Hangzhou Hysen is offering two main services now:
1) Our documentation department supplies a strong support on documentation for API as well as pharmaceutical intermediates related to DMF requirement, and as the bridge between the manufacturers and buyers, we can offer the service of explaining the questions concerned the complaints of the product quality and processing if be concerned and be allowed by the manufacturer, assists the application of the COS in EDQM for European market and registration in the United State market, supply the service of the activities related to the inspection of the manufacturer site by EDQM and FDA. And also provide the assistance on the registration of DMF in other market, such as India, Korea etc.