{
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    "changes" : "changes.html"
  },
  {
    "version" : "2.0.0-alpha",
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    "fhirversion" : "4.0.1",
    "date" : "2026-02-25",
    "desc" : "This publication is a quality assurance (QA) preview release provided in support of the Xt-EHR Projectathon.",
    "descmd" : "This publication is a quality assurance (QA) preview release provided in support of the Xt-EHR Projectathon. It is not intended for production use and should not be used as a reference implementation. The content of this publication is subject to change without notice as it is being actively developed and tested. Feedback from users is welcome to help improve the quality and functionality of the final release."
  },
  {
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    "path" : "http://hl7.eu/fhir/laboratory/0.1.1",
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    "date" : "2025-03-25",
    "desc" : "This is the Edition 1 STU 1.1"
  },
  {
    "version" : "0.1.0",
    "path" : "http://hl7.eu/fhir/laboratory/0.1.0",
    "status" : "trial-use",
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    "date" : "2024-02-26",
    "desc" : "This is the Edition 1 STU 1 release"
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  {
    "version" : "0.1.0-ballot",
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  "canonical" : "http://hl7.eu/fhir/laboratory",
  "title" : "HL7 Europe Laboratory Report",
  "category" : "Laboratory Report",
  "introduction" : "This guide defines a set of common rules to be applied to HL7 FHIR to define how to represent a Laboratory Report in the European Context. It coveres laboratory reports within the core fields of in-vitro diagnostics, for example clinical biochemistry, haematology, immunohematology, microbiology, immunology, while leaving out some specialised laboratory domains requiring specialised reporting structure like histopathology or medical genetics."
}
