28 - 29 August, 2012, Novotel Clarke Quay Hotel, Singapore
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"This event is a good start and will achieve another future milestone for years to come!"
- Director, Ministry of Health, Malaysia
"Good discussion on challenges in clinical trials."
- Regulatory Specialist, HSA, Singapore
"First-hand information on sharing among the experts in the field."
- Senior Manager, National University Health System, Singapore
"Good mix of topics on clinical trials."
- Senior CRM, Allergan
"Valuable practical scientific issues to be used back in the office!"
- Senior Clinical Scientist, Protech Pharmaservices Corporation
"Great opportunity to meet industry experts in Asia!"
- Clinical Research Manager, Daiichi Sankyo Taiwan
"IQPC brings together the experts you can learn from!"
- Director Patient Safety, Vanthys Pharmaceutical Development
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In March 2012, the number of clinical trials registered in Asia reached almost 19,922. Also, we have seen a significant increase in the number of early-phase clinical trials conducted in Asia with more and more multinational pharmaceutical and biopharmaceutical companies planning early phase clinical trials including First-in-Human trials in the next 2 years.
What strategies are you putting in place to reduce timelines and prevent early and late phase failures?
The 2nd Annual Early Phase Clinical Trials Asia 2012 summit is returning this August as a high-level platform to gather Heads of Clinical Development/Research, Medical Directors, Principle Investigators, Heads of R & D from pharmaceutical, biopharmaceutical companies and CROs from Mainland China, India, Taiwan, Korea, Hong Kong and other Southeast Asian countries. They will discuss the most efficient way to overcome regulatory, scientific and operational challenges in developing early phase clinical trials in Asian markets.
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