
Centering on quality, a risk-based quality system is established to continuously enhance the competitiveness and market reputation of the company's pharmaceuticals.

Good Manufacturing Practice (GMP) is a systematic engineering process involving multiple variables and dimensions. It encompasses a continuous ecosystem spanning drug development, production, logistics, and the entire product lifecycle, requiring a tightly coordinated and gap-free responsibility system.

Manufacturing is strictly organized in compliance with GMP standards. A dedicated quality oversight and inspection unit—the Quality Department—has been established, equipped with multiple advanced imported testing instruments and staffed by professional quality control personnel. Comprehensive monitoring throughout the entire process ensures the safety, efficacy, and consistency of drug quality.