Sponsor-CRO Practices That Facilitate the Creation of a High-Quality Pathology Report
Author:
Affiliation:
1. Eli Lilly and Company, Indianapolis, Indiana, USA
2. Abbott Laboratories, Abbott Park, Illinois, USA
3. Baxter Healthcare Corporation, Round Lake, Illinois, USA
Publisher
SAGE Publications
Subject
Cell Biology,Toxicology,Molecular Biology,Pathology and Forensic Medicine
Link
http://journals.sagepub.com/doi/pdf/10.1177/0192623311419525
Reference5 articles.
1. The no-observed-adverse-effect-level in drug safety evaluations: Use, issues, and definition(s)
2. Industry–Contract Research Organization Pathology Interactions
3. Recognition of Adverse and Nonadverse Effects in Toxicity Studies
4. Recommendations for Pathology Peer Review
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1. Practices to Optimize Generation, Interpretation, and Reporting of Pathology Data from Toxicity Studies;Haschek and Rousseaux's Handbook of Toxicologic Pathology;2022
2. Supportive care for animals on toxicology studies: An industrial best practices survey conducted by the IQ 3Rs TPS CRO Outreach Working Group;Toxicology Research and Application;2021-01-01
3. Selected Aspects of Ocular Toxicity Studies With a Focus on High-Quality Pathology Reports: A Pathology/Toxicology Consultant’s Perspective;Toxicologic Pathology;2020-08-20
4. Review of approaches to the recording of background lesions in toxicologic pathology studies in rats;Toxicology Letters;2014-08
5. Prestudy Preparation, the Protocol, Data Interpretation, and Reporting;The Role of the Study Director in Nonclinical Studies;2014-05-09
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