背景(考古学)
计算机科学
工作流程
最佳实践
转化式学习
质量(理念)
知识管理
概化理论
数据科学
人工智能
管理科学
心理学
工程类
政治学
哲学
认识论
古生物学
教育学
发展心理学
数据库
法学
生物
作者
Nadia Terranova,Didier Renard,Mohamed H. Shahin,Sujatha Menon,Youfang Cao,Cornelis E. C. A. Hop,Sean T. Hayes,Kumpal Madrasi,Sven Stodtmann,Thomas G. Tensfeldt,Pavan Vaddady,Nicholas Ellinwood,James Lu
摘要
Recent breakthroughs in artificial intelligence (AI) and machine learning (ML) have ushered in a new era of possibilities across various scientific domains. One area where these advancements hold significant promise is model‐informed drug discovery and development (MID3). To foster a wider adoption and acceptance of these advanced algorithms, the Innovation and Quality (IQ) Consortium initiated the AI/ML working group in 2021 with the aim of promoting their acceptance among the broader scientific community as well as by regulatory agencies. By drawing insights from workshops organized by the working group and attended by key stakeholders across the biopharma industry, academia, and regulatory agencies, this white paper provides a perspective from the IQ Consortium. The range of applications covered in this white paper encompass the following thematic topics: (i) AI/ML‐enabled Analytics for Pharmacometrics and Quantitative Systems Pharmacology (QSP) Workflows; (ii) Explainable Artificial Intelligence and its Applications in Disease Progression Modeling; (iii) Natural Language Processing (NLP) in Quantitative Pharmacology Modeling; and (iv) AI/ML Utilization in Drug Discovery. Additionally, the paper offers a set of best practices to ensure an effective and responsible use of AI, including considering the context of use, explainability and generalizability of models, and having human‐in‐the‐loop. We believe that embracing the transformative power of AI in quantitative modeling while adopting a set of good practices can unlock new opportunities for innovation, increase efficiency, and ultimately bring benefits to patients.
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