XZ
Xia Zheng
Suzhou Xishan Zhongke Drug R&D Co.,Ltd.
13 Experiences in establishing & operating GLP system. Experience in quality Assurance of toxicity studies for pharmaceutical, chemical and pesticides, and data management in computerized system. Experience of GLP audit/ inspection from regulatory agency of CFDA, MEP and MOA-ICAMA. Knowledge of regulatory agency requirement (Good Laboratory Practice standards of FDA, OECD, EPA).