• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

[Assessment of stability variation among batches, packaging, and formulations--application of matrixing and bracketing].

作者信息

Yoshioka S, Aso Y, Kojima S

出版信息

Kokuritsu Iyakuhin Shokuhin Eisei Kenkyusho Hokoku. 1998(116):192-4.

PMID:10097539
Abstract

Assessment of shelf-life equivalence among batches, packaging or formulations of pharmaceutical products, which was based on the range of shelf-life estimates, was proposed as an alternative method to an analysis of variance (ANOVA). The power of this analysis was not significantly affected by assay error, whereas that of ANOVA decreased markedly as assay error increased. Thus, ANOVA exhibites a tendency to overlook the stability variation from stability data of a larger assay error, but this is not the case for the proposed method.

摘要

相似文献

1
[Assessment of stability variation among batches, packaging, and formulations--application of matrixing and bracketing].
Kokuritsu Iyakuhin Shokuhin Eisei Kenkyusho Hokoku. 1998(116):192-4.
2
[Shelf-life estimation of pharmaceutical products by matrixing].[通过矩阵法估算药品保质期]
Eisei Shikenjo Hokoku. 1996(114):143-4.
3
Shelf life determination based on equivalence assessment.基于等效性评估的保质期测定。
J Biopharm Stat. 2003 Aug;13(3):431-49. doi: 10.1081/BIP-120022765.
4
An alternative approach to evaluation of poolability for stability studies.一种用于稳定性研究的可合并性评估的替代方法。
J Biopharm Stat. 2006;16(1):1-14. doi: 10.1080/10543400500406421.
5
Estimating drug shelf-life with random batches.用随机批次估计药品保质期。
Biometrics. 1991 Sep;47(3):1071-9.
6
International Conference on Harmonisation: guidance on Q1D bracketing and matrixing designs for stability testing of new drug substances and products; availability. Notice.国际协调会议:关于新药原料药和制剂稳定性试验的Q1D分组和矩阵设计指南;可获取性。通知。
Fed Regist. 2003 Jan 16;68(11):2339-40.
7
Comparison of bracketing and matrixing designs for a two-year stability study.两年稳定性研究中括弧法和矩阵法设计的比较。
J Biopharm Stat. 2000 May;10(2):217-28. doi: 10.1081/BIP-100101023.
8
Overview of stability study designs.稳定性研究设计概述。
J Biopharm Stat. 2003 Aug;13(3):337-54. doi: 10.1081/BIP-120022759.
9
Equivalence tests for shelf life and average drug content in stability studies.稳定性研究中保质期和平均药物含量的等效性试验。
J Biopharm Stat. 2008;18(5):985-95. doi: 10.1080/10543400802287230.
10
Pooling data for stability studies: testing the equality of batch degradation slopes.汇集稳定性研究数据:检验批次降解斜率的相等性。
Biometrics. 1991 Sep;47(3):1059-69.