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Pharmacist Shared Medicines List (PSML)
Services
Topics
ID
DG-3130
Type
Guide
Version
1.1
Status
Active
Created date
Updated date
The Pharmacist Shared Medicines List (PSML) is a clinical document type supported by the My Health Record system.
Pharmacist Shared Medicines List v1.1.1
Pharmacist Shared Medicines List
Services
Topics
ID
EP-2924:2020
Type
Product
Version
1.1.1
Access
Open access
Status
Active
Created date
Updated date
PSML documents help ensure the continuity of medicine management for consumers across different care settings. PSML documents allow pharmacists in both hospital and community pharmacy settings to record the outcome of consumer consultations regarding their current medications for upload to the My Health Record system. This specification references or…
Pharmacist Shared Medicines List - My Health Record Conformance Profile v1.1.1
My Health Record Conformance Profile
ID
DH-2926:2020
Type
Component
Version
1.1.1
Status
Active
Created date
Updated date
This document lists the conformance requirements for producing systems and consuming systems of Pharmacist Shared Medicines List (PSML) documents that connect to the My Health Record system. It contains the conformance requirements specific for the PSML document type that are in addition to those stated in the Common Conformance Profile and provides…
Pharmacist Shared Medicines List - Product Data Sheet v1.1
Product Data Sheet
ID
DH-2802:2020
Type
Component
Version
1.1
Status
Active
Created date
Updated date
PSML documents allow pharmacists in both hospital and community pharmacy settings to document the outcome of consumer consultations regarding their current medications and upload it to the My Health Record system. The product data sheet provides information for implementers about the Pharmacist Shared Medicines List features and supporting CDA…
Pharmacist Shared Medicines List - Template Package Library v1.2
Template Package Library
ID
DH-2925:2020
Type
Component
Version
1.2
Status
Active
Created date
Updated date
The template package library provides validation rules for Pharmacist Shared Medicines List documents to help identify points of non-conformance to the relevant specifications. The template packages contained in this library will be used by the My Health Record system, other clinical information systems and the Agency's Clinical Package Validator. Template…
Pharmacist Shared Medicines List - Release Note v1.1.1
Release Note
ID
DH-2927:2020
Type
Component
Version
1.1.1
Status
Active
Created date
Updated date
PSML documents allow pharmacists in both hospital and community pharmacy settings to document the outcome of consumer consultations regarding their current medications and upload it to the My Health Record system. This is the first public release of this end product. It contains the conformance profile, validation rules and implementation guides for the…
Pharmacist Shared Medicines List - Conformance Test Specification v1.1.1
Conformance Test Specification
ID
DH-3018:2020
Type
Component
Version
1.1.1
Status
Active
Created date
Updated date
The Conformance Test Specification describes a series of test cases, each of which is a discrete test and a statement of expected behaviour. Developers can use the documented test cases to assess the conformance of their software that is producing or consuming PSML documents.
Pharmacist Shared Medicines List - Implementation Guidance for Download and View PSML (Mobile) v1.0
Implementation Guidance for Download and View PSML (Mobile)
ID
DH-2762:2018
Type
Component
Version
1.0
Status
Active
Created date
Updated date
Guidance for mobile applications which provide My Health Record viewing functionality using the mobile gateway. Configuration changes to such mobile apps might be required to download and display PSML documents from the My Health Record system.
Pharmacist Shared Medicines List - Implementation Guidance for Download and View PSML (B2B) v1.0
Implementation Guidance for Download and View PSML (B2B)
ID
DH-2761:2018
Type
Component
Version
1.0
Status
Active
Created date
Updated date
Guidance for software vendors and healthcare organisations who provide My Health Record viewing functionality in their local clinical information systems. Configuration changes to such systems might be required to download and display PSML documents from the My Health Record system.
My Health Record FHIR® Mobile Gateway - Clinical Document Service
Category
Guidance Document
Services
Topics
Organisation
ADHA
ID
DG-3048
Type
Guide
Standard
Version
1.0
Status
Active
Created date
Updated date
In this guide, we will be accessing Prescription and Dispense List and Allergies List contained in a patient’s clinical document service
List of Excluded Medicinal Items reference set
Category
Reference Sets
Organisation
SNOMED
ID
1545561000168103
Type
Standard
Version
20241231
Access
Open
Status
Active
This reference set supports the identification of Australian Medicines Terminology Medicinal Product Unit of Use and Medicinal Product Pack concepts associated with the List of Excluded Medicinal Items reference set.
Shared Health Summary v1.5.2
Shared Health Summary
Category
Specification
Topics
Organisation
ADHA
ID
EP-3013:2019
Type
Standard
Product
Version
1.5.2
Access
Open access
Status
Active
Created date
Updated date
Shared Health Summary documents are sourced from an individual’s nominated healthcare provider and contain key summary information about the individual’s health status.
List of Medicines for Brand Consideration reference set
Category
Reference Sets
Organisation
SNOMED
ID
1495581000168106
Type
Standard
Version
20241231
Access
Open
Status
Active
This reference set supports the identification of Australian Medicines Terminology Medicinal Product Unit of Use and Medicinal Product Pack concepts associated with the List of Medicines for Brand Consideration that forms part of the Active Ingredient Prescribing initiative.
Health informatics – Identification of medicinal products – Data elements and structures for the unique identification and exchange of regulated medicinal product information
Category
Standard
Organisation
ISO
ID
ISO 11615:2017
Type
Standard
Version
2
Access
Fees apply to access
Status
Active
Created
Oct-17
This standard defines the data elements and structural relationships required for the unique identification and detailed description of medicinal products.
Health informatics — Categorial structures of clinical findings in traditional medicine — Part 1: Traditional Chinese, Japanese and Korean medicine
Category
Specification
Organisation
ISO
ID
ISO/TS 16277-1:2015
Type
Standard
Version
1
Access
Fees apply to access
Status
Active
Created
May-15
This specification defines a categorial structure for clinical findings in terminological systems for traditional Chinese medicine, traditional Japanese medicine and traditional Korean medicine.
IHE Pathology and Laboratory Medicine Technical Framework Supplement: Transfusion Medicine – Administration (TMA) v2.1
Category
Supplementary Resource
Organisation
IHE
Type
Standard
Version
2.1
Access
Open
Status
Trial
Created
Oct-19
This document is a supplement to the IHE Pathology and Laboratory Medicine (PaLM) Technical Framework. It describes the Transfusion Medicine – Administration (TMA) profile.
Health informatics — Profiling framework and classification for Traditional Medicine informatics standards development — Part 1: Traditional Chinese Medicine
Category
Specification
Organisation
ISO
ID
ISO/TS 18790-1:2015
Type
Standard
Version
1
Access
Fees apply to access
Status
Active
Created
May-15
This specification establishes common concepts and a vocabulary for describing the complex domain of various traditional Chinese medicine informatics standards initiatives and their supporting artefacts.
My Health Record FHIR® Mobile Gateway - Patient Details and Record List
Category
Guidance Document
Services
Organisation
ADHA
ID
DG-3083
Type
Guide
Standard
Version
1.0
Status
Active
Created date
Updated date
We will use the token received from MyGov to access the patient’s My Health Record
Health informatics – Identification of medicinal products – Data elements and structures for the unique identification and exchange of regulated medicinal product information – Amendment 1
Category
Standard
Organisation
ISO
ID
ISO 11615:2017/Amd 1:2022
Type
Standard
Version
2
Access
Fees apply to access
Status
Active
Created
Aug-22
This document adds an additional annex to ISO 11615:2017. The annex specifies class name and attribute translations and synonyms for the identification of medicinal products.
Specialist Letter v1.4
Specialist Letter
Topics
ID
EP-3486:2022
Type
Product
Version
1.4
Access
None
Status
Active
Created date
Updated date
Specialist Letter documents are used in replying to a referral or reporting on a health event and contain information related to the event or the requested diagnosis or treatment by a specialist. When a specialist creates a Specialist Letter document, it will be sent directly to the intended recipient, as per current practices. A copy may also be sent to…
Queensland Health QScript Schedule 4 monitored medicines reference set
Category
Reference Sets
Organisation
SNOMED
ID
1489271000168107
Type
Standard
Version
20241231
Access
Open
Status
Active
This reference set supports the identification of the Australian Medicines Terminology Trade Product Unit of Use, Containered Trade Product Pack, Medicinal Product Unit of Use and Medicinal product pack concepts associated with Schedule 4 medicines that are monitored by the Queensland Health QScript Real-Time Prescription Monitoring solution.
Western Australia Health Schedule 4 restricted medicines for public hospitals reference set
Category
Reference Sets
Organisation
SNOMED
ID
1655261000168109
Type
Standard
Version
20241231
Access
Open
Status
Active
This reference set supports the identification of the Australian Medicines Terminology Trade Product Unit of Use, Containered Trade Product Pack, Medicinal Product Pack and Medicinal Product Unit of Use concepts that have additional storage and handling requirements in public hospitals within Western Australia Health (WA Health), as per WA Health policies.
Therapeutic Goods Order No. 91 - Standard for labels of prescription and related medicines
Category
Standard
Organisation
TGA
ID
F2023C00458 (C03)
Type
Standard
Access
Open
Status
Active
Created
Apr-23
This document sets out the labelling requirements for prescription medicines and composite packs containing a subscription medicine. It includes general labelling requirements, information that must be present, information that must be on the main label, and exemptions from the labelling requirements.
Specialist Letter - Release Note v1.4
Release Note
ID
DH-3484:2022
Type
Component
Version
1.4
Status
Active
Created date
Updated date
This minor release of the Specialist Letter specification bundle includes the following change to the Specialist Letter – My Health Record Conformance Profile: Document subtyping introduced to improve clinical document discoverability. The following change was also made to the Specialist Letter – Template Package Library: List of non-critical…
Standard for serialisation and data matrix codes on medicines v1.0
Guidance for TGO 106
Category
Supplementary Resource
Organisation
TGA
Type
Standard
Version
V 1.0
Access
Open
Status
Active
Created
Mar-21
This guidance is for sponsors and manufacturers supplying medicines in Australia that are serialised or have data matrix codes. It describes the requirements in the Therapeutic Goods (Medicines – Standard for Serialisation and Data Matrix Codes) (TGO 106) Order 2021.
Shared Health Summary - My Health Record Conformance Profile v1.6.1
My Health Record Conformance Profile
ID
DH-3016:2019
Type
Component
Version
1.6.1
Status
Active
Created date
Updated date
This document provides the requirements for producers and consumers of Shared Health Summary documents that connect to the My Health Record system. It lists the specific conformance requirements for Shared Health Summary documents in the context of the My Health Record system and provides references to all other documents that specify requirements…
Specialist Letter - My Health Record Conformance Profile v1.6
My Health Record Conformance Profile
ID
DH-3483:2022
Type
Component
Version
1.6
Status
Active
Created date
Updated date
NOTE: The document presentation has been enhanced to align with current branding guidelines, however the content has not been changed. This document provides the requirements for producers and consumers of Specialist Letter documents that connect to the My Health Record system. It lists the specific conformance requirements for Specialist Letter documents…
Medicine labels: Guidance on TGO 91 and TGO 92 v2.3
Category
Supplementary Resource
Organisation
TGA
Type
Standard
Version
2.3
Access
Open
Status
Active
Created
Mar-21
This document provides extensive guidance for medicine labelling rules TGO 91 and TGO 92. It clarifies and elaborates on the mandatory requirements and provides best practice recommendations for medicine labels.
LOINC Search Syntax: Answer List Search
Category
User guide
Organisation
LOINC
Type
Standard
Access
Open
Status
Active
This document describes the RELMA Answer List Search screen and explains how to conduct a search and interpret the results.
Electronic Prescribing - Conformance Test Specifications - Active Script List Registry v3.0.4
Conformance Test Specifications - Active Script List Registry
ID
DH-3948:2024
Type
Component
Version
3.0.4
Status
Active
Created date
Updated date
Electronic Prescribing - Conformance Test Specifications - Active Script List Registry v3.0.4 includes conformance test specifications related to Active Script List Registry.
Therapeutic Goods Order No. 92 - Standard for labels of non-prescription medicines vC02
Category
Standard
Organisation
TGA
ID
F2023C00456 (C02)
Type
Standard
Version
C02
Access
Open
Status
Active
Created
Apr-23
This document sets out the labelling requirements for non-prescription medicines. It includes general labelling requirements, information that must be present, information that must be on the main label, and exemptions from the labelling requirements.
Australian Medicines Terminology v2 Model - UML Class Diagram v1.1
UML Class Diagram
ID
NEHTA-0168:2008
Type
Component
Version
1.1
Status
Active
Created date
Updated date
The Australian Medicines Terminology (AMT) delivers standard identification of branded and generically equivalent medicines and their components. It also provides standard naming conventions and terminology to accurately describe medications. The terminology is for use by medication management computer systems, in both primary and secondary healthcare. …
Electronic Prescribing - Contact list for software developers v3.0
Contact list for software developers
ID
DH-3248:2020
Type
Component
Version
3.0
Status
Active
Created date
Updated date
The Electronic Prescribing developer contact list provides a list of key contacts that are useful for software developers throughout the development and implementation of electronic prescribing functionality.
Specialist homelessness services annual report 2022-23 v7.0
Category
Reference Table
Organisation
AIHW
ID
Cat. no: HOU 333
Type
Standard
Version
7
Access
Open
Status
Active
Updated
Feb-24
This specialist homelessness services annual report summarises the characteristics of clients receiving support from specialist homelessness services throughout 2022-23.
Electronic Prescribing - National Prescription Delivery Service and Active Script List Registry Conformance Profile v3.1
National Prescription Delivery Service and Active Script List Registry Conformance Profile
ID
DH-3939:2024
Type
Component
Version
3.1
Status
Active
Created date
Updated date
Electronic Prescribing – National Prescription Delivery Service and Active Script List Registry Conformance Profile v3.1 document includes requirements related to National Prescription Delivery Service and Active Script List Registry.
Australian Medicines Terminology v2 Model - Editorial Rules v4.0
Editorial Rules
ID
NEHTA-0851:2011
Type
Component
Version
4.0
Status
Active
Created date
Updated date
The AMT Editorial Rules (v2 model) has been updated to reflect a number of changes. The Australian Medicines Terminology (AMT) delivers standard identification of branded and generically equivalent medicines and their components. It also provides standard naming conventions and terminology to accurately describe medications. The terminology is for use by…
Australian Medicines Terminology v2 Model - Technical Specification Guide v4.0
Technical Specification Guide
ID
NEHTA-0883:2012
Type
Component
Version
4.0
Status
Active
Created date
Updated date
This document specifies the data model for the AMT (v2 model), giving special attention to how the concepts, relationships and descriptions are structured in the AMT. This document should be read in conjunction with: Australian Medicines Terminology UML Class Diagrams v7.0 (05 March 2008) Australian Medicines Terminology Editorial Rules (v2 model) …
Health informatics – Identification of medicinal products – Data elements and structures for the unique identification and exchange of regulated information on substances
Category
Standard
Organisation
ISO
ID
ISO 11238:2018
Type
Standard
Version
2
Access
Fees apply to access
Status
Active
Created
Jul-18
This document provides an information model that enables the definition and identification of substances within medicinal products or substances used for medicinal purposes, including dietary supplements, foods and cosmetics.
Health informatics — Requirements for international machine-readable coding of medicinal product package identifiers
Category
Specification
Organisation
ISO
ID
ISO/TS 16791:2020
Type
Standard
Version
2
Access
Fees apply to access
Status
Active
Created
Sep-20
This specification provides guidelines on identification and labelling of medicinal products from the point of manufacture of packaged medicinal product to the point of dispensing the product.
IHE Radiology Technical Framework Supplement – Prioritization of Worklists for Reporting (POWR)
Category
Supplementary Resource
Organisation
IHE
Type
Standard
Version
1.1
Access
Open
Status
Trial
Created
Aug-23
This document describes the Prioritisation of Worklists for Reporting (POWR) Profile, which standardises data interfaces to provide details relevant to the prioritisation of studies on a medical imaging reading worklist.
National Product Catalogue - Supplier Agreement Checklists v1.0
Supplier Agreement Checklists
ID
NEHTA-0309:2008
Type
Component
Version
1.0
Status
Archived
Created date
Updated date
The following items are a suggested checklist to use when negotiating an e-Procurement relationship with a supplier. It is also suggested that this relationship be managed at three levels. At a Business level to ensure that there is an ongoing relationship that is beneficial to the jurisdiction. At an Operational level to ensure that the day to day…
SNOMED CT Medicinal Product Model Specification v4.0
Category
Specification
Organisation
SNOMED
Type
Standard
Version
4
Access
Open
Status
Active
Updated
Nov-21
SNOMED CT is a standard for data elements used in the electronic exchange of clinical information. This document specifies the concept model for representation of pharmaceutical and biological products in the international edition of SNOMED CT.
IHE Patient Care Coordination (PCC) Technical Framework Supplement: Paramedicine Care Summary (PCS) v1.1
Category
Supplementary Resource
Organisation
IHE
Type
Standard
Version
1.1
Access
Open
Status
Trial
Created
Sep-18
This document defines the Paramedicine Care Summary (PCS) profile, which makes ambulance-based patient assessments and paramedicine interventions available electronically to hospital or emergency room staff, either when the patient arrives or in advance of the patient’s arrival to the hospital.
Specialist Letter - Core Information Components v1.0
Core Information Components
ID
NEHTA-0973:2011
Type
Component
Version
1.0
Status
Active
Created date
Updated date
This document presents the core information components of the Specialist Letter 1.0.4 package release, which are recommended for use when sending electronic responses from specialists back to the referring general practitioners within Australia.
Health informatics — Identification of medicinal products — Core principles for maintenance of identifiers and terms
Category
Technical Report
Organisation
ISO
ID
ISO/TR 14872:2019
Type
Standard
Version
1
Access
Fees apply to access
Status
Active
Created
Jul-19
This document describes the core principles and a proposed service-delivery model for terminology maintenance services in support of 5 International Standards on the Identification of Medicinal Products (IDMP).
Shared Health Summary - Structured Content Specification v1.2
Structured Content Specification
ID
NEHTA-1839:2015
Type
Component
Version
1.2
Status
Active
Created date
Updated date
This document describes the structured component specifications and guidelines to be adopted when producing electronic Shared Health Summary documents for sharing within the Australian healthcare community. This specification references or contains excerpts of intellectual property (IP) owned by the Regenstrief Institute, IHTSDO, or HL7 International…
Specialist Letter - Structured Content Specification v1.1
Structured Content Specification
ID
NEHTA-0983:2011
Type
Component
Version
1.1
Status
Active
Created date
Updated date
This document specifies the information structure of Agency-compliant Specialist Letters in order to support the transfer of information about a specialist consultation initiated by a referral. This specification references or contains excerpts of intellectual property (IP) owned by the Regenstrief Institute, IHTSDO, or HL7 International. Applicable IP…
Therapeutic Goods (Medicines-Standard for Serialisation and Data Matrix Codes) (TGO 106) Order 2021
Category
Standard
Organisation
TGA
ID
F2021L00333
Type
Standard
Access
Open
Status
Active
Created
Mar-21
This document is the standard for serialisation and data matrix code use in relation to medicines.