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Access China Management Consulting Ltd. Research

logo Access China is a professional provider of managements and consulting services specifically designed to provide overseas clients a virtual gateway to enter the lucrative market of China. Access China is headquartered in Nanjing, Jiangsu Province, Eastern China. Access China offers managements and consulting services in three major areas: International Trade,Strategic Investment,and Market Research .

Found 20 Research Reports
Latest Guidebook for Chinese Medical Device GMP Regulations
US $1495.00

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, Chinese hea...

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November 3, 2015 217 pages
Latest Chinese Guidance for Development, Evaluation, License Approval of Biosimilars
US $750.00

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....

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May 18, 2015 48 pages
Latest Regulations on Pharmaceutical International Multi-Center Clinical Trials in China
US $1495.00

China’s healthcare market is indispensable for overseas and multinational pharmaceutical companies, but Chinese regulations on pharmaceutical clinical trials are undergoing sharp changes....

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March 27, 2015 101 pages
Chinese Special Examination and Approval Procedures for Innovative Medical Devices: speed up overseas innovative medical devices entry into Chinese market
US $750.00

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 innovative ...

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January 28, 2015 32 pages
Guide to Prepare Application Dossiers for Oversea Medical device registration and recordation in China
US $1250.00

Guide to Prepare Application Dossiers for Oversea Medical device registration and recordation in China not only provided a comprehensive and thorough knowledge of the overall new requirements of application dossiers for medical device registration or...

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November 15, 2014 190 pages
Latest Guidebook for Conducting Medical Device Clinical Evaluation and Clinical Trial in China: From Regulations to Practices
US $1495.00

China’s regulatory framework for medical devices is undergoing radical changes. The country’s new leaders have recognized that the regulations for supervision and administration of medical devices are far from perfect along with rapid population ...

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October 15, 2014 199 pages
Latest Chinese Guidebook for Application and Approval of Imported In-vitro Diagnostic Reagent Registration: From Regulations to Practices
US $1495.00

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....

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September 28, 2014 208 pages
Latest Chinese Guidebook for Application and Approval of Imported Medical Device Registration: From Regulations to Practices
US $1250.00

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 thor...

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August 25, 2014 194 pages
Latest Guidebook for Conducting Pharma Clinical Trials in China: From Regulations to Practice
US $1495.00

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....

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July 25, 2014 191 pages
Latest Guide to Chinese Pharmaceutical GMP Regulations
US $750.00

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....

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July 20, 2014 135 pages
China Pharmaceutical Guidebook:Latest Chinese Regulations for Imported Drug Registration
US $1495.00

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, thes...

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June 20, 2014 245 pages
China’s Guidebook for Pharmaceutical Patent Protection
US $1495.00

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....

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May 20, 2014 230 pages
Material and Clinical Trial Requirements of Application and Approval for Imported Drug Registration: A Guidebook of Registration Application for Imported Traditional Chinese Medicines and Natural Medicines:China Pharmaceutical Guidebook Series (4)
US $750.00

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 imported t...

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May 20, 2014 118 pages
Material and Clinical Trial Requirements of Application and Approval for Imported Drug Registration: A Guidebook of Registration Application for Imported Biological Products:China Pharmaceutical Guidebook Series (3)
US $750.00

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 products....

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May 10, 2014 168 pages
Material and Clinical Trial Requirements of Application and Approval for Imported Drug Registration: A Guidebook of Registration Application for Imported Chemical Drugs
US $750.00

This is the second guidebook of the China Pharmaceutical Guidebook Series. It will provide a detailed introduction of CFDA’s requirements for materials and clinical trials of application and approval for imported chemical drug registration, includi...

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April 20, 2014 121 pages
Latest Chinese Regulations for Imported Drug Registration: A Comprehensive Guidebook for Foreign Pharmaceutical Companies
US $750.00

This is the first guidebook of the China Pharmaceutical Guidebook Series. It will provide a detailed introduction of the latest Chinese regulations for imported drug registration, and guide overseas pharmaceutical manufacturers and producers to file ...

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April 10, 2014 116 pages
Latest guidebook for Chinese Drug Recall Regulations (2014 Edition)
US $750.00

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....

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March 28, 2014 26 pages
Chinese guidebook for Medical Device Adverse Event Reporting and Monitoring Regulations (2014 Edition)
US $750.00

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....

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March 28, 2014 69 pages
Chinese guidebook for Adverse Drug Reaction Reporting and Monitoring Regulations (2014)
US $750.00

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....

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March 25, 2014 50 pages
Latest guidebook for Chinese Medical Device Recall Regulations (2014 Edition)
US $750.00

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....

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February 3, 2014 34 pages
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