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China Pharmaceutical Guidebook Series, Volume 1 (Access China)
Report #07-AC2
Publication Date: February 2007
Page Count: 40
Single User Electronic Copy:$750
Electronic Copy with Site License: $3,500
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Latest Chinese Regulations for Imported Drug Registration:A Comprehensive Guidebook for Foreign Pharmaceutical Companies
In China, the process of application and approval for imported drug registration is very complex, because the Chinese pharmaceutical authorities administer and control this process by exorbitant administrative measures and regulations, moreover, these exorbitant administrative regulations are variable and lack of transparency. Therefore, a comprehensive knowledge of the Chinese latest regulations for imported drug registration has been become an essential prerequisite for overseas pharmaceutical manufacturers and producers to achieve a successful application for their products entry into the Chinese drug market.
This is the first guidebook of the China Pharmaceutical Guidebook Series. It will provide a detailed introduction of the Chinese latest regulations for imported drug registration, and guide overseas pharmaceutical manufacturers and producers to file the application for their drugs with the Chinese pharmaceutical authorities.
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