Executing clinical studies using risk-based Monitoring (RBM) methodologies is reducing risks in clinical development, while improving patient safety and study quality. Clinical trial site engagement is a critical component relating to a study’s performance and ultimately, its success.
Hear directly from a leading investigator site on how they are using RBM methods to optimize monitoring efforts, improve data cleaning efficiencies, and reduce study risks. Understand what factors impact study site performance and engagement and how more engaged sites are more responsive, resolving queries faster, enrolling more subjects and responding to monitoring requests.
You will hear recent results from numerous studies demonstrating improvements in Missing Pages, Data Entry time & accuracy, Query Response Times, Aged Queries, and higher overall satisfaction from Sites working with RBM methodologies.
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