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The Analyst Magazine:
Clinical Research in Asia : Gaining Ground
 
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Many pharmaceutical and biotech companies are moving their clinical trials abroad, and Asia is quickly becoming a primary region of choice.


The cost of conducting clinical research in US is steadily escalating, largely because of unsuccessful domestic subject recruitment, leading to costly time delays. This is forcing pharmaceutical and biotech companies to look abroad for solutions. In fact, 86% of the US clinical studies fail to recruit the required number of subjects on time, according to Thomson Center-Watch statistics. As a result, many companies are currently outsourcing all the phases of clinical research. Phase III clinical trials, in particular, are increasingly moving to non-US markets due to the increased demand for multiple trials and larger subject pools. If one considers that more than 40% of product development costs are incurred during the clinical trial process, this growing trend of outsourcing clinical research to countries, where costs are dramatically reduced, is understandable.

Despite the similarity in environmental and disease traits, there are striking differences between various Asian countries as far as the pharmaceutical market size and health expenditures are concerned. This difference is primarily due to the differences in regulatory and business environments. Tables 1 and 2 bring out these differences across Asian countries. The Japanese and Chinese pharmaceutical markets are huge and hence, attract a lot of investment. However, there are striking differences in the per capita health expenditure between Asian countries, which varies significantly from $27 in India to $2,662 in Japan. Considering the huge population base in Asian countries, it still offers a huge value proposition for the pharmaceutical industry to undertake clinical trials and market its products in the Asian countries.

 
 

 

The Analyst Magazine, Clinical Research, Pharmaceutical Markets, Clinical Trials, Healthcare Regulations, Healthcare Systems, Clinical Research Industries, Regulatory Environment, Good Clinical Practices, GCP, United States Food and Drug Administration, USFDA, Global Regulations, Clinical Data Management.