论文部分内容阅读
医学实验仪器的质量直接关系到食品、药品研究与检测等领域中科研数据和检测结果的公正性、科学性和有效性。本文从计量溯源性要求出发,提出了对医学检测仪器实施期间核查的必要性,从不同角度解释了期间核查的定义,总结出了医学实验仪器期间核查实施的一般要求、具体实施方案、核查结果处理,重点阐述了核查对象的确定、期间核查时机的选择、核查方法的编写,为医学实验仪器的期间核查提出了切实的解决策略,对实验室规范开展此项工作具有指导意义。
The quality of medical experimental apparatus is directly related to the impartiality, scientificness and validity of scientific research data and test results in the fields of food and drug research and testing. Based on the requirement of measuring traceability, this paper puts forward the necessity of verification during the implementation of medical testing instruments, explains the definition of period verification from different angles, summarizes the general requirements for verification during medical laboratory instruments, the specific implementation plan, the verification results Processing, focusing on the verification of the object to determine the timing of the verification period, the preparation of verification methods for the medical laboratory equipment during the inspection proposed practical solutions to the norms of laboratory work to carry out this guidance.