Navigate to the program of interest by selecting a logo below for additional information:
CareAware Validation Overview
CareAware Validation is an active approach to collaboration across development, sales, marketing, and support. It creates a unique relationship that emphasizes the best of both companies and helps to better address mutual client needs.
Through the Validation process Cerner can:
Jointly advance and develop device integrations
Expand the CareAware driver library
Test validity of data transfer to CareAware iBus
Provide seamless integration with CareAware Solutions and Workflows
Achieve scalable integration for broad market adoption
Coordinate support efforts to ensure client satisfaction
High Level Overview of CareAware Validation Process
Initial screening/value proposition through request process
Complete non-disclosure agreement
Fully vet technical and workflow feasibility of product
Execute contractual agreement
Prioritize and slate validation efforts
Complete development and workflow validation
Documentation completion and code released
Cerner updates marketing materials and sends validation letter
Jointly identify pilot site
Release code as generally available once integrated at a client site
Benefits of joining CareAware Validation
Engineering and product management alignment
Availability to integrate in all countries where the CareAware iBus is available
Scalable integration for broad market adoption; not effort spent to address a singular implementation
Driver development prioritization
Ongoing maintenance, including release coordination to deliver a validated version to mutual clients
Coordinated support efforts so clients and partners can make a single call for connected sub-systems
Increased sales and marketing opportunities
Recognition as a Validation Partner in marketing materials and promotions to clients
Opportunity for annual meetings around initiatives and overall business relationship
Tighter strategic integration between companies
Ability to have an extensive portfolio of validated devices
"Memorial wrapped up a very successful CareAware VitalsLinks® project, finishing on time and under budget. We expanded our use of the Welch Allyn devices housewide, thus eliminating the need to manually enter vital signs into our system. This is another significant step in our journey to automate clinical workflows, thus improving quality and patient care."
ECG Management Validation ensures the DICOM interoperability between devices and Cerner ECG Management for DICOM Modality Worklist and DICOM Storage of 12-Lead ECG and DICOM pdf. By utilizing the DICOM (digital imaging communications in medicine) standards, Cerner ECG Management can integrate with any validated ECG Cart, Stress or Holter System. The goal of this program is to allow clients options for the acquisition of devices that fit their organizational needs and to actively engage with participating partners to continuously validate devices and workflows.
Through ECG Management Validation process Cerner can:
Jointly advance and develop device integrations
Expand device options for ECG Management clients
Test validity of data transfer to ECG Management
Provide seamless integration with ECG Management
Achieve scalable integration for broad market adoption
Coordinate support efforts to ensure client satisfaction
High Level overview of ECG Validation Process
Initial screening/value proposition through request process
Complete non-disclosure agreement
Fully vet DICOM capabilities to determine feasibility
Execute contractual agreement
Prioritize and slate validation efforts
Complete testing and workflow validation
Documentation completion
Cerner updates marketing materials and sends validation letter
Benefits of Joining ECG Validation
Engineering and product management alignment
Availability to integrate in all countries where ECG Management is available
Scalable integration for broad market adoption; not effort spent to address a singular implementation
Testing prioritization
Ongoing maintenance, including release coordination to deliver a validated version to mutual clients
Coordinated support efforts so clients and partners can make a single call for connected sub-systems
Increased sales and marketing opportunities
Recognition as a Validation Partner in marketing materials and promotions to clients
Opportunity for annual meetings around initiatives and overall business relationship
Technology validation is a fee-for-service offering available to manufacturers who evaluate
devices for compatibility with Cerner Millennium applications. The process includes the development of necessary
operating systems scripts, libraries, installation and support documentation and training of Cerner support
associates. The device types available for validation include printers, scanners and barcode scanners.
