Industry Leading Health IT Providers Collaborate to Demonstrate Interoperability with Clinical Sites, Research Sponsors and Regulators through Utilization of RFD Standard
CARROLLTON, Ga., June 19 /PRNewswire/ -- Greenway Medical Technologies, a leading provider of an integrated electronic health record (EHR), practice management and interoperability solution, today announced its participation in the Drug Information Association's (DIA) 45th annual convention taking place in San Diego, June 21-25.
During the DIA convention, Greenway(R), with its industry leading and 08 CCHIT Certified(R) electronic heath record (EHR), PrimeSuite 2008, will be participating in the Clinical Data Interchange Standards Consortium's (CDISC) live healthcare link demonstration at booth 1915. At the exhibit, Greenway will showcase its collaboration with the retrieve form for data capture's (RFD) integration profile, which facilitates data interoperability between clinical research and clinical care providers by integrating the processes and workflows of electronic data capture (EDC), spontaneous adverse event (AE) reporting and EHRs such as PrimeSuite(R).
Currently, Greenway is the only leading EHR provider to fully embrace RFD in multiple real-world situations including several registry studies with Outcome Sciences and a multi-site retrospective study with Nextrials. Greenway also allows for the capabilities of the ASTER (Adverse Drug Event Spontaneous Triggered Electronic Reporting) study, which enhances pharmacovigilance whereby negative or adverse drug reactions can be reported instantly to the FDA, who can then report any issues or warnings to the public. Participation in demonstrations like those held at DIA help facilitate other real-world interoperability collaborations.
Greenway will be participating in two scenarios at DIA, a clinical research scenario and a drug safety
|SOURCE Greenway Medical Technologies|
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