| Literature DB >> 27631784 |
Síle F Molloy1, Patricia Henley2.
Abstract
This article describes the processes and procedures involved in planning, conducting and reporting monitoring activities for large Clinical Trials of Investigational Medicinal Products (CTIMPs), focusing on those conducted in resource-limited settings.Keywords: Buenas Prácticas Clínicas; Good Clinical Practice; bonnes pratiques cliniques; clinical trial; ensayo clínico; essai clinique; lugar con recursos limitados; monitoreo basado en los riesgos; monitoring; monitorización; resource-limited setting; risk-based monitoring; régions à ressources limitées; suivi; surveillance basée sur les risques
Mesh：
Year: 2016 PMID： 27631784 DOI： 10.1111/tmi.12781
Source DB: PubMed Journal: Trop Med Int Health ISSN： 1360-2276 Impact factor: 2.622