Benefits of Integrating ePRO & eClinical Systems for Clinical Studies
Sponsors conducting clinical research are demanding integrated solutions and increased work efficiencies. An integrated eClinical environment in which systems share data in near real time responds to these needs. Integrating ePRO and eClinical systems enhance and streamline clinical trials by:
- Improved oversight of the trial
- Providing more timely access to all data for analysis and cleaning purposes
- Reducing data management workload and associated costs for Sponsors and help speed time to database lock at study close
- Allowing sites and Sponsors to see all real-time patient data within one system, for:
- More efficient and timely monitoring of subject data
- Easier correlation of information from different sources to detect adverse events, identifying causality, study drug intake or use, concomitant medication change, and other data
- More efficient drug accountability
CRF Health Launches an Open ePRO Integration Interface
The TrialMax Synapse open integration interface enables Sponsors and CROs to integrate their own eClinical systems (EDC, IVR, other back end clinical data system) with CRF Health's acclaimed ePRO platform, TrialMax®, to provide data collected from patients in real time to all study stakeholders. This integration is provided via a Public Output Interface as well as system-specific interfaces, such as for Medidata Rave®. The TrialMax Synapse integration interface is currently used in several live studies.
TrialMax Synapse provides 3rd parties with the following benefits:
- Public Output Interface enables Sponsors and CROs to integrate with the TrialMax® platform
- CDISC compliant interface for transferring ePRO data into a 3rd party system
- Ability to provide data collected from patients in real time to all study stakeholders
- Enables sites to view all study data in one system
- Provides efficient tools for setting up a reusable integration framework for each Sponsor according to their specific needs
- Enables quick configuration of integration for individual clinical studies
- Provides powerful yet easy-to-use tools for exception handling and robust maintenance of each study integration
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