National Health Act 1953 - Amendment special arrangements under subsection 100(1) - Highly Specialised Drugs Program (No. PB 55 of 2008)

Administered by Department of Health, Disability and Ageing

Legislation au F2008L01390 Not in force Legislative Instrument

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EXPLANATORY STATEMENT

INSTRUMENT NUMBER PB 55 of 2008

NATIONAL HEALTH ACT 1953

AMENDMENT SPECIAL ARRANGEMENTS UNDER SUBSECTION 100(1)

HIGHLY SPECIALISED DRUGS PROGRAM

 

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 and the restrictions, if any, that apply to the prescribing of such drugs and medicinal preparations as pharmaceutical benefits. 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 is a set of Arrangements made under subparagraph 100(b)(i) 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 private hospitals as non-admitted patients, day admitted patients or patients on discharge.

This legislative instrument amends the Arrangements made under subparagraph 100(b)(i) (PB 92 of 2007) which came into effect on 1 December 2007.  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 June 2008, was made on 1 May 2008.

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 June 2008.

Paragraph 2:  provides that Schedule 1 amends PB 92 of 2007.

Schedule 1: provides for the following amendments: 

 

SCHEDULE 1

Alteration of Circumstances

Tacrolimus

 

SCHEDULE 2

Deletion of Form

Apomorphine

Injection containing apomorphine hydrochloride 10 mg in 1 mL

 

Addition of Brand

Apomorphine

Injection containing apomorphine hydrochloride 20 mg in 2 mL (Apomine)

 

Overview

The National Health Act 1953, as amended by the instrument F2008L01390, aims to address the gap in providing reliable, timely, and affordable access to highly specialised drugs for Australians receiving treatment in private hospitals. This Act, enacted by the Commonwealth Parliament, establishes the legislative framework for the Pharmaceutical Benefits Scheme (PBS), which is overseen by the Minister for Health and Ageing. The primary policy objective of this amendment is to ensure that an adequate supply of highly specialised drugs is available to patients who are receiving treatment in private hospitals as non-admitted, day admitted, or discharged patients, where the standard provisions of the PBS are inadequate or cannot be efficiently applied. This legislative instrument, which came into effect on 1 June 2008, amends the previous arrangements made under the Act to include specific drugs such as Tacrolimus and Apomorphine under the Highly Specialised Drugs Program, thereby expanding the scope of treatments available through this initiative.

Scope and Application

The National Health Act 1953, specifically under Part VII, forms the legislative foundation for the Pharmaceutical Benefits Scheme (PBS), ensuring Australians have access to a broad range of affordable and timely medicines. The Act allows the Minister to declare which drugs and medicinal preparations are covered under the PBS through legislative instruments, listing them as pharmaceutical benefits. The Act's application extends to providing special arrangements under subsection 100(1) for individuals in isolated areas or receiving medical treatment where standard PBS provisions are inadequate, thereby ensuring an adequate supply of necessary pharmaceutical products. The Highly Specialised Drugs Program, established under this Act, specifically caters to patients receiving highly specialised drug treatments in private hospitals, ensuring these patients receive the necessary medications despite the unique challenges of their treatment circumstances. This instrument, effective from 1 June 2008, amends the existing arrangements, reflecting changes in the Highly Specialised Drugs Program as recommended by the Pharmaceutical Benefits Advisory Committee and the Commonwealth/State Highly Specialised Drugs Working Party.

Key Provisions

The main operative sections of this legislation (sections 100(1) and 100(3)) establish the framework for the Highly Specialised Drugs Program, which is a provision under the National Health Act 1953, designed to ensure that an adequate supply of special pharmaceutical products is available to certain individuals. Specifically, section 100(1) allows the Minister for Health to make special arrangements for providing such pharmaceutical products to individuals living in isolated areas or those receiving medical treatment where conventional pharmaceutical benefits are inadequate or cannot be efficiently supplied under the existing scheme. Section 100(3) further clarifies that the operation of the Pharmaceutical Benefits Scheme under Part VII of the Act is subject to any special arrangements made under section 100(1). These provisions impose several obligations and requirements on the relevant parties. For instance, the Minister must ensure that the special arrangements meet the needs of individuals in isolated areas or those receiving highly specialised treatments. Additionally, the Pharmaceutical Benefits Advisory Committee (PBAC) plays a critical role in recommending drugs that should be listed for the Highly Specialised Drugs Program. The PBAC's recommendations are based on factors such as the medical conditions for which the medicine is approved, its clinical effectiveness, safety, and cost-effectiveness compared to alternative treatments. Furthermore, the Commonwealth/State Highly Specialised Drugs Working Party (HSDWP) advises the PBAC on the suitability of certain drugs for the program, considering both funding and administrative aspects. The Act also includes provisions that outline the consequences for breaches. While the explanatory statement does not explicitly mention offences or penalties, it is implied that failure to comply with the special arrangements or recommendations by the relevant authorities could lead to legal ramifications. Such breaches might result in civil or criminal consequences, although the specific penalties are not detailed in the text provided. The Act's overarching aim is to ensure that the Highly Specialised Drugs Program effectively serves the needs of those who require highly specialised pharmaceutical treatments.

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