China Medical Device Recall Regulations Highlighted by Access China Management Consulting in New Report Published at MarketPublishers.com
11 Feb 2014 • by Natalie Aster
LONDON – China is ranked as the leading and fastest-growing global economies with a fifth largest population in the world. The country has the largest healthcare market across the globe. Supported by the stable population and economic growth, the Chinese healthcare market has witnessed an annual average growth rate of nearly 16% during the past several years.
Medical devices formed the mostly dynamic sector. By 2013, the value of the sector amounted to RMB 179 billion. Furthermore, it is poised to see sustained growth in the upcoming years and exceed RMB 340 billion by 2015. China’s medical devices market will likely outrun Japan’s market and become the 2nd largest medical devices market after the US. The country is anticipated to attract more foreign medical device producers to penetrate the highly promising market.
New research report “Latest guidebook for Chinese Medical Device Recall Regulations (2014 Edition)” worked out by Access China Management Consulting provides a comprehensive and detailed overview of the Chinese medical device recall regulations.
The study reviews the organizational structure of the country’s regulatory authorities, highlights all the important details and steps of the recall process, describes the Chinese regulations for voluntary and mandatory recall of medical devices, and also clarifies the entire process of both types of recalls. The research report contains a case study of recall of the US company’s medical device, grants access to a whole set of the Chinese and English bilingual forms associated with medical device recall, as well as features the latest changes in the national medical device recall regulations.
Latest guidebook for Chinese Medical Device Recall Regulations (2014 Edition)
Published: February, 2014
Price: US$ 750.00
Other In-demand Reports by Access China Management Consulting Include:
- China Pharmaceutical Guidebook: (2013 Edition) Latest Chinese Regulations for Imported Drug Registration 2013 Edition Material and Clinical Trial Requirements of Application and Approval for Imported Drug Registration: A Guidebook of Registration Application for Imported Chemical Drugs
- Latest Guide to Chinese Medical Device GMP Regulations
- Latest Guide to Chinese Pharmaceutical GMP Regulations
- Latest Chinese Guide to Industrial Access for Foreign Companies and Investors
More in-demand research reports by the publisher can be found at Access China Management Consulting page.