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Overview China has an indispensable in-vitro diagnostic reagent market for overseas and multinational in-vitro diagnostic reagent companies. Chinese healthcare market has maintained annually average growth rate above 16 % since 1990s. Among them, in-vi.....

No Of Pages : 134
Publication Date: Nov, 2015
Single User Price : US$ 750.00
Latest Guidebook for Chinese Medical Device GMP Regulations by Access China Management Consulting Ltd

Summary China is one of the fastest growing global economies with a fifth population in the world, and is one of the largest healthcare markets around the world. Along with sustained economic and population growth as well as an ageing population, Chine.....

No Of Pages : 217
Publication Date: Nov, 2015
Single User Price : US$ 1,495.00

Synopsis Responding to strong desire of overseas and multinational pharmaceutical manufacturers and domestic pharmaceutical manufacturers to carry out research and development of biosimilar products, this is first time in history, Chinese pharmaceutica.....

No Of Pages : 48
Publication Date: May, 2015
Single User Price : US$ 750.00

Synopsis This is first time in history, Chinese pharmaceutical authorities officially issued a guidance on international multi-center clinical trials of drugs in China, which has begun to be implemented on March 1, 2015. The guidance provides an opport.....

No Of Pages : 101
Publication Date: Mar, 2015
Single User Price : US$ 1,495.00

Synopsis Chinese regulatory authorities ---- China Food and Drug Administration unprecedentedly set a special examination and approval procedures for innovative medical devices since March 1, 2014, which provides a opportunity to speed up overseas inno.....

No Of Pages : 32
Publication Date: Jan, 2015
Single User Price : US$ 750.00

Synopsis China’s regulatory framework for in-vitro diagnostic reagents is undergoing earthshaking changes. It will bring overseas and multinational in-vitro diagnostic reagent manufacturers the maximum challenges and opportunities. How do you in .....

No Of Pages : 208
Publication Date: Sep, 2014
Single User Price : US$ 1,495.00

Synopsis Now, Chinese regulations on medical devices are undergoing earthshaking changes. Latest Chinese Guidebook for Application and Approval of Imported Medical Device Registration?From Regulations to Practices not only provided a comprehensive and .....

No Of Pages : 194
Publication Date: Aug, 2014
Single User Price : US$ 1,250.00
Latest Guide to Chinese Pharmaceutical GMP Regulations by Access China Management Consulting Ltd

Synopsis Latest Guide to Chinese Pharmaceutical GMP Regulations provides a comprehensive and thorough knowledge of the Chinese pharmaceutical GMP regulations to guide overseas pharmaceutical companies and multinational pharmaceutical companies to achie.....

No Of Pages : 135
Publication Date: Jul, 2014
Single User Price : US$ 750.00

Synopsis 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, moreove.....

No Of Pages : 245
Publication Date: Jun, 2014
Single User Price : US$ 1,495.00
China’s Guidebook for Pharmaceutical Patent Protection by Access China Management Consulting Ltd

Synopsis China’s Guidebook for Pharmaceutical Patent Protection is an essential resource for overseas and multinational pharmaceutical companies to achieve a successful patent protection for their intellectual property in China. This guidebook, t.....

No Of Pages : 230
Publication Date: May, 2014
Single User Price : US$ 1,495.00

Synopsis This is the fourth guidebook of the China Pharmaceutical Guidebook Series. It will provide a detailed introduction of the Chinese pharmaceutical authorities’ requirements for materials and clinical trials of application and approval for .....

No Of Pages : 118
Publication Date: May, 2014
Single User Price : US$ 750.00

Synopsis This is the third guidebook of the China Pharmaceutical Guidebook Series. It provides a detailed introduction of CFDA’s requirements for materials and clinical trials of registration application and approval for imported biological produ.....

No Of Pages : 168
Publication Date: May, 2014
Single User Price : US$ 750.00