2, where the introduction of the hospital has not yet carried out the new technology, new projects, should strictly abide by the access system.
3, the new medical technology is divided into the following three categories:
(1) explore the use of technology, refers to the introduction of medical institutions or independent development of new technologies not yet used in the country.
((2) limited system of use of technology (difficult, high-tech), refers to the need to limit the scope and have
-certain conditions before the use of technology
difficult, technically demanding medical technology.
(3) general diagnostic and therapeutic techniques, in addition to the national or provincial health administrative departments to limit the use of common diagnostic and therapeutic items, specifically in the country has been carried out and basically mature or fully mature medical technology.
(4) The hospital encourages the research, development and application of new medical technology, and encourages the introduction of advanced medical technology at home and abroad; prohibits the use of technology that has been significantly outdated or is no longer applicable, and needs to be eliminated or technical, safety, efficacy, economy, and social ethics and legal aspects of the protection of the citizens' health is not compatible with the technology.
(5) Hospital led by the Medical Department to set up the hospital's new technology management committee (consisting of members of the hospital's main business backbone) and departmental medical new technology management team (consisting of departmental director and departmental business backbone of 3-5 people), is fully responsible for the theoretical and technological demonstration of the new technology projects and provide authoritative evaluation. Including:Proposing medical technology access policy recommendations;Proposing recommendations for limited system use technology projects and related technical specifications and access standards;Being responsible for exploring and limited system use technology wood project technology evaluation and issuing evaluation reports;Evaluating the effect and social impact of the implementation of major technology access projects, and other consulting work related to technology access.
(6) strictly regulate the clinical access system of new medical technologies, where the introduction of the hospital has not yet carried out the new technology, new projects, first of all, must be carried out by the Department of feasibility studies, in order to confirm its safety, effectiveness and including ethical and moral aspects of the assessment of the basis of the scientific attitude of seeking truth from facts to guide clinical practice, and at the same time, to have the appropriate technical conditions, personnel and facilities, after a centralized discussion and consent of the head of the Department. After centralized discussion and consent of the head of the department, the department will fill in the "application form for new technology and new projects" and submit it to the Medical Education Department for review and collective assessment.
6.1 Department of the new general diagnostic and treatment technology projects only need to fill out the "application form" to the Medical Services Section to apply for the hospital's "Medical Practice Permit" within the scope of the medical education organization review and collective assessment; new projects for the hospital's "Medical Practice Permit" outside of the scope of the medical education to the District Health Bureau to declare, the Health Bureau to organize the review, and the Medical Services Section to review and evaluate the new projects. By the Health Bureau to organize the review, the Medical Section is responsible for liaison and urging the practice of registration.
6.2 Application to carry out the exploration of the use of limited system of use of technology must be submitted to the following materials:
6.2.1 medical institutions (including the number of beds, departments set up, technical personnel, equipment and technical conditions, etc.) and the legitimacy of the medical institution a copy of the materials;
6.2.2 to carry out the new technology project related to technical conditions, equipment conditions, the project responsible for physician qualification certificates and
6.2.2 to carry out new technology projects related to technical conditions, equipment conditions, project responsible for physician qualification certificates and the project responsible for the project. Conditions, the project is responsible for the qualification of physicians and technical personnel
6.2.3 to carry out new technology projects related regulations, technical specifications and operating procedures;
6.2.4 to carry out the feasibility of exploring the use of technology projects report;
6.2.5 health administrative departments or provincial medical associations provide for the submission of other materials.
6.3 Exploration of the use of technology, limited system of use of technology project evaluation and reporting:
6.3.1 Acceptance of the declaration by the Medical Education Department to conduct a formal review;
6.3.2 first by the Department of Medical Education Department of Medical Technology Management Group relying on the Department of Medical Technology based on the relevant technical specifications and access criteria for the initial technical assessment;
6.3.3 departments Declaration materials perfected within 15 working days by the Medical Education Department to organize the hospital's new technology management committee experts to assess and issue a technical assessment report;
6.3.4 by the Department of Medical Services to the Provincial Department of Health to declare the Department of Health and the Provincial Medical Association to organize the audit, the Medical Education Department is responsible for liaison and urging the practice of registration.
7, the hospital medical department responsibilities:
(1) hospital medical department is responsible for the organization and management of the hospital medical technology access work, the system set the relevant medical technology access policy, planning, coordination and supervision of the implementation of this system.
(2) in accordance with the "Regulations on the Administration of Medical Institutions", "Medical Practice License" and other regulatory requirements,
Organization of the audit of new technology projects
whether the scope of practice, such as belonging to the over-scope of the practice of the Medical Department to the District Health Bureau to declare the District Health Bureau to organize the audit, the medical
(3) Medical Department of the Department of Medical Services to organize the Department of medical management group of new medical technologies and other functional departments, with reference to the provincial or domestic hospitals of the same level of charges, fill out the fee standard declaration form to report to the Price Bureau.
(4) The medical department of the hospital is responsible for implementing the daily supervision and management of medical technology access in the whole hospital, including tracking the new medical technologies that have been declared and carried out, understanding their progress, assisting in the training of the relevant personnel, inviting experts from outside the hospital for guidance, and solving the problems and difficulties in the progress.
8. Every year, each department will report the new medical technology projects planned to be carried out in the current year
to the Department of Medical Education according to the specified time, and approve and implement the main person in charge of the new medical technology and the main participants, and fill in the relevant application materials. Department of new medical technology management team to organize and supervise the implementation of medical technology according to the plan, regular contact with the competent departments to ensure the smooth implementation of new medical technology. The person in charge of the new medical technology project should pay attention to the technical projects that have been carried out at any time to pay attention to the development of domestic and foreign
provincial and international developments, collect
collecting information, organizing various types of academic exchanges, and summarizing and improving in a timely manner.
9, in the implementation of new technologies, new projects before the patient or his proxy must obtain consent and written signature for the record.
10, declared the medical new technology achievement award:
(1) declared the department at the end of the new technology, new projects will be carried out to summarize, fill out the new technology, new project selection application form, reported to the Medical Department to participate in the hospital's annual evaluation. Reporting materials are required to be complete, accurate and factual, including the completion and effect of the technology, the number of completed cases and the necessary medical records (clinical effects and the necessary control), the status of domestic and international and provincial applications, thesis publication.
(2) At the end of each year, the Medical Affairs Department organizes the experts of the hospital's New Technology Management Committee to review the new medical technologies that have been carried out and achieved results using efficient and fair procedures, and grants awards to the very valuable projects among them and promotes them to the higher-level departments.
(3) At the end of each year, the Medical Affairs Department organizes the experts of the Hospital New Technology Management Committee to conduct retrospective summaries and evaluations of the social and economic benefits of the new medical technologies that have been carried out or awarded in the past, and draws the corresponding conclusions on the medical technologies that have lost their practical value or ceased.
11, violation of the provisions of this approach, without access to the management of unauthorized medical technology projects approved, in accordance with the "Regulations on the Management of Medical Institutions", "Regulations on the Implementation of the Regulations on the Management of Medical Institutions" and other relevant laws and regulations to be punished, and bear the corresponding legal responsibility.
12, violation of the provisions of this approach to physicians, in accordance with the "People's Republic of China **** and the State Practitioners Law" and other relevant laws and regulations to be punished, and bear the corresponding legal responsibility.
13. If there is any conflict between this system and the relevant medical technology access system of the state administrative department, the system shall be implemented according to the relevant medical technology access system of the state administrative department.
14. Medical technology access programs or experimental medical programs otherwise stipulated by the state administration shall be implemented in accordance with the relevant state regulations.
Legal basis:
"Regulations for the Implementation of the Regulations on Medical Institutions"