首页> 美国卫生研究院文献>AAPS PharmSci >Ligand Binding Assay Critical Reagents and Their Stability: Recommendations and Best Practices from the Global Bioanalysis Consortium Harmonization Team
【2h】

Ligand Binding Assay Critical Reagents and Their Stability: Recommendations and Best Practices from the Global Bioanalysis Consortium Harmonization Team

机译:配体结合测定关键试剂及其稳定性:全球生物分析联合会协调小组的建议和最佳实践

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

The L4 Global Harmonization Team on reagents and their stability focused on the management of critical reagents for pharmacokinetic, immunogenicity, and biomarker ligand binding assays. Regulatory guidance recognizes that reagents are important for ligand binding assays but do not address numerous aspects of critical reagent life cycle management. Reagents can be obtained from external vendors or developed internally, but regardless of their source, there are numerous considerations for their reliable long-term use. The authors have identified current best practices and provided recommendations for critical reagent lot changes, stability management, and documentation.
机译:L4全球试剂协调小组及其稳定性专注于药物动力学,免疫原性和生物标志物配体结合测定的关键试剂的管理。监管指南认识到试剂对于配体结合测定很重要,但并未涉及关键试剂生命周期管理的许多方面。试剂可以从外部供应商处获得或内部开发,但无论其来源如何,长期可靠使用都有许多考虑因素。作者已经确定了当前的最佳实践,并为关键试剂批号更改,稳定性管理和文档提供了建议。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号