Acuity is a powerful and flexible data aggregation, visualization and analytics platform driving actionable knowledge in real time. Acuity improves productivity and minimizes risk in clinical research by providing a clear vision of clinical and operational data.
Through efficient aggregation of data and a sophisticated use of visualizations and analytics, users can data mine retrospective events, monitor real-time clinical trial activity and predict future performance. Acuity allows you to transform data into knowledge and knowledge into actions that drive evaluations of drugs, diseases and performance.
Rapid deployment | Secure cloud | Regulatory compliant | Designed and supported by industry experts | Built for Pharma, Biotech, CRO and academic research.
“Acuity has enabled us to implement an end-to-end risk-based approach to monitoring. The ability to provide data-driven solutions by utilizing a combination of technology and deep domain expertise in clinical monitoring has added significant value for a global organization like ours from a quality, cost and study governance perspective.” -- Deputy General Manager, Clinical Development, Global Midsized Pharma
To learn about how today's regulatory requirements affect you, and how risk planning can help avoid pitfalls, download our White Paper: Understanding the New ICH-GCP Landscape.
Ensure teams work together to capture risks, and develop mitigation strategies and KRIs in a transparent way. All key players can access a study's risk profile online as it develops over time. Acuity RBM™ makes sure everything that you need to focus on gets the attention it requires.
Reduce regulatory risk and improve quality and compliance with real-time insight. Access your portfolio views of compounds or therapeutic areas in your organization. Site profiles integrate clinical and operational data to give a comprehensive view of site performance. Subject profiles give detailed views of subject data across domains, including visit information, safety data, medical history, vitals, imaging and core labs, exposure to IP and more.
View protocol performance across a range of measures from regulatory submission to recruitment. Drill-down from global views to regional, country and site levels.
Choose what parameters matter and benchmark site performance. Use our statistical models or your own to forecast future performance.
Get an up-to-date and detailed view of a subject across critical data domains.
Acuity's highly flexible architecture can connect with multiple data sources and aggregate data into streamlined and controlled views. Commonly used data integration adapters for Acuity Insights™ include EDC, CTMS, IRT and eCOA.
The portfolio view combines data from multiple studies. Portfolios can give a view for all studies under a compound or therapeutic area. Monitor across studies with a common oversight strategy without losing sight of individual protocol needs.
Your libraries will save time and money, and produce consistency across studies; but every protocol is unique. Customize dashboards and visualizations when you need them; add them to your library if you want to use them again.