You expect an interoperability platform to gather data for better informed decisions and to help you work more efficiently. But those simple expectations often crash into a more complicated reality, especially in fragmented healthcare systems. Differences in data nomenclature and formatting, missing data elements or values, duplications and other hazards block the path to usable interoperability. Simply aggregating data produces patient records with “unhealthy” information that can’t be trusted. And as that data is shared with payers, allied health providers, and social services organizations it impacts the entire experience of care.
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