Corporate Profile | Suzhou Tianji Biopharma – New Manufacturing Campus at a Glance

2026-08-14

A core pharmaceutical arm of Suzhou Tianma Pharma Group, Suzhou Tianji Biopharma has specialized in peptide therapeutics for more than 26 years, with a fully integrated value chain spanning peptide APIs and finished dosage forms. Our pipeline spans high-growth franchises, including Tirzepatide, Semaglutide, and other GLP-1 receptor agonists; the oral cyclic peptide Linaclotide; and Peptide-Drug Conjugates (PDCs).

 

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New Production Campus – Changshu New Materials Industrial Park

Metric

Detail

Site Area

80 mu (~5.3 hectares)

Total GFA

53,564 m²

API Workshops

4 international-standard units (2 peptide APIs + 2 small-molecule APIs)

Formulation Workshops

6 GMP-compliant integrated lines

Dedicated Topical Unit

1,500 m² (planned)

Designed and built to global regulatory standards — cGMP, FDA, ICH, and EMA.




Production Capacity Highlights

Category

Capacity & Specs

Peptide APIs

Annual output ≥ 2,000 kg; Synthesizers: 10L–3,000L; Batch scale: 100g to tens of kg

Small-Molecule APIs

Reactors: 500L–5,000L; Temp range: –20°C to 145°C; Batch scale up to metric ton level

Injectables

>300 million units/year (≥200M lyophilized vials + ≥100M small-volume injections)

Topical Dosage Forms

Additional hormonal/non-hormonal capacity in pipeline




Strategic Advantages

· Location: Yangtze River Delta hub — superior logistics and supply-chain connectivity

· Scale: Metric-ton API capacity paired with 100M+ units of annual formulation output

· Compliance: Automated, validated manufacturing lines meeting major global regulatory standards