Updated China Pharmaceutical Market Guides Published by MarketPublishers.com
24 May 2011 • by Natalie Aster
LONDON - Market Publishers Ltd informs that updated in-demand Access China Management Consulting Ltd guides to Chinese pharmaceutical markets have been added to its catalogue.
China’s Guidebook for Pharmaceutical Patent Protection. China is expected to become the fifth largest drug market in the world by 2010 with a growth rate of 20-25 percent per annum in next three years. The guidebook provides a comprehensive and thorough knowledge of the Chinese patent system relating to pharmaceuticals, the detailed administrative, civil and criminal judicial pathways for protections of patent right, and the design for composition of optimized protection strategies …
China Pharmaceutical Guidebook: Latest Chinese Regulations for Imported Drug Registration. The Chinese drug market is expected to grow with a growth rate of 20-25 percent per annum in next five years. China is expected to become the fifth largest drug market in the world by 2010. The aim of the guidebook is to guide overseas pharmaceutical manufacturers and producers to achieve a successful application and approval for their imported drug registration …
Material and Clinical Trial Requirements of Application and Approval for Imported Drug Registration: A Guidebook of Registration Application for Imported Chemical Drugs China Pharmaceutical Guidebook. The report provides an overview of the classification of drug registration formulated by the SFDA (The State Food and Drug Administration in China). The study addresses the requirements for materials and clinical trials of registration application and approval for imported biological products, the material and clinical trial requirements for application of radioactive pharmaceuticals …
Latest Chinese Regulations for Imported Drug Registration: A Comprehensive Guidebook for Foreign Pharmaceutical Companies China Pharmaceutical Guidebook Series (1) (3rd edition). The report provides a detailed introduction of the latest Chinese regulations for imported drug registration, and guides overseas pharmaceutical manufacturers and producers to file the application for their drugs with the Chinese pharmaceutical authorities. Many useful resources of law and regulations are included …
Material and Clinical Trial Requirements of Application and Approval for Imported Drug Registration: A Guidebook of Registration Application for Imported Biological Products China Pharmaceutical Guide. The guidebook introduces SFDA’s requirements for materials and clinical trials of registration application for imported biological products. The report highlights the significant suggestions for overseas pharmaceutical manufacturers and producers looking to achieve a successful application for their biopharmaceuticals registration in China …
More new and updated market research reports by Access China Management Consulting Ltd can be found at https://marketpublishers.com/members/access_china/info.html
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