CDMO Services
Our Foshan facility spans 4,700 m2, including 1,600 m2 of GMP workshops for nucleic acid, virus, stem cell, and immune cell manufacturing along with dedicated QC areas.
As a trusted CDMO partner, we provide end-to-end solutions from IND-enabling studies to clinical sample production, under a robust quality management system that meets international GMP standards.
With five core technology platforms, we offer comprehensive capabilities that accelerate product development, ensure regulatory compliance, and enable global clinical translation.
Through advanced technologies and automated systems, we provide biotech companies, research institutes, and clinical centers with scalable, reliable, and high-quality CDMO services for next-generation therapies.
State-of-the-art GMP manufacturing platform with modular design and large-scale capacity, enabling high-quality, traceable, and compliant production from IND submission through Phase I/II clinical trials.
_edited_edited.png)
Get a Quote
Tell us about your project needs and our team will provide a tailored CDMO solution.