The Agency’s Electronic Signatures Recommendations document explores the legal context for eSignatures on clinical documents, explains key concepts relating to eSignatures, and analyses the clinical and business risks.
Reading & Development: 2 hours. In this guide, we will cover; How to implement CIS to NPP into your software, Solution overview and Conformance Test Requirements
Reading 15 minutes, Registration 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
Specifications, guidance and associated collateral applicable to all types of clinical documents.
Reading & Development: 2 hours. In this guide, we will cover; How to implement CIS to NPP into your software, Solution overview and Conformance Test Requirements
Reading 15 minutes, Registration 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
On this page find information on SNOMED® CT-AU, National Clinical Terminology Service and Open Source Software.
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.
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.
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.
The Detailed Clinical Model Library is a suite of logical models that underpins the national My Health Record system.
The Agency’s Electronic Signatures Recommendations document explores the legal context for eSignatures on clinical documents, explains key concepts relating to eSignatures, and analyses the clinical and business risks.
Specifications, guidance and associated collateral applicable to all types of clinical documents.
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.
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.
This recording provides an introduction to the NCTS products and services. Topics in this recording include:
The Australian Digital Health Agency has released version 3.2 of the Clinical Package Validator.
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).
