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2013 Chinese Pharmaceutical Guidebook: Drug Registration Rules
Date:4/10/2013

, the clinical investigation for application of imported drug registration to the time limits in drug registration. Chapter 4 introduces the procedures of application and approval for imported drug registration, including the procedures of the initial application and approval for imported drugs, the supplementary application and approval for imported drugs, and the application and approval for clinical trials relating to imported drugs. Chapter 5 provides an English version of Application Form for Imported Drug Registration in order to facilitate overseas audience to easily file the application of imported drug registration with the SFDA. The guidebook concludes in chapter 6 by highlighting the significant suggestions for overseas pharmaceutical manufacturers and producers looking to achieve a successful application of their drug registration in China. The appendices in chapter 7 include the Drug Administration Law of the People's Republic of China, the Regulations for Implementation of Drug Administration Law of the People's Republic of China, and the Chinese Good Clinical Practice of Pharmaceutical Products.

Comprehensive Table of Contents and more on the report can be explored @ http://www.marketreportsonline.com/232497-china-pharmaceuti.html.

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