The content of the Administrative Measures for the Clinical Application of Medical Technology

The administrative measures for the clinical application of medical technology are as follows:

The Measures for the Administration of Clinical Application of Medical Technology are measures formulated in accordance with relevant laws and regulations to strengthen the management of clinical application of medical technology. On August 13, 2018, Decree No. 1 of the National Health Commission of the People's Republic of China was promulgated, which came into force on November 1, 2018.

Medical institutions and medical personnel shall comply with these Measures when carrying out the clinical application of medical technology. The clinical application of medical technology shall follow the principles of science, safety, standardization, effectiveness, economy, and ethics. Medical institutions must not carry out clinical application of medical technology whose safety and effectiveness are uncertain.

The state shall establish a negative list management system for the clinical application of medical technologies, implement negative list management for medical technologies that are prohibited for clinical application, and carry out key management of some medical technologies that require strict supervision. Other medical technologies applied at the top of clinical orders are self-managed by the medical institution that decides to use them.

Medical institutions bear the main responsibility for the clinical application and management of medical technology in their own institutions. Medical establishments carrying out medical technology services shall be commensurate with their technical capabilities. The main person in charge of the medical institution is the first person responsible for the management of the clinical application of medical technology in the institution.

The National Health Commission is responsible for the management of the clinical application of medical technology nationwide.

The local health administrative departments at or above the county level shall be responsible for the supervision and management of the clinical application of medical technology within their respective administrative areas. Health industry organizations are encouraged to participate in the quality control of the clinical application of medical technology, standardized training and technical evaluation, and the administrative departments of health at all levels shall create conditions for health industry organizations to participate in the management of clinical application of medical technology.

The administrative department of health shall periodically review the clinical application of medical technology in medical institutions. In the course of regular audits, if violations are found, a decision is made on whether to cancel the registration of the medical technology under the diagnosis and treatment subjects of the medical institution, and to continue or stop the clinical application of the medical technology.

Legal basis: Administrative Measures for the Clinical Application of Medical Technology on the Supervision and Administration of Clinical Application of Medical Technology

Article 45 The local health administrative departments at or above the county level shall strengthen the supervision and management of the clinical application of medical technology in medical institutions.

Article 46 When the administrative department of health at or above the county level conducts supervision and inspection, it has the right to take the following measures: (1) If it enters the work site to understand the situation, it will investigate and collect evidence; (2) Inspecting and reproducing relevant materials; (3) Order medical establishments to immediately correct violations of laws and regulations.

The clinical application of medical technology shall follow the principles of science, safety, standardization, effectiveness, economy, and compliance.

Principles of clinical diagnosis and treatment.

According to the purpose of clinical diagnosis and treatment, the principle is divided into two aspects, on the one hand, it is beneficial to the patient, and on the other hand, it is for the medical staff.

The aspects that are beneficial to patients include: (1) the principle of patient first: it means that medical staff always take patients as the center in the process of diagnosis and treatment, and put the interests of patients in the first place.

2) Optimization principle: (merit principle) refers to the decision that medical personnel should obtain the maximum effect at the minimum cost when choosing a diagnosis and treatment plan. Under the condition of limited diagnosis and treatment, the diagnosis and treatment measures taken should make the patient suffer the least pain, the least cost, the least cost, the best effect, and the highest safety.

3) The principle of informed consent: It means that medical personnel should obtain the patient's informed and free choice and decision when selecting and determining the diagnosis and treatment plan of the disease. For some special examinations, special tests, special procedures, and surgeries are based on the signature of the patient or the patient's family.

For this reason, medical personnel are asked to provide information. If the patient makes a mistake, the medical staff has the responsibility and obligation to perform the guidance. (4) The principle of confidentiality and trustworthiness.

It means that medical staff should keep the confidentiality and privacy of patients during the diagnosis and treatment of patients and beyond, and abide by the ethical code of integrity. This includes keeping information confidential about adverse diagnoses that should not be disclosed to patients. (5) Principle of autonomy:

In the process of diagnosis and treatment, patients have the autonomy to inquire about their condition, accept or reject them, or choose treatment options.

The requirements for medical personnel include: (1) the principle of timeliness: medical personnel are required to make a diagnosis of the disease as soon as possible, take the initiative to act quickly, and respond to the patient's requirements and disease changes in a serious and timely manner.

2) The principle of accuracy: medical personnel are required to actively and fully use the actual conditions to make serious and serious judgments that are in line with the actual conditions.

Summary. Hello dear! <> The catalogue of clinical application management of medical technology is an important part of China's "Regulations on the Supervision and Administration of Medical Devices", which belongs to the specific implementation provisions of laws and regulations.

The Regulations on the Supervision and Administration of Medical Devices are regulations jointly issued by the National Health Commission of China and the State Drug AdministrationThe Regulations on the Supervision and Administration of Medical Devices are administrative regulations, so in terms of effectiveness, it is above the departmental regulations.

Hello dear! <> medical technology clinical application management catalogue is an important part of China's "Regulations on the Supervision and Administration of Medical Devices", which belongs to the specific implementation provisions of laws and regulations. The Regulations on the Supervision and Administration of Medical Devices is a regulation jointly issued by the National Health Commission of China and the National Medical Products Administration, and the Regulations on the Supervision and Administration of Medical Devices are administrative regulations.

Legal basis: In order to strengthen the management of the clinical application of medical technology, establish a wide access and management system for medical technology, promote the development of medical science and medical technology, improve the quality of medical care, and ensure medical safety, in accordance with the Law on Medical Practitioners, the Regulations on the Administration of Medical Institutions, the Regulations on the Careful Handling of Medical Accidents and other relevant laws, regulations and rules.

Summary. Hello dear! The Administrative Measures for the Clinical Application of Medical Technology are normative documents that belong to administrative regulations, and their effectiveness levels are: higher than departmental regulations, local regulations, administrative rules and military regulations, and lower than laws.

Hello Kiss, Fierce Front! The Administrative Measures for the Clinical Application of Medical Technology are the normative Wenzhen Zhilun parts that belong to the administrative regulations, and their effectiveness level is higher than that of departmental regulations, local regulations, administrative rules and military regulations, and lower than that of Yuxin laws.

The full text of the Administrative Measures for the Clinical Application of Medical Technology compiled by the Medical Education Network is as follows; Article 1 These measures are formulated in accordance with the "Law on Medical Practitioners", "Regulations on the Administration of Medical Institutions", "Regulations on the Handling of Medical Accidents" and other relevant laws, regulations and rules, in order to strengthen the management of the clinical application of medical technology, establish a system for access and management of medical technology, promote the development of medical science and medical technology progress, improve the quality of medical care, and ensure medical safety. Article 2 The term "medical technology" in these measures refers to the diagnosis and measures taken by medical institutions and their medical personnel for the purpose of diagnosing and eliminating diseases, alleviating diseases, alleviating pain, improving functions, prolonging life, and helping patients recover their health.