- -Formulation Development
- -Pharmaceutical Analysis
- -Drug Registration
- -Single Dosage Sterilized Preparation Manufacturing
Our two production workshops, which meets China and EU's GMP standards and equipped with world class integrated BFS system, the automatic liquid mixing and distribution system and the Nikka pinhole inspector, have an annual production capacity of 80,000,000 pcs.
Our labs are constructed in accordance with the GLP standard of China, Europe and America, and managed with the LIMS system which is an industry
well-recognized laboratory information management system.
We could provide GMP qualitative and quantitative analysis service and stability research on drug substance, excipients, package, and intermediates to our customer.
Besides, our professionals could also provide superior services on analytical method development, validation, and transfer.