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Vendor Neutral Archives (VNA)

This content is draft for consultation. 

 

Definition:

Medical imaging technology that provides a centralised storage solution for medical images and associated data. Its standard format and interface allows it to be accessed in a vendor-neutral manner by other systems. 

Standards and specifications

General requirements

Cyber security

The software must demonstrate ability to effectively achieve mitigation strategies in line with ‘Essential 8’.

Privacy

Data collected about an individual by medical software is likely to constitute health information. Due to the sensitive nature of this information, it generally has a higher degree of privacy protection than other personal information, under relevant federal, state and territory legislations.

The software must demonstrate adherence to relevant federal, state or territory privacy legislation for example, the Privacy Act 1988 (Federal) or Health Records and Information Privacy Act 2002 (NSW).

The applicable federal legislation is the Privacy Act 1988.

Details of the relevant state and territory legislations are contained under the State and territory requirements section below.

Core requirements

Standards for identification

The software must:  

  • be able to discover and validate Individual Healthcare Identifiers (IHI) via the Healthcare Identifier (HI) Service Business-2-Business web services
  • utilise Individual Healthcare Identifiers (IHIs) to integrate and link records into the local patient record
  • support adherence to Patient Identification best practices as outlined by the Australia Commission on Safety and Quality in Health Care.

Australian Core Data for Interoperability (AUCDI)

The software should support the use of AUCDI Release 1.

Note: The focus of the AUCDI Release 1 is the representation of the clinical content necessary for each of the data groups identified within the Release 1 scope.

Development is continuing to enhance AUCDI.

Standards for data sharing

The software should:

  • support the DICOM standard
  • support the consumption of clinical documents in Fast Healthcare Interoperability Resources (FHIR®) formats.
  • capable of using HL7 FHIR-compliant API when sending clinical information.
  • should be capable of using HL7 FHIR-compliant API when receiving clinical information.

Standards for terminology, code sets and classifications

The system must:

  • support Systematised Nomenclature of Medicine-Clinical Terms AU (SNOMED CT-AU)
  • support Logical Observation Identifiers Names and Codes (LOINC®).

The system should:

  • support person and provider identification in healthcare National Best Practice Data Set.

National Safety and Quality Health Service (NSQHS) Standards

Implementation of NSQHS is mandated in all hospitals, day procedure services and public dental services across Australia.

The system must:  

  • support adherence to best practices related to Informed Consent  
  • support adherence to all relevant National Safety and Quality Health Service Standards in accordance with the intended scope of the system being procured. These may include, but not limited to the following standards:  
    • Partnering with Consumers Standard
    • Communicating for Safety Standard
    • Comprehensive Care Standard
    • Blood Management Standard
    • Medication Safety Standard
    • Clinical Governance Standard.
  • support adherence to all relevant Clinical Care Standards.  

Other Standards

National

The system should:

Connections to National Systems

HI Service

If the software is expected to deal with healthcare identifiers (e.g. in a hospital environment) then it must either:

  • be able to discover and validate Individual Healthcare Identifiers (IHI) via the Healthcare Identifier (HI) Service, or

Where the enterprise utilises an enterprise wide system for discover and validation of Individual Healthcare Identifiers (IHI) the software must:  

  • be able to manage and interface with this middleware in order to enable discovery and validation of Individual Healthcare Identifiers (IHI).

My Health Record

The software must:

  • be able to respect patient instruction not to upload at a patient and document level when contributing clinical information to the My Health Record system
  • be able to access record information from the My Health Record as required
  • be able to upload an Event Summary to the My Health Record system, if required
  • support patient instruction not to upload.

Note: If the system is not connecting to My Health Record, then My Health Record requirements above can be removed.

Conformance

The software must:

  • have production access to the My Health Record
  • have production access to the Health Identifiers Service.

State and territory requirements

The following state and territory requirements must be upheld based on location.

Date last updated: 20 January 2025