I.S. EN 14822-3:2005
Current
The latest, up-to-date edition.
HEALTH INFORMATICS - GENERAL PURPOSE INFORMATION COMPONENTS - PART 3: CLINICAL
Hardcopy , PDF
English
01-01-2005
For Harmonized Standards, check the EU site to confirm that the Standard is cited in the Official Journal.
Only cited Standards give presumption of conformance to New Approach Directives/Regulations.
Foreword
Introduction
1 Scope
2 Normative references
3 Terms and definitions
4 Abbreviations
5 Rules governing the use of general purpose
information components
6 General Purpose Information Components -
an overview
7 General Purpose Information Components
7.1 Analysable Object GPICs
7.1.1 Analysable Object
7.1.2 Analysable Object In Use
7.1.3 Specimen
7.1.4 Related Analysable Object
7.1.5 Manufactured Specimen
7.1.6 Specimen Treatment
7.1.7 Related Specimen Treatment
7.1.8 Associated Specimen Treatment
7.1.9 Study Product
7.1.10 Object Characteristic
7.1.11 Preservation Material
7.1.12 Acquired Analysable Object
7.1.13 Analysable Object Acquisition
7.1.14 Related Object Acquisition
7.1.15 Acquisition Procedure
7.1.16 External Data Reference
7.2 Clinical Information GPICs
7.2.1 Clinical Information
7.2.2 Clinical Information Complex
7.2.3 Clinical Information Context
7.2.4 Related Clinical Information Complex
7.2.5 Clinical Information Item
7.2.6 Related Clinical Information
7.3 Clinical Observation GPICs
7.3.1 Clinical Observation
7.3.2 Related Patient Condition
7.4 Clinical Procedure GPICs
7.4.1 Clinical Procedure
7.4.2 Patient Preparation Procedure
7.4.3 Patient Preparation Substance
7.5 Counselling GPICs
7.5.1 Counselling
7.6 Unclassified Clinical Information GPICs
7.6.1 Unclassified Clinical Information
7.7 Laboratory And Diagnostic Investigation GPICs
7.7.1 Investigation Request
7.7.2 Related Investigation Request
7.7.3 Investigation Result Item
7.7.4 Related Investigation Result
7.7.5 Reference Limit
7.7.6 Reference Population
7.7.7 Investigation Specification
7.7.8 Body System
7.7.9 Related Body System
7.7.10 Measurement Procedure
7.8 Medication GPICs
7.8.1 Utilisation Guide
7.8.2 Medication Treatment
7.8.3 Medication Supply
7.8.4 Medicinal Product
7.8.5 Ingredient
7.8.6 Medicinal Product in Use
7.8.7 Medicinal Product Pack
7.8.8 Medicinal Product Pack in Use
7.8.9 Medication Appliance
7.8.10 Medication Appliance in Use
7.8.11 Medication Treatment Regimen
7.8.12 Dose Administration
7.8.13 Medication Treatment Condition
7.9 Treatment Routing GPICs
7.9.1 Routing Option
7.9.2 Routing Device
7.9.3 Care Encounter GPICs
7.9.3 Care Service Request
7.9.4 Related Service Request
7.9.5 Care Service Report
7.9.6 Related Service Report
7.9.7 Care Encounter
7.9.8 Related Care Encounter
7.10 Care Service Delivery GPICs
7.10.1 Care Service Delivery
7.10.2 Previous Related Activity
8 Acts, their context and inheritance
8.1 Introduction
8.2 Inheritance of Act Context
8.2.1 Method
8.2.2 Participation
8.2.3 Act Relationship
9 Structural vocabularies
9.1 Act class
9.2 Act mood
9.3 Act status
9.4 Act Relationship
9.5 Context Control Act Relationship
9.6 Context Control Participation
Annex A (informative) Rationale for this document on
general purpose information
components
Annex B (informative) How to read the models
B.1 Introduction
B.2 Classes
B.3 Associations between classes
B.4 Generalisation/Specialisation
Annex C (informative) Health Level 7 (HL7) reference
information model
Annex D (informative) Common features of the general
purpose information components
Annex E (informative) Localisation of the general purpose
information components
Bibliography
Defines the definition and structuring of information relating to entities that are commonly encountered in communications with and between clinical information computer systems.
DocumentType |
Standard
|
Pages |
212
|
PublisherName |
National Standards Authority of Ireland
|
Status |
Current
|
Standards | Relationship |
BS EN 14822-3:2005 | Identical |
EN 14822-3:2005 | Identical |
DIN EN 14822-3:2006-05 | Identical |
UNI EN 14822-3 : 2006 | Identical |
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