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CMO/CDMO


With QMS compliant with international standard (USFDA/EMA/PMDA/NMPA), we are able to manufacture APIs and INTs under GMP for clinical study and commercialization use.

 

With the project from early stage development to commercial production, the highly experienced operation teams including project management and customer service teams can ensure the seamless connection between different stages of the project to maximize the production efficiency and reduce the cost.

 

PRODUCION CAPABILITIES

  • More than 100 reactors from 100L to 5000L

  • Special reaction at Low temperature (-70oC), high temperature (250oC) and high pressure (hydrogenation)

  • 4 independent API production lines

  • New GMP plant under construction. Capabilities will be upgraded in the future.


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