GlobalCODE® gives translational medicine, assay management, specimen management and data teams unique views into their often large and disparate data sources for a unified view of their specimen data.
GlobalCODE infuses best practices into discovery and clinical development processes, protocol procedures, as well as informed consent, regulatory and specimen management processes.
GlobalCODE fully tracks and manages specimens virtually, and enables real-time custom visual dashboard reports of trial and specimen bank data. GlobalCODE guides users to actionable insights and in-life intervention for best of class clinical trial execution.
GlobalCODE is built on secure, reliable, accessible Software-as-a-Service (SaaS) technology. Highly flexible, GlobalCODE can accommodate client process requirements across the clinical trial and beyond. GlobalCODE easily imports data from multiple data sources in little time, providing immediate robust unified views of pipeline data.
- Fully tracks and manages specimens virtually
- Enables real-time custom visual dashboard reports
- Guides users to actionable insights and in-life interventions
- Seamlessly imports data from multiple data sources
- Easily accommodates client process requirements
- Built on secure, reliable, accessible SaaS technology
Real-time point-of-collection (eReq)
Real-time specimen, informed consent & clinical data tracking and analytics
Full LIMS workflow automation