National Health (IVF Program) Special Arrangement Amendment Instrument 2024 (No. 1)

Administered by Department of Health, Disability and Ageing

Legislation au F2024L01398 Not in force Legislative Instrument

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EXPLANATORY STATEMENT

NATIONAL HEALTH ACT 1953

NATIONAL HEALTH (IVF PROGRAM) SPECIAL ARRANGEMENT AMENDMENT INSTRUMENT 2024 (No. 1)

PB 117 of 2024

 

Purpose

This is the National Health (IVF Program) Special Arrangement Amendment Instrument 2024 (No. 1) (this Instrument). The purpose of this Instrument, made under subsection 100(2) of the National Health Act 1953 (the Act), is to amend the National Health (IVF Program) Special Arrangement 2015 (PB 60 of 2015) (the Special Arrangement), to make changes to the Special Arrangement relating to the IVF Program.

The purpose of the Special Arrangement is to ensure that an adequate supply of pharmaceutical benefits is available for patients who require in vitro fertilisation treatment. Restrictions on the provision of this treatment mean that these pharmaceutical benefits can more conveniently or efficiently be supplied under a special arrangement.

The amendments made by this Instrument reflect amendments to the National Health (Listing of Pharmaceutical Benefits) Instrument 2024 (PB 26 of 2024), which commence on the same day. The National Health (Listing of Pharmaceutical Benefits) Instrument 2024 (PB 26 of 2024) is made under sections 84AF, 84AK, 85, 85A, 88 and 101 of the Act.

Schedule 1 to this Instrument provides for the addition of a form of the listed drug choriogonadotropin alfa to the Special Arrangement. Schedule 1 also reformats the table at Schedule 1 of the Special Arrangement to display the listed drug, form and manner of administration in every row of the table.

This change is summarised, by subject matter, in the Attachment.

Authority

Subsection 100(1) of 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).

Consultation

The amendments made by this Instrument accord with recommendations made by the Pharmaceutical Benefits Advisory Committee (PBAC).

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 PBAC.

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. 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 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 PBAC, and that would enable them to contribute meaningfully to the deliberations of PBAC. In addition, an industry nominee has been appointed to the PBAC membership. When recommending the listing of a medicine on the Pharmaceutical Benefits Scheme (PBS), 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.

Pharmaceutical companies were consulted throughout the process of changes to the listings on the PBS. This includes consultation through the PBAC process.

Further consultation for this Instrument was considered unnecessary due to the nature of the consultation that has already taken place in the decision to list the medications outlined under ‘Purpose’.

General

Details of this instrument are set out in the Attachment.

This Instrument commences on 1 November 2024.

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


ATTACHMENT

PROVISION-BY-PROVISION DESCRIPTION OF NATIONAL HEALTH (IVF PROGRAM) SPECIAL ARRANGEMENT AMENDMENT INSTRUMENT 2024 (No. 1)

Section 1 Name of Instrument

This section provides the name of this instrument as the National Health (IVF Program) Special Arrangement Amendment Instrument 2024 (No. 1) and may also be cited as PB 117 of 2024.

Section 2 Commencement

This section provides that this instrument commences on 1 November 2024.

Section 3 Authority

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

Section 4  Schedules

This section 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 amendment in Schedule 1 involves the addition of a form of a listed drug to the Special Arrangement. This change is summarised below.

SUMMARY OF CHANGES TO THE NATIONAL HEALTH (IVF PROGRAM) SPECIAL ARRANGEMENT 2015 MADE BY THIS INSTRUMENT

Form Added

Listed Drug

Form

Choriogonadotropin alfa

Solution for injection 250 micrograms in 0.5 mL pre-filled syringe (S19A)


Statement of Compatibility with Human Rights

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

National Health (IVF Program) Special Arrangement
Amendment Instrument 2024 (No. 1)

(PB 117 of 2024)

This 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 Instrument

The purpose of this Instrument, made under subsection 100(2) of the National Health Act 1953 (the Act), is to amend the National Health (IVF Program) Special Arrangement 2015 (PB 60 of 2015) (the Special Arrangement), to make changes to the Special Arrangement relating to the IVF Program.

The purpose of the Special Arrangement is to ensure that an adequate supply of pharmaceutical benefits is available for patients who require in vitro fertilisation treatment. Restrictions on the provision of this treatment mean that these pharmaceutical benefits can more conveniently or efficiently be supplied under a special arrangement.

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 UN Committee on Economic Social and Cultural Rights (the Committee) reports that there is a strong presumption that retrogressive measures taken in relation to the right to social security are prohibited under ICESCR. In this context, a retrogressive measure would be one taken without adequate justification that had the effect of reducing existing levels of social security benefits, or of denying benefits to persons or groups previously entitled to them. However, it is legitimate for a Government to re-direct its limited resources in ways that it considers to be more effective at meeting the general health needs of all society, particularly the needs of the more disadvantaged members of society.

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 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 National Health (Listing of Pharmaceutical Benefits) Instrument 2024 (the Listing Instrument), that affect the pharmaceutical benefits that may be supplied under the Special Arrangement, are made concurrently. This Instrument provides for the addition of a form of the listed drug choriogonadotropin alfa to the Special Arrangement.

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.

Conclusion

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

Nikolai Tsyganov

Assistant Secretary

Pricing and PBS Policy Branch

Technology Assessment and Access Division

Department of Health and Aged Care

Overview

The National Health (IVF Program) Special Arrangement Amendment Instrument 2024 (No. 1) was introduced to amend the National Health (IVF Program) Special Arrangement 2015 under subsection 100(2) of the National Health Act 1953. The purpose of this amendment is to ensure that an adequate supply of pharmaceutical benefits is available for patients who require in vitro fertilisation treatment, particularly by making changes to the Special Arrangement that facilitate the supply of these benefits. The National Health Act 1953 allows the Minister to make special arrangements for the supply of pharmaceutical benefits, and this amendment is made in response to changes to the National Health (Listing of Pharmaceutical Benefits) Instrument 2024. This amendment involves the addition of a form of the listed drug choriogonadotropin alfa to the Special Arrangement and reflects recommendations made by the Pharmaceutical Benefits Advisory Committee (PBAC). This instrument is compatible with human rights, specifically advancing the rights to social security and health as outlined in the International Covenant on Economic, Social and Cultural Rights. The amendment ensures that the changes to the pharmaceutical benefits that may be supplied under the Special Arrangement are made concurrently with the changes to the National Health (Listing of Pharmaceutical Benefits) Instrument 2024.

Scope and Application

The National Health (IVF Program) Special Arrangement Amendment Instrument 2024 (No. 1) applies to the amendment of the National Health (IVF Program) Special Arrangement 2015 under the National Health Act 1953. This Act pertains to the regulation and administration of health services, including the provision of pharmaceutical benefits, across the Commonwealth of Australia. The Instrument's amendments ensure that an adequate supply of pharmaceutical benefits, specifically for in vitro fertilisation treatment, remains available and efficiently supplied. This special arrangement caters to patients needing such treatments and is designed to operate within the framework of the Pharmaceutical Benefits Scheme (PBS), which is managed under the Act. The changes introduced by this Instrument reflect adjustments made to the National Health (Listing of Pharmaceutical Benefits) Instrument 2024, which are implemented to ensure the provision of necessary medications under the IVF Program. The Instrument does not explicitly outline exclusions or exemptions but operates within the constraints and provisions defined in the overarching National Health Act. The scope of this Instrument extends to altering the Special Arrangement to incorporate specific pharmaceutical benefits, ensuring they align with the amendments in the PBS listings. The amendments, which include the addition of a form of choriogonadotropin alfa to the Special Arrangement, are made in accordance with recommendations from the Pharmaceutical Benefits Advisory Committee (PBAC). This committee's role in advising the Minister ensures that the amendments are evidence-based and align with the principles of providing equitable access to necessary health treatments. The Instrument does not specify any additional subordinate instruments for extending or restricting its application, indicating that its provisions are standalone and directly amend the Special Arrangement as outlined.

Key Provisions

The National Health (IVF Program) Special Arrangement Amendment Instrument 2024 (No. 1) (Instrument) amends the National Health (IVF Program) Special Arrangement 2015 (Special Arrangement) to reflect changes to the National Health (Listing of Pharmaceutical Benefits) Instrument 2024 (Listing Instrument) (sections 1-4). This Instrument introduces a new form of the drug choriogonadotropin alfa to the Special Arrangement, which is designed to ensure an adequate supply of pharmaceutical benefits for patients requiring in vitro fertilisation treatment. This addition is detailed in Schedule 1 of the Instrument (Schedule 1). The purpose of these amendments is to align the Special Arrangement with the updated listings on the Pharmaceutical Benefits Scheme (PBS), thereby facilitating more efficient and convenient supply of necessary pharmaceutical benefits (Schedule 1). The Instrument imposes several obligations on the parties involved. Firstly, it mandates that the Special Arrangement must be updated to reflect changes in the Listing Instrument, ensuring that the pharmaceutical benefits available to IVF patients remain current and effective (Schedule 1). Additionally, the Instrument requires that the Pharmaceutical Benefits Advisory Committee (PBAC) recommendations be followed in determining which drugs and forms should be included in the Special Arrangement. This ensures that decisions about pharmaceutical benefits are evidence-based and take into account factors such as clinical effectiveness, safety, and cost-effectiveness (section 100A). The Instrument also requires ongoing consultation with stakeholders, including pharmaceutical companies, to ensure that the Special Arrangement meets the needs of patients and remains aligned with broader health policy objectives (section 100A). Failure to comply with the requirements set out in this Instrument could result in legal consequences. While the Instrument itself does not specify particular offences or penalties, non-compliance with the Special Arrangement could potentially lead to civil or criminal consequences under the National Health Act 1953 (the Act). For example, unauthorised supply of pharmaceutical benefits not included in the Special Arrangement could be considered a breach of the Act, leading to penalties including fines and imprisonment (sections 100-100C). Additionally, failure to follow PBAC recommendations could undermine the evidence-based approach intended by the Act, potentially leading to legal challenges or regulatory action. In summary, the National Health (IVF Program) Special Arrangement Amendment Instrument 2024 (No. 1) updates the Special Arrangement to include a new form of choriogonadotropin alfa, ensuring that patients requiring IVF treatment have access to necessary pharmaceutical benefits. The Instrument imposes obligations on parties to align the Special Arrangement with changes in the Listing Instrument and to follow PBAC recommendations. Non-compliance with these obligations could lead to legal consequences under the Act, including fines and imprisonment for unauthorised supply of pharmaceutical benefits.

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