Our History

With the aim of helping the human community access high-quality medicines at affordable prices.

Necessary to undergo regulatory review and be approved by relevant agencies such as the FDA before it can be commercialized.

Conducting pre-clinical and clinical trials to determine the safety and efficacy of a new drug candidate, also involves the large-scale production of the drug in accordance with good manufacturing practices (GMP).

Monitoring the safety and effectiveness of the drug once it has been commercialized, and making necessary changes to ensure patient safety.