TEMPO™ eClinical Platform, a private cloud-based application, serves as the technology foundation to all of Clinipace’s clinical development service teams. Through its one platform-one database approach, Clinipace and client study teams leverage TEMPO to improve study visibility, control deliverables and documents, and reduce costs from start-up to close-out. TEMPO replaces the need for multiple disparate technologies such as CTMS, EDC, TMF, Safety, and Portals, which are bolt-on applications that increase trial complexity, cost, and “friction” points between functional groups.
I’ve been in this industry a long time and this is the first tool I’ve seen with the flexibility we needed to manage our research processes.
– John Ely, VP, Regulatory Affairs at On-X Life Technologies
Clinipace introduces the concept of Configurable Modules, which are a set of predefined workflows, forms, and reports bundled together as a unit on the same platform within one database. These flexible modules enable study teams to deploy the right set of functionality to support the unique needs of a single study and support more functions without the need for costly data duplication or systems integration.
Published modules include:
- TEMPO™ Trial Manager
- TEMPO™ Trial Master File (eTMF)
- TEMPO™ EDC
- TEMPO™ Patient Reported Outcomes (ePRO)
- TEMPO™ Monitoring
- TEMPO™ Safety Management
- TEMPO™ Clinical Event Committee (CEC)
- TEMPO™ Drug Accountability
- TEMPO™ Medical Imaging
- TEMPO™ Study Portal
The ability to provide cross-function and cross-trial management and visibility without excessive and expensive IT infrastructure is a huge benefit to clients. Through the TEMPO framework Clinipace can more rapidly deploy innovative services that enhance quality, while creating additional efficiencies that continuously improve study visibility without lengthy development cycles.
Key Platform Features
Together with TEMPO, Clinipace Worldwide offers data management services that ensure clean, accessible, quality data. Data Management Services are designed to ensure:
- Data validation and cleansing
- Quality assurance
- Database auditing
- Data reconciliation
- Export Management
I was able to significantly reduce the time it would have taken to identify sites and eligible patients by mining the registry data through TEMPO. The collaborative nature of our relationship with Clinipace as well as the flexible workflow processes and real-time reporting enabled the project team to complete the research phase in as little as 7.5 months. Without the collaboration, a similar project would have taken me 3 years.
- Andrew Asimos, MD, Director of Emergency Stroke Care, Carolinas Medical Center, North Carolina Collaborative Stroke Registry