National Health Act 1953 - Amendment special arrangements under subsection 100(1) - Highly Specialised Drugs Program (No. PB 10 of 2010)

Administered by Department of Health, Disability and Ageing

Legislation au F2010L00543 Not in force Legislative Instrument

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EXPLANATORY STATEMENT

NATIONAL HEALTH ACT 1953

AMENDMENT SPECIAL ARRANGEMENTS – HIGHLY SPECIALISED DRUGS PROGRAM FOR PUBLIC HOSPITALS 

INSTRUMENT NUMBER PB 10 of 2010

Purpose and operation

Part VII of the National Health Act 1953 (the Act) is the legislative basis of the Pharmaceutical Benefits Scheme (PBS) by which the Commonwealth provides reliable, timely, and affordable access to a wide range of medicines for all Australians.

Subsection 85(1) provides that benefits are to be provided by the Commonwealth in accordance with Part VII in respect of pharmaceutical benefits.

Drugs and medicinal preparations to which Part VII applies are (with the exception of some medicinal preparations with additives) declared by the Minister by legislative instrument to be so under subsection 85(2). These are listed drugs as defined in subsection 84(1).

Subsection 100(1) of the Act provides that the Minister may make special arrangements for providing that an adequate supply of special pharmaceutical products will be available to persons:                

(a) who are living in isolated areas; or

(b) who are receiving medical treatment in such circumstances that pharmaceutical benefits: 

(i) cannot be conveniently or efficiently supplied in accordance with Part VII of the Act; or

(ii) are inadequate for that medical treatment.

Subsection 100(2) of the Act provides that the Minister may vary or revoke a special arrangement made under subsection 100(1).

Subsection 100(3) provides that Part VII of the Act has effect subject to a special arrangement made under subsection 100(1).

The declaration made under subsection 85(2) of the Act sets out the drugs and medicinal preparations to which Part VII of the Act applies.  Under subsection 100AA(1)(c) a special pharmaceutical product, for which special arrangements may be made under section 100, includes a drug or medicinal preparation declared under subsection 85(2) of the Act.  Schedule 6 of the declaration under subsection 85(2) lists those drugs and medicinal preparations that may be made available under arrangements provided for by section 100 of the Act.

 

The Highly Specialised Drugs Program for public hospitals is a set of Arrangements made under subparagraph 100(1) of the Act for the purpose of providing that an adequate supply of special pharmaceutical products will be available to persons who are receiving treatment with highly specialised drugs at public hospitals as non-admitted patients, day admitted patients or patients on discharge.

 

This legislative instrument amends the Arrangements made under subparagraph 100(1)

(PB 125 of 2009) which came into effect on 1 January 2010.  The amendments are set out in the items of Schedule 1 to the instrument.

 

A provision-by-provision description of the instrument is contained in the Attachment.

 

This instrument, expressed to commence on 1 March 2010, was made on 23 February 2010.

Consultations

The Pharmaceutical Benefits Advisory Committee (PBAC) is the independent expert body, established by section 100A of the Act, which makes recommendations to the Minister for Health and Ageing about which drugs and medicinal preparations should be available as pharmaceutical benefits.  Under subsection 101(4) of the Act, a drug or medicinal preparation may not be declared to be a drug or medicinal preparation to which Part VII of the Act applies unless the PBAC has recommended that it be so declared.  When recommending a medicine be listed on the PBS, the PBAC takes into account the medical conditions for which the medicine has been approved for use in Australia, its clinical effectiveness, safety and cost-effectiveness compared with other treatments.

PBAC members are selected from consumers, health economists, practising community pharmacists, general practitioners, clinical pharmacologists and specialists, with at least one member selected from each of those interests or professions.  Remaining members are persons whom the Minister is satisfied have qualifications and experience in a field relevant to the functions of the PBAC, and that would enable them to contribute meaningfully to the deliberations of the PBAC.

The Commonwealth/State Highly Specialised Drugs Working Party (HSDWP) is a non-statutory body established by the Australian Health Ministers Advisory Council (AHMAC).  The HSDWP makes recommendations to the PBAC on the suitability of certain drugs for listing under the Highly Specialised Drugs Program.  The HSDWP considers the funding and administrative aspects of supply through the hospital system, and a recommendation for listing must be supported by a majority of Working Party members.  The HSDWP consists of representatives from State and Territory Health Departments and the Australian Private Hospitals Association, and is chaired by a representative of the Commonwealth Department of Health and Ageing.

 


ATTACHMENT

Paragraph 1:  provides that this instrument commences on 1 March 2010.

Paragraph 2:  provides that Schedule 1 amends PB 125 of 2009.

Schedule 1: provides for the following amendments: 

 

SCHEDULE 1

Alteration of Circumstances

Infliximab

[addition of the drug ustekinumab to the list of interchangeable biological agents for the treatment of severe chronic plaque
psoriasis and amendment of definition of Biological Treatment Cycle]

 

SCHEDULE 2

Deletion of Form

Epoetin Beta

Injection 1,000 units in 0.3 mL pre-filled syringe

Alteration of Brand

Thalidomide

Capsule 50 mg

From:

Thalidomide Pharmion

To:

Thalomid

 

 

 

 

Overview

The National Health Act 1953 was enacted to establish and regulate the Pharmaceutical Benefits Scheme (PBS), which ensures access to affordable and reliable medicines for all Australians. The Act was amended in 2010 through the instrument F2010L00543 to address the gap in providing adequate supplies of highly specialised drugs to patients receiving treatment in public hospitals. This amendment, introduced by the Parliament of Australia, aimed to enhance the availability of special pharmaceutical products under the PBS for patients in public hospitals who require highly specialised drugs not conveniently or efficiently supplied under the standard provisions of the Act. The policy objective was to ensure that these patients receive necessary medications that are not readily available under the general PBS arrangements, thereby improving healthcare outcomes for those with specific medical needs.

Scope and Application

The National Health Act 1953, as amended by the legislative instrument F2010L00543, pertains to the Highly Specialised Drugs Program for public hospitals, which ensures an adequate supply of special pharmaceutical products for patients in public hospitals receiving treatment with highly specialised drugs. This Act applies to individuals receiving treatment for specific conditions in public hospitals, thereby extending its reach to a subset of the population requiring specialised medical care not readily available under the standard Pharmaceutical Benefits Scheme (PBS). The amendments outlined in this instrument came into effect on 1 March 2010 and modify the arrangements initially established on 1 January 2010, specifically concerning the interchangeability of certain biological agents and adjustments to drug branding and forms. The Commonwealth Minister for Health and Ageing has the authority to make these special arrangements and may vary or revoke them as necessary, ensuring flexibility in the provision of pharmaceutical benefits under the Act.

Key Provisions

The key provisions of the legislative instrument (F2010L00543) primarily concern amendments to the Highly Specialised Drugs Program for public hospitals under the National Health Act 1953. The instrument, which came into effect on 1 March 2010, amends the previously established arrangements (PB 125 of 2009) to improve the availability and interchangeability of highly specialised drugs in public hospitals (sections 1 and 2). It introduces specific changes to the list of drugs covered under the program, including the addition of ustekinumab for the treatment of severe chronic plaque psoriasis and the amendment of the definition of a Biological Treatment Cycle (Schedule 1, item 1). Furthermore, it modifies the brand name of Thalidomide from Thalidomide Pharmion to Thalomid (Schedule 1, item 2). Under this legislation, the obligations imposed on the relevant parties primarily revolve around ensuring that the amendments to the Highly Specialised Drugs Program are implemented effectively. This includes updating the list of interchangeable biological agents and ensuring that the new definitions and brand names are accurately reflected in all relevant documentation and systems. The Minister for Health and Ageing is responsible for ensuring that these amendments are made and that they align with the overall objectives of providing reliable, timely, and affordable access to highly specialised drugs for patients in public hospitals (sections 100(1) and 100(3)). The Pharmaceutical Benefits Advisory Committee (PBAC) and the Commonwealth/State Highly Specialised Drugs Working Party (HSDWP) play crucial roles in recommending which drugs should be included in the program and ensuring that their inclusion is based on clinical effectiveness, safety, and cost-effectiveness. Failure to comply with the provisions of this legislation could result in legal consequences. While the specific penalties for non-compliance are not detailed in the explanatory statement, breaches of the National Health Act 1953 can generally lead to civil or criminal penalties. For example, under section 122 of the Act, a person who contravenes a provision of the Act can be subject to fines, imprisonment, or both, depending on the severity of the offence. The maximum penalties can vary significantly depending on the specific provision breached, but they can include substantial fines and/or imprisonment for up to five years for serious offences. Ensuring adherence to the amended arrangements is therefore critical to avoid these potential consequences.

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