National Health Act 1953 - Amendment special arrangements under subsection 100(1) - Highly Specialised Drugs Program (No. PB 82 of 2009)

Administered by Department of Health, Disability and Ageing

Legislation au F2009L03154 Not in force Legislative Instrument

Legislation content

EXPLANATORY STATEMENT

INSTRUMENT NUMBER PB 82 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 September 2009, was made on 10 August 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 September 2009.

Paragraph 2:  provides that Schedule 1 amends PB 54 of 2009.

Schedule 1: provides for the following amendments: 

 

SCHEDULE 1

Alteration of Circumstances

Thalidomide

 

 

 

 

Overview

The National Health Act 1953, enacted by the Australian Parliament, serves as the legislative foundation for the Pharmaceutical Benefits Scheme (PBS), ensuring all Australians have reliable, timely, and affordable access to a broad range of medicines. Section 100(1) of the Act enables the Minister to create special arrangements for providing an adequate supply of special pharmaceutical products to individuals in isolated areas or those receiving medical treatment where conventional pharmaceutical benefits under the Act are inadequate. This instrument amends the Highly Specialised Drugs Program arrangements, which cater to individuals receiving treatment with highly specialised drugs as non-admitted, day admitted, or discharge patients in private hospitals. The amendments, which came into effect on 1 September 2009, are designed to refine the existing arrangements (PB 54 of 2009) to better address the needs of those requiring highly specialised drugs, thereby improving the overall efficacy and reach of the PBS. The policy objective of these amendments is to ensure that an adequate supply of necessary pharmaceutical products is maintained, particularly for those in remote areas or undergoing specialised treatments.

Scope and Application

The National Health Act 1953, as amended by the legislative instrument F2009L03154, primarily applies to the Pharmaceutical Benefits Scheme (PBS) under which the Commonwealth provides access to a range of medicines for all Australians. This Act governs the provision of pharmaceutical benefits in accordance with Part VII, with drugs and medicinal preparations being declared by the Minister. The Highly Specialised Drugs Program, an amendment under subsection 100(1) of the Act, is designed to ensure an adequate supply of special pharmaceutical products for individuals in isolated areas or receiving treatment where conventional pharmaceutical benefits are inadequate. This includes patients in private hospitals as non-admitted, day admitted patients, or those on discharge. The amendments to the existing arrangements, effective from 1 September 2009, are detailed in Schedule 1 of the instrument, which includes changes related to specific drugs such as Thalidomide. These amendments are subject to the overarching provisions of Part VII, and the Pharmaceutical Benefits Advisory Committee (PBAC) plays a crucial role in recommending the inclusion of drugs on the PBS based on clinical effectiveness, safety, and cost-effectiveness.

Key Provisions

The main operative sections of the instrument (F2009L03154) amend the previously established Highly Specialised Drugs Program under the National Health Act 1953 (the Act). Specifically, section 100(1) of the Act allows the Minister to make special arrangements for providing an adequate supply of special pharmaceutical products to certain groups, including those receiving medical treatment under circumstances where pharmaceutical benefits cannot be conveniently or efficiently supplied in accordance with Part VII of the Act or are inadequate for their medical treatment. This legislative instrument modifies the arrangements made under paragraph 100(b)(i) (PB 54 of 2009), which came into effect on 1 July 2009, and sets out these amendments in Schedule 1. The instrument commences on 1 September 2009. The obligations and requirements imposed by the Act on the parties it governs include the declaration of drugs and medicinal preparations under subsection 85(2), with the Pharmaceutical Benefits Advisory Committee (PBAC) recommending these declarations under subsection 101(4). The PBAC, established by section 100A, comprises experts from various relevant fields, including consumers, health economists, and practising medical professionals. Additionally, the Commonwealth/State Highly Specialised Drugs Working Party (HSDWP) recommends the suitability of drugs for listing under the Highly Specialised Drugs Program. The HSDWP, a non-statutory body, 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. Any offences, penalties, or civil/criminal consequences for breach under this legislation are not explicitly detailed in the explanatory statement. However, given the nature of the Act and the legislative instrument, breaches could potentially lead to administrative or legal consequences. For instance, failure to comply with the special arrangements or recommendations made by the PBAC and HSDWP could result in the non-provision of necessary pharmaceutical benefits to eligible patients, leading to potential disputes or legal challenges. While specific penalties are not mentioned, the seriousness of ensuring adequate medical treatment could imply significant consequences for non-compliance, including possible civil or administrative penalties as determined by relevant authorities.

Legal classification tags

Area of Law
Health Law
Pharmaceutical Law
Instrument
Amending Act
Concepts
Definitions & Interpretation
Offence Provisions
Licensing & Registration
Compliance Obligations

Interactions

Authorises

All Versions

Sourced from the Federal Register of Legislation at 26 August 2026. For the latest information on Australian Government law please go to https://www.legislation.gov.au.