SEND harmonization & cross-study analysis: A proposal to better harvest the value from SEND data
Author:
Publisher
Elsevier BV
Subject
Toxicology,General Medicine
Reference9 articles.
1. Common Issues in CDISC-SEND Data in FDA Toxicology Review;Anderson,2019
2. Making sense of SEND; the standard for Exchange of nonclinical data;Briggs;Regul. Toxicol. Pharmacol.,2017
3. The standard for Exchange of nonclinical data (SEND): challenges and promises;Choudhary;Toxicol. Pathol.,2018
4. Concordance of the toxicity of pharmaceuticals in humans and in animals;Olson;Regul. Toxicol. Pharmacol.,2000
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2. Cross study analyses of SEND data: toxicity profile classification;Toxicological Sciences;2024-06-08
3. The Preparation of a Preclinical Dossier to Support an Investigational New Drug Application and First-In-Human Clinical Trial;A Comprehensive Guide to Toxicology in Nonclinical Drug Development;2024
4. An extension of the BioAssay Ontology to include pharmacokinetic/pharmacodynamic terminology for the enrichment of scientific workflows;Journal of Biomedical Semantics;2023-08-11
5. NCI-EVS: Building the Semantic Infrastructure to Support CDISC Data Standards and Real-World Data;Journal of the Society for Clinical Data Management;2023-06-19
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