p—MEC中国制药峰会
The 2nd P-MEC Summit, focusing on the implementation of CFDA regulations and the quality assurance in pharma manufacturing, will gather nearly 200 decision makers from multinational pharmaceutical companies, government agencies, technology solution providers, and provide an unparalleled platform of communication and cooperation for professionals specialized in pharma manufacturing.
第二届P-MEC中国制药工程峰会,将汇聚来自全球领先制药企业、政府机构、技术解决方案供应商等近两百位决策人员,共同聚焦CFDA政策实施进展以及药品生产质量监控,为从事药品生产的专业人士提供交流与展示的平台,促进交流与合作。
Date: June 24,2015 Venue: Hall N 1 2015.6.24 地点:N3-M43馆
序号 | Time/时间 | Topic/主题 | Speaker/演讲人 | Company Name/公司名称 |
10:00 - 10:10 |
大会主席致开幕辞 Address from Chairman |
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H1 | 10:10 - 10:40 | GMP检查趋势看质量管理信息化的效益 |
许哲毓 执行总监 |
洛施德企业管理咨询 (上海) 有限公司 Soltoris Lifescience Management Consultants Co., Ltd. |
H2 | 10:40 – 11:10 |
洁净服高品质风险管控 |
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H3 | 11:10 – 11:40 |
案例分析:在质量体系中建立风险管理机制 Case Study: Establishing Risk Management in the Quality System |
李树德 高级副总裁 Michael Lee Senior Vice President |
瑞华药业集团 TDW Pharmaceuticals, Inc. |
H4 | 13:00 – 13:30 |
污染控制对制药设备的挑战和机遇 Challenges and opportunities with Pollution control on pharmaceutical equipment |
王俊华 项目负责人 Junhua Wang Head of Healthcare-Process |
拜耳公司 Bayer Technology and Engineering (Shanghai) Company Limited |
H5 | 13:30 – 14:00 |
可靠质量导向的制药工程项目以及与运行、维护安全周期整合管理 Reliable Quality oriented pharmaceutical Project and its operation, maintenance life cycle integration management |
郭红星 副经理 Hong-Xing Guo vice-manager |
上海罗氏制药工程部 Roche |
H6 | 14:00 – 14:30 |
应用DOE对丙酸氟替卡松的筛选研究 Screening Studies for Flucticasone Propionate with DOE |
刘哲生,资深质量和法规顾问 Liu Zhesheng, Head of Regulatory Center | 江苏恒盛药业 Hspharm |
H7 | 14:30 – 15:30 |
小组讨论:加强质量管理,达到法规标准 Panel Discussion: Enhancing Quality Management to Meet Heightened Regulatory Standards |
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H8 | 15:30 | 大会结束 End of the Conference |
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