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This guide will walk through the steps to create and upload clinical documents

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…

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…

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 in the context of the My Health Record system and provides references to all other documents that specify requirements applicable to…

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…

This document provides a guide to implementing the 'logical' model detailed by the Agency's Specialist Letter Structured Content Specification as an HL7 Clinical Document Architecture Release 2 (CDA) XML document. The primary aim of the guide is to take implementers step by step through the mapping of each data component of the structured content…

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.

This template package library provides validation rules for Specialist Letter documents to identify points of non-conformance to the relevant specifications. The template packages contained in this library can be used by the My Health Record system and the Agency's Clinical Package Validator.

This document defines the service interfaces and associated conformance points for the provider-to-provider (P2P) delivery of Specialist Letter CDA document packages.

This Developer Guide is for the use of developers whose products connect to the Healthcare Identifiers (HI) Service, My Health Record, Electronic Prescribing and Secure Messaging with a National Authentication Service for Health (NASH) PKI Certificate.

The following steps will assist prescribing and dispensing Clinical Information System (CIS) software developers connect to the national Prescription Delivery Service (PDS) and declare software conformance with the Agency’s Electronic Prescribing technical framework.

The FAQs are guidance material for implementation. They are to be used for clarification purposes and to support existing documentation.

The HIPS product enables the seamless integration of digital health systems with national digital health infrastructure services, such as the Healthcare Identifiers Service, the My Health Record system. The product data sheet provides information for implementers about the capabilities of the HIPS end product and its product components.

A mobile intermediary system is a software product that a mobile application uses to connect to, and interact with, Open Prescription Delivery Services (PDS) and/or Active Script List Registry (ASLR) Services. 

This FAQ answers: What identity information contained in a production or test NASH certificate should I use when validating a signature And What will be the impact on the CCA status of any SMD product that was tested with code that used the URI in the test NASH certificates issued before June 2012

The following steps will assist Clinical Information System (CIS) software developers with a direct Prescription Delivery Service (PDS), declare software conformance with the Agency’s Electronic Prescribing technical framework.

HIPS Mobile is a mobile web application that may be added to an existing HIPS v7.1 or higher instance operated by a HIPS site, enabling users to list, download and display CDA™ documents and views from a patient’s My Health Record on their mobile or tablet device. The product data sheet provides information for implementers about the…

A guide for vendors already in production. It covers topics such as incident management and software changes and upgrades. This document outlines the process for liaising with the My Health Record System Operator (SO) about production incidents and events requiring notification to the SO, such as changes and upgrades to software that connects to the My…

A guide for vendors already in production. It covers topics such as incident management and software changes and upgrades. This document outlines the process for liaising with the My Health Record System Operator (SO) about production incidents and events requiring notification to the SO, such as changes and upgrades to software that connects to the My…

The Clinical Document Data Extractor Library simplifies the development process by providing vendors with a simple interface for extracting data from a range of CDA documents. The library uses the information from Agency-developed CDA implementation guides. This product component was previously called CDA Data Extractor Library - Product Data…

The My Health Record B2B Client Library provides vendors with a sample implementation for integration with the B2B web services provided by the My Health Record system.This product data sheet provides more detailed information about the capabilities and components of this library. "My Health Record" is the new name of the system previously known as "PCEHR"…

The Clinical Document Packaging Library provides a sample implementation of how to package CDA documents (and any attachments) following the Agency specifications. This product component was previously called CDA Packaging Library - Product Data Sheet.

A mobile application or web-based application is used by a subject of care or carer to manage prescriptions and to present an electronic prescription token to a pharmacy.

The following steps will assist software developers who provide open Prescription Delivery Service (PDS) and/or Active Script List Registry capabilities to declare software conformance with the Agency’s Electronic Prescribing technical framework.