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Classifying Free Texts Into Predefined Sections Using AI in Regulatory Documents: A Case Study with Drug Labeling Documents

[Image: see text] The US Food and Drug Administration (FDA) regulatory process often involves several reviewers who focus on sets of information related to their respective areas of review. Accordingly, manufacturers that provide submission packages to regulatory agencies are instructed to organize...

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Detalles Bibliográficos
Autores principales: Gray, Magnus, Xu, Joshua, Tong, Weida, Wu, Leihong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2023
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10445280/
https://www.ncbi.nlm.nih.gov/pubmed/37487037
http://dx.doi.org/10.1021/acs.chemrestox.3c00028

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