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The Annual Meeting program is subject to change. Speakers are added as confirmations are received.
Please  note that Quality College workshops require separate registration.

Please review the Safety Rules and Guidelines.
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).