Responsibilities:
1. All equipment related to quality

2. All quality files should be approved by this dept.

3. As an independent department subordinated general manager to lead, we have such responsibilities:
1)  The permission of APIs
2)  The permission of pharmaceutical intermediates, packing materials and label system
3) Production records and QC records before the drug levels factory
4)  Investigate big deviation and solve it
5)  Approve standard, specification and SOP
6)  Help internal audit
7)  Approve the changes that may affect the qualities of APIs and intermediates
8)  Check and Approve test solution and report
9)  Help investigate and solve quality complaints
10)  Help maintain small system and adjust key instruments

Contact: Zhang Qing      Tel: 0512-88169855　   Email: zhangqing@lixinpharm.com