Chinese Medical Device GMP Regulations Guidebook 2015 Report

24 Nov, 2015, 10:30 ET from Market Reports Online

PUNE, India, November 24, 2015 /PRNewswire/ --

MarketReportsOnline.com adds Latest Guidebook for Chinese Medical Device GMP Regulations industry research report of 217 pages published in November 2015 to the medical devices market data collection of its online business intelligence library at http://www.marketreportsonline.com/226134.html.

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 healthcare market has maintained annually average growth rate above 16 % since 1990s. Among them, medical devices represented dynamical growth since 2000s. By 2014, total value of medical devices on Chinese healthcare market has reached 255.6 billion RMB (about 40.25 billion US dollars). Medical devices have been widely used in the process of disease prevention, diagnosis, therapy, care and rehabilitation. On the Chinese medical device market, imported overseas medical devices made by overseas and multinational medical device market manufacturers account for about a half, in which the high-tech and high-valued medical devices, such as magnetic resonance imaging (MRI) equipment's, computed tomography (CT) equipment's are almost monopolized by GE, Siemens, Philips and other overseas and multinational companies. It is estimated that Chinese medical device market will be likely to be more than 340 billion RMB (about 53.15 billion US dollars) by 2015, and will surpass Japan to become the second largest medical device market behind the United States.

Order a copy of this Chinese medical device GMP regulations guidebook report at http://www.marketreportsonline.com/contacts/purchase.php?name=226134.

Company Coverage of Medical Devices Market: GE, Siemens and Philips.

Key Reasons to Buy 

China's medical device market is indispensable for overseas and multinational medical device manufacturers. It's definitely a field worth playing on, but Chinese regulatory framework for medical devices has undergone significantly changed. Since October 2014, China Food and Drug Administration (CFDA) issued the latest Chinese Good Manufacturing Practice (GMP) Regulations for Medical Devices, the latest Implementation Regulations of Good Manufacturing Practice (GMP) for Sterile Medical Devices and the Implementation Regulations of Good Manufacturing Practice (GMP) for Implantable Medical Devices as the appendices of the latest Chinese Good Manufacturing Practice (GMP) Regulations for Medical Devices, as well as the latest On-site Inspection Guideline of Good Manufacturing Practice (GMP) for medical devices market, On-site Inspection Guideline for Sterile Medical Device GMP Implementation Regulations, and On-site Inspection Guideline for Implantable Medical Device GMP Implementation Regulations. Everything changed.

Facing sharp changes of medical devices GMP regulations, how do you in compliance with the latest Chinese medical device GMP regulations, how do you operate business smoothly in China?

Latest Guidebook for Chinese Medical Device GMP Regulations is an essential resource for overseas and multinational medical device manufacturers to achieve a successful entry into the Chinese medical device market, and to operate business smoothly in China, which provides not only a comprehensive and thorough knowledge of the latest Chinese Medical Device GMP Regulations, but also the practical operation how to comply with the latest Chinese Medical Device GMP Regulations, how to smoothly pass through the extremely stringent on-site inspection and verification process of GMP rules and the relevant assorted GMP implementation regulations.

Major points from Table of Contents (http://www.marketreportsonline.com/226134-toc.html) are listed below:

Chapter 1 Executive Summary

Chapter 2 Chinese Regulatory Authorities for Medical Device GMP Regulations

Chapter 3 An Overview of Good Manufacturing Practice (GMP) for Medical Devices

Chapter 4 Implementation Regulations of Good Manufacturing Practice (GMP) for Sterile Medical Devices

Chapter 5 Implementation Regulations of Good Manufacturing Practice (GMP) for Implantable Medical Devices

Chapter 6 On-site Inspection of Good Manufacturing Practice (GMP) for Medical Devices

Chapter 7 Inspection Items and Inspection Contents of Good Manufacturing Practice (GMP) for Medical Devices

Chapter 8 Inspection Items and Inspection Contents for Sterile Medical Device GMP Implementation Regulations

Chapter 9 Inspection Items and Inspection Contents for Implantable Medical Device GMP Implementation Regulations

Company's Brief Introduction

Explore more related reports on medical devices market at http://www.marketreportsonline.com/cat/medical-devices-market-research.html.

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