Hande uses a well-established process for the separation of natural Paclitaxel and taxane derivatives.

1996 - This process has been FDA approved since 1996. There is an excellent, well proven quality control system. Quality management and quality control are strictly performed in the whole process including material selection, in compliance with cGMP requirements.

Hande has introduced state-of-art instruments from other countries. The HPLC/UV, GC, IR, microbe test and chemical analysis methods have been well established. Hande has ranked among the advanced enterprises in terms of adopting advanced technology.

world-class quality control systems, state-of-the-art instruments and a US FDA approved production line. 

• Well established HPLC/UV, GC, IR, microbe test and chemical analysis methods.
• Rigorous quality management and quality control from material authentication through to shipment and sales compliance.