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6th International Pharmaceutical China R&D Summit

 
  December 15, 2010  
     
 
IBC Life Sciences & BayHelix, Grand Hyatt Shanghai
11-13 April 2011


Clinical & Regulatory Summit·  Changing Regulatory Environment in China·  Global Regulatory Harmonization ·  Clinical Trials and Regulatory/Quality Compliance Comparison Between US/EU and China·  Bringing Forward Product Launch and Approval for Innovative Compounds·   Phase I Clinical Trials in China ·  Proof-of-Concept Studies in China·  Clinical Development Strategies for Bioequivalence/Biocomparability Studies of Biologic Compounds in China·  Real-world Evidence Studies·  Patient Safety/Pharmacovigilence·  Global Simultaneous Development and Bridging China Data with Global Data·  Clinical Site Management & Monitoring Discovery to PreClinical Development & Partnerships·  Drug Discovery & PreClinical Development Update/Status Report in China·  Creating Value Through Partnerships·  Update on Current NCE Development in China from Domestic and Foreign-funded Biotechs·  Challenges in GLP Toxicology ·  Challenges in Drug Metabolism and Pharmacokinetics·  Innovative Drug Discovery Platforms in Academia·  Comparison of Local vs Global CROs Biologics & Biosimilars Development·  SFDA Regulatory Update on Biologics·  Global Pharma’s Strategies for Large Molecules Worldwide and in China·  Showcase of Companies Developing Biologics in China·  Companies with commercialized products·  Companies with soon-to-be commercialized products·  Companies with products launching in 2-3 years·  Biosimilars vs. Biobetters – Comparison of the Challenges of Developing Biosimilars vs. Bio-betters in China·  Manufacturing & Process Development Challenges
 
 
Organized by: IBC Life Sciences & Bay Helix
Invited Speakers:

A never-before line-up of over 80 Speakers from international pharma, MNCs in China, and domestic Chinese pharma/biotechs will be sharing their expert opinions and experiences on transformation & innovation in China, clinical challenges, regulatory updates , NCE discovery efforts, preclinical partnerships, biosimilars development and more!

 Plenary Sessions and Overall Program
Steve Yang, Ph.D., Vice President, Head of R&D, Asia, Pfizer Global Research & Development
Tony Zhang, Ph.D., Vice President, Global External R&D, Asia, Eli Lilly & Co.
Xian-Ping Lu, Ph.D., CEO & Chief Scientific Officer, Shenzhen Chipscreen Biosciences, Ltd.
Kewen Jin, M.D., General Manager, Preclinical Services, Charles River Laboratories Greater China
Li Chen, Ph.D., Chief Executive Officer, Hua Medicine

Clinical & Regulatory Summit
-- Ruiping Dong, M.D., Ph.D., Senior Vice President, Head of Emerging Markets R&D, Merck Research Laboratories
-- Maria Song, Ph.D., M.D., R. Pharmacist, M.A., President, VPS-CRO Group
-- Ling Su, Ph.D., Senior Vice President, Head of Development Greater China, Novartis Pharma
-- Karen Atkin, M.D., Vice President, R&D, AstraZeneca China
-- Li Ding, MSc., China Site Head, Clinical Data Management, Sanofi-aventis
-- Frank Shen, Ph.D., Head, Biometrics (Biostatistics & Data Management), Actemra China Development Champion, Roche Global Pharma Development Center, Asia Pacific
-- Dan Zhang, M.D., MPH, Co-Founder & CEO, Fountain Medical Development 

AND MANY MORE!

 
Deadline for Abstracts: 01/02/2011
 
Registration:

WEB: www.IBCLifeSciences.com/China

Customer Service Hotline: +65 6508 2401

FAX: +65 6508 2407

E- MAIL: register@ibcasia.com.sg

E-mail: rita.parasurum@ibcasia.com.sg
 
   
 
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