National Health (Efficient Funding of Chemotherapy) Special Arrangement Amendment Instrument 2022 (No. 1)

Administered by Department of Health, Disability and Ageing

Legislation au F2022L00089 Not in force Legislative Instrument

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EXPLANATORY STATEMENT

NATIONAL HEALTH ACT 1953

NATIONAL HEALTH (EFFICIENT FUNDING OF CHEMOTHERAPY)
SPECIAL ARRANGEMENT AMENDMENT INSTRUMENT 2022 (No. 1)

PB 6 of 2022

 

Purpose

The purpose of this Instrument, made under subsection 100(2) of the Act, is to amend the National Health (Efficient Funding of Chemotherapy) Special Arrangement 2011 (PB 79 of 2011) (the Special Arrangement) to make changes relating to the Efficient Funding of Chemotherapy.

The Special Arrangement achieves greater efficiency in payment for the supply of injected or infused chemotherapy medicines (‘chemotherapy pharmaceutical benefits’) to eligible patients being treated for cancer, to reflect the 2010 Budget measure titled ‘Revised arrangements for the efficient funding of chemotherapy drugs’.  The Special Arrangement also relates to the supply of medicines associated with the side-effects of cancer and cancer treatment (‘related pharmaceutical benefits’) at certain public hospitals.

This Instrument makes amendments to the Special Arrangement to reflect changes made to the National Health (Listing of Pharmaceutical Benefits) Instrument 2012 (PB 71 of 2012) which commences on the same day. 

Schedule 1 to this Instrument provides for the addition of brands of the listed drug bortezomib to the Special Arrangement. It also provides for the alteration of a responsible person code for a brand of the listed drug doxorubicin - pegylated liposomal, the alteration of the name of a brand of the drug daratumab, and for the addition of two responsible persons to the list of responsible persons. These changes are summarised, by subject matter, in the Attachment.

Authority

Subsection 100(1) of the National Health Act 1953 (the Act) enables the Minister to make special arrangements for the supply of pharmaceutical benefits.  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) of the Act provides that Part VII of the Act, and instruments made for the purposes of Part VII, have effect subject to a special arrangement made under subsection 100(1).

Consultations

An ongoing and formal process of consultation in relation to matters relevant to the Special Arrangement includes the involvement of interested parties through the membership of the Pharmaceutical Benefits Advisory Committee (PBAC).  The PBAC is an independent expert body established by section 100A of the Act which makes recommendations to the Minister about which drugs and medicinal preparations should be available as pharmaceutical benefits.  Part VII of the Act only applies to drugs or medicinal preparations recommended by the PBAC.  When recommending the listing of a medicine on the Pharmaceutical Benefits Scheme, the PBAC takes into account the medical conditions for which the medicine has been approved for use in Australia and its clinical effectiveness, safety and cost-effectiveness compared with other treatments.

PBAC members are appointed following nomination by prescribed organisations and associations from consumers, health economists, practising community pharmacists, general practitioners, clinical pharmacologists and specialists, with at least one member selected from each of these 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.

Pharmaceutical companies are consulted throughout the process for additions and changes to listings on the Pharmaceutical Benefits Scheme (PBS), including consultation through the PBAC process and agreement to final listing details.

It was considered that further consultation for this Instrument was unnecessary due to the nature of the consultation that has already taken place.

General

A provision-by-provision description of this instrument is contained in the Attachment.

This Instrument commences on 1 February 2022.

This Instrument is a legislative instrument for the purposes of the Legislation Act 2003.


ATTACHMENT

PROVISION-BY-PROVISION DESCRIPTION OF NATIONAL HEALTH (EFFICIENT FUNDING OF CHEMOTHERAPY) SPECIAL ARRANGEMENT AMENDMENT
INSTRUMENT 2022 (No. 1)

Section 1 Name of Instrument

This section provides the name of this Instrument as the National Health (Efficient Funding of Chemotherapy) Special Arrangement Amendment Instrument 2022 (No. 1) and may also be cited as
PB 6 of 2022.

Section 2 Commencement

This section provides that this Instrument commences on 1 February 2022.

Section 3 Authority

This section states that this instrument is made under subsection 100(2) of the National Health Act 1953.

Section 4  Schedules

Section 4 provides that each instrument that is specified in a Schedule to the Instrument is amended or repealed as set out in the applicable items in the Schedule concerned, and any other item in a Schedule to the Instrument has effect according to its terms.

Schedule 1 Amendments

The amendments in Schedule 1 involve the addition of brands, the alteration of responsible person codes for brands of pharmaceutical benefits, the alteration of a brand name, and the addition of two responsible persons to the list of responsible persons. These changes are summarised below.

 

SUMMARY OF CHANGES TO THE EFFICIENT FUNDING OF
CHEMOTHERAPY PROGRAM MADE BY THIS INSTRUMENT

 

Brands Added

Listed Drug

Form and Brand

Bortezomib

Powder for injection 1 mg (Bortezomib Accord)

Powder for injection 2.5 mg (DBL Bortezomib)

Powder for injection 3 mg (DBL Bortezomib)

Powder for injection 3.5 mg (Bortezom; Bortezomib Accord; Bortezomib Sandoz;
Bortezomib-Dr.Reddy's; BORTEZOMIB-TEVA; DBL Bortezomib)

Alteration of Responsible Person Code

Listed Drug

Form

Brand Name

Responsible Person

Doxorubicin - pegylated liposomal

Suspension for I.V. infusion containing pegylated liposomal doxorubicin hydrochloride 20 mg in 10 mL

Caelyx

From: JC

To: BX

Suspension for I.V. infusion containing pegylated liposomal doxorubicin hydrochloride 50 mg in 25 mL

Caelyx

From: JC

To: BX

Alteration of Brand Name

Listed Drug

Form

Brand Name

Daratumumab

Solution for subcutaneous injection containing daratumumab 1800 mg in 15 mL

From: Darzalex
 

To: Darzalex SC

Addition of Responsible Person Code

Pharmacor Pty Limited (CR)

Dr Reddy's Laboratories (Australia) Pty Ltd (RI)


Statement of Compatibility with Human Rights

Prepared in accordance with Part 3 of the Human Rights (Parliamentary Scrutiny) Act 2011

National Health (Efficient Funding of Chemotherapy) Special Arrangement
Amendment Instrument 2022 (No. 1)

(PB 6 of 2022)

This Legislative Instrument is compatible with the human rights and freedoms recognised or declared in the international instruments listed in section 3 of the Human Rights (Parliamentary Scrutiny) Act 2011.

Overview of the Legislative Instrument

The purpose of this Legislative Instrument, made under subsection 100(2) of the National Health Act 1953 (the Act), is to amend the National Health (Efficient Funding of Chemotherapy) Special Arrangement 2011 (PB 79 of 2011) (the Special Arrangement) to make changes relating to the Efficient Funding of Chemotherapy.

The Special Arrangement achieves greater efficiency in payment for the supply of injected or infused chemotherapy medicines (‘chemotherapy pharmaceutical benefits’) to eligible patients being treated for cancer, to reflect the 2010 Budget measure titled ‘Revised arrangements for the efficient funding of chemotherapy drugs’.  The Special Arrangement also relates to the supply of medicines associated with the side-effects of cancer and cancer treatment (‘related pharmaceutical benefits’) at certain public hospitals.

This Instrument provides for amendments to the Special Arrangement to ensure that the Special Arrangement accurately reflects changes to the National Health (Listing of Pharmaceutical Benefits) Instrument 2012, made under sections 84AF, 84AK, 85, 85A, 88 and 101 of the Act, which commences on the same day.

Human Rights Implications

This Instrument engages Articles 9 and 12 of the International Covenant on Economic Social and Cultural Rights (ICESCR), specifically the rights to social security and health.

The Right to Social Security

The right to social security is contained in Article 9 of the ICESCR. It requires that a country must, within its maximum available resources, ensure access to a social security scheme that provides a minimum essential level of benefits to all individuals and families that will enable them to acquire at least essential health care. Countries are obliged to demonstrate that every effort has been made to use all resources that are at their disposal in an effort to satisfy, as a matter of priority, this minimum obligation.

The Right to Health

The right to the enjoyment of the highest attainable standard of physical and mental health is contained in Article 12(1) of the ICESCR. The UN Committee on Economic Social and Cultural Rights (the Committee) has stated that the right to health is not a right for each individual to be healthy, but is a right to a system of health protection which provides equality of opportunity for people to enjoy the highest attainable level of health.

The Committee reports that the ‘highest attainable standard of health’ takes into account the country’s available resources. This right may be understood as a right of access to a variety of public health and health care facilities, goods, services, programs, and conditions necessary for the realisation of the highest attainable standard of health.


Analysis

This Instrument advances the right to health and the right to social security by ensuring that the amendments to the Listing Instrument, that affect the pharmaceutical benefits that may be supplied under the Special Arrangement, are made concurrently.

The Listing Instrument determines the pharmaceutical benefits that are on the Pharmaceutical Benefits Scheme (PBS) through declarations of drugs and medicinal preparations, and determinations of forms, manners of administration and brands. The PBS is a benefit scheme which assists with advancement of these human rights by providing for subsidised access by patients to medicines. The recommendatory role of the Pharmaceutical Benefits Advisory Committee (PBAC) ensures that decisions about subsidised access to medicines on the PBS are evidence-based. 

This Instrument provides for the addition of brands for the listed drug bortezomib to the Special Arrangement. It also provides for the alteration of responsible person codes for brands of pharmaceutical benefits, the alteration of a brand name of a pharmaceutical benefit, and for the addition of two responsible persons to the list of responsible persons.

Conclusion

This Legislative Instrument is compatible with human rights because it advances the protection of human rights.

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

David Laffan

Assistant Secretary

Pharmacy Branch

Technology Assessment and Access Division

Department of Health

Overview

The National Health (Efficient Funding of Chemotherapy) Special Arrangement Amendment Instrument 2022 (No. 1) amends the National Health (Efficient Funding of Chemotherapy) Special Arrangement 2011 to update the efficient funding of chemotherapy pharmaceutical benefits. This Instrument, made under the National Health Act 1953, facilitates the incorporation of amendments to the National Health (Listing of Pharmaceutical Benefits) Instrument 2012, which also commenced on 1 February 2022. This update is crucial to ensure the Special Arrangement accurately reflects changes in the pharmaceutical benefits that may be supplied under the Arrangement. The policy objective is to achieve greater efficiency in payment for the supply of injected or infused chemotherapy medicines to eligible patients being treated for cancer, as well as the supply of related pharmaceutical benefits at certain public hospitals. Consultations were conducted through the Pharmaceutical Benefits Advisory Committee (PBAC), an independent expert body established under the Act, which makes recommendations to the Minister about which drugs and medicinal preparations should be available as pharmaceutical benefits. The PBAC, which includes members from various relevant sectors, ensures that decisions about subsidised access to medicines on the Pharmaceutical Benefits Scheme (PBS) are evidence-based. The amendments to the Special Arrangement include the addition of brands for the listed drug bortezomib, alteration of responsible person codes for brands of pharmaceutical benefits, alteration of a brand name, and addition of two responsible persons to the list of responsible persons.

Scope and Application

The National Health (Efficient Funding of Chemotherapy) Special Arrangement Amendment Instrument 2022 (No. 1) amends the National Health (Efficient Funding of Chemotherapy) Special Arrangement 2011, made under the National Health Act 1953. This Act applies to the Commonwealth of Australia, and the Instrument itself reflects changes made to the National Health (Listing of Pharmaceutical Benefits) Instrument 2012. The Instrument seeks to achieve greater efficiency in payment for the supply of injected or infused chemotherapy medicines to eligible patients being treated for cancer, and also concerns the supply of medicines associated with the side-effects of cancer and cancer treatment at certain public hospitals. The amendments involve the addition of brands, the alteration of responsible person codes for brands of pharmaceutical benefits, the alteration of a brand name, and the addition of two responsible persons to the list of responsible persons. The changes are designed to ensure that the Special Arrangement accurately reflects the updated Pharmaceutical Benefits Scheme (PBS), and are made under the authority provided by subsection 100(2) of the Act. The Instrument engages Articles 9 and 12 of the International Covenant on Economic, Social and Cultural Rights, specifically the rights to social security and health, by ensuring that the amendments to the Listing Instrument, which affect the pharmaceutical benefits that may be supplied under the Special Arrangement, are made concurrently. This Instrument is made under the authority provided by subsection 100(2) of the National Health Act 1953, which enables the Minister to make special arrangements for the supply of pharmaceutical benefits. The Instrument is compatible with the human rights and freedoms recognised or declared in the international instruments listed in section 3 of the Human Rights (Parliamentary Scrutiny) Act 2011, as it advances the right to health and the right to social security by ensuring that the amendments to the Listing Instrument, which affect the pharmaceutical benefits that may be supplied under the Special Arrangement, are made concurrently. The Pharmaceutical Benefits Advisory Committee (PBAC) plays a recommendatory role in decisions about subsidised access to medicines on the PBS, ensuring that such decisions are evidence-based. The Instrument provides for the addition of brands for the listed drug bortezomib to the Special Arrangement, alteration of responsible person codes for brands of pharmaceutical benefits, alteration of a brand name, and addition of two responsible persons to the list of responsible persons. The amendments are designed to ensure that the Special Arrangement accurately reflects the updated Pharmaceutical Benefits Scheme, thus facilitating efficient funding of chemotherapy and related pharmaceutical benefits.

Key Provisions

The National Health (Efficient Funding of Chemotherapy) Special Arrangement Amendment Instrument 2022 (No. 1) (the Instrument) is made under subsection 100(2) of the National Health Act 1953 (the Act) and is intended to amend the National Health (Efficient Funding of Chemotherapy) Special Arrangement 2011 (the Special Arrangement) (s 3). This amendment is to ensure that the Special Arrangement accurately reflects changes made to the National Health (Listing of Pharmaceutical Benefits) Instrument 2012, which also commences on 1 February 2022 (s 4). The changes involve the addition of brands of the listed drug bortezomib to the Special Arrangement, alterations to responsible person codes for brands of pharmaceutical benefits, the alteration of a brand name, and the addition of two responsible persons to the list of responsible persons (Schedule 1). The Special Arrangement aims to achieve greater efficiency in the payment for the supply of injected or infused chemotherapy medicines (chemotherapy pharmaceutical benefits) to eligible patients being treated for cancer, reflecting the 2010 Budget measure titled ‘Revised arrangements for the efficient funding of chemotherapy drugs’ (Explanatory Statement). It also pertains to the supply of medicines associated with the side-effects of cancer and cancer treatment (related pharmaceutical benefits) at certain public hospitals (Explanatory Statement). The obligations imposed by the Act and the Instrument include ensuring that the Special Arrangement accurately reflects the changes made to the National Health (Listing of Pharmaceutical Benefits) Instrument 2012 (s 4). The Instrument further requires the addition of brands of the listed drug bortezomib to the Special Arrangement, the alteration of responsible person codes for brands of pharmaceutical benefits, the alteration of a brand name, and the addition of two responsible persons to the list of responsible persons (Schedule 1). The Instrument does not explicitly outline offences, penalties, or civil/criminal consequences for breach. However, the legislative framework within which the Act operates and the nature of the amendments suggest that non-compliance with the provisions of the Act or the Instrument could result in legal consequences. The Instrument’s purpose is to ensure that the Special Arrangement is kept up to date with changes in the Pharmaceutical Benefits Scheme, and failure to comply with the requirements could potentially impact the efficient funding of chemotherapy treatments and related pharmaceutical benefits, which are critical for patient care.

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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.