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Toxicol Pathol ; 41(8): 1159-69, 2013.
Artículo en Inglés | MEDLINE | ID: mdl-23531793

RESUMEN

This article reviews the regulatory guidelines that provide for the inclusion of recovery groups in toxicology studies, presents the challenges in the design and interpretation of nonclinical recovery studies, and summarizes the best practices for the role of an anatomic pathologist regarding toxicology studies with recovery groups. Evaluating the potential recovery of histopathologic findings induced by a biopharmaceutical requires the active participation of one or more anatomic pathologists. Their expertise is critical in risk assessment regarding the potential for recovery as well as providing scientific guidance in the design and evaluation of studies with recovery groups.


Asunto(s)
Pruebas de Toxicidad/métodos , Pruebas de Toxicidad/normas , Animales , Biofarmacia/normas , Guías como Asunto , Patología/métodos , Patología/normas , Proyectos de Investigación , Toxicología/métodos , Toxicología/normas
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