National Health Act 1953 - Amendment Special Arrangements under subsection 100(1) - Highly specialised drugs program for public hospitals (No. PB 72 of 2009)

Administered by Department of Health, Disability and Ageing

Legislation au F2009L02969 Not in force Legislative Instrument

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EXPLANATORY STATEMENT

INSTRUMENT NUMBER PB 72 of 2009

NATIONAL HEALTH ACT 1953

AMENDMENT SPECIAL ARRANGEMENTS UNDER SUBSECTION 100(1)

HIGHLY SPECIALISED DRUGS PROGRAM FOR PUBLIC HOSPITALS

 

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(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 public 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 61 of 2009) which came into effect on 1 July 2009.  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 August 2009, was made on 23 July 2009.

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 August 2009.

Paragraph 2:  provides that Schedule 1 amends PB 61 of 2009.

Schedule 1: provides for the following amendments: 

 

Preamble paragraphs:

Paragraphs 22 and 23 are amended to reflect the removal of the “grandfather” restrictions for the listed drugs bosentan and sitaxentan.

SCHEDULE 1

Alteration of Circumstances

Bosentan

 

Epoprostenol

 

Iloprost

 

Sildenafil

 

Sitaxentan

 

 

SCHEDULE 2

Addition of Forms

Apomorphine

Injection containing apomorphine hydrochloride 50 mg in 5 mL

Etanercept

Injection 50 mg in 1 mL single use injection pen, 4

 

SCHEDULE 4

Price Decrease

All drugs listed in Schedule 4 reflect a price decrease in Column 5 — Approved price and Column 6 — Price claimed by manufacturer.

 

 

 

 

 

Overview

The National Health Act 1953, enacted by the Parliament of Australia, provides the legislative framework for the Pharmaceutical Benefits Scheme (PBS), ensuring that all Australians have reliable, timely, and affordable access to a broad range of medicines. To address specific needs not fully met by the general provisions of the PBS, subsection 100(1) of the Act allows the Minister for Health to make special arrangements for the provision of pharmaceutical benefits to individuals in particular circumstances, such as those living in isolated areas or undergoing medical treatment where standard PBS provisions are inadequate. The Highly Specialised Drugs Program for Public Hospitals, established under these special arrangements, ensures that patients receiving treatment with highly specialised drugs in public hospitals have access to necessary medications. This program was introduced to address the gap in the standard PBS provisions for patients requiring highly specialised drugs for their medical treatment.

Scope and Application

The National Health Act 1953, as amended by the instrument PB 72 of 2009, pertains to the Highly Specialised Drugs Program for Public Hospitals, which is designed to ensure the availability of special pharmaceutical products for individuals receiving treatment in public hospitals who cannot be conveniently or efficiently supplied with these products under the Pharmaceutical Benefits Scheme (PBS). This Act applies to patients in public hospitals who are receiving medical treatment and require highly specialised drugs not readily available or adequately covered under the standard PBS provisions. The Act's reach is national, governed by the Commonwealth, with the Minister for Health and Ageing having the authority to make special arrangements and amendments to the program. The Highly Specialised Drugs Program for Public Hospitals is subject to changes and adjustments through subordinate instruments, as evidenced by the amendments listed in Schedule 1 of PB 72 of 2009, which include updates to drug listings, pricing, and specific circumstances under which the drugs are provided. The program excludes certain drugs unless recommended by the Pharmaceutical Benefits Advisory Committee (PBAC) and approved by the Commonwealth/State Highly Specialised Drugs Working Party (HSDWP).

Key Provisions

The legislative instrument F2009L02969, which amends the Highly Specialised Drugs Program for Public Hospitals under the National Health Act 1953, introduces several key provisions. Section 100(1) of the Act allows the Minister to make special arrangements to ensure an adequate supply of special pharmaceutical products for specific groups, including those receiving treatment in circumstances where the Pharmaceutical Benefits Scheme (PBS) is inadequate or cannot be efficiently supplied (subsection 100(1)(b)). These amendments, effective from 1 August 2009, focus on altering the eligibility criteria and pricing of certain highly specialised drugs available through the program. The amendments are detailed in Schedule 1, which modifies the existing arrangements established in PB 61 of 2009. Under these amendments, the program now removes “grandfather” restrictions for certain drugs, specifically bosentan and sitaxentan, allowing broader access to these treatments. Additionally, new drugs such as apomorphine and etanercept have been added to the program, expanding the range of treatments available to patients. The instrument also includes price adjustments for listed drugs, reflecting decreases in the approved prices and prices claimed by manufacturers. These changes are intended to ensure that the program remains responsive to the needs of patients requiring highly specialised drugs and to maintain the cost-effectiveness of the scheme. The obligations imposed by this Act on the parties involved include ensuring that the listed drugs are supplied under the terms of the special arrangements and that the pricing reflects the agreed-upon costs. Public hospitals participating in the program must adhere to the criteria set forth in the amendments, ensuring that they provide the necessary treatments to eligible patients. The Commonwealth is obligated to monitor and adjust the pricing of drugs to ensure they remain within the approved limits. For breaches of the provisions set out in this Act, there are potential civil and criminal consequences. While the specific penalties are not detailed in the explanatory statement, breaches of the National Health Act can generally result in substantial fines and, in severe cases, imprisonment. The penalties for non-compliance can vary depending on the nature and severity of the breach but may include financial penalties, corrective actions, or other measures deemed necessary by the relevant authorities to ensure compliance with the Act.

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