LANGUAGE
X

SITEMAP

CDMO

About US

Contact

The largest CDMO in Korea

Manufacturing process

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.

  • step. 01

    Cleaning / sterilization / preparation

    CAPA: 150L, 500L
    CAPA: 2㎥
  • step. 02

    Filling

    CAPA: 18,000amp/h
  • step. 03

    Lyophilization

    CAPA : Ice Capa 450Kg * 4대
  • step. 04

    Sealing

    CAPA: 18,000amp/h
  • step. 05

    Foreign matters inspection

    CAPA: 14,400amp/h
  • step. 06

    Labeling/Packing

    CAPA : 6,000V/h
  • step. 07

    Weight selection

    CAPA : 6,000Case/h
  • step. 08

    2D barcode process

    CAPA : 6,000Case/h