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South Korea Operations & Management Taiwan Manufacturing Facilities

Vials

  • Liquid Vials
  • Lyophilized (Powder) Vials

Cartridges

  • Liquid Configurations

Supplements

  • Capsules / Tablets
  • Sublinguals
  • Dermal Patches

Manufacturing configuration support includes:

  • Peptide compatibility assessment
  • Stability and excipient assessment
  • Lyophilization process coordination
  • Production parameter assessment
  • Coordinated quality-control processes across manufacturing operations

Quality & Testing

  • Dedicated QC & QA oversight
  • Raw material qualification & verification
  • Appearance & clarity assessment
  • HPLC identity & purity verification
  • pH and endotoxin testing
  • Stability testing under controlled conditions
  • Batch review & QA-approved final release

Manufacturing & Packaging

  • Aseptic manufacturing environments (ISO 5 / ISO 7)
  • Vials, cartridges, and sterile production formats
  • Sterile filtration procedures (0.22μm)
  • Lyophilization processes — batch and continuous operations
  • Secondary packaging and labeling operations
  • Temperature-controlled packaging procedures
  • Private-label packaging coordination
1

Supply Coordination

Manufacturing and sourcing activities are coordinated across multi-region production operations.
2

Production Planning

Integrated testing and coordinated production procedures support manufacturing timelines across production stages.
3

Sourcing Operations

International sourcing activities support raw material procurement within documented manufacturing procedures.
4

Long-Term Supply Coordination

Manufacturing infrastructure supports ongoing production activities and manufacturing documentation procedures.