Statement of Principles concerning haemochromatosis No. 21 of 2012

Administered by Department of Veterans' Affairs

Legislation au F2012L00450 Not in force Legislative Instrument

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REPATRIATION MEDICAL AUTHORITY

 

INSTRUMENT NO. 21 of 2012

 

VETERANS’ ENTITLEMENTS ACT 1986

MILITARY REHABILITATION AND COMPENSATION ACT 2004

 

EXPLANATORY NOTES FOR TABLING

 

 

  1. The Repatriation Medical Authority (the Authority), under subsection 196B(8) of the Veterans' Entitlements Act 1986 (the VEA), revokes Instrument No. 5 of 1997, determined under subsection 196B(2) of the VEA concerning haemochromatosis.

 

2.             The Authority is of the view that there is sound medical-scientific evidence that indicates that haemochromatosis and death from haemochromatosis can be related to particular kinds of service.  The Authority has therefore determined pursuant to subsection 196B(2) of the VEA a Statement of Principles, Instrument No. 21 of 2012 concerning haemochromatosis.  This Instrument will in effect replace the revoked Statement of Principles.

 

3.             The provisions of the Military Rehabilitation and Compensation Act 2004 (the MRCA) relating to claims for compensation commenced on 1 July 2004.  Claims under section 319 of the MRCA for acceptance of liability for a service injury sustained, a service disease contracted or service death on or after 1 July 2004 are determined by the Military Rehabilitation and Compensation Commission by reference to Statements of Principles issued by the Authority pursuant to the VEA.

 

4.             The Statement of Principles sets out the factors that must as a minimum exist, and which of those factors must be related to the following kinds of service rendered by a person:

 

 operational service under the VEA;

 peacekeeping service under the VEA;

 hazardous service under the VEA;

 British nuclear test defence service under the VEA;

 warlike service under the MRCA;

 non-warlike service under the MRCA,

 

before it can be said that a reasonable hypothesis has been raised connecting haemochromatosis or death from haemochromatosis, with the circumstances of that service.

 

5.             This Instrument results from an investigation notified by the Authority in the Government Notices Gazette of 25 June 2008 concerning haemochromatosis in accordance with section 196G of the VEA.  The investigation involved an examination of the sound medical-scientific evidence now available to the Authority, including the sound medical-scientific evidence it has previously considered.

 

6.             The contents of this Instrument are in similar terms as the revoked Instrument.  Comparing this Instrument and the revoked Instrument, the differences include:

 

  • adopting the latest revised Instrument format, which commenced in 2005;
  • deleting the ICD code from the Instrument header;
  • revising the definition of 'haemochromatosis' in clause 3;
  • revising factor 6(a) concerning 'consuming alcohol' for males;
  • revising factor 6(b) concerning 'consuming alcohol' for females;
  • new factor 6(c) concerning 'hepatitis C virus' for clinical worsening only;
  • new factor 6(d) concerning 'chronic blood transfusional overload' for clinical worsening only;
  • new definitions of 'alcohol', 'chronic blood transfusional overload', 'death from haemochromatosis', 'ICD-10-AM code' and 'terminal event' in clause 9;
  • revising the definition of 'relevant service' in clause 9;
  • deleting definitions of 'alcohol (contained within alcoholic drinks)' and 'ICD code'; and
  • specifying a date of effect for the Instrument in clause 11.

 

7.             Further changes to the format of the Instrument reflect the commencement of the MRCA and clarify that pursuant to subsection 196B(3A) of the VEA, the Statement of Principles has been determined for the purposes of both the VEA and the MRCA.

 

8.             Prior to determining this Instrument, the Authority advertised its intention to undertake an investigation in relation to haemochromatosis in the Government Notices Gazette of 25 June 2008, and circulated a copy of the notice of intention to investigate to a wide range of organisations representing veterans, service personnel and their dependants.  The Authority invited submissions from the Repatriation Commission, organisations and persons referred to in section 196E of the VEA, and any person having expertise in the field.  No submissions were received for consideration by the Authority during the investigation.

 

9.             This instrument is compatible with the Human Rights and Freedoms recognised or declared in the International Instruments listed in Section 3 of the Human Rights (Parliamentary Scrutiny Act 2011).

 

10.         The determining of this Instrument finalises the investigation in relation to haemochromatosis as advertised in the Government Notices Gazette of 25 June 2008.

 


11.         A list of references relating to the above condition is available to any person or organisation referred to in subsection 196E(1)(a) to (c) of the VEA.  Any such request must be made in writing to the Repatriation Medical Authority at the following address:

 

The Registrar

Repatriation Medical Authority Secretariat

GPO Box 1014

BRISBANE    QLD    4001

Overview

The Repatriation Medical Authority Instrument No. 21 of 2012, enacted under the Veterans' Entitlements Act 1986 and the Military Rehabilitation and Compensation Act 2004, addresses the problem of clarifying the relationship between haemochromatosis, a genetic disorder causing iron overload in the body, and military service. The Authority, acting under subsection 196B(2) of the VEA, established a Statement of Principles to determine the minimum factors required to link haemochromatosis to specific types of military service. This Instrument revokes the previous Statement of Principles, Instrument No. 5 of 1997, and incorporates the latest medical-scientific evidence available. It aims to ensure that claims for compensation related to haemochromatosis are assessed consistently and fairly, aligning with the provisions of the MRCA for claims commencing on or after 1 July 2004. The Authority conducted an investigation, advertised in the Government Notices Gazette on 25 June 2008, and determined the Instrument based on the available evidence, while ensuring compatibility with human rights standards.

Scope and Application

The Repatriation Medical Authority Instrument No. 21 of 2012, concerning haemochromatosis, applies to veterans and service personnel under the Veterans' Entitlements Act 1986 (VEA) and the Military Rehabilitation and Compensation Act 2004 (MRCA). Specifically, it governs claims for compensation relating to service injuries, diseases, and deaths on or after 1 July 2004, focusing on the connection between haemochromatosis or death from haemochromatosis and certain types of service, such as operational, peacekeeping, hazardous, British nuclear test defence, warlike, and non-warlike service. The Instrument revokes the previous Statement of Principles from 1997 and provides a new framework for determining these claims, detailing the medical and scientific factors that must exist to establish a connection. This Instrument is applicable nationally, with its provisions extending to all veterans and service personnel across Australia. While it does not specify any exclusions or thresholds, the determination of liability for compensation claims will still require a detailed examination of individual cases to ensure the criteria outlined in the Instrument are met.

Key Provisions

The key sections of the Repatriation Medical Authority Instrument No. 21 of 2012, issued under the Veterans' Entitlements Act 1986 (VEA) and the Military Rehabilitation and Compensation Act 2004 (MRCA), primarily revolve around the establishment of a Statement of Principles concerning haemochromatosis. This Statement of Principles outlines the factors that must exist to connect haemochromatosis or death from haemochromatosis with specific types of military service, such as operational, peacekeeping, hazardous, and nuclear test defence service under the VEA, as well as warlike and non-warlike service under the MRCA (Section 4). The instrument replaces the previously revoked Instrument No. 5 of 1997 and adopts a revised format, aligning with more recent standards and omitting certain outdated definitions and codes (Section 6). Furthermore, it specifies a date of effect and clarifies the applicability of the Statement of Principles for both the VEA and the MRCA (Section 7). The obligations and requirements imposed by this Act are primarily directed towards the Repatriation Medical Authority (the Authority), which must determine the Statement of Principles concerning haemochromatosis based on sound medical-scientific evidence. The Authority must ensure that the Statement of Principles is compatible with human rights and freedoms as recognised in international instruments (Section 9). Additionally, the Authority is required to advertise its intention to investigate and solicit submissions from relevant parties, although it is noted that no submissions were received for this particular investigation (Section 8). The Authority also has the responsibility to provide references relating to the condition upon written request (Section 11). Breaches of the provisions outlined in the Act may not explicitly state specific penalties or consequences within the text provided. However, under the broader legislative frameworks of the VEA and the MRCA, there are potential civil and criminal penalties for non-compliance or misuse of the entitlements provided. Typically, these penalties may include fines or imprisonment for fraudulent claims or misrepresentations. The exact penalties would be determined in accordance with the relevant sections of the VEA and the MRCA, although the maximum penalties are not specified in the text provided.

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