The iX Payer Solution is used by our clients to consolidate, curate, and de-silo the healthcare data to create a new standards-based centralized Member Data Repository (MDR), which is the source of member data including new and existing clinical, claims, and other member relevant data.
The MDR is populated with member data from internal and external data sources such as providers, pharmacies, labs, wearable devices etc.
InteropX offers iX EHR Solution to enable Cure Act compliance and certification for single or multi-tenant EHR software. iX EHR Solution is based on the mandated US Core Data for interoperability (USCDI). Once the iX EHR Solution is integrated, configured, and tested, the InteropX team will support the certification testing of the EHR software.
The Mandatory Disclosure statement of costs and any additional transparency information for our certified product(s) is posted as required by Cures Act g (10) certification requirements.
As part of the Conditions and Maintenance of Certification introduced with the 21st Century Cures Act Final Rule, the Office of the National Coordinator for Health IT (ONC) adopted an annual requirement for developers of certified health IT to demonstrate the successful interoperability of their certified software in real world use. Real World Testing is demonstrated through annual Real World Testing plans outlining how the certified developer will be demonstrating the successful interoperability for each pertinent certified capability, and corresponding Real World Testing results. Provided below are InteropX annual Real World Testing plans and results organized by calendar year:
|Real World Testing Plan
|Real World Testing Results
|2022 InteropX Real World Testing Plan
|Pending CY 2022 test plan execution
|2024 InteropX Real World Testing Plan
|Pending CY 2024 test Plan execution