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IHE Radiology Technical Framework Supplement – Post-Acquisition Workflow (PAWF)

Category
Supplementary Resource
Organisation
IHE
Type
Standard
Access
Open
Status
Trial
Created
Jun-12
This document describes the Post-Acquisition Workflow (PAWF) Profile, which addresses the need to schedule, distribute and track the status of typical post-acquisition workflow steps such as Computer-Aided Detection or Image Processing.

IHE Radiology Technical Framework Supplement – Results Distribution (RD)

Category
Supplementary Resource
Organisation
IHE
Type
Standard
Version
1.2
Access
Open
Status
Active
Created
Aug-19
This supplementary resource provides a profile that sends radiology results (that is, radiology reports) between systems, such as from a report management system to an electronic healthcare record system.

IHE Radiology Technical Framework Supplement – Standardized Operational Log of Events (SOLE)

Category
Supplementary Resource
Organisation
IHE
Type
Standard
Version
1.3
Access
Open
Status
Active
Created
Jun-23
Healthcare providers’ efforts to increase throughput and efficiency depend on capturing workflow events and applying business intelligence tools. This supplementary resource defines a way to exchange information about business activities that can be collected, analysed and displayed using standard methods.

IHE Radiology White Paper – AI Interoperability in Imaging

Category
Supplementary Resource
Organisation
IHE
Type
Standard
Version
1.1
Access
Open
Status
Active
Created
Oct-21
This supplementary resource aims to document what artificial intelligence (AI) in medical imaging encompasses and provide a comprehensive map of interoperability needs, problems and challenges that must be addressed to achieve an ecosystem of interoperable products that support all the processes and tasks that make up AI in medical imaging.

IT Infrastructure (ITI) White Paper – Survey of Network Interfaces Form

Category
Supplementary Resource
Organisation
IHE
Type
Standard
Version
1.1
Access
Open
Status
Active
Created
May-20
This supplementary resource describes the need for, value of and approach for establishing a central data source of technical connectivity details for HL7 v2, XD, DICOM and FHIR endpoints to support search and retrieval of services and endpoints.

Privacy Consent on FHIR (PCF)

Category
Supplementary Resource
Organisation
IHE
Type
Standard
Version
1.1.0
Access
Open
Status
Active
Created
Feb-24
This supplementary resource provides support for patient privacy consents and access control where a FHIR application programming interface (API) is used to access Document Sharing Health Information Exchanges.

Sample RCS-C CDA Document

Category
Supplementary Resource
Organisation
IHE
Type
Standard
Access
Open
Status
Trial
This supplementary resource provides a sample Registry Content Submission – CathPCI V4.4 (RCS-C) Clinical Document Architecture (CDA) document.

Sample RCS-C Data Collection Form

Category
Supplementary Resource
Organisation
IHE
Type
Standard
Access
Open
Status
Trial
This supplementary resource provides a sample Registry Content Submission – CathPCI V4.4 (RCS-C) data collection form.

SDPi Requirements Compilation

Category
Supplementary Resource
Organisation
IHE
Type
Standard
Access
Open
Status
Trial
This supplementary resource provides a compilation of Service-oriented Device Point-of-care Interoperability (SDPi) requirements.

XML Schemas (ITS-XML) Component - 2.0.0

Category
Specification
Organisation
openEHR
Type
Standard
Version
2.0.0
Access
Open
Status
Trial
Created
Apr-21
This resource provides the latest released specifications of XML Schemas (ITS-XML) Component.

Example EMR EHR Requirements Guide

Category
User guide
Organisation
SNOMED
Type
Standard
Access
Open
Status
Active
Updated
Jul-19
This user guide presents high-level examples of categories and requirements to consider when procuring a SNOMED CT-enabled electronic medical record or electronic health record system.

SNOMED CT National Release Center Guide

Category
User guide
Organisation
SNOMED
Type
Standard
Access
Open
Status
Active
Updated
Sep-24
This user guide introduces SNOMED International and SNOMED CT for those working in or planning to develop a National Release Center. It is also applicable to countries considering joining SNOMED International and existing Members.

Practical Guide to Reference Sets

Category
User guide
Organisation
SNOMED
Type
Standard
Access
Open
Status
Active
Updated
May-24
This user guide provides a high-level introduction to SNOMED CT reference sets and explains the different types of reference sets and their usage. It also introduces the reference set format and provides guidance on the development and management of reference sets.

Requirements for External Editors of SNOMED CT International Release

Category
User guide
Organisation
SNOMED
Type
Standard
Access
Open
Status
Active
Created
Sep-19
Updated
Dec-21
This user guide describes the knowledge, skills, abilities, education, experience and certification required for individuals external to SNOMED International to author content directly into the SNOMED CT International release.

SNOMED CT - SQL Practical Guide

Category
User guide
Organisation
SNOMED
Type
Standard
Access
Open
Status
Active
Updated
Sep-24
This user guide provides a simple and practical example of how a relational database can be used to enable effective access to the content and features of SNOMED CT. It includes tested SQL scripts for loading release files into a relational database, searching the terminology and querying the terminology for concepts that meet simple but useful constraints.

Edition URI Examples

Category
Supplementary Resource
Organisation
SNOMED
Type
Standard
Access
Open
Status
Active
Updated
Sep-24
This resource provides the focus module ID and edition URI for several national and international editions of SNOMED CT.

SNOMED CT Editorial Guide

Category
User guide
Organisation
SNOMED
Type
Standard
Access
Open
Status
Active
This user guide provides the information needed to model concepts in SNOMED CT. The guide’s primary audience is those who edit content in the International Release, but it may also be useful to those creating extensions.

Software & tooling

Category
User guide
Organisation
SNOMED
Type
Standard
Access
Open
Status
Active
SNOMED International offers a range of software and tools to use and work with SNOMED CT, as well as supporting a growing community of developers. This resource lists SNOMED CT software and tools.

AS 4700.1.2.4:2014 Implementation of Health Level Seven (HL7) Version 2.4, Part 1.2.4: Patient administration

Category
Standard
Organisation
Standards Australia
Type
Standard
Access
Fees apply to access
Status
Active
Created
May-14
This standard defines a uniform implementation of chapter 3 of the HL7 Version 2.4 protocol. It aims to enable the greatest degree of standardisation possible in the exchange of patient administration data among various healthcare computer applications in Australia using HL7 Version 2.4.

AS 4700.1.2.5:2014 Implementation of Health Level Seven (HL7) Version 2.5 and Version 2.5.1, Part 1.2.5: Patient administration

Category
Standard
Organisation
Standards Australia
Type
Standard
Access
Fees apply to access
Status
Active
Created
May-14
This standard defines a uniform implementation of chapter 3 of the HL7 Version 2.5 and Version 2.5.1 protocols. It aims to enable the greatest degree of standardisation possible in the exchange of patient administration data among various healthcare computer applications in Australia using HL7 Version 2.5, as well as HL7 Version 2.5.1 where applicable.

AS 4700.2-2012 Implementation of Health Level Seven (HL7) Version 2.4, Part 2: Pathology and diagnostic imaging (diagnostics)

Category
Standard
Organisation
Standards Australia
Type
Standard
Access
Fees apply to access
Status
Active
Created
Dec-12
This standard provides requirements and guidance for implementing electronic messages to exchange information on pathology and diagnostic imaging orders and results using the HL7 Version 2.4 protocol. It aims to specify message formats and code sets for communicating such orders and results within and between Australian healthcare settings.

AS 4700.3:2014 Implementation of Health Level Seven (HL7) Version 2.5, Part 3: Electronic messages for exchange of information on medicines prescription

Category
Standard
Organisation
Standards Australia
Type
Standard
Access
Fees apply to access
Status
Active
Created
Aug-14
This standard covers implementing electronic messages to exchange information on medicines prescriptions in the community and hospital environment using the HL7 Version 2.5 protocol. It covers implementation of the protocol for communication between prescribers, dispensers and their healthcare trading partners in Australia.

AS 4700.6-2013 Implementation of Health Level Seven (HL7) Version 2.5, Part 6: Referral, discharge and health record messaging

Category
Standard
Organisation
Standards Australia
Type
Standard
Access
Fees apply to access
Status
Active
Created
May-13
This standard provides guidance for implementing communication of clinical patient-centred information between health service providers using the HL7 Version 2.5 protocol. It focuses on the HL7 discharge and referral, shared care and event summary messages.

AS 5021-2005 The language of health concept representation

Category
Standard
Organisation
Standards Australia
Type
Standard
Access
Fees apply to access
Status
Active
Created
Jun-05
This standard provides agreed definitions of terms used for health concept representation in Australia and a coherent vocabulary of the central concepts of terminology.

ATS 5546-2013 E-health endpoint location service

Category
Specification
Organisation
Standards Australia
Type
Standard
Access
Fees apply to access
Status
Active
Created
Dec-13
This standard defines the technical service specification for the Endpoint Location Service and contains the requisite datatypes and interfaces and behaviours. It also provides conformance criteria intended for unambiguous operation between clients and service providers.

RCPA – Pathology Terminology and Information Models Release Note

Category
Supplementary Resource
Organisation
ADHA
ID
EP-3596:2022
Type
Standard
Version
1.6
Access
Open
Status
Superseded
Created
Feb-22
This release note summarises the RCPA – Pathology Terminology and Information Models v1.6 package, an updated version of the Requesting Pathology Terminology Reference Set.

GS1 EDI Healthcare Guidelines

Category
Guideline
Organisation
GS1
Type
Standard
Access
Open
Status
Active
The GS1 Electronic Data Interchange (EDI) Healthcare Guidelines provide global standards for electronic business messaging in the healthcare sector. This resource includes a model for healthcare supply chain processes, detailed descriptions of these processes and a set of specifications describing the information that should be included in electronic documents sent between business systems.

Application of risk management for IT-networks incorporating medical devices – Part 1: Safety, effectiveness and security in the implementation and use of connected medical devices or connected health software

Category
Standard
Organisation
ISO
ID
IEC 80001-1:2021
Type
Standard
Version
2
Access
Fees apply to access
Status
Active
Created
Sep-21
This document specifies general requirements for organisations in the application of risk management before, during and after the connection of a health IT system within a health IT infrastructure.

Health software – Part 1: General requirements for product safety

Category
Standard
Organisation
ISO
ID
IEC 82304-1:2016
Type
Standard
Version
1
Access
Fees apply to access
Status
Active
Created
Oct-16
This document sets out the safety and security requirements for manufacturers of health software products that are designed to operate on general computing platforms without dedicated hardware.

Application of risk management for IT-networks incorporating medical devices – Part 2-1: Step by Step Risk Management of Medical IT-Networks; Practical Applications and Examples

Category
Technical Report
Organisation
ISO
ID
IEC/TR 80001-2-1:2012
Type
Standard
Version
1
Access
Fees apply to access
Status
Active
Created
Jul-12
This technical report is a step-by-step guide for the application of practical risk management when creating or changing a medical IT network. It is intended for use in conjunction with the IEC 80001-1 risk management standard.

Application of risk management for IT-networks incorporating medical devices – Part 2-2: Guidance for the communication of medical device security needs, risks and controls

Category
Technical Report
Organisation
ISO
ID
IEC/TR 80001-2-2:2012
Type
Standard
Version
1
Access
Fees apply to access
Status
Active
Created
Jul-12
This technical report creates a framework for the disclosure of security-related capabilities and risks necessary for managing risk when connecting medical devices to IT networks. It also supports the security dialogue surrounding IEC 80001-1 and informs the responsibility agreements specified in that standard.

Application of risk management for IT-networks incorporating medical devices – Part 2-4: General implementation guidance for Healthcare Delivery Organizations

Category
Technical Report
Organisation
ISO
ID
IEC/TR 80001-2-4:2012
Type
Standard
Version
1
Access
Fees apply to access
Status
Active
Created
Nov-12
This technical report helps healthcare delivery organisations assess the impact of IEC 80001-1 on the organisation and establish a series of business-as-usual processes to manage risk in the creation, maintenance and upkeep of medical IT networks.

Application of risk management for IT-networks incorporating medical devices – Part 2-5: Application guidance – Guidance for distributed alarm systems

Category
Technical Report
Organisation
ISO
ID
IEC/TR 80001-2-5:2014
Type
Standard
Version
1
Access
Fees apply to access
Status
Active
Created
Dec-14
This technical report provides guidance for responsible organisations, medical device manufacturers and providers of other information technology in the application of IEC 80001-1:2010 for the risk management of distributed alarm systems.

Application of risk management for IT-networks incorporating medical devices – Part 2-8: Application guidance – Guidance on standards for establishing the security capabilities identified in IEC 80001-2-2

Category
Technical Report
Organisation
ISO
ID
IEC/TR 80001-2-8:2016
Type
Standard
Version
1
Access
Fees apply to access
Status
Active
Created
May-16
This technical report provides guidance to health delivery organisations and medical device manufacturers on the application of the framework outlined in IEC/TR 80001-2-2 for the communication of medical device security needs, risks and controls.

Application of risk management for IT-networks incorporating medical devices – Part 2-9: Application guidance – Guidance for use of security assurance cases to demonstrate confidence in IEC/TR 80001-2-2 security capabilities

Category
Technical Report
Organisation
ISO
ID
IEC/TR 80001-2-9:2017
Type
Standard
Version
1
Access
Fees apply to access
Status
Active
Created
Jan-17
This technical report establishes a security case framework and provides guidance to healthcare delivery organisations and medical device manufacturers for identifying, developing, interpreting, updating and maintaining security cases for networked medical devices.

Health informatics – HL7 Electronic Health Record-System Functional Model

Category
Standard
Organisation
ISO
ID
ISO 10781:2023
Type
Standard
Version
2.1
Access
Fees apply to access
Status
Active
Created
Nov-23
This document describes the EHR-S Functional Model (EHR-S FM), which sets out standardised functional profiles for different healthcare settings (e.g. intensive care, cardiology, office practice in one country or primary care in another country).

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