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Chinese pharma-biotech dragon rears its head

forward aggressively to implement common drug development parameters existing in countries such as the U.S. and Europe; in September 2003, they put into place Good Clinical Practice (GCP) standards. This measure alone has significant impact on the performance of clinical trials in China in a manner consistent with world-class standards.

The impact of GCP means not only the potential usabi......

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Source:wistechnology.com By Michael Rosen 09/11/06


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