National Health Act 1953 - Amendment Special Arrangements under subsection 100(1) - Highly specialised drugs program for public hospitals (No. PB 94 of 2009)

Administered by Department of Health, Disability and Ageing

Legislation au F2009L03701 Not in force Legislative Instrument

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EXPLANATORY STATEMENT

INSTRUMENT NUMBER PB 94 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 October 2009, was made on 28 September 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 October 2009.

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

Schedule 1: provides for the following amendments: 

 

SCHEDULE 1

Alteration of Circumstances

Filgrastim [additional indication]

Pegfilgrastim [additional indication]

SCHEDULE 2

Deletion of Forms

Epoetin Beta

Injection 30,000 units in 0.6 mL pre-filled syringe

Indinavir

Capsule 100 mg (as sulfate)

Capsule 200 mg (as sulfate)

Ribavirin and Peginterferon Alfa-2a

Pack containing 84 tablets ribavirin 200 mg and 4 pre-filled syringes peginterferon alfa-2a injection 180 micrograms

 

SCHEDULE 3

Deletion of Form

Ribavirin and Peginterferon Alfa-2a

Pack containing 84 tablets ribavirin 200 mg and 4 pre-filled syringes peginterferon alfa-2a injection 180 micrograms

 

 

Overview

The National Health Act 1953, as amended by the instrument F2009L03701, addresses the need to ensure reliable, timely, and affordable access to a wide range of medicines for all Australians, particularly focusing on the provision of highly specialised drugs to those receiving treatment in public hospitals. This legislation, enacted by the Australian Parliament, establishes the legal framework for the Pharmaceutical Benefits Scheme (PBS) and allows the Minister for Health to make special arrangements under subsection 100(1) to provide access to pharmaceutical products that are not conveniently or efficiently supplied under the standard PBS arrangements. The policy objective of this Act is to ensure that individuals in isolated areas or those receiving medical treatment where standard PBS benefits are inadequate have access to necessary medications. The instrument F2009L03701, which came into effect on 1 October 2009, amends the previously established Highly Specialised Drugs Program for Public Hospitals. This amendment introduces additional indications for certain drugs, such as Filgrastim and Pegfilgrastim, while also removing certain forms of other drugs like Epoetin Beta and Ribavirin and Peginterferon Alfa-2a from the program. These changes aim to ensure that the program remains effective and relevant to the current medical needs of patients in public hospitals. The amendments are made following recommendations from the Pharmaceutical Benefits Advisory Committee and the Commonwealth/State Highly Specialised Drugs Working Party, ensuring that the drugs included in the program are clinically effective, safe, and cost-effective.

Scope and Application

The National Health Act 1953, as amended by the instrument F2009L03701, pertains specifically to the Highly Specialised Drugs Program for Public Hospitals, which is designed to ensure an adequate supply of special pharmaceutical products for certain patients receiving medical treatment in public hospitals. This Act applies to individuals who are receiving treatment with highly specialised drugs at public hospitals, either as non-admitted patients, day admitted patients, or patients on discharge. These special pharmaceutical products include drugs and medicinal preparations declared under subsection 85(2) of the Act, and the Act allows the Minister to make special arrangements under subsection 100(1) for ensuring their availability. The Act extends nationally, governed by the Commonwealth, and is subject to variations or revocations by the Minister under subsection 100(2). It is worth noting that while the Act broadly covers these special arrangements, specific details and amendments are provided in Schedule 1 of the instrument, which came into effect on 1 October 2009. This includes alterations to the conditions for certain drugs such as Filgrastim and Pegfilgrastim, and deletions of specific forms of drugs such as Epoetin Beta, Indinavir, and Ribavirin and Peginterferon Alfa-2a.

Key Provisions

The main operative sections of this legislation are sections 100(1) and 100(2) of the National Health Act 1953, which allow the Minister to make special arrangements for providing that an adequate supply of special pharmaceutical products will be available to specific groups of people, and to vary or revoke these arrangements. The legislative instrument provides for the amendment of the Highly Specialised Drugs Program for Public Hospitals, which is a set of arrangements made under section 100(1)(b)(i) of the Act for the purpose of providing an adequate supply of special pharmaceutical products to certain patients receiving treatment at public hospitals. The amendments outlined in Schedule 1 of the instrument include the addition of new indications for filgrastim and pegfilgrastim and the deletion of certain forms of epoetin beta, indinavir, ribavirin, and peginterferon alfa-2a. The Act imposes obligations and requirements on the Minister for Health and Ageing to make special arrangements for providing an adequate supply of special pharmaceutical products to the specified groups of people. The Pharmaceutical Benefits Advisory Committee (PBAC) and the Commonwealth/State Highly Specialised Drugs Working Party (HSDWP) play roles in recommending which drugs and medicinal preparations should be available as pharmaceutical benefits and their suitability for listing under the Highly Specialised Drugs Program. The Minister must consider these recommendations when making special arrangements under section 100(1) of the Act. Offences, penalties, or consequences for breach of the Act are not explicitly stated in the provided text. However, the Act's provisions are likely to be enforced through administrative or regulatory means, such as the suspension or revocation of special arrangements made under section 100(1). The Minister may also take legal action against any person or entity that breaches the requirements of the Act or the special arrangements made under section 100(1). The penalties for such breaches would depend on the specific circumstances and the relevant laws governing the enforcement of the Act.

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