崔强：无菌工艺模拟试验要点
崔强，费卡华瑞制药有限公司QC高级经理（微生物）
崔强，华瑞制药有限公司，微生物部经理
Cui Qiang, General Manager of Microbiological Department, SINO-SWED PHARMACEUTICAL CORP. LTD
毕业于沈阳药科大学制药系微生物制药专业，现任华瑞制药有限公司微生物高级质量控制经理。长期从事制药行业微生物污染控制工作，熟悉实验室管理。CFDA 高级研修学院客座教授，无锡药学会工业制剂专业委员会委员，曾参与编写《无菌药品GMP 指南》一书，并参加美国PDA 协会的环境监测、参数放行、干热灭菌等技术报告的撰写讨论工作。
Mr Cui Qiang graduated from the College of Pharmacy, Shenyang Pharmaceutical University, and was majored in microbial pharmaceutics, and now she works for SINO-SWED PHARMACEUTICAL CORP.LTD as the Manager of Microorganism Senior Quality Control.Mr Cui has been engaged in microbiological contamination control in pharmaceutical industry over a long time, and is familiar with the lab management. He is a Visiting Professor of CFDA Institute of Executive Development and a member of Professional Committee of Industrial Preparations, Wuxi Pharmaceutical Society. And he took part in the preparation of the Guide to Sterile Drugs GMP, and also participated in the preparation and discussion about the environmental monitoring, parametric release, dry heat sterilization and other technical reports.
2001-2009Vogel Industry Media版权所有 京ICP备12020067号-15 京公网安备110102001177号
加载更多