如果您是中国本土的合同研究组织(CRO),请致电或来函索取参会优惠价格——
不要错过向国际药厂和合同研究组织展示自己合作伙伴潜力的机会
If you are a CRO company from China offering data management or relevant services, request a preferred rate with us to meet with your potential partners at this gathering of global pharmaceutical and CRO companies. Contact us at

电话Tel: +65 6722 9388l
电邮Email: enquiry@iqpc.com.sg

Equip yourself with the necessary skill-sets to become a data management leader in emerging markets- attend the post-conference workshop on 26th of November led by the Pfizer global data management team! Click here for details

    Confirmed Speakers include:

  • Linda M. Talley CCDM.
    Global Director – Biopharmaceutics
    Exploratory and Program Medical – Clinical Project Management, Eli Lilly and Company
  • Bruce Xue
    Biostatistical Manager, Medical Affairs Department
    Xian-Janssen Pharmaceutical Ltd.
  • Joanne Liu
    Regional Director, Asia Pacific for Global Data Management & Standards
    MSD (Shanghai) Pharmaceuticals Consultancy Co. Ltd
  • Teng Lot Yin
    Head of Biometrics and Medical Writing
    Lundbeck
  • Andrew Taylor
    Asia-Pacific Head, Clinical Data Management
    Roche
  • Bhavesh Acharya
    Senior. Director, Clinical Data Management and Regional Head
    Quintiles China
  • Jessie Jessie Chen
    Head of Global Clinical Data Services GCDS Department
    Pfizer, China

Stay ahead of the competition by drastically improving clinical trial data quality and reducing data processing time. Gain comprehensive insights into the industry’s best practices in Asia

Key themes for Data Collection and Management in Clinical Trials Asia 2010:

  • What opportunities does Asia offer in managing global data for clinical trials; how should global pharmaceutical companies address the challenges and seize the opportunities from this increasingly important hub for clinical trials.
  • How can pharmaceutical companies and sponsors stay abreast of clinical trial practices by improving efficiency and reducing cost in collecting and managing clinical data;
  • How should CROs organize themselves to address sponsors’ requirements and play the role of a strategic partner in reducing trial time and complying with regulatory requirements;
  • What regulatory considerations should the industry bear in mind in the process of data collection, transmission and in regards to data security;
  • What are the software and hardware developments to date, and how should pharmaceutical and CRO companies leverage such development to improve the efficiency of data collection and management for clinical trials

The Data Collection and Management in Clinical Trials Asia 2010 is the first event exclusively focusing on patient compliance and data management strategies in Asia, an area of increasing popularity for building world-class data management centres. The event will gather key pharmaceutical companies, CROs, regulatory officials, as well as data capturing and management solution providers together under one roof. It will discuss opportunities and form strategic partnerships to leverage the enormous amount of opportunities the region has to offer.

What our expert speakers say about key learning objectives of this conference:

In 2010, the Asia Pacific region is home to more than 45 percent of the world’s population. As a result, there is a major need for medications and therapies to meet the medical needs of the region. Clinical trials conducted in Asia can yield information to help prevent mega illnesses, improve preventive care, predict which treatments have higher likelihood of success, reduce mortality rates and create a healthcare environment that is based on data, outcomes and best practices employed in other countries. As Clinical Data Managers working in a global economy, we have a keen interest in making clinical data bast practices, tools, and data analyses readily available where they are not today.
- Linda M. Talley, CCDM, Global Director - Biopharmaceutics, Exploratory and Program Medical - Clinical Project Management, Eli Lilly and Company
I’m excited to attend this first event exclusively focusing on clinical trial data management in Asia. I look forward to hearing new technology, sharing best practices of developing a world-class data management organization, and seeking partnerships of enlarging the talent pool of data management capacity in the region.
- Chen Zhao Hua, Head of Global Clinical Data Services, Pfizer China R&D Center
In the face of rapidly evolving clinical trial opportunities in Asia, critical issues in clinical data management across borders need to be urgently addressed. I look forward to sharing the most up-to-date information and best practices in this field with many outstanding speakers and colleagues at the conference from the academic research perspective.
- Prof. Yuji Sato, VP, Japanese Association of Pharmaceutical Medicine; Director, Center for Clinical Research, Keio University School of Medicine

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

Call (65) 6722 9388 to discuss how you can showcase your company’s offerings to reduce clinical trial data collection and management at the Data Collection and Management in Clinical Trials in Asia 2010. Placing yourself as the preferred partner of choice puts you way ahead of the game in a market where major sponsors are expanding. If you are not yet ready to register, feel free to request a reminder nearer the time.

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