Product component
Identifier: 
DH-2895:2019

This document is a guide for developers, testers and analysts who use version 1.6 of the Information Quality Rules (‘the IQ Rules’). 

Identifier: 
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.

Identifier: 
EP-2903:2020

Version 2.8 of 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.

Product component
Identifier: 
DH-2906:2020

This document describes the system requirements, administrator rights, and supporting software needed for installing and configuring the Clinical Package Validator (Validator).

Product component
Identifier: 
DH-2904:2020

This document describes the use of the Clinical Package Validator (Validator) for helping vendors test whether a clinical document conforms with eHealth specifications.

Identifier: 
EP-2965:2019

SOFTWARE DOWNLOADS 

For access to binary executable code for the HIPS product please email [email protected] or call 1300 901 001.

 

Product component
Identifier: 
DH-2855:2019

HIPS Documentation Packages contains a comprehensive set of product documentation, including license terms for incorporated third-party products.

Product component
Identifier: 
DH-2874:2019

HIPS Documentation Packages contains a comprehensive set of product documentation, including license terms and conditions for the Binary Software Package and the Source Code Software Package.

Product component
Identifier: 
DH-2801:2019

HIPS Documentation Package contains a comprehensive set of product documentation, including license terms and conditions for the Binary Software Package and the Source Code Software Package.

Product component
Identifier: 
DH-2737:2018

This document describes the use of the Clinical Package Validator (Validator) for helping vendors test whether a clinical document conforms with eHealth specifications.

Pages

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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