More knowledge, better compliance, higher quality
Respond faster to your studies’ changing needs
Effective clinical trial management requires timely access to accurate data. How are the sites performing? Which need additional resources? Are things running efficiently? Where are the budgetary risks?
Clinical research associates play a big role in identifying issues and shortfalls, and our CRAs are among the best — but their time is better spent addressing issues that support the collection of high-quality data. Likewise, project managers need to maintain a broad view and avoid getting mired in the details. We’ve answered these needs with eMonitoring, a data driven, systematic approach to clinical monitoring.
eMonitoring makes information on every trial readily available to those who need. It continually assesses 30 to 40 key risk indicators, and a central monitor assigns issues to the right people for research and resolution. CRAs stay focused on ensuring high-quality clinical data are provided by sites — and with consistent access to high-quality data, project managers have better visibility into how the study is performing and can better respond to changing needs.