Repeat Analysis and Incurred Sample Reanalysis: Recommendation for Best Practices and Harmonization from the Global Bioanalysis Consortium Harmonization Team

被引:0
|
作者
Eric Fluhler
Faye Vazvaei
Puran Singhal
Petra Vinck
Wenkui Li
Jignesh Bhatt
Theo de Boer
Ajai Chaudhary
Masahiro Tangiuchi
Vinicius Rezende
Dafang Zhong
机构
[1] Pfizer,Roche Pharma Research and Early Development, Pharmaceutical Sciences, Global DMPK and Bioanalytical R&D
[2] PDM-NBE,R&D Centre
[3] Roche Innovation Center New York,Department of Bioanalysis
[4] Alkem Laboratories Ltd.,Bio
[5] Janssen R&D,Evaluation Center
[6] Novartis Institutes for Biomedical Research,Department of Hematology, School of Medicine
[7] Drug Metabolism and Pharmacokinetics,Chinese Academy of Sciences
[8] Torrent Pharmaceutical Ltd.,undefined
[9] Analytical Biochemical Laboratory BV,undefined
[10] Merck Research Laboratories,undefined
[11] PPDM,undefined
[12] SCAS-BTT Bioanalysis Company Ltd.,undefined
[13] University of Sao Paulo,undefined
[14] Shanghai Institute of Materia Medica,undefined
[15] Pfizer R&D,undefined
来源
The AAPS Journal | 2014年 / 16卷
关键词
harmonization; incurred sample reanalysis; regulated bioanalysis; repeat analysis;
D O I
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学科分类号
摘要
The A7 harmonization team (A7 HT), a part of the Global Bioanalysis Consortium (GBC), focused on reviewing best practices for repeat analysis and incurred sample reanalysis (ISR) as applied during regulated bioanalysis. With international representation from Europe, Latin America, North America, and the Asia Pacific region, the team first collated common practices and guidance recommendations and assessed their suitability from both a scientific and logistical perspective. Subsequently, team members developed best practice recommendations and refined them through discussions and presentations with industry experts at scientific meetings. This review summarizes the team findings and best practice recommendations. The few topics where no consensus could be reached are also discussed. The A7 HT recommendations, together with those from the other GBC teams, provide the basis for future international harmonization of regulated bioanalytical practices.
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页码:1167 / 1174
页数:7
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