Search for standards based on keywords, categories, and organisations. You can also search more broadly for other resources or all content.
Implementation Guide - Manufacturer's Catalog Number and Lot Number (items other than containers) v1.0.1
Category
Implementation Guide
Organisation
ICCBBA
ID
ICCBBA IG-019
Type
Standard
Version
1.0.1
Access
Open
Status
Active
Created
May 2017
This document provides background information and examples of the use of the Manufacturer and Catalog Number: Items Other Than Containers [Data Structure 021] and the Lot Number: Items Other Than Containers [Data Structure 022].
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].
Implementation Guide - Use of Flexible Date and Time [Data Structure 031] v1.2.0
Category
Implementation Guide
Organisation
ICCBBA
ID
ICCBBA IG-024
Type
Standard
Version
1.2.0
Access
Open
Status
Active
Created
February 2019
This document provides guidance in the use of the Flexible Date and Time [Data Structure 031] in cellular therapy, ocular tissue, regenerated tissues and organ transplantation.
Implementation Guide - US guidance on printing text associated with red cell antigens v1.1.0
Category
Implementation Guide
Organisation
ICCBBA
ID
ICCBBA IG-025
Type
Standard
Version
1.1.0
Access
Open
Status
Active
Created
February 2024
This document provides guidance for printing text and coding red blood cell antigen test results on the affixed blood label.
Implementation Guide - Use of Dimensions [Data Structure 029] v1.3.0
Category
Implementation Guide
Organisation
ICCBBA
ID
ICCBBA IG-026
Type
Standard
Version
1.3.0
Access
Open
Status
Active
Created
February 2019
This document provides implementation guidance for users and software developers who wish to implement Dimensions [Data Structure 029].
Implementation Guide - Use of Red Cell Antigens with Test History [Data Structure 030] v1.2.0
Category
Implementation Guide
Organisation
ICCBBA
ID
ICCBBA IG-027
Type
Standard
Version
1.2.0
Access
Open
Status
Active
Created
July 2016
This document provides implementation guidance for users and software developers who wish to implement Red Cell Antigens with Test History [Data Structure 030].
Implementation Guide - Use of ISBT 128 by North American tissue banks v1.4.0
Category
Implementation Guide
Organisation
ICCBBA
ID
ICCBBA IG-028
Type
Standard
Version
1.4.0
Access
Open
Status
Active
Created
June 2020
This document provides guidance for the final labelling of human tissue products in a way that is compliant with the ISBT 128 Standard in North American tissue banks.
Implementation Guide - Choosing an on-demand label printer v1.0.2
Category
Implementation Guide
Organisation
ICCBBA
ID
ICCBBA IG-029
Type
Standard
Version
1.0.2
Access
Open
Status
Active
Created
February 2019
This document provides guidance for laboratory and hospital users who wish to procure on_demand label printers for blood product container labels.
Implementation Guide - Use of the Processing Facility Information Code [Data Structure 033] v1.1.0
Category
Implementation Guide
Organisation
ICCBBA
ID
ICCBBA IG-031
Type
Standard
Version
1.1.0
Access
Open
Status
Active
Created
September 2016
This document provides specific guidance for cellular therapy and tissue (including ocular) facilities to implement and use the Processing Facility Information Code [Data Structure 033].
Implementation Guide - ISBT 128 Facility Identification Number v1.3.0
Category
Implementation Guide
Organisation
ICCBBA
ID
ICCBBA IG-034
Type
Standard
Version
1.3.0
Access
Open
Status
Active
Created
June 2023
The Facility Identification Number (FIN) found in many ISBT 128 data structures. This document describes how the FIN is assigned and maintained, the database supporting the FIN, and how the FIN is used within ISBT 128 data structures to identify an organisation responsible for an action.
Implementation Guide - Use of ISBT 128 in North American Eye Banks v1.4.0
Category
Implementation Guide
Organisation
ICCBBA
ID
ICCBBA IG-040
Type
Standard
Version
1.4.0
Access
Open
Status
Active
Created
November 2016
The Eye Bank Association of America (EBAA) requires its accredited eye banks to use ISBT 128. This document provides guidance to North American and other eye banks accredited by the EBAA to help them implement ISBT 128.
Implementation Guide - Use of ISBT 128 in resource_limited countries v1.0.2
Category
Implementation Guide
Organisation
ICCBBA
ID
ICCBBA IG-041
Type
Standard
Version
1.0.2
Access
Open
Status
Active
Created
September 2022
This document provides guidance for implementing the ISBT 128 Standard for blood transfusion in resource_limited countries. It provides options to allow facilities to promote safety, traceability and efficiency without needing to implement all features of the ISBT 128 Standard.
Implementation Guide - A validation tool for ISBT 128 Data Structures v1.3.0
Category
Implementation Guide
Organisation
ICCBBA
ID
ICCBBA IG-043
Type
Standard
Version
1.3.0
Access
Open
Status
Active
Created
February 2023
This document provides a mechanism for users to validate their ISBT 128 barcode-reading software. It will help make users aware of how their system responds to a given data structure. Regulatory and compliance staff, as well as software developers, may find this guidance document helpful when developing certain validation test plans.
ISBT 128 Standard - Technical specification v6.2.2
Category
Technical Specification
Organisation
ICCBBA
ID
ICCBBA ST-001
Type
Standard
Version
6.2.2
Access
Open
Status
Active
Created
April 2023
The ISBT 128 Standard is an international standard to convey information about medical products of human origin clearly and accurately. The standard is continually updated based on new and changing user needs.
ISBT 128 Standard - Standard terminology for medical products of human origin v7.72
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.
ISBT 128 Standard - Labeling of medical products of human origin with INN and USAN nonproprietary names v1.0.0
Category
Standard
Organisation
ICCBBA
ID
ICCBBA ST-016
Type
Standard
Version
1.0.0
Access
Open
Status
Active
Created
March 2018
This document provides instructions for the labelling of medical products of human origin that have an approved International Nonproprietary Name (INN) or a United States Adopted Name (USAN), or both.
ISBT 128 Standard for XML - Electronic messaging: Standardized XML elements for medical products of human origin v1.1.0
Category
Standard
Organisation
ICCBBA
ID
ICCBBA ST-020
Type
Standard
Version
1.1.0
Access
Open
Status
Active
Created
November 2021
This standard provides specifications of XML elements for use in electronic messages that provide information about medical products of human origin.
ISBT 128 Standard - Use of Clinical Trials Product Description Codes (PDCs) v1.0.1
Category
Standard
Organisation
ICCBBA
ID
ICCBBA ST-022
Type
Standard
Version
1.0.1
Access
Open
Status
Active
Created
November 2022
This document provides guidance on the use of Clinical Trials Product Description Codes (PDCs) and describes the structure of the Clinical Trials PDC Database.
ISBT 128 Standard for base labels v1.0.1
Category
Standard
Organisation
ICCBBA
ID
ICCBBA ST-023
Type
Standard
Version
1.0.1
Access
Open
Status
Active
Created
August 2023
This document provides specifications for base labels that carry ISBT 128 Data Structures. It applies to base labels of containers that are intended to hold medical products of human origin, such as blood and cells.
IHE IT Infrastructure Technical Framework Supplement: Advanced Patient Privacy Consents (APPC) Rev 1.4
Category
Supplementary Resource
Organisation
IHE
Type
Standard
Version
1.4
Access
Open
Status
Trial
Created
July 2021
This profile describes the semantics needed to enable patient consent to be captured, managed and communicated between systems and organisations.
IHE IT Infrastructure Technical Framework Supplement: Asynchronous AS4 Option Rev 1.3
Category
Supplementary Resource
Organisation
IHE
Type
Standard
Version
1.3
Access
Open
Status
Trial
Created
August 2023
This supplement introduces an Asynchronous Web Services (WS) Exchange stack based on the OASIS Applicability Statement 4 (AS4). The AS4 Specification provides a robust option to support cross-border e-health information exchange.
IHE IT Infrastructure Technical Framework Supplement: Care Services Discovery (CSD)
Category
Supplementary Resource
Organisation
IHE
Type
Standard
Access
Open
Status
Trial
Created
September 2016
The CSD Profile supports queries across related directories that contain data about organisations, facilities, services and providers.
IHE IT Infrastructure Technical Framework Supplement: Cross-Community Document Reliable Interchange (XCDR) Rev 1.6
Category
Supplementary Resource
Organisation
IHE
Type
Standard
Version
1.6
Access
Open
Status
Trial
Created
August 2023
This profile introduces the capability to send documents from a source community with enough information to direct the documents through gateways to a designated target community.
IHE IT Infrastructure Technical Framework Supplement: Cross-Community Fetch (XCF) Rev 1.6
Category
Supplementary Resource
Organisation
IHE
Type
Standard
Version
1.6
Access
Open
Status
Trial
Created
July 2019
The Cross-Community Fetch (XCF) Profile defines a single transaction for accessing medical data between gateways that facilitate multiple dimensions of communication.
IHE IT Infrastructure Technical Framework Supplement: Cross-Community Patient Discovery (XCPD) Health Data Locator and Revoke Option Rev 1.3
Category
Supplementary Resource
Organisation
IHE
Type
Standard
Version
1.3
Access
Open
Status
Trial
Created
May 2023
This document adds 2 optional capabilities to the XCPD Profile. The Health Data Locator option locates communities that hold patient-relevant health data. The Revoke option supports the means to indicate a patient match should be revoked.
IHE IT Infrastructure Technical Framework Supplement: Cross-Enterprise Document Workflow Extension for Cross-Community Environment
Category
Supplementary Resource
Organisation
IHE
Type
Standard
Access
Open
Status
Trial
Created
August 2015
This supplement extends the Cross-Enterprise Document Workflow (XDW) Profile with several additions to support the XDW Profile in cross-community environments.
IHE IT Infrastructure Technical Framework Supplement: Document Encryption (DEN) Rev 1.4
Category
Supplementary Resource
Organisation
IHE
Type
Standard
Version
1.4
Access
Open
Status
Trial
Created
July 2019
This supplement provides end-to-end confidentiality to workflows where a document progresses in unanticipated paths, where workflows use many different types of transport, or where workflows involve storage systems such as USB media.
IHE IT Infrastructure Technical Framework Supplement: Extensions to the Document Metadata Subscription (DSUB) Profile Rev 1.5
Category
Supplementary Resource
Organisation
IHE
Type
Standard
Version
1.5
Access
Open
Status
Trial
Created
August 2023
This profile describes a subscription and notification mechanism for use within an XDS (Cross-Enterprise Document Sharing) Affinity Domain and across communities.
IHE IT Infrastructure Technical Framework Supplement: Healthcare Provider Directory (HPD) Rev 1.8
Category
Supplementary Resource
Organisation
IHE
Type
Standard
Version
1.8
Access
Open
Status
Trial
Created
August 2020
This profile describes the minimum foundational attribute set required for defining a provider information directory.
IHE IT Infrastructure Technical Framework Supplement: Internet User Authorization (IUA) Rev 2.3
Category
Supplementary Resource
Organisation
IHE
Type
Standard
Version
2.3
Access
Open
Status
Trial
Created
May 2024
This profile describes the authorisation of network transactions when using HTTP RESTful transports.
IHE IT Infrastructure Technical Framework Supplement: Mobile Alert Communication Management (mACM) Rev 3.1
Category
Supplementary Resource
Organisation
IHE
Type
Standard
Version
3.1
Access
Open
Status
Trial
Created
December 2019
The mACM Profile provides the infrastructure components needed to send short, unstructured text alerts to human recipients, record interactions and provide feedback on alert status.
IHE IT Infrastructure Technical Framework Supplement: Patient Location Tracking (PLT)
Category
Supplementary Resource
Organisation
IHE
Type
Standard
Access
Open
Status
Trial
Created
August 2015
The Patient Location Tracking (PLT) Integration Profile collects patient location information within a single facility, and provides the patient's recently recognised location to other systems.
IHE IT Infrastructure Technical Framework Supplement: Remove Metadata and Documents (RMD) Rev 1.6
Category
Supplementary Resource
Organisation
IHE
Type
Standard
Version
1.6
Access
Open
Status
Trial
Created
August 2023
The Remove Metadata and Documents (RMD) Profile allows for the removal of metadata from the Document Registry and documents from a Document Repository that are no longer required to be discoverable within a patient's care record.
IHE IT Infrastructure Technical Framework Supplement: Restricted Metadata Update (RMU) Rev 1.3
Category
Supplementary Resource
Organisation
IHE
Type
Standard
Version
1.3
Access
Open
Status
Trial
Created
July 2021
The Restricted Metadata Update (RMU) Profile provides a mechanism for changing Document Sharing metadata both within and across community boundaries in a controlled way.
IHE ITI Technical Framework Supplement: XCA Deferred Response Option, XCA Support For Two 2-way Messaging Rev 1.1
Category
Supplementary Resource
Organisation
IHE
Type
Standard
Version
1.1
Access
Open
Status
Trial
Created
August 2019
The Deferred Response Option is needed when the Responding Gateway needs extensive time for processing (days or weeks). This option splits the request and response into 2 separate 2-way exchanges.
IHE IT Infrastructure Technical Framework Supplement: XDS Metadata Update Rev 1.14
Category
Supplementary Resource
Organisation
IHE
Type
Standard
Version
1.14
Access
Open
Status
Trial
Created
August 2023
This supplement updates the XDS (Cross-Enterprise Document Sharing) and XDR (Cross-Enterprise Document Reliable Interchange) Profiles to add support for updating metadata.
IHE IT Infrastructure White Paper: A Service-Oriented Architecture (SOA) View of IHE Profiles
Category
Supplementary Resource
Organisation
IHE
Type
Standard
Access
Open
Status
Active
Created
September 2009
This white paper is for SOA practitioners who want to take advantage of the IHE profiles in their implementations. It shows how IHE profiles can be used in SOA design, and explores issues, challenges and benefits, with examples.
IHE IT Infrastructure White Paper: Enabling Document Sharing Health Information Exchange Using IHE Profiles Rev 2.2
Category
Supplementary Resource
Organisation
IHE
Type
Standard
Version
2.2
Access
Open
Status
Active
Created
May 2024
This white paper provides an overview of the collection of IHE profiles that communities can use for exchanging health information, and shows how the various profiles work together.
IHE IT Infrastructure White Paper: mCSD White Paper Rev 1.1
Category
Supplementary Resource
Organisation
IHE
Type
Standard
Version
1.1
Access
Open
Status
Active
Created
November 2021
This white paper describes some common uses where the Mobile Care Services Discovery (mCSD) Profile can be used to help implementation of services discovery using registries or directories.
IHE IT Infrastructure Technical Framework Supplement: Secure Retrieve (SeR) Rev 2.1
Category
Supplementary Resource
Organisation
IHE
Type
Standard
Version
2.1
Access
Open
Status
Trial
Created
October 2022
The Secure Retrieve Profile defines a mechanism to convey authorisation decisions between actors in the community.
IHE IT Infrastructure White Paper: Access Control
Category
Supplementary Resource
Organisation
IHE
Type
Standard
Access
Open
Status
Active
Created
September 2009
This document is a white paper providing policy recommendations on data sharing and access control in healthcare networks. It includes a policy review, a design methodology for access control systems, and an example use case.
Medicine labels: Guidance on TGO 91 and TGO 92 v2.3
Category
Supplementary Resource
Organisation
TGA
Type
Standard
Version
2.3
Access
Open
Status
Active
Created
March 2021
This document provides extensive guidance for medicine labelling rules TGO 91 and TGO 92. It clarifies and elaborates on the mandatory requirements and provides best practice recommendations for medicine labels.
Therapeutic Goods (Medicines-Standard for Serialisation and Data Matrix Codes) (TGO 106) Order 2021
Category
Standard
Organisation
TGA
ID
F2021L00333
Type
Standard
Access
Open
Status
Active
Created
March 2021
This document is the standard for serialisation and data matrix code use in relation to medicines.
Therapeutic Goods (Standard for Biologicals-Labelling Requirements) (TGO 107) Order 2021
Category
Standard
Organisation
TGA
ID
F2021L01325
Type
Standard
Access
Open
Status
Active
Created
September 2021
This document sets out the labelling requirements for biologicals and human cell and tissue materials.
Therapeutic Goods Order No. 91 - Standard for labels of prescription and related medicines
Category
Standard
Organisation
TGA
ID
F2023C00458 (C03)
Type
Standard
Access
Open
Status
Active
Created
April 2023
This document sets out the labelling requirements for prescription medicines and composite packs containing a subscription medicine. It includes general labelling requirements, information that must be present, information that must be on the main label, and exemptions from the labelling requirements.
Therapeutic Goods Order No. 92 - Standard for labels of non-prescription medicines vC02
Category
Standard
Organisation
TGA
ID
F2023C00456 (C02)
Type
Standard
Version
C02
Access
Open
Status
Active
Created
April 2023
This document sets out the labelling requirements for non-prescription medicines. It includes general labelling requirements, information that must be present, information that must be on the main label, and exemptions from the labelling requirements.
Clinical care for Aboriginal and Torres Strait Islander peoples using aged care services
Category
Standard
Organisation
ACSQHC
Type
Standard
Access
Open
Status
Active
Created
March 2024
This literature review provides recommendations for aged care services to provide high-quality clinical care in a culturally safe and responsive environment for older Aboriginal and Torres Strait Islander people.
Electronic Prescribing
Category
Guideline
Organisation
ADHA
Type
Standard
Access
Open
Status
Active
This guideline outlines steps for software developers who wish to build products that support electronic prescribing.