The most costly impact on clinical study timelines and budgets is the recruitment and retention of patients and the management of clinical study sites. Spotfire addresses these challenges by helping identify enrollment issues and drop-out issues early. Site management can be maximized by identifying protocol violations by data-driven monitoring via links to study management systems to identify sites with dirty data saving thousands of dollars per problem patient. Using Spotfire, patient enrollment by region or therapeutic area as well as clinical resource requirements can be obtained. This includes specific headcount estimates for individual studies and their component stages. Spotfire can be utilized at both the study and portfolio level for patient and resource estimation and to manage operational aspects associated with a portfolio of clinical programs.
Spotfire enables the balancing of resources and budgets across an entire portfolio of clinical studies.
Spotfire’s dynamic, visual review environment where live clinical and operational data can be combined and analyzed together via dashboards showing key performance indicators (KPIs) including trial enrollment and site performance with drill down to root-cause understanding enables an optimal pay for performance relationship with various outsourced providers, clinical sites and investigators. Spotfire’s ability to enable informative in stream monitoring of complex clinical and operational data creates considerable efficiencies in clinical trial operations, analysis and decision-making. This drives a highly productive drug development culture across clinical development organizations, leading to shorter development cycles and fast, safe product approvals.