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CPhI Conferences 2013

Welcome to NextGen China 2013!
Confirmed Speakers
  Dr. Wu Xihan

Dr. Wu Xihan
COO
PharmaBlock

  Tan Xuehai

Tan Xuehai
PhD,CEO&President
HD Biosciences(China) Co.,ltd

  Dr.Song Yue

Dr.Song Yue
Senior Liquid Mass Application Engineer
Agilent Technologies

  Dr.Frank Cheng

Dr.Frank Cheng
President
NovoScience Consulting

  Rajni Jha

Rajni Jha
Senior General Manager
Indswift Laboratories

  Douglas Andrews

Douglas Andrews
CEO
Stravencon Ltd.

  Zhou Weicheng

Zhou Weicheng
Zhou Weicheng
Zhou Weicheng

  Deepak Hegde

Deepak Hegde
VP of Pharmaceutical Services
WuXi AppTec Co. Ltd.

  Ling Ye

Ling Ye
General Manager
Cenway Pharmaceutical

  Christopher Pelloni

Christopher Pelloni
Former Chair, Former Vice President
US GPhA Scientific Committee, Global Generic Research & Development, TEVA

  Shi Licheng

Shi Licheng
Medicine Partner
Allpku Management Consulting Group

  Nicola Travierso

Nicola Travierso
Managing Director
NTC Srl

  Gurpreet Sandhu

Gurpreet Sandhu
Managing Director
REVA PHARM

  Xie Mufeng

Xie Mufeng
Deputy Director of the Pharmacist
Shanghai Institute for Food and Drug Control,SIFDC

 
   
 
  Background and Key Topics

The generic drug market makes up over 40% of the global drug market. Currently, the global generic drug market has a value of 80 billion US dollars and is growing at a rate of 8% while the generic drug industry of China is growing at a tremendous rate of 25%. As the 12th Five-Year Plan stipulates that the quality of generic drugs should be enhanced comprehensively, China’s generic drug market will change its strategy from “mere imitating” to “innovation”. Undoubtedly, the huge domestic market of generic drugs will be subject to the market criterion of “survival of the fittest”. In recent years, new drugs are getting fewer on overseas market and the world’s bulk drug industry is gradually shifting itself towards developing countries. The next few years will see the peak period of patent expiry for international drugs. China and many other developing countries will become major transfer destinations of the generic drug industry for further growth. In such a situation, generic drugs promise to become a “footboard” for China’s pharmaceutical industry. Pharmaceutical enterprises may combine imitation with manufacture and have much to do in process innovation on China’s generic drug market, which is characterized by “domestication of international competition and internationalization of domestic competition”.

More     

  Why Should You Attend?

Delving into road-map of generics regulatory updates, process quality & R&D channels;
Concern-solving & insights hearing from 25+ domestic and overseas speakers under CPhl resources;
Getting on-spot answers to your critical business by 2-day’s 15+ industry issue interactive sharing and peer networking;
Covering 3 hot topics: Seminar of international & domestic regulatory concerning generic drugs; Analysis of process quality & innovation of generic drugs; New ideas of cooperation & R&D for generic drugs;
Networking with 120+ decision makers from 30+ China’s pharmaceutical companies and 20+ MNCs in the category of drug manufacturing;
Brainstorming domestic and overseas generics qualifying standards so as to seek out market growing performances and the assessment approval of generics consistency + 2 leaders’ think tank about generic pharma operational methodologies to find out the new opportunities in the generics value chain

  Who Should Attend?

Decision makers/R&D/QA,QC/Product Development/Regulatory Affairs/BD/Marketing
From:  Generics Manufacturers/Innovator Pharma Manufacturers/CRO,CMO/Ingredient & Material Suppliers/Equipment Suppiers/Government Associations/Analytical Laboratories

  Past Review
On-site pictures:
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  Past attendees’comments:

 2-day conference made me in deeper understanding of China generics technology dynamics and networking with many industrial professionals and peers。
                                                                                                                                           -- Zhao Xiaowei, Project Manager, FERGUSON
Getting to acquire generics impurity spectrum technical qualifications, the assessment of generics consistency, USP Pharmacopoeia knowledge
                                                                                                                --Zhang Suoqing, R&D Manager, North China Pharmaceutical
Getting to know the latest standards for domestic pharmaceutical research progressing
                                                      --Zhu Dequan, Assistant President/BD Director,SICHUAN HUIYU PHARMACEUTICAL CO., LTD

  Past Participants Analysis:


 

Manager
Director
General Manager
Vice General Manager
Executive
Specilist
VP
Minister
Dean
Chief Engineer
CEO
Senior Manager
Project Manager
Chief Scientis
Business Development
Product Development
R&D
Technical Department
Sales Department
Marketing Department
 
Regulatory Affairs
QA/QC
Pharmaceutical Development
■IPR
laboratory
Generic Manufacturers
Innovator Pharma Manufacturers
Ingredient and Material Suppliers
Biopharma Manufacturers
CRAMS
Machinery Manufacturers
Drug Delivery Platform Providers
Analytical Laboratories
Life Sciences Companies
Government agencies
Media Partners
 
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