Release date: 2010-01-11 Capsules Capsules Excellent Health Products Co.,Ltd. , https://www.sino-excellent.com
Recently, the "Food and Drug Safety and Supervision Policy Research Report (2009)" prepared by the Shanghai Food and Drug Safety Research Center and published by the Social Science Literature Publishing House was officially released in Beijing. The book comprehensively reflects the research and progress of food and drug safety and regulatory policies at all levels of government departments, institutions and society, especially the improvement of food and drug safety supervision at the institutional and institutional level. I believe these studies are The revision and improvement of China's food and drug safety supervision policy will play a certain role in promoting, have a positive guiding role in food and drug regulatory practice, and play a positive guiding role in food and pharmaceutical enterprises' research and implementation of government policies.
The 2009 Blue Book on Food and Drugs pointed out that medical devices, as modern science and technology products, have been widely used in disease prevention, diagnosis, treatment, health care and rehabilitation, and have become an important means of diagnosis and treatment in the field of modern medicine. In recent years, with the development of the medical device industry, the public has put forward higher requirements for the safety and effectiveness of medical device products, and the standard is the most basic means to ensure the safety and effectiveness of medical device products, thus strengthening medical device standards. Management work is important.
The Blue Book pointed out that medical devices, as modern science and technology products, have been widely used in disease prevention, diagnosis, treatment, health care and rehabilitation, and have become an important means of diagnosis and treatment in the field of modern medicine. In recent years, with the rapid development of China's medical device industry, the public has put forward higher requirements for the safety and effectiveness of medical device products. In addition, in the context of economic globalization, the barriers to trade in medical device technology have also become an important factor affecting the development of medical devices in China.
Technical standards are the basic means to ensure the safety and effectiveness of medical devices, and are also an important basis for the government to exercise supervision and management powers. It is also a prerequisite for China's medical device products to explore the international market. At present, China's medical device standard work has entered a stage of rapid development and has begun to show its scale. However, there are still some important problems in the management of medical device standards. Based on the summary of the status quo of medical device technology standards in China, this paper analyzes the problems existing in standard management and puts forward further suggestions. (Midi Medical Network)