1. To carry out the new technology, new projects should be in line with relevant state laws and regulations and rules and regulations. 2. To carry out the new project should be scientific, effective, safe, innovative and beneficial. 3. To carry out the new technology, new business of medical instruments used in the medical instrument must have "medical instrument manufacturer license", "medical instrument business enterprise license", "medical instrument product registration certificate" and product qualification certificate, and provide a copy of the seal stamped with the company for verification; the use of qualified documents to carry out new projects, medical instruments, and the use of qualified documents, and the use of medical instruments to carry out new projects, the main content of the management system. Registration Certificate" and product certification, and provide a copy of the seal stamped with the enterprise for inspection; the use of medical equipment to carry out new projects do not have all the qualification documents, are refused to enter the 4. To carry out the new project of the use of pharmaceutical products must have a "Drug Manufacturing License", "Drug License" and the product certification, imported drugs must have a "burst of the port license", and provide a copy of the seal stamped with the enterprise for inspection; the use of Qualification documents are not full of drugs to carry out new projects, are not allowed to burst. Fourth, new technology, new business procedures
l. Declaration Declaration should have an associate physician or equivalent associate physician and above professional title of the hospital's clinical, medical technology, nursing staff, must carefully fill out the "new technology, new business application," the undergraduate discussion and review, signed by the section chief sent to the Medical Education Department. 2. Audit Medical Education Department on the "new technology, new business application," to review and qualify, and then submitted to the medical education department. Audit qualified, reported to the hospital technical committee review, assessment, after full justification and agreed to allow people to report to the President for approval. 3. Approval of the proposed new technology, new business reported to the President and the relevant departments of the higher level for approval, by the Office of the management is responsible for the municipal pricing department to declare the charges, approved before implementation; health insurance reimbursement or not, by the Office of the higher level of health insurance department for approval. V, the main content of the feasibility study
Including new technologies, new sources of business, domestic and international to carry out the project's current situation, to carry out the purpose, content, methodology, quality indicators, to ensure that the conditions and funding, the expected results and benefits, and so on. Sixth, monitoring measures
1. new technology, new business after approval must be implemented according to the plan, where the increase or withdrawal of the project needs to be approved by the Technical Committee review and approval, reported to the hospital leadership approval before proceeding. 2. medical textbooks every six months to carry out routine inspection of the new project once, the project leader every six months to the medical textbooks written report on the implementation of the new project. 3. new projects that can not be completed by the due date, the project The applicant must explain the reasons in detail to the Technical Committee. The technical committee has the right to question the project applicant according to the specific circumstances, criticism or punishment. 4. new technology, new business permits people to implement the relevant technical information should be properly preserved; new project acceptance, the technical summary should be submitted to the medical science archives copies of the thesis for the record.