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This Roadmap Item has been updated to refer to specification 1.1.0 following comments and points of clarification from Suppliers. |
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GP Connect: New Update Record - ITK3 |
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GP Connect currently includes the following Standards:
The current GP Connect Specifications are:
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Patient Information Maintenance - GP: New Epic |
E00440 - GP Connect- Update Patient RecordAs a Health or Care Professional I want to receive structured clinical updates for Patients from other Healthcare Organisations So that structured clinical updates from other Healthcare Organisations can be stored in Electronic Patient Records (EPRs) Acceptance criterion 1: view received structured clinical updatesGiven that structure clinical updates for a Patient have been sent to the Healthcare Organisation When the Health or Care Professional selects to view the Electronic Patient Record (EPR) Then the received Patient encounter information is displayed And the received Patient observations are displayed And the received Patient medications are displayed E00440 - Additional Implementation DetailsSolutions MUST comply with the following when implementing this Epic:
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Full Specification
/wiki/spaces/GPITFDS/pages/12477792439GP Connect Standard v5.1.0
Patient Information Maintenance - GP v5.1.0
Assurance Approach
Assurance of the GP systems (i.e., recipients of the Update Record) will follow the Solution Assurance (SA) risk-based assurance approach. Suppliers will be provided in advance of onboarding for assurance, a SA Risk log listing risk items for the technical Interoperability, functional, non-functional, clinical, Information Governance and Security areas pertaining to this roadmap item. The SA Risk log will also explicitly state for each of the risk items in the risk log as to what are the risk mitigations expected from an onboarding GP system Supplier from a testing perspective. The GP system suppliers will also be provided access to the ITK Toolkit Workbench (TKW) test tooling for testing with their systems to mitigate the identified technical interoperability risks where possible to do so with the test tooling. Suppliers will also be provided with a manual test pack containing high level generic (i.e., system agnostic) test scenarios for risks items which cannot be tested using the ITK TKW test tooling. GP system suppliers are accountable for the testing of their solution and are expected to have also developed their internal test suite in addition to the SA supplied test tooling and test packs as these are supplier system agnostic and cannot be expected to cover specific supplier system functionality. There will be some risk items which would be more appropriate to assure through online demonstration sessions setup by the supplier and these would be explicitly specified in the SA risk log . The completed SA risk log submission from the supplier with all the completed risk mitigation asks would be reviewed and signed off by Solution assurance in conjunction with the Direct Care APIs Programme.
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