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Hear from 19+ leading experts including:

  • Wang Jinhua
    Clinical Operations Head, GCO-MAO Asia Pacific, Global Clinical Operations
    Johnson & Johnson
  • Dr. Yan Cai
    Director of Clinical Operations
    Novo Nordisk, China
  • Susan Chen
    Head of Clinical Operations
    Roche, China
  • Dr Yan Wu
    Medical & Clinical Development, Director
    Biogen Idec, China
  • Eva Yang
    Head of Clinical Operations
    Bayer Healthcare China
  • Tracy Han
    Project Management Supervisor
    GSK, China

Strengthening clinical trial supply chain practices in China to shorten trial timeline, reduce waste and minimize costs

With more clinical trials being held in China than ever before, clinical trial supply systems need to become increasingly sophisticated in order to cope with local regulations, importation and exportation guidelines, obtainment of licenses, transit, packaging and labelling requirements, temperature-controlled storage and transportation and local distribution. With this in mind, the Clinical Trials Supply China 2010 will create a high-level platform from which to find answers to these challenges and more.

This is the ONLY CONFERENCE GLOBALLY that will focus on clinical trial supply issues and challenges in China! NO OTHER CONFERENCE GLOBALLY will provide you with the opportunity to meet senior level decision makers looking after clinical trial supply in China. Don’t miss it!

From effective outsourcing and ensuring a streamlined distribution network to the latest regulatory updates and developments in clinical trials supply technology, this conference will provide ample opportunities for discussion and networking with pharmaceutical, biotechnology companies, hospitals and clinical trial sponsors in order to establish best practice methods for approaching this complex issue in China.


Special offer for Chinese companies!!

If you look after clinical trial supply in a Chinese pharmaceutical company/hospital, you will qualify for the complimentary pass at this event. To find out more, please email Yip Teck Chee at yip.teckchee@iqpc.com.sg

Key Conference Highlights include:

  • Overcoming challenges faced in regulatory approval processes - obtaining drug/clinical supplies import licenses in China
  • Ensuring temperature-controlled storage and distribution of clinical supplies
  • Eliminating key inefficiencies in the clinical trial supply chain in China
  • Establish the decision criteria for partnering with the right vendors in China
  • Hear best practices for planning and forecasting of clinical supplies in China

Other benefits of attending include:

  • Cost effective clinical supply packaging
  • Optimal planning for clinical trial supply management in China
  • Incorporating risk management into the clinical trial supply chain strategy in China
  • Implementing temperature monitoring processes and technologies to enhance clinical trial supply and distribution
  • Depot strategies to delivering supplies in a timely and cost-effective manner in China

Clinical Trials Supply China 2010 is a forum for year long discussion between thought leaders and new entrants.

Want to be an exhibitor, sponsor or even the Event Partner for 2010?

Call (+65) 6722 9388 to discuss how the Clinical Trials Supply China 2010 can become an ideal platform to showcase your company’s offerings to senior level decision makers who look after clinical trials supply in China. In these tough times, it is crucial that your company be portrayed as the preferred partner of choice. This annual event attracts the most active players in the market, giving you access to your target market, and the opportunity to strengthen your market share, increase your corporate profile and achieve business growth. As a sponsor at the Clinical Trials Supply China 2010, we are providing you with the opportunity to do so in front of your business prospects!

If you are not yet ready to register, feel free to request a reminder nearer the time.

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