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International Patient Access (IPA) is the emerging global standard that allows patients and medical apps to easily access and share health information across countries. It builds upon existing FHIR (Fast Healthcare Interoperability Resources) standards but adds important improvements for secure, reliable, and consistent data exchange.
Why Do We Need IPA?
Many countries already use FHIR, but IPA addresses crucial limitations: Secure Access: IPA ensures that only authorized users and apps can access health information, protecting patient privacy. It defines how apps get permission to access data using standard methods (like OAuth 2.0). Standardized Data: IPA creates a common set of data types and formats. This means medical apps can work consistently across different systems worldwide, simplifying development and improving interoperability.
Key Features of IPA:
IPA uses FHIR profiles (specifications for how specific data is structured) to define a globally harmonized set of core health information. Countries can then expand on this base information to meet their unique needs: Patient Profiles: Basic demographics and identifiers.
IPA also defines server capabilities to help medical apps easily access and use this information. Benefits of IPA:
Who is driving the IPA project?
The IPA initiative is driven by HL7 International, a not-for-profit organization dedicated to developing standards for the exchange of electronic health information. As a global leader in health data interoperability, HL7’s work is largely made possible through the contributions of volunteers from various sectors in the healthcare and technology industries.
Participating Organizations and Individuals:
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