This package contains the conformance test specifications for Prescribing systems, Dispensing Systems, Open Prescription Delivery Services (PDS) and all associated test data.
Specifications, guidance and associated collateral applicable to all types of clinical documents.
The Agency’s Secure Messaging provides software developers with information and tools to assist in the implementation of Secure Message Delivery (SMD) and Endpoint Location Service (ELS).
These test have been written against the specified requirements in the Electronic Prescribing - Participating Software Conformance Profile document.
These test have been written against the specified requirements in the Electronic Prescribing - Participating Software Conformance Profile document.
These test have been written against the specified requirements in the Electronic Prescribing - Participating Software Conformance Profile document.
This package contains the conformance test specifications for Prescribing systems, Dispensing Systems, Open Prescription Delivery Services (PDS) and all associated test data.
The prescription test data file contains a comprehensive list of pharmaceutical test data for use by software vendors wishing to test their electronic prescribing functionality.
The Healthcare Provider Identifier-Organisation (HPI-O) Test Data file contains a comprehensive list of HPI-O test data for use by software vendors wishing to test their electronic prescribing functionality.
The Healthcare Provider Identifier - Individual (HPI-I) Test Data file contains a comprehensive list of HPI-I test data for use by software vendors wishing to test their electronic prescribing functionality.
These test cases have been written against the specified requirements in the Electronic Prescribing - Participating Software Conformance Profile document.
These test cases have been written against the specified requirements in the Electronic Prescribing - Participating Software Conformance Profile document.
These test have been written against the specified requirements in the Electronic Prescribing - Participating Software Conformance Profile document.
These test have been written against the specified requirements in the Electronic Prescribing - Participating Software Conformance Profile document.
These test have been written against the specified requirements in the Electronic Prescribing - Participating Software Conformance Profile document.
The subjects of care test data file contains a comprehensive list of subjects of care (Patient) test data for use by software vendors wishing to test their electronic prescribing functionality.
The prescribe and dispense personas file contains a list of medical practitioners that may be a part of the electronic prescribing lifecycle.
This package contains the conformance test specifications for Prescribing systems, Dispensing Systems, Open Prescription Delivery Services (PDS) and all associated test data.
The prescription test data file contains a comprehensive list of pharmaceutical test data for use by software vendors wishing to test their electronic prescribing functionality.
The subjects of care test data file contains a comprehensive list of subjects of care (Patient) test data for use by software vendors wishing to test their electronic prescribing functionality.
These test have been written against the specified requirements in the Electronic Prescribing - Participating Software Conformance Profile document.
These test have been written against the specified requirements in the Electronic Prescribing - Participating Software Conformance Profile document.
These test have been written against the specified requirements in the Electronic Prescribing - Participating Software Conformance Profile document.
The prescribe and dispense personas file contains a list of medical practitioners that may be a part of the electronic prescribing lifecycle.
The Healthcare Provider Identifier-Organisation (HPI-O) Test Data file contains a comprehensive list of HPI-O test data for use by software vendors wishing to test their electronic prescribing functionality.
The Healthcare Provider Identifier - Individual (HPI-I) Test Data file contains a comprehensive list of HPI-I test data for use by software vendors wishing to test their electronic prescribing functionality.
PSML documents help ensure the continuity of medicine management for consumers across different care settings.
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.
This release of the Conformance Test Specification for CDA Authoring Systems includes updated test cases in alignment with Common Conformance Profile v1.7.
Specifications, guidance and associated collateral applicable to all types of clinical documents.
Specifications, guidance and associated collateral applicable to all types of clinical documents.
Specifications, guidance and associated collateral applicable to all types of clinical documents.
This release of Conformance Test Specification for Authoring Systems includes updates to feature sets, improves the readability of the document, and addresses multiple issues raised during internal Agency reviews.
eHealth pathology reports can be used to share information about pathology tests via an individual's digital health record. The Pathology Report PDF may contain one or more tests that are uploaded by the pathology provider to the individual's digital health record.
Specifications, guidance and associated collateral applicable to all types of clinical documents.
eHealth diagnostic imaging reports can be used to share information about diagnostic imaging examinations via an individual's digital health record.
Conformance Test Specification for Authoring Systems provides a significant expansion of the authoring test cases previously available to developers in Clinical Documents - Conformance Test Specification for CDA Rendering v1.3 which contained test cases for authoring and rendering. This previous
This Conformance Test Specification consists of a series of test cases, each of which is a discrete test and a statement of expected behaviour. Vendors can use the documented test cases to assess the conformance of their pathology eHealth software.
This Conformance Test Specification consists of a series of test cases, each of which is a discrete test and a statement of expected behaviour. Vendors can use the documented test cases to assess the conformance of their diagnostic imaging eHealth software.
eHealth diagnostic imaging reports can be used to share information about diagnostic imaging examinations via an individual's digital health record.
eHealth pathology reports can be used to share information about pathology tests via an individual's digital health record. The Pathology Report PDF may contain one or more tests that are uploaded by the pathology provider to the individual's digital health record.
Specifications, guidance and associated collateral applicable to all types of clinical documents.
Overviews, guides and CCA material relating to the My Health Record system (formerly the PCEHR system).
Specifications, guidance and associated collateral applicable to all types of clinical documents.
One of the key foundations for a national approach to eHealth is a standard process across the health sector to consistently identify everyone involved in a healthcare event:
This page contains implementation collateral that is related to the AMT v3 model.
Specifications, guidance and associated collateral applicable to all types of clinical documents.
NOTE: The sample code previously available in this end product is now available in:
Specifications, guidance and associated collateral applicable to all types of clinical documents.
NOTE: The sample code previously available in this end product is now available in two new packages:
Specifications, guidance and associated collateral applicable to all types of clinical documents.
NOTE: The sample code previously available in this end product is now available in two new packages:
Overviews, guides and CCA material relating to the My Health Record system.
Overviews, guides and CCA material relating to the My Health Record system.
Specifications, guidance and associated collateral applicable to all types of clinical documents.
NOTE: The sample code previously available in this end product is now available in:
One of the key foundations for a national approach to eHealth is a standard process across the health sector to consistently identify everyone involved in a healthcare event:
Specifications, guidance and associated collateral applicable to all types of clinical documents.
Specifications, guidance and associated collateral applicable to all types of clinical documents.
One of the key foundations for a national approach to eHealth is a standard process across the health sector to consistently identify everyone involved in a healthcare event:
Specifications, guidance and associated collateral applicable to all types of clinical documents.
Specifications, guidance and associated collateral applicable to all types of clinical documents.
Specifications, guidance and associated collateral applicable to all types of clinical documents.
One of the key foundations for a national approach to eHealth is a standard process across the health sector to consistently identify everyone involved in a healthcare event:
Specifications, guidance and associated collateral applicable to all types of clinical documents.
Specifications, guidance and associated collateral applicable to all types of clinical documents.
Specifications, guidance and associated collateral applicable to all types of clinical documents.
One of the key foundations for a national approach to eHealth is a standard process across the health sector to consistently identify everyone involved in a healthcare event:
Material such as Frequently Asked Questions relevant to clinical documents.
The supporting documents on this page provide background and guidance for healthcare provider organisations, and conformance, compliance and accreditation requirements for vendors.
Overviews, guides and conformance material relating to the My Health Record system.
The conformance tests to be applied when testing a health software system for conformance to the requirements for use of healthcare identifiers.
The conformance tests to be applied when testing a health software system for conformance to the requirements for use of healthcare identifiers.
This test specification contains test cases for use by software testers to assess the conformance of their software to the conformance requirements for use of healthcare identifiers.
An amendment to the conformance test specification for clinical information systems connecting to the My Health Record system for assisted registration of an eHealth record for an adult, child or newborn.
The Agency has a Compliance, Conformance and Accreditation (CCA) program that supports clinical safety and quality in health software. CCA provides leadership, guidance and materials for assessing the conformance of software that implements e-health specifications and standards.
An amendment to the conformance test specification for clinical information systems connecting to the My Health Record system; for assisted registration of an adult and child.
The conformance test specification contains test cases for assessing clinical information systems for conformance with the following PCEHR usability recommendations (published as part of the Clinical Usability Programme (CUP) Release 3):
Specifies test cases for the assessment of conformance of clinical information systems with requirements related to CDA packaging.
Conformance Test Specification for CDA Packaging
All SNOMED CT-AU and AMT resources, including implementation collateral, are now available to download from the document library on the National Clinical Term
This conformance test specification supports the currently published My Health Record views specifications and their conformance requirements. It provides a targeted set of test cases, managed using a Microsoft Excel workbook.
This document mentions the NPDR.
Conformance test specification for clinical documents
This version of Conformance Test Specification provides clarifications for many of the test cases, improves the readability of the document, and adds a number of test cases to support recently published Pathology Report and Diagnostic Imaging Report conformance profiles.
Conformance test specification for CDA rendering.
Tests for assessing the conformance of a clinical information system to the My Health Record clinical information system requirements.
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).
