Guidelines for the validation of qualitative screening methods for the detection of residues of veterinary drugs in milk and milk products
文件核验信息(付费前可核对)
标准范围(官方英文摘要)
This document describes general workflows and protocols for the validation and the verification of qualitative screening tests for the detection of residues of veterinary drugs in liquid milk (raw, pasteurized, UHT and reconstituted milk powders and whey protein extracts) including biological methods. This guideline does not cover the validation of residue analysis by HPLC, UHPLC or LC-MS/MS.
This document is intended to be useful for manufacturers of screening test kits, laboratories validating screening methods or tests, competent authorities and dairies or end users of reagents or tests for the detection of veterinary drug residues in milk products. This document facilitates and improves the validation and verification of screening methods. The goals of this document are a harmonization in validation of methods or test kits in order for all stakeholders to have full trust in the result of residue screening and to limit the overlap and multiplication of validation work in different laboratories by sharing the validation results generated by an independent laboratory. Furthermore, a harmonized validation and verification procedure allows for comparison of the performance of diffe
标准信息
- 标准号
- ISO/TS 23758:2021
- 英文标题
- Guidelines for the validation of qualitative screening methods for the detection of residues of veterinary drugs in milk and milk products
- 发布单位
- —
- 技术委员会
- ISO/TC 34/SC 5
- 版本 / 版次
- 1
- 状态
- 现行
- 发布日期
- 2021
- ICS 分类
- 67.100.01 奶和奶制品综合
- 页数
- 34 页
- 官方定价
- CHF 151
同分类下的其他标准
相关标准
怎么获取 ISO/TS 23758:2021 全文
这份标准属于 ISO/IEC 发布,全文 34 页,语言为 EN。如果你只需要核对条款、做合规对照或者写方案引用,直接在线支付 2 元即可获得 PDF 全文,支付成功后立即给出下载链接(24 小时内有效,之后凭购买记录也能随时重新下载,不再收费)。
如果你要长期、大量使用这类标准,包年会员更合适:39 元一年每天可下 10 份,69 元一年每天 50 份,999 元一年不限次数。会员下载过的标准可以随时免费重下,不占用每日次数。按单份均价 3 元估算,一年下 13 份以上就已经回本。
需要注意的是,标准正文的著作权归 ISO、IEC 及各国家成员体所有。本站提供的是文献检索与代传服务,建议在正式项目、投标或认证场景中同时通过官方渠道核验标准的最新版本,避免使用已废止版本造成合规风险。