中国医疗器械监管力度逐渐加大 法规日臻完善（Chinas medical device supervision has gradually increased, and the regulations are improving day by day）.docVIP

中国医疗器械监管力度逐渐加大 法规日臻完善（Chinas medical device supervision has gradually increased, and the regulations are improving day by day） Chinas medical device supervision has gradually increased, and the regulations are improving day by day Source: Bio Valley Science News Network Editor: Sharon 2012, 04, 28 Keyword: medical device supervision regulations Chinese Medical Devices Market from 2000 to 2009 ten years CAGR of 21%, to 2010 China medical equipment market reached 120 billion yuan, a huge potential for growth, in January 18, 2012, the Ministry issued a medical technology industry 12th Five-Year special plan, indicating 12th Five-Year during the key direction of products, medical equipment industry key layout tasks and policy measures, is expected to 12th Five-Year during new medical value of 200 billion yuan to pull, the formation of 8-10 value more than 5 billion yuan of large medical equipment industry group, effectively meet the primary medical and conventional medical treatment. This means that by 2015, Chinas entire medical equipment and equipment market is expected to be nearly 340 billion yuan. And the current global medical equipment accounted for 42% of the total market size of medicine, while China accounted for only 14% of the total size of the pharmaceutical market, it can be described as enormous potential. In China and the world, medical devices are highly regulated industries, policies and regulations not only affect the scale of the development of the industry, mode and direction, but also affect all aspects of enterprise management behavior. Therefore. In order to reduce risk and improve efficiency in the field of medical equipment such as high supervision, high risk, high technology and high profit, the most important problem is to understand the regulatory and regulatory environment. The definition of MD Devices (Medical) in China According to the 2000 release of medical equipment supervision and management regulations chapter third, medical devices,