Legal analysis: The Regulations clarify the supervision and management of the process of using the medical insurance fund; clarify the center of the people's health, provide all participants with a level of protection compatible with economic and social development, and supervision in accordance with the law; highlighting the "safe" "effective The two key words "safe" and "effective" are emphasized. Fund "safety" is the foundation, "effective" operation is the goal. It clearly defines the behavioral norms related to the use of the fund by the "two institutions" and the insured; puts forward the measures that can be taken by the medical insurance department to implement supervision and inspection; lists the various illegal behaviors that may cause the loss of the medical insurance fund, providing a standard for the implementation of supervision and management and the characterization of events; and establishes the penalties for the relevant illegal behaviors and the processing of the law. The law also defines the penalties and methods of handling related violations.
Legal basis: "Regulations for the Supervision and Administration of Medical Devices"
Article 7: Medical device products shall comply with the mandatory national standards for medical devices; if there are no mandatory national standards, they shall comply with the mandatory industry standards for medical devices.
Article VIII The state develops medical device industry planning and policy, medical device innovation into the development of key, innovative medical devices to be prioritized for review and approval, to support the clinical promotion and use of innovative medical devices, and to promote the high-quality development of the medical device industry. The drug supervision and management department of the state council shall cooperate with the relevant departments of the state council, the implementation of the national medical device industry planning and guiding policies.
Article IX The State shall improve the medical device innovation system, support the basic and applied research of medical devices, promote the promotion and application of new technologies of medical devices, and support scientific and technological projects, financing, credit, bidding and purchasing, and medical insurance. Support enterprises to set up or jointly set up research and development institutions, encourage enterprises to cooperate with universities, research institutes and medical institutions to carry out research and innovation of medical devices, strengthen the protection of intellectual property rights of medical devices, and improve the capability of independent innovation of medical devices.
Article 10 The state to strengthen the supervision and management of medical devices information construction, improve the level of online government services, for the administrative licensing of medical devices, filing to provide convenience.
Article XI medical device industry organizations should strengthen industry self-discipline, promote the construction of integrity system, supervise enterprises to carry out production and management activities in accordance with the law, and guide enterprises to be honest and trustworthy.
Article XII of the research and innovation in medical devices to make outstanding contributions to the units and individuals, in accordance with relevant state regulations to give recognition and reward.