National Health Act 1953 - Amendment Special Arrangements under subsection 100(1) - Highly Specialised Drugs Program (No. PB 24 of 2009)

Administered by Department of Health, Disability and Ageing

Legislation au F2009L01115 Not in force Legislative Instrument

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EXPLANATORY STATEMENT

INSTRUMENT NUMBER PB 24 of 2009

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 120 of 2008) which came into effect on 1 December 2008.  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 April 2009, was made on 3 March 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 April 2009.

Paragraph 2:  provides that Schedule 1 amends PB 120 of 2008.

Schedule 1: provides for the following amendments: 

 

SCHEDULE 1

Alteration of Circumstances

Filgrastim [chemotherapy for B-cell chronic lymphocytic leukaemia]

Infliximab [initial treatment of adult patients with severe active psoriatic arthritis]

Pegfilgrastim [chemotherapy for B-cell chronic lymphocytic leukaemia]

 

 

Overview

The National Health Act 1953, as amended by the instrument F2009L01115, was enacted to address the need for an efficient and reliable supply of highly specialised drugs for patients receiving medical treatment in circumstances where conventional pharmaceutical benefits under the Pharmaceutical Benefits Scheme (PBS) are inadequate. The Commonwealth Parliament established the legislative framework to ensure timely and affordable access to a wide range of medicines for all Australians through the PBS. Under subsection 100(1) of the Act, the Minister for Health was empowered to make special arrangements for providing an adequate supply of special pharmaceutical products for persons living in isolated areas or receiving medical treatment under circumstances where conventional pharmaceutical benefits cannot be conveniently or efficiently supplied or are inadequate. This instrument amends the arrangements made under subparagraph 100(b)(i) to include certain highly specialised drugs, effective from 1 April 2009. The policy objective of these amendments is to enhance the availability of necessary drugs for patients in need of highly specialised treatments, ensuring that they receive appropriate medical care despite logistical challenges or the limitations of the standard PBS provisions.

Scope and Application

The Highly Specialised Drugs Program, as outlined in the National Health Act 1953, is designed to ensure that Australians who require highly specialised drugs for their medical treatment have access to these medications, particularly in cases where the standard Pharmaceutical Benefits Scheme (PBS) does not adequately cover their needs. This program applies to individuals who are either residing in isolated areas or receiving medical treatment under circumstances where the conventional pharmaceutical benefits cannot be conveniently or efficiently supplied, or are inadequate for their treatment. The Highly Specialised Drugs Program specifically addresses the needs of patients treated at private hospitals, whether as non-admitted, day admitted, or discharge patients. The legislation allows for the Minister to make special arrangements to ensure the availability of these highly specialised drugs, and these arrangements can be varied or revoked as necessary. The program operates under the overarching framework of the National Health Act 1953, which governs the PBS and the availability of pharmaceutical benefits across the Commonwealth.

Key Provisions

The National Health Act 1953, as amended by the instrument PB 24 of 2009, introduces specific provisions regarding the Highly Specialised Drugs Program under section 100(1)(b)(i) of the Act. This program is designed to ensure an adequate supply of special pharmaceutical products for patients receiving treatment with highly specialised drugs at private hospitals as non-admitted patients, day admitted patients, or patients on discharge. The legislative instrument amends the previous arrangements established under PB 120 of 2008, effective from 1 December 2008, and the amendments are detailed in Schedule 1 of the current instrument, which commences on 1 April 2009. Under the National Health Act, the Minister for Health and Ageing is empowered to make special arrangements for the provision of pharmaceutical benefits in certain circumstances, such as when patients are in isolated areas or when their medical treatment requires pharmaceutical benefits that cannot be efficiently supplied under the general provisions of Part VII of the Act. The Minister can also vary or revoke these special arrangements as necessary. The Highly Specialised Drugs Program is an application of these provisions, ensuring that specific highly specialised drugs are available to those who need them in non-traditional hospital settings. The obligations imposed by this Act on the relevant parties include ensuring that the special pharmaceutical products are provided as per the arrangements laid out in the legislation. The Minister must work in conjunction with the Pharmaceutical Benefits Advisory Committee (PBAC) to recommend and approve drugs for inclusion in the Highly Specialised Drugs Program. The PBAC, composed of experts from various healthcare-related fields, must recommend any drug or medicinal preparation for inclusion on the Pharmaceutical Benefits Scheme (PBS) before it can be declared under the Act. Additionally, the Commonwealth/State Highly Specialised Drugs Working Party (HSDWP) assists the PBAC by evaluating the suitability of drugs for the program based on funding and administrative considerations. Violations of the provisions of the National Health Act or the special arrangements under section 100 can lead to both civil and criminal consequences. While the specific offences and penalties are not detailed in the explanatory statement, breaches of the Act could potentially result in fines or imprisonment under general provisions for contravention of statutory instruments. The penalties for such breaches would depend on the nature and severity of the offence, with potential maximum penalties varying according to the specific provisions of the Act and related legislation.

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