Patented formulas. GMP floors. No outsourced R&D.
Three automated lyophilization lines. Proprietary peptide actives at clinically validated concentrations. Every batch documented from raw material to release.
Proprietary actives, not licensed ingredients
ONo third-party licencing, no outsourced compounding.
Lab infrastructure covers peptide synthesis, stability testing, and lyophilization-cycle optimisation。
Three automated lines, zero quality shortcuts
ISO-class clean rooms, automated lyophilization cycles, and in-line environmental monitoring. Every batch passes in-process and final-release inspection before leaving the facility.
Capacity scales from 1 kg sampling runs to multi-tonne annual contracts. Same GMP gates, same documentation, same 72-hour sample turnaround regardless of order size.
Evidence available on request
GMP Certified
1 kg – 1,000 kg
72-Hour Sampling
Confirmed turnaround from formula brief to physical sample. Third-party test reports included with every sample shipment.
GMP-standard workshops with third-party audit records.
Annual capacity supports small-batch sampling through large-volume production contracts with identical quality gates.