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Doing Business in China: Research on Chinese Good Manufacturing Practice Regulations for Medical Devices
Date:3/27/2013

Manufacturing Practice (GMP) Regulations for Medical Devices.

Highlights from the guidebook include: an overview of medical device GMP, details of inspection regulations, implementation guidelines and inspection criteria for both sterile and implantable medical devices, and a complete set of English and Chinese bilingual application and inspection forms of Good Medical Device Manufacturing Practice.

Learn more about the guidebook and request free sample pages at http://www.giiresearch.com/report/acmc264331-latest-guide-chinese-medical-device-gmp.html

For additional medical device market research reading, Global Information (GII) also recommends "The Medical Device Market: China". The report supplies a wealth of statistical data and analysis of key medical market drivers. 5-year market forecasts, national data projections, market outlook and key developments such as regulation, health facilities and government policy are provided in addition to extensive background information, population trends, health status, health expenditure, organization and administration, hospital services, medical personnel, healthcare development, market access information, trade data and essential industry contacts.

Learn more about Espicom's report on medical devices in China and request free sample pages at http://www.giiresearch.com/report/es26125-medical.html

Ophthalmic devices and In Vitro Diagnostics (IVD) account for a major portion of the medical device market in China. Ophthalmic surgery devices will be driven by a combination of China's large population of patients suffering from cataracts and government-backed insurance schemes t
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SOURCE Global Information, Inc.
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