Scientific and Regulatory Policy Committee Points to Consider: Integration of Clinical Pathology Data With Anatomic Pathology Data in Nonclinical Toxicology Studies-Reference-Cited by-同舟云学术

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Scientific and Regulatory Policy Committee Points to Consider: Integration of Clinical Pathology Data With Anatomic Pathology Data in Nonclinical Toxicology Studies

Published:2022-08-17 Issue:3 Volume:51 Page:311-329
ISSN:0275-6382
Container-title:Veterinary Clinical Pathology
language:en
Short-container-title:Veterinary Clinical Pathol

Author:

Siska William¹^ORCID,Schultze Albert Eric²,Ennulat Daniela³,Biddle Kathleen⁴^ORCID,Logan Michael⁵,Adedeji Adeyemi O.⁶^ORCID,Arndt Tara⁷^ORCID,Aulbach Adam⁸

Affiliation:

1. Charles River Laboratories, Inc. Reno Nevada USA

2. Eli Lilly and Company Indianapolis Indiana USA

3. GlaxoSmithKline Collegeville Pennsylvania USA

4. Pfizer Groton Connecticut USA

5. AbbVie Chicago Illinois USA

6. Genentech, Inc. South San Francisco California USA

7. Labcorp Drug Development Madison Wisconsin USA

8. Inotiv, Maryland Heights Missouri USA

Publisher

Wiley

Subject

General Veterinary

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/vcp.13167

Reference89 articles.

1. Best Practices for Reporting Pathology Interpretations within GLP Toxicology Studies

2. Evaluation of Clinical Pathology Data

3. Interpreting and Integrating Clinical and Anatomic Pathology Results

4. Interpretative considerations for clinical pathology findings in nonclinical toxicology studies

5. Plant and Animal Toxins

Cited by 1 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Clinical Pathology in Nonclinical Toxicity Studies;A Comprehensive Guide to Toxicology in Nonclinical Drug Development;2024

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