eve Conference Variant Block
- Nov. 16th 2011
- 9:00-9:10 Opening speech
- 9:10-10:00 Internationalization of Chinese Pharmaceutical-Significance of publishing in western journals& the increased requirements of cGMP that will come with increased exports
- （Seth J Goldenberg）
- 10:00-10:30 A Fast Drug Development and Approval Pathway in the US（Andrew JIANG）
- 10:30-11:00 Coffee Break
- 11:00-11:30 Development trends and strategies of Generics R&D （Huijun GAO）
- 11:30-12:00 DMF regulation for pharmaceutical packaging material （Huimin SUN）
- 12:00-13:30 Luncheon
- 13:30-14:15 CRO development & Preclinical safety evaluation of Biopharmaceuticals （Conglin ZUO ）
- 14:15-15:00 Application of new environmental plasticizer in pharmaceutical manufacturing （Pingping JIANG）
- 15:00-15:30 Coffee Break
- 15:30-16:15 Pharmaceutical Automation and Supervisory Control of Drug Quality （Jiliang TANG ）
- 16:15-16:30 Panel discussion & Closure of Day 1
-
- Nov. 17th 2011
- 9:00-9:45 R&D of new dosage form of pharmaceutical formulations （Qineng PING）
- 9:45-10:30 Pharmaceutical excipients screening and using （Jiangsheng TU）
- 10:30-11:00 Coffee Break
- 11:00-11:30 Hutchison
- 11:30-12:00 Combination of TCM and Western medicine and R&D of TCM dosage innovation （Guoping ZHAO ）
- 12:00-13:30 Luncheon
- 13:30-14:15 R&D of New Dosage Forms of Traditional Chinese Medicine （Jianxin WANG ）
- 14:15-15:00 The Development and FDA review of TCM （Andrew Jiang）
- 15:00-15:30 Coffee Break
- 15:30-16:00 Brain storm & Lucky Draw
