首页|我国24家检验检测机构洁净环境照度检测能力验证

我国24家检验检测机构洁净环境照度检测能力验证

扫码查看
目的 评价我国检验检测机构对洁净环境照度的检测能力。方法 回顾性分析中国食品药品检定研究院于 2022 年在全国范围内首次设计并组织实施的洁净环境照度能力验证项目。基于洁净环境检测的行业特点,该项目分为笔试和实际操作(简称实操)两部分。笔试部分,共 3 题(限时 40 min完成),考察参加测试(简称参测)实验室对检测标准正确理解和掌握的程度,根据专家商议确定的评分标准评分(满分 50 分)。实操部分,以该院药用辅料和包装材料检定所的 2 台洁净工作台为现场考核样品,以参测实验室的现场测试结果考察参测实验室的仪器操作和实验水平(限时 5 min完成),以Z值进行评价(︱Z︱≤2,>2~<3,≥3分别为满意、有问题、不满意)并打分(满分 50 分)。以笔试和实操评分之和评价参测实验室的检测能力(≥60分为合格)。结果 共 24 家实验室参加了能力验证并按要求提交了结果报告。笔试,评分为 45~50 分,满分 21 家(87。50%)。实操,样品A,满意 21 家(87。50%),有问题 3 家(12。50%);样品B,满意 23 家(95。83%),有问题 1 家(4。17%),2 个样品均无不满意的实验室。24 家实验室总评分均合格。结论 该次能力验证结果显示,各实验室的检测能力维持良好,但部分实验室存在对标准的理解和掌握仍有欠缺或未按校准周期对照度计进行计量等问题,建议检测人员加深对洁净环境检测标准的理解,相应机构重视仪器的校准,持续提高检测能力。
Proficiency Testing for Illuminance Detection of Clean Environment of 24 Inspection and Testing Institutes in China
Objective To evaluate the proficiency of Chinese inspection and testing institutes on the illuminance detection of clean environment.Methods A proficiency testing program for illuminance detection of pharmaceutical clean environment firstly designed and implemented nationwide by National Institutes for Food and Drug Control in 2022 was retrospectively analyzed.Based on the characteristics of clean environment testing industry,this program included written examination and practical operation.The written examination consisted of three questions(limited to 40 min to complete),aiming to assess the correct understanding and mastery degree of participating laboratories on testing standards,and it was evaluated according to the scoring criteria determined by experts(a maximum of 50 points).Two clean workbenches from the Institute for Pharmaceutical Excipients and Packaging Materials Control,National Institutes for Food and Drug Control were used as the samples in practical operation to assess the instrument operation and testing level of participating laboratories(limited to 5 min to complete).The results of on-site testing were evaluated by Z-value(︱Z︱≤2,2<︱Z︱<3,︱Z︱≥3 refer to satisfactory,questionable and unsatisfactory results)and scored(a maximum of 50 points).The testing capacity of participating laboratories was evaluated based on the sum of written examination and practical operation scores,with≥60 points as qualification.Results A total of 24 laboratories participated in this proficiency testing and submitted reports as required.The score of written examination was in the range of 45 to 50 points,with 21 laboratories getting full scores(87.50%).For sample A,the practical operation of 21 laboratories was satisfactory(87.50%),while that of three was questionable(12.50%);for sample B,that of 23 laboratories was satisfactory(95.83%),while that of one was questionable(4.17%),and there was no unsatisfactory result for both samples.The total score of 24 laboratories was all qualified.Conclusion This proficiency testing shows that the testing capacity of each laboratory is good.However,some laboratories still lack understanding and mastery of the standards or do not meter the lumeter according to the calibration cycle.It is suggested that the testing personnel should increase understanding of clean environment testing standards,and corresponding institutes should pay attention to instrument calibration to continuously improve the testing capability.

inspection and testing instituteclean environmentilluminanceproficiency testing

田霖、刘雅丹、项新华、谢兰桂、杨会英

展开 >

国家药品监督管理局药用辅料质量研究与评价重点实验室·中国食品药品检定研究院,北京 100050

检验检测机构 洁净环境 照度 能力验证

中国食品药品检定研究院学科带头人培养基金立项课题

2023X9

2024

中国药业
重庆市食品药品监督管理局

中国药业

CSTPCD
影响因子:1.369
ISSN:1006-4931
年,卷(期):2024.33(2)
  • 12