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eHealth Pathology Report (pathology PDF only) v1.2.3

eHealth Pathology Report (pathology PDF only)
ID
EP-3399:2021
Type
Product
Version
1.2.3
Access
None
Status
Active
Created date
Updated date
eHealth pathology reports can be used to share information about pathology tests via a consumer's My Health Record.  The Pathology Report PDF may contain one or more tests that are uploaded by the pathology provider to the consumer's My Health Record. This specification references or contains excerpts of intellectual property (IP) owned by the…

eHealth Pathology Report (pathology PDF plus results data) v2.1.1

eHealth Pathology Report (pathology PDF plus results data)
Topics
Clinical documents
ID
EP-3986:2024
Type
Product
Version
2.1.1
Access
None
Status
Active
Created date
Updated date
eHealth Pathology Report documents can be used to share information about pathology test results via a consumer's My Health Record. Such a report may contain one or more tests that are uploaded by a pathology provider to the consumer’s My Health Record. Reports will be in a PDF format but test results data may also be presented in another format. This…

RCPA - Pathology Terminology and Information Models v1.0

RCPA - Pathology Terminology and Information Models
ID
EP-2353:2016
Type
Product
Version
1.0
Access
SNOMED License Holder
Status
Withdrawn
Created date
Updated date
This end product contains terminology and information model resources developed and owned by the Royal College of Pathologists of Australasia (RCPA) and have been developed as part of The National Pathology Terminology and Information Standardisation Plan. The intellectual property rights of the RCPA pathology terminology and information models are owned…

eHealth Pathology Report View v1.1

eHealth Pathology Report View
Topics
Clinical documents
ID
EP-2053:2015
Type
Product
Version
1.1
Access
Open access
Status
Active
Created date
Updated date
eHealth pathology reports can be used to share information about pathology tests via an individual's digital health record. A pathology report PDF may contain one or more tests that are uploaded by the pathology provider to the individual's digital health record. The eHealth Pathology Report View provides a mechanism to list, group and sort those…

Electronic Prescribing - CIS to NPDS or ASLR

Services
Electronic Prescribing
ID
DG-3045
Type
Guide
Version
1.0
Status
Active
Created date
Updated date

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

RCPA - APUTS Surgical Pathology Report Information Model Terminology v2.3

APUTS Surgical Pathology Report Information Model Terminology
ID
DH-2365:2016
Type
Component
Version
2.3
Status
Withdrawn
Created date
Updated date
RCPA - APUTS Surgical Pathology Report Information Model Terminology provides a set of terms for reporting surgical pathology in Australia and their associated codes. Specifically, it provides a structured report model and preferred terms for surgical pathology reporting, which can be used in the electronic communication of a pathology report.

RCPA - APUTS Cytopathology Report Information Model Terminology v2.3

APUTS Cytopathology Report Information Model Terminology
ID
DH-2362:2016
Type
Component
Version
2.3
Status
Withdrawn
Created date
Updated date
RCPA - APUTS Cytopathology Report Information Model Terminology provides a set of terms for reporting cytopathology in Australia and their associated codes. Specifically, it provides a structured report model and preferred terms for reporting cytopathology test results, which can be used in the electronic communication of a pathology report.

RCPA - APUTS Chemical Pathology Terminology Reference Set v2.3

APUTS Chemical Pathology Terminology Reference Set
ID
DH-2355:2016
Type
Component
Version
2.3
Status
Withdrawn
Created date
Updated date
RCPA  - APUTS Chemical Pathology Terminology Reference Set provides a set of terms for reporting chemical pathology in Australia and their associated codes and preferred units. Specifically, it provides preferred terms and units for reporting chemical pathology test results, which can be used in the electronic communication of a pathology report…

RCPA - APUTS Immunopathology Terminology Reference Set v2.3

APUTS Immunopathology Terminology Reference Set
ID
DH-2357:2016
Type
Component
Version
2.3
Status
Withdrawn
Created date
Updated date
RCPA - APUTS Immunopathology Terminology Reference Set provides a set of terms for reporting immunopathology in Australia and their associated codes and preferred units. Specifically, it provides preferred terms and units for reporting immunopathology test results, which can be used in the electronic communication of a pathology report.

HIPS - Product Data Sheet v8.3

Product Data Sheet
ID
DH-3603:2022
Type
Component
Version
8.3
Status
Active
Created date
Updated date
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.

Supporting Document Library - Communicating a Request Not to Upload a Pathology or Diagnostic Imaging Report to the My Health Record System Implementation Guide v1.0

Communicating a Request Not to Upload a Pathology or Diagnostic Imaging Report to the My Health Record System Implementation Guide
ID
DH-2951:2019
Type
Component
Version
1.0
Status
Active
Created date
Updated date
This guide explains how a requesting clinician can communicate to a pathology or diagnostic imaging provider that they should not upload a report to the patient’s My Health Record. The intended audience includes developers and vendors of digital health systems that generate pathology and/or diagnostic imaging requests. Background Pathology and…

Implementation Guide - Use of Product Divisions [Data Structure 032] v1.2.0

Category
Implementation Guide
Organisation
ICCBBA
ID
ICCBBA IG-023
Type
Standard
Version
1.2.0
Access
Open
Status
Active
Created
November 2018
This document provides guidance to users and software developers on the use of the Product Divisions [Data Structure 032] for cellular therapy and regenerated tissue products, when used with the Product Code [Data Structure 003].

ISBT 128 Standard - Standard terminology for medical products of human origin v7.72

For use with product description code database
Category
Technical Specification
Organisation
ICCBBA
ID
ICCBBA ST-002
Type
Standard
Version
7.72
Access
Open
Status
Active
Created
January 2024
This document provides a standard terminology for describing transfusion and transplantation products. It helps users distinguish between products when required for safety, clinical practice, or inventory management.

SNOMED CT Medicinal Product Model Specification v4.0

Category
Technical Specification
Organisation
SNOMED
Type
Standard
Version
4
Access
Open
Status
Active
Updated
November 2021
SNOMED CT is a standard for data elements used in the electronic exchange of clinical information. This document specifies the concept model for representation of pharmaceutical and biological products in the international edition of SNOMED CT.

RCPA - APUTS Requesting Pathology Terminology Reference Set v2.2

APUTS Requesting Pathology Terminology Reference Set
ID
DH-2361:2016
Type
Component
Version
2.2
Status
Withdrawn
Created date
Updated date
RCPA - APUTS Requesting Pathology Terminology Reference Set v2.2, which provides a set of terms for requesting pathology in Australia and their associated SNOMED CT codes. It is intended to provide request terminology reference set for the most commonly requested terms used in both public and private practice.

NASH - Obtaining Identity From a Production or Test NASH Certificate v1.0

Obtaining Identity From a Production or Test NASH Certificate
ID
NEHTA-1281:2013
Type
Component
Version
1.0
Status
Active
Created date
Updated date
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

Clinical Document Data Extractor Library - Product Data Sheet v1.1

Product Data Sheet
ID
NEHTA-2130:2015
Type
Component
Version
1.1
Status
Active
Created date
Updated date
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…

Clinical Document Packaging Library - Product Data Sheet v1.2

Product Data Sheet
ID
NEHTA-2131:2015
Type
Component
Version
1.2
Status
Active
Created date
Updated date
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.

My Health Record - Managing Your B2B Software In Production v1.6

Managing Your B2B Software In Production
Services
My Health Record B2B Gateway
ID
DH-3849:2023
Type
Component
Version
1.6
Status
Active
Created date
Updated date
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…

Common - Continuity of Care - FAQ Undifferentiated Pathology and Radiology Results v1.3

FAQ Undifferentiated Pathology and Radiology Results
ID
NEHTA-1459:2013
Type
Component
Version
1.3
Status
Active
Created date
Updated date
The CDA implementation guides that include diagnostic service reports (eReferral, Specialist Letter, Event Summary, and Discharge Summary) divide the reports into pathology and radiology. This FAQ answers the question: What should we do if our system cannot distinguish between pathology and radiology reports

My Health Record - Managing Your B2B Software In Production v1.6

My Health Record - Managing Your B2B Software In Production
Services
My Health Record B2B Gateway
ID
EP-3850:2023
Type
Product
Version
1.6
Access
Open access
Status
Active
Created date
Updated date
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…

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