National Health Act 1953 - Amendment special arrangements under subsection 100(1) - Highly Specialised Drugs Program (No. PB 92 of 2009)

Administered by Department of Health, Disability and Ageing

Legislation au F2009L03547 Not in force Legislative Instrument

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EXPLANATORY STATEMENT

INSTRUMENT NUMBER PB 92 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.  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 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 54 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 10 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 54 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, amended by the instrument PB 92 of 2009, addresses the need for special arrangements to ensure an adequate supply of highly specialised drugs for certain medical treatments. The Act, enacted by the Parliament of Australia, is the foundation of the Pharmaceutical Benefits Scheme (PBS), aiming to provide affordable access to a wide range of medicines. The specific amendment under subsection 100(1) targets special pharmaceutical products, ensuring they are available to those in isolated areas or receiving treatment where standard PBS provisions are inadequate. The policy objective is to facilitate timely and efficient access to critical medications for those in unique medical circumstances. The instrument, which came into effect on 1 October 2009, involves amendments to the Highly Specialised Drugs Program, overseen by the Pharmaceutical Benefits Advisory Committee and the Commonwealth/State Highly Specialised Drugs Working Party, ensuring recommendations are evidence-based and consider both clinical and economic factors.

Scope and Application

The National Health Act 1953, as amended, governs the availability of pharmaceutical benefits through the Pharmaceutical Benefits Scheme (PBS), providing Australians with access to affordable and reliable medicines. The Act applies to drugs and medicinal preparations declared by the Minister, which are listed as pharmaceutical benefits under the Act. It also applies to special arrangements for highly specialised drugs made under subsection 100(1) of the Act, which provide an adequate supply of these drugs to individuals in isolated areas or receiving medical treatment where conventional pharmaceutical benefits are inadequate or cannot be efficiently supplied. The Highly Specialised Drugs Program, which falls under these special arrangements, ensures that patients receiving treatment in private hospitals as non-admitted, day admitted, or discharge patients have access to highly specialised drugs. This Act has a national reach, as it is a Commonwealth legislation, and applies to all individuals and entities involved in the provision of these pharmaceutical benefits across Australia. While the Act primarily applies to drugs and medicinal preparations listed under the PBS, there are exclusions and thresholds set by the Minister, and the Pharmaceutical Benefits Advisory Committee (PBAC) makes recommendations to the Minister regarding the suitability of drugs for inclusion on the PBS. The Act allows for the extension or restriction of its application through subordinate instruments, such as the amendment of special arrangements under section 100(1) as seen in the legislative instrument PB 92 of 2009.

Key Provisions

The National Health Act 1953 Amendment Special Arrangements Under Subsection 100(1) Highly Specialised Drugs Program (F2009L03547) primarily amends the existing Highly Specialised Drugs Program under section 100 of the National Health Act. This program facilitates the provision of an adequate supply of special pharmaceutical products to specific groups, including those living in isolated areas or undergoing medical treatments where standard pharmaceutical benefits are inadequate or inefficiently supplied (section 100(1)). The amendments focus on updating the list of drugs and medicinal preparations eligible for special arrangements, which are detailed in Schedule 1 of the instrument. For example, it adds new indications for filgrastim and pegfilgrastim (Schedule 1) and removes certain forms of epoetin beta, indinavir, and ribavirin and peginterferon alfa-2a (Schedules 2 and 3). The instrument comes into effect on 1 October 2009, amending the previous arrangements made on 1 July 2009 (PB 54 of 2009). The Act imposes specific obligations on the Minister for Health and Ageing, including the responsibility to make special arrangements for the provision of special pharmaceutical products under section 100(1). This includes considering recommendations from the Pharmaceutical Benefits Advisory Committee (PBAC) and the Commonwealth/State Highly Specialised Drugs Working Party (HSDWP). The Minister must ensure that any special arrangements are made in accordance with the legislative framework and take into account the clinical effectiveness, safety, and cost-effectiveness of the drugs. Additionally, the Minister must ensure that the arrangements are subject to the provisions of Part VII of the Act (subsection 100(3)). The Act also outlines potential consequences for non-compliance with the special arrangements. While the specific penalties are not detailed in the provided text, breaches of the National Health Act can generally result in civil or criminal penalties, depending on the nature and severity of the breach. Civil penalties can include fines, and in severe cases, criminal penalties can include imprisonment. The exact penalties would be determined based on the specific breach and the provisions of the Act. The Act empowers courts to impose these penalties to ensure compliance and the effective provision of pharmaceutical benefits.

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