National Health (Listed Drugs on F1 or F2) Amendment Determination 2023 (No. 3)

Administered by Department of Health, Disability and Ageing

Legislation au F2023L00492 Not in force Legislative Instrument

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EXPLANATORY STATEMENT

 

National Health Act 1953

 

National Health (Listed Drugs on F1 or F2) Amendment Determination 2023 (No. 3)

 

PB 39 of 2023

 

Authority

 

This instrument, made under subsection 85AB(1) of the National Health Act 1953 (the Act), amends the National Health (Listed Drugs on F1 or F2) Determination 2021 (PB 33 of 2021)  (the Principal Determination).

 

The Principal Determination provides for the allocation of drugs to the F1 and F2 formularies of the Pharmaceutical Benefits Scheme (PBS).

 

Purpose

 

This instrument makes amendments to the Principal Determination.

 

The Act provides that PBS listed drugs may be assigned to formularies identified as F1 and F2. F1 is intended for single branded drugs and F2 for drugs that have multiple brands, or are in a therapeutic group with other drugs with multiple brands. Drugs on F2 are subject to the provisions of the Act relating to price disclosure and guarantee of supply.

 

Section 84AC of the Act provides that a drug is on F1 or F2 if there is a determination in force under section 85AB that the drug is on F1 or F2.

 

Subsection 85AB(1) of the Act empowers the Minister (or delegate) to determine by legislative instrument that a listed drug is on F1 or F2.  For a drug to be on F1, it must satisfy the criteria in subsection 85AB(4). This requires that there are no listed brands of pharmaceutical items that have the drug that are bioequivalent or biosimilar, and no listed brands of pharmaceutical items that have another drug in the same therapeutic group as the first drug that are bioequivalent or biosimilar. It also requires that the drug was not on F2 the day before the determination comes into effect. A drug may only be determined to be on F2 if it does not satisfy one or more of the criteria for F1 (subsection 85AB(3)).

 

When subsection 85AB(5) of the Act applies, which relates to listed drugs with a single brand combination item on the PBS, the listed drug is not placed on F1 or F2, but on the administrative combination drug list (CDL).

 

This instrument amends the Principal Determination by adding to F1 two new drugs, asciminib and vosoritide from 1 May 2023.

 

Variation and revocation

 

Unless there is an express power to revoke or vary PB 33 of 2021 cited in this instrument, subsection 33(3) of the Acts Interpretation Act 1901 is relied upon to revoke or vary PB 33 of 2021.

 

Consultation

 

This instrument affects pharmaceutical companies with new medicines listing on the PBS.

Asciminib and vosoritide meet the criteria for F1 under subsection 85AB(4).

 

Before a drug is PBS listed and allocated to a formulary, there are detailed consultations about the drug with the responsible person and recommendations from the Pharmaceutical Benefits Advisory Committee (PBAC). Any PBAC recommendation is made following receipt of a submission made by the affected pharmaceutical company. Two-thirds of the PBAC membership is from the following interests or professions: consumers, health economists, practising community pharmacists, general practitioners, clinical pharmacologists and medical specialists.

 

No additional consultation with experts was undertaken regarding this determination because consultation with the affected responsible person and the PBAC drew on the knowledge of persons with relevant expertise.

 

Commencement

 

This instrument commences on 1 May 2023.

 

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


Statement of Compatibility with Human Rights

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

National Health (Listed Drugs on F1 or F2) Amendment Determination 2023 (No. 3)
(PB 39 of 2023)

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

This legislative instrument is made pursuant to subsection 85AB(1) of the National Health Act 1953 (the Act), which relates to listed drugs on F1 or F2.  This instrument amends the National Health (Listed Drugs on F1 or F2) Determination 2021 (PB 33 of 2021) (the Principal Determination) which provides for the allocation of drugs to the F1 and F2 formularies of the Pharmaceutical Benefits Scheme (PBS).

 

This instrument amends the Principal Determination by adding to F1 two new drugs, asciminib and vosoritide from 1 May 2023.

 

Human rights implications

This legislative instrument engages Articles 2 and 12 of the International Covenant on Economic, Social and Cultural Rights by assisting with the progressive realisation by all appropriate means of the right of everyone to the enjoyment of the highest attainable standard of physical and mental health.

The PBS assists with the advancement of this human right by providing for subsidised access of medicines to patients. The recommendatory role of the Pharmaceutical Benefits Advisory Committee ensures that decisions about subsidised access to medicines on the PBS are evidence-based.

The right to social security is contained in Article 9 of the International Covenant on Economic Social and Cultural Rights (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 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.

 


Conclusion

 

This legislative instrument is compatible with human rights. Human rights continue to be protected by retaining clinically important medicines on the PBS and placing them in formularies that ensure the most cost-effective pricing for supply of each medicine to Australians.

 

 

 

Nikolai Tsyganov

  Assistant Secretary

Pricing and PBS Policy Branch

Technology Assessment and Access Division

Department of Health and Aged Care

 

Overview

The National Health (Listed Drugs on F1 or F2) Amendment Determination 2023 (No. 3), enacted by the Australian government, is an amendment to the National Health Act 1953. This legislation was introduced to address the need for an updated allocation of drugs within the Pharmaceutical Benefits Scheme (PBS) formularies, specifically F1 and F2. The National Health Act 1953, administered by the Australian Parliament, establishes the framework for the PBS, which subsidises access to essential medicines for Australians. The policy objective of this determination is to ensure that drugs meeting specific criteria are appropriately allocated to either F1 or F2 formularies to maintain cost-effective pricing and guarantee supply for the benefit of patients. This amendment determination specifically adds two new drugs, asciminib and vosoritide, to the F1 formulary, effective from 1 May 2023, following consultations with relevant stakeholders and recommendations from the Pharmaceutical Benefits Advisory Committee.

Scope and Application

The National Health (Listed Drugs on F1 or F2) Amendment Determination 2023 (No. 3) amends the National Health (Listed Drugs on F1 or F2) Determination 2021 under subsection 85AB(1) of the National Health Act 1953. This amendment pertains to the allocation of drugs within the Pharmaceutical Benefits Scheme (PBS) by adding two new drugs, asciminib and vosoritide, to the F1 formulary, effective from 1 May 2023. The National Health Act 1953 governs the PBS, which subsidises access to medicines for Australians, and it applies to all entities and individuals involved in the provision and administration of PBS listed drugs, including pharmaceutical companies, healthcare providers, and patients. The Act's provisions are applicable across Australia, encompassing the Commonwealth, states, and territories. The determination ensures that the drugs added to the F1 formulary meet specific criteria, such as having no bioequivalent or biosimilar listed brands and not having been on the F2 formulary previously. This legislative instrument ensures compatibility with human rights by facilitating access to essential health services through the PBS, thereby contributing to the progressive realisation of the right to the highest attainable standard of physical and mental health as recognised under international covenants.

Key Provisions

The National Health (Listed Drugs on F1 or F2) Amendment Determination 2023 (No. 3) amends the National Health (Listed Drugs on F1 or F2) Determination 2021, adding two new drugs, asciminib and vosoritide, to the F1 formulary of the Pharmaceutical Benefits Scheme (PBS) from 1 May 2023. Section 85AB(1) of the National Health Act 1953 empowers the Minister (or delegate) to determine by legislative instrument that a listed drug is on F1 or F2. For a drug to be on F1, it must meet specific criteria, including the absence of bioequivalent or biosimilar brands within the same therapeutic group and not having been on F2 the day before the determination comes into effect. In this case, asciminib and vosoritide meet the criteria for F1 as stated in subsection 85AB(4) of the Act. The obligations imposed by this Act primarily concern pharmaceutical companies involved with new medicines being listed on the PBS. The responsible person for the drug must consult with the Pharmaceutical Benefits Advisory Committee (PBAC), which provides recommendations following a submission by the pharmaceutical company. The PBAC, composed of experts from various relevant fields, ensures decisions about the drug's listing and formulary allocation are evidence-based. Additionally, this instrument adheres to the human rights obligations under international treaties, ensuring that decisions about the availability and affordability of medicines respect and promote the right to health. Breaching the provisions of the National Health Act 1953 or the determinations made under it may lead to civil or criminal consequences, although specific offences, penalties, or consequences are not detailed within this instrument. The Act provides for the enforcement of its provisions, and breaches may result in legal action, which could include fines or other penalties as prescribed by law. The maximum penalties for such breaches would be in accordance with the relevant sections of the Act and any other applicable legislation. The National Health (Listed Drugs on F1 or F2) Amendment Determination 2023 (No. 3) ensures that asciminib and vosoritide are added to the F1 formulary of the PBS from 1 May 2023, promoting equitable access to these essential medicines while adhering to evidence-based practices and human rights obligations. The instrument ensures that these drugs are priced and supplied in the most cost-effective manner, thus maximising the benefits to Australian patients.

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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.