Physiologically Based Pharmacokinetic Model Qualification and Reporting Procedures for Regulatory Submissions: A Consortium Perspective.

Physiologically Based Pharmacokinetic Model Qualification and Reporting Procedures for Regulatory Submissions: A Consortium Perspective.
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DOI:
10.1002/cpt.1013
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发表时间:
2018-07
影响因子:
6.7
通讯作者:
Rowland M
Rowland M
中科院分区:
医学2区
文献类型:
--
作者:
Shebley M;Sandhu P;Emami Riedmaier A;Jamei M;Narayanan R;Patel A;Peters SA;Reddy VP;Zheng M;de Zwart L;Beneton M;Bouzom F;Chen J;Chen Y;Cleary Y;Collins C;Dickinson GL;Djebli N;Einolf HJ;Gardner I;Huth F;Kazmi F;Khalil F;Lin J;Odinecs A;Patel C;Rong H;Schuck E;Sharma P;Wu SP;Xu Y;Yamazaki S;Yoshida K;Rowland M

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This work provides a perspective on the qualification and verification of physiologically based pharmacokinetic (PBPK) platforms/models intended for regulatory submission based on the collective experience of the Simcyp Consortium members. Examples of regulatory submission of PBPK analyses across various intended applications are presented and discussed. European Medicines Agency (EMA) and US Food and Drug Administration (FDA) recent draft guidelines regarding PBPK analyses and reporting are encouraging, and to advance the use and acceptability of PBPK analyses, more clarity and flexibility are warranted.
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