • Automatic transfer system
    • Filter : 10inch(0.2 ~ 0.22㎛)
  • step. 02

    Filling

    CAPA : 18,000V/h
    • Consisting of RABS + Clean Booth
    • HEPA Filter : 0.2㎛(99.997%)
    • 24Ø, 30Ø, 35Ø
    • 100% IPC 8 EA
  • step. 03

    Lyophilization

    CAPA: Ice Capa 550Kg * 3 EA
  • step. 04

    Sealing

    CAPA : 24,000V/h
    • Consisting of RABS + Clean Booth
    • HEPA Filter : 0.2㎛(99.997%)
    • 24Ø, 30Ø, 35Ø
  • step. 05

    Foreign matters inspection

    CAPA : 2,400V/h
    • 24Ø, 26Ø, 30Ø, 38Ø
  • step. 06

    Labeling

    CAPA : 9,000V/h
    • 24Ø, 26Ø, 30Ø, 38Ø
  • step. 07

    Packaging

    CAPA : 900Case/h
    • 24Ø, 26Ø, 30Ø, 38Ø
  • step. 08

    Weight selection

    CAPA : 900Case/h
    • 24Ø, 26Ø, 30Ø, 38Ø
  • step. 09

    2D barcode process

    CAPA : 900Case/h
    • 24Ø, 26Ø, 30Ø, 38Ø