首页|微生物限度检查能力验证组织及解读

微生物限度检查能力验证组织及解读

扫码查看
目的 通过组织非无菌药品微生物限度检查能力验证,掌握云南省药品生产企业和药检机构的检验检测能力,并通过对不满意结果的分析讨论,提高参加实验室该项目的检验检测能力和质量管理水平。方法 根据中国合格评定国家认可委员会(CNAS)相关文件要求,定性项目以制备值阳性或阴性为指定值,计数项目以对数中位值作为指定值,采用稳健统计方法,Z值作为评定参数,4个项目全部为满意的,总结论为满意,反之则为不满意,仅部分项目满意的为部分满意。结果 全省共152家实验室参加本次能力验证,其中116家满意,占76。31%;33家部分满意,占21。71%;3家不满意,占1。97%。按实验室性质统计药检机构满意率为88。23%;药品生产相关机构满意率为74。81%。结论 参加实验室的非无菌药品微生物限度检查的检测能力较好,能够保证该项目的顺利开展和结果的准确、有效。少数实验室的检测能力和质量管理水平有待改进提高。
Implementation and interpretation for proficiency testing of microbiological examination
Objective To understand the testing performance of drug manufacturers and testing institute in Yunnan province by organizing proficiency testing of microbiological examination of non-sterile drugs,and to improve the testing performance and quality management level of participants by interpretation of unsatisfactory results.Methods According to the requirements of relevant China National Accreditation Service for Conformity Assessment (CNAS),preparation values of positive or negative was determined as assigned values for qualitative items,and the median value was as assigned value for enumeration items.Using robust statistical methods and Z-score for assessment,if all the 4 items were satisfactory,it would be assessed as overall satisfactory performance,and contrariwise,it would be assessed as unsatisfactory performance.If partial item were satisfactory,it would be assessed as partially satisfactory performance.Results 152 laboratories participated in this proficiency testing program,116 laboratories obtained satisfactory performance and the satisfactory rate was 76.31%;33 laboratories obtained partially satisfactory performance,and the partially satisfactory rate was 21.71%;3 laboratories obtained unsatisfactory performance and the unsatisfactory rate was 1.97%.To classify the participants with type,the satisfactory rate for drug control institute was 88.23% and the satisfactory rate of drug manufacturers was 74.81%.Conclusion The testing performance of participating laboratories in microbiological examination of non-sterile drugs is generally good,which can ensure the smooth implementation of the program and the accuracy and effectiveness of the results.The testing capacity and quality management level of a few laboratories need to be improved.

Proficiency testingNon-sterile drugsMicrobiological examinationImplementation and interpretation

李志远、张景仪、王思琪、李哲媛、刘屹、邹伟斌

展开 >

云南省食品药品监督检验研究院,工业和信息化部产业技术基础公共服务平台,昆明 650106

艾吉析科技(上海)有限公司,上海 200041

能力验证 非无菌药品 微生物限度检查 组织与解读

2024

中国药师
国家药品监督管理局高级研修学院,武汉医药(集团)股份有限公司

中国药师

CSTPCD
影响因子:0.944
ISSN:1008-049X
年,卷(期):2024.28(10)