Overview and considerations for the reporting of clinical pathology interpretations in nonclinical toxicology studies-Reference-Cited by-同舟云学术

Overview and considerations for the reporting of clinical pathology interpretations in nonclinical toxicology studies

Published:2019-09 Issue:3 Volume:48 Page:389-399
ISSN:0275-6382
Container-title:Veterinary Clinical Pathology
language:en
Short-container-title:Vet Clin Pathol

Author:

Aulbach Adam¹,Vitsky Allison²,Arndt Tara³,Ramaiah Lila⁴,Logan Michael⁵,Siska William⁶,Cregar Laura¹,Tripathi Niraj³,Adedeji Adeyemi⁷,Provencher Anne⁸,Gupta Ara⁹,Jordan Holly³,Bounous Denise¹⁰,Boone Laura³

Affiliation:

1. Charles River Laboratories Mattawan MI USA

2. Pfizer Inc. San Diego CA USA

3. Covance Laboratories Inc. Madison WI USA

4. Bristol‐Myers Squibb New Brunswick NJ USA

5. AbbVie Chicago IL USA

6. Charles River Laboratories, Inc. Reno NV USA

7. Genentech Inc. San Francisco CA USA

8. Charles River Laboratories Senneville Quebec Canada

9. Boehringer Ingelheim Animal Health USA Inc. Duluth GA USA

10. Bristol‐Myers Squibb Lawrenceville NJ USA

Publisher

Wiley

Subject

General Veterinary

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/vcp.12772

Reference28 articles.

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

2. - Toxicokinetics and Drug Disposition

3. Plant and Animal Toxins

4. - Toxicokinetics and Drug Disposition

5. Deciphering Sources of Variability in Clinical Pathology—It’s Not Just about the Numbers

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