In the pharmaceutical bulks and its' intermediates manufacturing, Everything should be run under professional standards, such as ISO9002, GMP, DMF, FDA etc., starting from the laboratory to pilot & Industrial scale, including the final refining, baking & packaging.

Besides the above hardware, we strictly improve ourselves by the environment protection, enterprise culture background, internal training and perfect service.

The constant Innovatory QA & QC is the key to each procedure.

Quality Analysis
Provided with varied advanced analysis equipment, such as High performance liquid chromatography, Gas chromatography, GC-Mass spectrometry, Nuclear magnetic resonance, Inferred spectrometry and Ultraviolet spectrometry etc., and some chemical analysis facilities, we can always obtain continuously high quality products.

Quality Control
In 1999, We were qualified for the ISO9002.