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Latest Guide to Chinese Medical Device GMP Regulations
Latest Guide to Chinese Medical Device GMP RegulationsSynopsis
Latest Guide to Chinese Medical Device GMP Regulations is an essential resource for overseas medical device manufacturers and producers to achieve a successful entry into the Chinese medical device market, which provides a detailed guidance of comprehensive and thorough knowledge of the latest Chinese Good Manufacturing Practice (GMP) Regulations for Medical Devices.
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Latest Guide to Chinese Medical Device GMP RegulationsSummary China is one of the fastest growing global economies with a
fourth population in the world, and is one of the largest healthcare markets around the world. Along with sustained economic and population growth, Chinese healthcare market has maintained annually average growth rate above 16 % since 1990s. Among them, medical devices represented dynamical growth since 2000s. By 2012, total value of medical devices on Chinese healthcare market has reached 138 billion RMB.
In 2009, the Chinese government vigorously launched “China’s Health-Care Reform”, developed an ambitious blueprint, in which health care system has covered about 1.28 billion people by 2012. Medical devices have been widely used in the process of disease prevention, diagnosis, therapy, care and rehabilitation. It is estimated that within the next few years, Chinese medical device market will be likely to be more than 600 billion RMB, and will surpass Japan to become the second largest medical device market following the United States. The Chinese medical device market will attract more and more overseas medical device manufacturers and producers to penetrate such market.
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Reasons To Buy Overseas medical device companies wishing to enter a
lucrative drug market in China. Overseas medical device companies interested in
understanding the latest Chinese Medical Device GMP Regulations.
Senior executive officers engaging in regulatory affairs expecting to understand the latest Chinese Medical Device GMP regulations.
Senior executive officers engaging in regulatory affairs for quality control, quality assurance, and production management for medical device manufacture.
Non-Chinese pharmaceutical consultative companies engaging in agent service for application and inspection of Medical Device GMP with the Chinese government authorities.
Non-Chinese universities, colleges, academic & research institutions
Non-Chinese university library, public library. Non-Chinese Chamber of Commerce.
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Latest Guide to Chinese Medical Device GMP Regulations
Latest Guide to Chinese Medical Device GMP RegulationsScope Latest Guide to Chinese Medical Device GMP Regulations is
an essential resource for overseas medical device manufacturers and producers to achieve a successful entry into the Chinese medical device market, which provides a detailed guidance of comprehensive and thorough knowledge of the latest Chinese Good Manufacturing Practice (GMP) Regulations for Medical Devices, covering the organizational structure of Chinese regulatory authorities for medical device GMP regulations, an overview of Good Manufacturing Practice (GMP) for Medical Devices, from design, development and manufacturing to sales and after-sale service, the details of the Regulations on Inspection of Good Manufacturing Practice (GMP) for Medical Devices, the Implementation Guidelines and Inspection Criteria of Good Manufacturing Practice (GMP) for Sterile Medical Devices in detail, as well as the detailed comprehensive guidance of Implementation Guidelines and Inspection Criteria of Good Manufacturing Practice (GMP) for Implantable Medical Devices.
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Latest Guide to Chinese Medical Device GMP Regulations
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