Attend Clinical Trial Supply Asia 2012 and get to:
• Understand regulatory requirements and approval processes of clinical trial supply to reduce your clinical trial timelines, especially so in China, India, Taiwan, Philippines and other Asian countries
• Determine the best clinical trial supply structure for your operations to optimise efficiency and cost – central setup vs regional setup?
• Establish the most cost-effective cold chain management for your network of clinical products in Asia
For more information, contact us at enquiry@iqpc.com.sg or at +65 6722 9388.
Further details and to register