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     2011 will witness a higher level of development of China’s pharmaceutical industry. The pharmaceutical industry will be listed as one of key industries for developing national economy in China’s 12th Five-Year Plan for Social and Economic Development. Recently, the State Council of China has issued several favorable policies for the pharmaceutical industry, which will greatly inspire domestic pharmaceutical enterprises to usher in the prime period of development in the future ten years.  

Good policy environment serves as the driving force for booming development of the industry. Concerted efforts for great-leap-forward development should be made by the entire industry to transform China from a big pharmaceutical nation into a powerful pharmaceutical nation. For this purpose, this Forum will cater to the needs of the industry and follow the developments in the industry, bring industry insiders together and pool authoritative views about the industry for becoming a specialized academic forum.

Given the promulgation and implementation of new version of GMP and pharmacopeia, SFDA officials will be invited to make in-depth analysis of the key points of new version of GMP and pharmacopeia FDA and EMEA officials will be present to introduce new developments in cGMP in U.S and Europe on this Forum. Subject to the concept of “Quality by Design”, the development level of pharmaceutical engineering determines to some extent the success of implementation of new version of GMP, thus how to promote overall development of the field of pharmaceutical engineering in China will be given a top priority. This Forum will be held under the “1+4” mode namely the mode of one main forum + four sub-forums to strive to create the professional and academic atmosphere for giving prominence to the key points and well defining key subjects. The four sub-forums covering solid preparations, active pharmaceutical ingredients, sterile preparations, biologicals and pharmaceutical factories will address the specific production needs of respective fields and will be available for discussing international advanced philosophy of pharmaceutical engineering and sharing the cases of applications of domestic and foreign current state-of-art core processes, technologies and equipment for jointly pushing forward overall development of domestic pharmaceutical industry and international technical exchange.

This Forum will continue the splendor based on the success of previous two international forums on pharmaceutical engineering. This Forum will focus on the current most-watched topics concerning product quality and production safety in China for discussions between guest speakers and listeners, thus providing an open harmonious platform for extensive communication and exchanges in the industry.

We hope that this Forum will be of great benefit for you!

 
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Deputy Director of State Administration of Traditional Chinese Medicine
PROCESS Publisher
Pharm-Tech (Tianjin) Co., Ltd, general manager, holding a current post in Tasly Group as engineering and technology general director
Guangzhou Pharmaceutical General Factory,Director of EU Accreditation Office
Manager and Chief Engineer, Equipment Division of Pharm-Tech (Tianjin) Co., Ltd
IMA Active Area & Product Manager
SeJong Pharmatech Company,Oversea Sales Manager
British Matcon Co., Ltd, China General Manager
JGC Corporation
L.B. Bohle, Area-manager
General Manager of Lonza Guangzhou Engineering & Consulting Co., Ltd
Tianjin Beechan Pharmaceutical Service Ltd ,Partner/ Tianjin ILE pharmaceutical materials Ltd. ,Member of board
 

Review of 2010 Pharmaceutical Engineering International Forum
Subforum: Automation of Pharmaceutical Manufacturing
Vogel Night
Subforum: Aseptic Preparation
Subforum: Solid Preparation and API