Statement of Principles concerning photocontact dermatitis No. 108 of 2011

Administered by Department of Veterans' Affairs

Legislation au F2011L01741 Not in force Legislative Instrument

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REPATRIATION MEDICAL AUTHORITY

 

INSTRUMENT NO. 108 of 2011

 

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. 63 of 1997, determined under subsection 196B(2) of the VEA concerning photocontact dermatitis.

 

2.             The Authority is of the view that there is sound medical-scientific evidence that indicates that photocontact dermatitis and death from photocontact dermatitis 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. 108 of 2011 concerning photocontact dermatitis.  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;

 warlike service under the MRCA;

 non-warlike service under the MRCA,

 

before it can be said that a reasonable hypothesis has been raised connecting photocontact dermatitis or death from photocontact dermatitis, 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 photocontact dermatitis 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 'photocontact dermatitis' in clause 3;
  • revising factors 6(a) & 6(d) concerning 'exposure of the affected area of skin to a phototoxic agent and light simultaneously';
  • revising factor 6(b) & 6(e) concerning 'exposure of the affected area of skin to a photoallergen and light simultaneously';
  • new factor 6(c) concerning 'exposure to the photoallergen responsible for the photocontact dermatitis and to light' for allergic photocontact dermatitis only;
  • new definitions of 'death from photocontact dermatitis', 'ICD-10-AM code' and 'terminal event' in clause 9;
  • revising definition of 'relevant service' in clause 9;
  • deleting definitions of 'ICD code', 'photoallergic contact dermatitis' and 'phototoxic contact dermatitis'; 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 photocontact dermatitis 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.             The determining of this Instrument finalises the investigation in relation to photocontact dermatitis as advertised in the Government Notices Gazette of 25 June 2008.


10.         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. 108 of 2011, issued under the Veterans' Entitlements Act 1986, was enacted to address the gap in the existing medical-scientific evidence concerning photocontact dermatitis and its relation to specific service conditions. This Instrument revokes the previous Statement of Principles, Instrument No. 63 of 1997, and establishes a new set of principles for determining liability for photocontact dermatitis and related deaths in veterans. The Instrument aims to ensure that the latest medical-scientific evidence is considered in assessing claims, and it reflects the revised Instrument format and definitions that align with the commencement of the Military Rehabilitation and Compensation Act 2004. The Authority, having reviewed the available evidence and consulted with relevant parties, determined that there is a sound basis for linking photocontact dermatitis to particular types of service, thus providing a clearer framework for processing claims.

Scope and Application

The Repatriation Medical Authority Instrument No. 108 of 2011, under the Veterans' Entitlements Act 1986 (VEA) and the Military Rehabilitation and Compensation Act 2004 (MRCA), outlines a Statement of Principles concerning photocontact dermatitis, replacing the previously revoked Instrument No. 63 of 1997. This Instrument applies to veterans and service personnel who have contracted photocontact dermatitis or died from it during or as a result of their service, specifically operational, peacekeeping, hazardous, warlike, or non-warlike service as defined by the VEA and MRCA. The Instrument determines the minimum factors required to establish a reasonable hypothesis connecting photocontact dermatitis or death from it with the service circumstances. It applies to claims for compensation for service injuries, diseases, or deaths occurring on or after 1 July 2004, which are assessed by the Military Rehabilitation and Compensation Commission. The Authority's determination is based on sound medical-scientific evidence, and the Instrument has been revised to adopt a new format, update definitions, and clarify its application under both the VEA and the MRCA.

Key Provisions

The Repatriation Medical Authority Instrument No. 108 of 2011 under the Veterans' Entitlements Act 1986 (VEA) and the Military Rehabilitation and Compensation Act 2004 (MRCA) establishes new Statement of Principles concerning photocontact dermatitis. This Instrument revokes the previous Instrument No. 63 of 1997 (subsection 196B(8) of the VEA). It details the minimum factors that must exist, and which of those factors must be related to specific service types, to establish a connection between photocontact dermatitis or death from photocontact dermatitis and service circumstances (subsection 196B(2) of the VEA). This includes operational, peacekeeping, and hazardous service under the VEA, and warlike and non-warlike service under the MRCA. The Statement of Principles sets out obligations for claimants to provide evidence linking their condition to their service. For instance, claimants must demonstrate exposure to a phototoxic agent and light simultaneously or a photoallergen and light simultaneously, depending on the type of photocontact dermatitis. Additionally, for allergic photocontact dermatitis, claimants must show exposure to the photoallergen responsible and to light. These obligations are crucial for the Military Rehabilitation and Compensation Commission to determine claims for compensation under section 319 of the MRCA. Non-compliance with the requirements set forth in the Statement of Principles can lead to claims being denied. Specifically, if a claimant fails to provide adequate evidence of the necessary factors, their claim may be rejected. This can result in the denial of compensation for service injuries, diseases, or deaths that would otherwise be covered under the VEA or MRCA. There are no specific offences or penalties mentioned in the document for failing to comply with the requirements, but the consequences are the denial of claims and thus the loss of potential compensation. The Authority's decision to determine this Instrument concludes the investigation into photocontact dermatitis, which was announced in the Government Notices Gazette on 25 June 2008. The Authority considered sound medical-scientific evidence in making this determination. This new Instrument provides clarity and updates the previous guidelines, ensuring that claimants and the Commission have the most current information to assess claims accurately. The Authority's decision is final, and claimants must adhere to the new Statement of Principles to seek compensation for photocontact dermatitis related to their service.

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