Market Research Reports, Inc. has announced the addition of “Latest Guidebook for Conducting Pharma Clinical Trials in China: From Regulations to Practice (2014 Edition)” research report to their offering. See more at- http://mrr.cm/Zss
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Introduction to Report
Launch Date: July 19, 2014
Number of Pages: 191
Geography Coverage: China
Available Format: PDF
Price For Single User License: USD 1,495
Price For Site User License: USD 4,995
Price For Global User License: USD 5,250
Delivery Time: Within 24 Hours (During Working Days)
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About the Report
This Latest Guidebook for Conducting Pharma Clinical
Trials in China: From Regulations to Practice (2014 Edition)
not only provided a comprehensive and thorough
knowledge of the latest Chinese regulations on clinical
trials for imported drug registration but also introdued
the practical operation how to comply with the Chinese
GCP to guide you use the Chinese trial venues to keep
drug development lean and agile in the “post-patent-cliff”
world step by step.
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Research Findings
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 aging population, Chinese healthcare market
has maintained annually average growth rate above 16 %
since 1990s.
By 2013, total value of drugs on Chinese healthcare
market has reached RMB 1114 billion. On the Chinese
healthcare market, imported drugs made by overseas and
multinational pharmaceutical manufacturers account for
about one fourth.
It is estimated that total value of drugs on Chinese
healthcare market will be likely to be more than RMB
1450 billion by 2015, and will surpass Japan to become
the second largest drug market following the United
States.
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Target Audience:
Overseas pharmaceutical companies wishing to enter
into the Chinese drug market.
Multinational pharmaceutical companies have
penetrated into the Chinese drug market.
Companies interested in understanding the latest
Chinese laws and regulations for pharmaceutical product
clinical trials.
Senior executive officers engaging in regulatory affairs
for imported drugs into Chinese lucrative drug market.
Senior executive officers engaging in conducting clinical
trials for imported drugs in China.
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Reasons To Buy
An overview of the Chinese applicable laws and
regulations for drug clinical trials.
An overview of organizational structure of Chinese
regulatory authorities for drug clinical trials to give the
direction of gateway for clinical trials of imported drugs.
The Chinese definitions of some basic terms used in
application and approval process of drug clinical trials for
drug registration, and the Chinese unique classification of
drug registration, from the chemical drugs,
Chinese unique every party’s responsibilities in clinical
trials for imported drug registration.
An entire process of application and approval procedures
for clinical trials of imported drug registration.
The full text in English of Drug Registration Application
Form for Imported Drug.
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Report Coverage
1. Executive Summary
2. Chinese Applicable Laws and Regulations for Drug Clinical
Trials
3. An Overview of Chinese Authorities for Drug Clinical Trials
4. Knowledge Preparation before conducting Imported Drug
Clinical Trials
5. General Regulations on Application and Approval for Clinical
Trials of Imported Drug Registration
6. Every Party’s Responsibilities in Clinical Trials for Imported
Drug Registration
7. Application and Approval Procedures for Clinical Trials of
Imported Drug Registration
8. Application Form for Imported Drug Registration
9. Practical Guidance for Clinical Trials of Imported Chemical
Drug Registration
10. Practical Guidance for Clinical Trials of Imported Biological
Product Registration
For more details regarding Report coverage see the last slide
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How To Buy This Report?
Visit following URL to see Table of Content and
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http://mrr.cm/Zss
About Market Research Reports, Inc.
Market Research Reports provides a customized set
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Contact : Amitava Sen
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