Health Insurance (Eligible Pathology Laboratories) Determination 2026

Administered by Department of Health, Disability and Ageing

Legislation au F2026L00272 In force Legislative Instrument

Legislation content

EXPLANATORY STATEMENT

 

HEALTH INSURANCE ACT 1973

 

Health Insurance (Eligible Pathology Laboratories) Determination 2026

 

Purpose and operation

 

The Health Insurance (Eligible Pathology Laboratories) Determination 2026 (the 2026 Determination) prescribes categories of accredited pathology laboratories as eligible pathology laboratories.

 

The 2026 Determination repeals and remakes the Health Insurance (Eligible Pathology Laboratories) Determination 2015 (the 2015 Determination). The 2015 Determination sunsets on 1 April 2026.

 

The 2026 Determination maintains the existing approach by prescribing laboratories allocated Category GX (General), Category GY (General) or Category S (Specialised) as eligible pathology laboratories.

 

Authority

 

Subsection 23DBA(1) of the Health Insurance Act 1973 (the Act) provides that the Minister may, by legislative instrument prescribe categories of accredited pathology laboratory for the purposes of the definition of an ‘eligible pathology laboratory’ in subsection 23DA(1) of the Act.

 

Subsection 23DBA(2) of the Act provides that the Minister may do so by applying, adopting or incorporating, with or without modification, the provisions of principles determined by the Minister under section 23DNA of the Act. These are currently, the Health Insurance (Accredited Pathology Laboratories-Approval) Principles 2017 (the Approval Principles).

 

Reliance on subsection 33(3) of the Acts Interpretation Act 1901

 

Under subsection 33(3) of the Acts Interpretation Act 1901, where an Act confers a power to make, grant or issue any instrument of a legislative or administrative character, the power includes a power to repeal, rescind, revoke, amend, or vary the instrument in the same manner and subject to the same conditions.

 

Background

 

Medicare benefits are payable for a pathology service only where the pathology specimen is collected from the patient at a location specified in subsection 16A(5AA) of the Act. One such location is an ‘approved collection centre,’ being a specimen collection centre approved by the Minister under section 23DNBA of the Act.

 

Section 23DNBA of the Act provides that the Minister:

  • may grant an approval to an approved pathology authority to operate an eligible collection centre on premises they own, lease, sub-lease or otherwise occupies, and
  • must determine, by legislative instrument, principles that apply to the granting of approvals of eligible collection centres. These are currently, the Health Insurance (Approvals for Eligible Collection Centres)Principles 2020.

 

Section 23DA of the Act defines an eligible collection centre as a collection centre on premises owned, leased or sub-leased by an approved pathology authority that is also the sole proprietor of at least one eligible pathology laboratory.

 

The 2026 Determination prescribes category GX(General), GY(General) or S(Specialised) accredited pathology laboratories for the definition of eligible pathology laboratory in subsection 23DA(1) of the Act.

 

The approval of premises as an accredited pathology laboratory under section 23DN of the Act specifies the category of accreditation allocated to the premises. These categories, and the criteria applying to them, are set out in section 17 of the Approval Principles, as in force from time to time.

 

Remake of the 2015 Determination and minor amendments

 

The 2026 Determination remakes the 2015 Determination with minor amendments to:

  • update references to the Approval Principles, and
  • exclude the grandfathered category in subsection 5(d) of the 2015 Determination.

 

The excluded provision related to a class of accredited pathology laboratory where:

  • the approved pathology authority, as the sole proprietor of that laboratory, had an arrangement with another approved pathology authority to use a category GX(General) or GY(General) accredited pathology laboratory; and
  • immediately before 1 December 2001, the approved pathology authority operated a collection centre that was in a rural or remote area that was not on the premises of a public hospital.

 

This provision does not align with current policy on the accreditation of pathology laboratories and approval of eligible collection centres.

 

Commencement

 

The 2026 Determination commences on 1 April 2026.

 

Consultation

 

The Department consulted the National Association of Testing Authorities (NATA) as part of its assessment to exclude the 25-year-old grandfathered provision from the 2026 Determination. NATA is the sole independent body responsible for assessing the conformity of laboratory premises with relevant accreditation standards. No broader consultation was completed. This is because the 2026 Determination remakes the sunsetting instrument in substantially the same form, with minor technical changes that are unlikely to affect approved pathology authorities currently operating approved collection centres, or patient access to specimen collection services.


General

 

The 2026 Determination is a legislative instrument for the purposes of the Legislation Act 2003.

 

Details of the 2026 Determination are set out in Attachment A.

 

The 2026 Determination is compatible with the human rights and freedoms recognised or declared under section 3 of the Human Rights (Parliamentary Scrutiny) Act 2011. A full statement of compatibility is set out in Attachment B.


ATTACHMENT A

 

Details of the Health Insurance (Eligible Pathology Laboratories) Determination 2026

Section 1  Name

Section 1 provides that the name of the instrument is the Health Insurance (Eligible Pathology Laboratories) Determination 2026.

Section 2  Commencement

Section 2 provides that the whole of the instrument commences on 1 April 2026.

Section 3  Authority

This section provides that the instrument is made under subsection 23DBA(1) of the Health Insurance Act 1973 (the Act).

Section 4  Schedules

Section 4 provides that the instrument specified in Schedule 1, the Health Insurance (Eligible Pathology Laboratories) Determination 2015 is repealed.

Section 5  Definitions

Section 5 defines key terms used in the instrument. Unless otherwise defined they have the same meaning as in the Act.

The instrument defines the relevant laboratory categories by reference to section 17 of the Health Insurance (Accredited Pathology Laboratories-Approval) Principles 2017, as in force from time to time. This incorporation is permitted by section 14 of the Legislation Act 2003, and that the provisions of the Act are incorporated as in force from time to time.

Section 6  Categories of eligible pathology laboratories

Section 6 prescribes the categories of accredited pathology laboratories for the purposes of the definition of eligible pathology in subsection 23DA(1) of the Act. These are laboratories allocated Category GX(General), Category GY(General) or Category S(Specialised) in the approval of premises as an accredited pathology laboratory given under section 23DN of the Act.


ATTACHMENT B

 

Statement of Compatibility with Human Rights

 

Prepared in accordance with Part 3 of the Human Rights (Parliamentary Scrutiny) Act 2011

 

Health Insurance (Eligible Pathology Laboratories) Determination 2026

 

This disallowable legislative 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.

 

Overview of the Disallowable Legislative Instrument

 

The Health Insurance (Eligible Pathology Laboratories) Determination 2026 (the 2026 Determination) remakes the Health Insurance (Eligible Pathology Laboratories) Determination 2015 (the 2015 Determination) which sunsets on 1 April 2026.

 

It prescribes categories of ‘accredited pathology laboratory’ for the purpose of the definition  of an ‘eligible pathology laboratory’ in subsection 23DA(1) of the Health Insurance Act 1973 (the Act).

 

Subsection 16A(5AA) of the Act provides that Medicare benefits are payable for pathology services rendered where, pathology specimens are collected in an ‘approved collection centre,’ or in other specified circumstances.

 

Section 23DNBA of the Act provides that the Minister may grant an approval to an approved pathology authority to operate an ‘eligible collection centre’ on premises owned, leased or otherwise occupied by the approved pathology authority. Once approved, an eligible collection centre becomes an approved collection centre.

 

Subsection 23DA(1) of the Act provides that an eligible collection centre is a collection centre on premises owned, leased or sub-leased by an approved pathology authority that is also the sole proprietor of at least one eligible pathology laboratory. Section 23DBA of the Act empowers the Minister, by determination in writing, to prescribe categories of accredited pathology laboratory for the purposes of the definition of an eligible pathology laboratory.

 

The 2026 Determination prescribes the categories of accredited pathology laboratories for the purposes of the definition of eligible pathology in subsection 23DA(1) of the Act. These are laboratories allocated category GX(General), GY(General) or S(Specialised) in the approval of premises as an accredited pathology laboratory given under section 23DN of the Act.

To align with the current policy for the accreditation of pathology laboratories and the approval of eligible collection centres, the 2026 Determination removes the grandfathered provision in subsection 5(d) of the 2015 Determination. The removed provision related to a class of accredited pathology laboratory in respect of which the approved pathology authority operated a collection centre:

  • in a rural or remote area that was not on the premises of a public hospital; and
  • before 1 December 2001.

 

Human rights implications

 

The 2026 Determination does not engage any of the applicable human rights or freedoms. It prescribes categories of accredited pathology laboratories that are eligible pathology laboratories.

 

It aligns with current policy for the accreditation of pathology laboratories and approval of eligible collection centres. It will not affect patient access to Medicare eligible pathology services.

 

Conclusion

 

The 2026 Determination  is compatible with human rights as it does not raise any human rights issues.

 

 

Mark Butler

Minister for Health and Ageing

 

Overview

The Health Insurance (Eligible Pathology Laboratories) Determination 2026 was enacted to address the need for updated criteria regarding the categories of accredited pathology laboratories that are eligible to provide pathology services under the Health Insurance Act 1973. The Determination, made under the authority of subsection 23DBA(1) of the Act, replaces the 2015 version and introduces minor amendments to align with current policy. The Minister for Health and Ageing, Mark Butler, asserts that the 2026 Determination is compatible with human rights as it does not adversely impact patient access to Medicare-eligible pathology services. The primary objective of this legislative instrument is to ensure that only those pathology laboratories meeting the specified criteria can claim Medicare benefits, thus maintaining the integrity and effectiveness of the healthcare system. The Determination was introduced by the Australian Government, specifically the Department of Health, following consultation with the National Association of Testing Authorities (NATA). The 2026 version removes a grandfathered provision from the 2015 Determination that no longer aligns with current policy on laboratory accreditation and collection centre approval. This change ensures that the criteria for eligibility remain consistent with contemporary standards and operational requirements. The instrument will come into effect on 1 April 2026, replacing the 2015 Determination, which sunsets on the same date.

Scope and Application

The Health Insurance (Eligible Pathology Laboratories) Determination 2026 (the 2026 Determination) applies to accredited pathology laboratories that are classified as eligible pathology laboratories for the purposes of the Health Insurance Act 1973 (the Act). The 2026 Determination specifies that only pathology laboratories allocated Category GX (General), Category GY (General), or Category S (Specialised) are eligible under the Act. The 2026 Determination has a national jurisdictional reach as it is a legislative instrument made under the authority of the Commonwealth of Australia. The Act extends its application through subordinate instruments, specifically the Health Insurance (Accredited Pathology Laboratories-Approval) Principles 2017, which detail the criteria for accreditation and approval. The 2026 Determination repeals and remakes the 2015 Determination, with minor amendments excluding a grandfathered category that no longer aligns with current policy. It will commence on 1 April 2026, ensuring that only those laboratories meeting the specified criteria will qualify for Medicare benefits, thus maintaining alignment with current health policies and ensuring continued access to pathology services for patients.

Key Provisions

The Health Insurance (Eligible Pathology Laboratories) Determination 2026 (the 2026 Determination) sets out the categories of accredited pathology laboratories that are recognised as eligible pathology laboratories under the Health Insurance Act 1973 (the Act). The 2026 Determination, which replaces the Health Insurance (Eligible Pathology Laboratories) Determination 2015, specifies that eligible pathology laboratories include those that have been allocated Category GX (General), Category GY (General), or Category S (Specialised) accreditation (Section 6). The authority to make this determination is provided under subsection 23DBA(1) of the Act, which empowers the Minister to prescribe categories of accredited pathology laboratories for the purposes of defining an eligible pathology laboratory (Section 3). The 2026 Determination imposes obligations on accredited pathology laboratories to meet the criteria for their specified category of accreditation. This includes maintaining compliance with the Health Insurance (Accredited Pathology Laboratories-Approval) Principles 2017, which outline the standards and requirements for laboratory accreditation (Section 17 of the Approval Principles). Approved pathology authorities, which are entities that operate eligible pathology laboratories, must ensure that their laboratories meet the necessary accreditation standards to qualify as eligible pathology laboratories. This includes adhering to the specific criteria for their allocated category of accreditation, as determined by the Minister under section 23DN of the Act. Breaches of the provisions outlined in the 2026 Determination may result in civil or administrative penalties under the Act. The specific penalties for non-compliance would depend on the nature and severity of the breach, as well as any relevant guidelines or regulations issued by the Minister. However, the 2026 Determination itself does not explicitly outline the penalties for non-compliance. It is important for accredited pathology laboratories and approved pathology authorities to familiarise themselves with the relevant legislation and guidelines to ensure compliance with the requirements of the 2026 Determination. The 2026 Determination is compatible with the human rights and freedoms recognised or declared under section 3 of the Human Rights (Parliamentary Scrutiny) Act 2011. A full statement of compatibility is set out in Attachment B of the explanatory statement. The compatibility assessment concludes that the 2026 Determination does not engage any of the applicable human rights or freedoms, as it prescribes categories of accredited pathology laboratories that are eligible pathology laboratories in alignment with current policy for the accreditation of pathology laboratories and approval of eligible collection centres. The 2026 Determination is also 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.

Legal classification tags

Area of Law
Health Law
Instrument
Legislative Instrument
Concepts
Definitions & Interpretation
Repeal & Amendment
Licensing & Registration

Interactions

Authorises

All Versions

Sourced from the Federal Register of Legislation at 26 August 2026. For the latest information on Australian Government law please go to https://www.legislation.gov.au.