Autor: |
Irizarry Rovira, Armando R., Foley, George L., Clemo, Frances A. |
Předmět: |
|
Zdroj: |
Toxicologic Pathology; Oct2011, Vol. 39 Issue 6, p1013-1016, 4p |
Abstrakt: |
The authors discuss contract research organization (CRO) and pharmaceutical sponsor practices that influence preclinical studies procedure and creation of pathology report. They stress that the success of CRO-sponsor relationship and the creation of high-quality pathology data depend on the communication throughout a toxicology study. Noted is the importance to data generation of the understanding of the capacity of CRO to handle time-sensitive requests. |
Databáze: |
Complementary Index |
Externí odkaz: |
|