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My Health Record CIS to NPP - Complete Implementation - Developer Guide

Developer Guides

Reading & Development: 2 hours

My Health Record CIS to NPP - Introduction

Developer Guides

Reading:       15 minutes
Register:       30 minutes

Learning objectives: In this guide, you'll learn, Introduction to CIS to NPP service, CIS to NPP Limitations, Register for CIS-to-NPP implementation, Testing, Vendor conformance process and Go Live requirements

Clinical Terminology

Developer Guides, Products, Sample Code, Specifications, Toolkits

On this page find information on SNOMED® CT-AU, National Clinical Terminology Service and Open Source Software. 

Common - Clinical Document v1.5.4

Products, Specifications | EP-3149:2020

Specifications, guidance and associated collateral applicable to all types of clinical documents.

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Information Quality Rules v1.6

Products, Specifications, Toolkits | EP-2895:2019

The Information Quality Rules (IQ Rules) is a tool that helps developers, testers and analysts determine the quality of clinical documents including the conformance of clinical documents to the My Health Record system conformance requirements.

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Participation Data Specification

Products

The participation data specification is a foundation document for the suite of data specifications that the Australian Digital Health Agency is developing for the Australian Health Informatics community across a range of health topics.

Clinical Package Validator

Products, Sample Code, Specifications, Toolkits

The Clinical Package Validator is a tool to automate some of the tests needed to assess conformance of clinical documents and clinical packages with the eHealth Specifications.

Data types in Agency specifications

Products

This document defines the Australian Digital Health Agency’s required data types as a logical level profile that conforms directly to the draft ISO 21090 standard. The detail included in this specification is less than that specified in the ISO document and the technical detail becomes relevant within the scope of this profile, during construction/implementation of Agency information products.

Detailed Clinical Model Library

Products

The Detailed Clinical Model Library is a suite of logical models that underpins the national My Health Record system. 

Developer Guides

My Health Record CIS to NPP - Complete Implementation - Developer Guide

Developer Guides

Reading & Development: 2 hours

My Health Record CIS to NPP - Introduction

Developer Guides

Reading:       15 minutes
Register:       30 minutes

Learning objectives: In this guide, you'll learn, Introduction to CIS to NPP service, CIS to NPP Limitations, Register for CIS-to-NPP implementation, Testing, Vendor conformance process and Go Live requirements

Products

Clinical Terminology

Developer Guides, Products, Sample Code, Specifications, Toolkits

On this page find information on SNOMED® CT-AU, National Clinical Terminology Service and Open Source Software. 

Participation Data Specification

Products

The participation data specification is a foundation document for the suite of data specifications that the Australian Digital Health Agency is developing for the Australian Health Informatics community across a range of health topics.

Clinical Package Validator

Products, Sample Code, Specifications, Toolkits

The Clinical Package Validator is a tool to automate some of the tests needed to assess conformance of clinical documents and clinical packages with the eHealth Specifications.

Data types in Agency specifications

Products

This document defines the Australian Digital Health Agency’s required data types as a logical level profile that conforms directly to the draft ISO 21090 standard. The detail included in this specification is less than that specified in the ISO document and the technical detail becomes relevant within the scope of this profile, during construction/implementation of Agency information products.

Detailed Clinical Model Library

Products

The Detailed Clinical Model Library is a suite of logical models that underpins the national My Health Record system. 

Specifications

Common - Clinical Document v1.5.4

Products, Specifications | EP-3149:2020

Specifications, guidance and associated collateral applicable to all types of clinical documents.

Login to download

Information Quality Rules v1.6

Products, Specifications, Toolkits | EP-2895:2019

The Information Quality Rules (IQ Rules) is a tool that helps developers, testers and analysts determine the quality of clinical documents including the conformance of clinical documents to the My Health Record system conformance requirements.

Login to download

Clinical Package Validator v3.2

Specifications | EP-3408:2020

The Clinical Package Validator (Validator) provides software developers with enhanced capabilities to achieve a greater degree of automation and depth of their conformance tests of clinical documents.

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Participation Data Specification v3.3

Specifications | EP-2499:2017
The Participation Data Specification is a foundation document for the suite of data specifications that the Agency is developing for the Australian health informatics community across a range of health topics. These specifications are generally agreed to be of high priority in order to achieve the benefits of semantic interoperability in the Australian healthcare setting.
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Medicare Records v1.0

Specifications | EP-2746:2018
The Medicare Records FHIR Implementation Guide specifies the format of FHIR-based representations of Medicare documents that is used for the upload of such documents into the My Health Record system.
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Digital Health Icon Library v1.0

Specifications | EP-2704:2018
The Icon Library is available as a resource for developers and implementers of digital health solutions and other interested parties.
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Detailed Clinical Model Library v4.5

Specifications | EP-2522:2017
May 2017 release of the Detailed Clinical Models
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Data Types in NEHTA Specifications v1.0

Specifications | EP-1135:2010
This document supports the Agency's detailed clinical model specifications and structured content specifications. It details a set of data types as a profile of the ISO 21090 data type specification.
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Common - Consumer Entered Information v1.2

Specifications | EP-1428:2013
Documents that are common to the Consumer Entered Information products.
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Common - P2P v1.1

Specifications | EP-1254:2012
Common documents for the secure point-to-point (P2P) delivery of clinical documents.
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FAQs

Introduction to the NCTS products and services - recording

FAQs, Webinars

This recording provides an introduction to the NCTS products and services. Topics in this recording include:

News

Clinical Package Validator v3.2 Released

News

The Australian Digital Health Agency has released version 3.2 of the Clinical Package Validator.

Tuesday, 12 January 2021

By operation of the Public Governance, Performance and Accountability (Establishing the Australian Digital Health Agency) Rule 2016, on 1 July 2016, all the assets and liabilities of NEHTA will vest in the Australian Digital Health Agency. In this website, on and from 1 July 2016, all references to "National E-Health Transition Authority" or "NEHTA" will be deemed to be references to the Australian Digital Health Agency. PCEHR means the My Health Record, formerly the "Personally Controlled Electronic Health Record", within the meaning of the My Health Records Act 2012 (Cth), formerly called the Personally Controlled Electronic Health Records Act 2012 (Cth).

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