WuXi Biologics
Offering End-to-End Solutions
GMP Drug Product Formulation, Fill and Lyophilization
ADC/Bioconjugate Drug Product(DP) GMP Manufacturing Capabilities
As a leading Contract Research, Development and Manufacturing Organization (CRDMO), we provide a variety of Drug Product GMP filling services not only for antibody drug conjugates and other bioconjugates but also cytotoxic compounds and small molecule products in WuXi XDC’s GMP manufacturing facility located in Wuxi, China. Our services include compounding, sterile filtration, filling, lyophilization, stoppering, capping, external washing, visual inspection and packaging. The filling line contains a fully isolated, automated aseptic system which can fill liquid and lyophilized products in vial sizes of 2R / 6R / 10R / 20R / and 50R. For more information on this state-of-the-art facility and our other extensive, global drug product manufacturing facilities and capacities – go here.
Fill System Capabilities
WuXi XDC Drug Product (DP) Manufacturing Capacity
Vial size (mL) | Filling speed (vials/hr) |
6 hrs forecasted output (Liquid) |
Lyophilizer (5 sqm) Capacity (vials/batch) |
Lyophilizer (20 sqm) Capacity (vials/batch) |
2R | 3,000 | 18,000 | 21,696 | 84,975 |
6R | 3,000 | 18,000 | 11,316 | 44,957 |
10R | 3,000 | 18,000 | 9,678 | 37,026 |
20R | 3,000 | 18,000 | 6,300 | 23,463 |
50R | 2,040 | 12,240 | 3,300 | 13,299 |
Also available
In addition to ADC/bioconjugate drug substance and drug product GMP manufacturing, WuXi XDC’s single-source bioconjugate platform includes non-GMP and GMP manufacture of all intermediates including the mAb/protein, payload and linkers. We also offer a library of ready-made payload and linker chemical compounds (available GMP and non-GMP)
All of our manufacturing operations are overseen by our comprehensive global Quality System that has been audited by multiple regulatory agencies including the FDA, EMA, NMPA, PMDA, MFDS, HSA, ANIVSA, HPRA and Health Canada.
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