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Latest Chinese Guidebook for Application and Approval of Imported Medical Device Registration: From Regulations to Practices
Date:9/3/2014

egulations on medical device registration. Otherwise, the restrictive legal requirements and approval delays eat up your time and energy to achieve a successful entry into such a lucrative medical device market, and cause trouble for your business smoothly in China.

Latest Chinese Guidebook for Application and Approval of Imported Medical Device Registration: From Regulations to Practices (2014 Edition) not only provides a comprehensive and thorough knowledge of the latest Chinese regulations for imported medical device registration but also introduces the practical operation of how to comply with the Chinese regulations to guide you to achieve a successful approval for your products entry into the Chinese medical device market.

For Sample Pages and Table of Contents: 

https://www.bharatbook.com/medical-devices-market-research-reports-228172/guidebook-application-approval-medical-device-registration-regulations.html

The organizations of this guidebook are arranged as follows. 

  • Chapter 2 provides the analysis and research for radical change of Chinese regulations on medical devices.
  • Chapter 3 Introduces the framework of the latest applicable Chinese regulations for medical device registration to provide a comprehensive and thorough knowledge of the latest Chinese regulations for medical device registration.
  • Chapter 4 provides an overview of the Chinese regulatory authorities -- China Food and Drug Administration (CFDA) being responsible for application and approval for imported overseas medical device registration and recordation to give the direction of gateway for imported overseas medical devices registration and recordation.
  • Chapter 5 elaborates on the knowled
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SOURCE Bharat Book Bureau
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