 0 Table of Contents |
  1 Home |
  2 Background |
  3 How to read this guide |
  4 Data types and references |
  5 Authoring rules |
  6 Known issues |
  7 Scope and Content |
  8 Ways of working |
  9 Obligations Framework |
  10 ePrescription |
  11 eDispensation |
  12 Patient Summary |
  13 Medical Test Results and Laboratory Report |
  14 Medical Images |
  15 Discharge Report |
  16 Download |
  17 Change Log |
  18 Artifacts Summary |
   18.1 Patient summary model |
   18.2 Medication dispense model |
   18.3 Medication prescription model |
   18.4 Laboratory observation model |
   18.5 Laboratory report model |
   18.6 Imaging report model |
   18.7 Imaging study model |
   18.8 Discharge Report model |
   18.9 Address model |
   18.10 Administered dosage model |
   18.11 Advance directive model |
   18.12 Alert model |
   18.13 Allergy intolerance model |
   18.14 Attachment model |
   18.15 Body structure model |
   18.16 Care plan model |
   18.17 Condition model |
   18.18 Current pregnancy status model |
   18.19 DataSet model |
   18.20 Device model |
   18.21 Device use model |
   18.22 Document model |
   18.23 Dosage model |
   18.24 Encounter model |
   18.25 Endpoint model |
   18.26 Health professional model |
   18.27 Human name model |
   18.28 Immunisation model |
   18.29 Location model |
   18.30 Medication administration model |
   18.31 Medication model |
   18.32 Medication use model |
   18.33 Observation model |
   18.34 Organisation model |
   18.35 Patient model |
   18.36 Pregnancy history model |
   18.37 Procedure model |
   18.38 Related person model |
   18.39 Service request model |
   18.40 Specimen model |
   18.41 Telecom model |
   18.42 Travel history model |
   18.43 Advance directive obligations |
   18.44 Alert obligations |
   18.45 AllergyIntolerance obligations |
   18.46 Condition obligations |
   18.47 Current pregnancy obligations |
   18.48 Device obligations |
   18.49 Device use obligations |
   18.50 Dosage obligations |
   18.51 Health professional obligations |
   18.52 Immunisation obligations |
   18.53 Medication model obligations |
   18.54 MedicationAdministration obligations |
   18.55 MedicationUse obligations |
   18.56 Observation Obligations |
   18.57 Organisation obligations |
   18.58 Patient obligations |
   18.59 Procedure obligations |
   18.60 Related person obligations |
   18.61 Patient summary obligations |
   18.62 Medication dispense model obligations |
   18.63 Medication prescription model obligations |
   18.64 Body structure laboratory specific obligations |
   18.65 Condition laboratory specific obligations |
   18.66 Device laboratory specific obligations |
   18.67 Health professional laboratory specific obligations |
   18.68 Immunisation laboratory specific obligations |
   18.69 Laboratory observation obligations |
   18.70 Laboratory Report Obligations |
   18.71 Medication Administration laboratory specific obligations |
   18.72 Medication laboratory specific obligations |
   18.73 Medication Use laboratory specific obligations |
   18.74 Organisation laboratory specific obligations |
   18.75 Patient laboratory specific obligations |
   18.76 Procedure laboratory specific obligations |
   18.77 Related person laboratory specific obligations |
   18.78 Service request laboratory specific obligations |
   18.79 Specimen Obligations |
   18.80 Imaging Report Obligations |
   18.81 Imaging Study Obligations |
   18.82 Discharge Report Obligations |
   18.83 Consumer |
   18.84 Producer |