Chinese Medical Device GMP Regulations Explored in Discounted Access China Report Now Available at

17 Nov 2015 • by Natalie Aster

LONDON – Being one of the swiftest growing economies, China can boast one of the largest healthcare marketplaces, as well. The latter one has grown by approximately 16 percent over the past several decades.

The medical devices segment has registered dynamical growth on an annual basis over the last 15 years. For instance, its value in the local healthcare market almost hit the RMB 256 billion mark by 2014.

Imported overseas devices account for around 50 percent of the Chinese medical devices marketplace. However, regulations related to medical devices have changed significant over the last year.

CFDA has issued some regulations that medical device manufacturers (overseas, international and local ones) must comply with.

Insightful study “Latest Guidebook for Chinese Medical Device GMP Regulations” developed by Access China provides a detailed guide to medical device GMP regulations in China. The report represents a unique source of information vital for manufacturers of medical devices willing to enter the Chinese marketplace and operate their business smoothly in the country. It provides an up-close look at the local regulatory authorities for medical device GMP regulations. The report sheds light on all essential regulations essential for medical device manufacturers, including the latest ones.  

Report Details:

Latest Guidebook for Chinese Medical Device GMP Regulations
Published: November, 2015
Pages: 217
Price: US$ 1,495.00 US$ 1,270.75

More new studies by the publisher can be found at Access China page


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Natalie Aster
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