Therapeutic Goods (Listing) Notice 2014 (No. 3)

Administered by Department of Health, Disability and Ageing

Legislation au F2014L01012 Not in force Legislative Instrument

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EXPLANATORY STATEMENT

THERAPEUTIC GOODS (LISTING) NOTICE 2014 (NO. 3)

Subsection 9A(5), Therapeutic Goods Act 1989

OUTLINE

Therapeutic Goods (Listing) Notice 2014 (No. 3) (the Listing Notice) is a notice made by the delegate of the Minister for Health under subsection 9A(5) of the Therapeutic Goods Act 1989 (the Act).

The Listing Notice has the effect of requiring that therapeutic goods that contain elemental ‘iron’ as a therapeutically active ingredient, subject to certain conditions, be included in the part of the Australian Register of Therapeutic Goods (the Register) for listed goods.

The Listing Notice commenced on the day after it was registered on the Federal Register of Legislative Instruments (FRLI).

BACKGROUND

The Act provides for the establishment and maintenance of a national system of controls for the quality, safety, efficacy and timely availability of therapeutic goods that are used in Australia or exported from Australia. The Therapeutic Goods Administration (the TGA) is responsible for administering the Act.

Unless specifically exempted or authorised under the Act, therapeutic goods are required to be included on the Register before being supplied in, imported into, manufactured in or exported from Australia (sections 19B and 19D of the Act refer). Medicines are either registered or listed on the Register, depending on the ingredients they contain and the therapeutic claims that are being made.

In general, products that contain low risk ingredients are referred to as listed medicines in Australia. Most listed medicines are considered to be of relatively low risk compared to other types of medicines, such as prescription and over-the-counter medicines, as they may only contain ingredients that have been approved by the TGA as being of low risk and may only make limited therapeutic claims.

Part 1 of Schedule 4 to the Therapeutic Goods Regulations 1990 (the Regulations) sets out those therapeutic goods that are required to be included in the part of the Register for listed goods. Part 1 of Schedule 4 does not currently include goods containing elemental ‘iron’ as a therapeutically active ingredient.

Subsection 9A(5) of the Act authorises the Minister for Health to publish a notice in the Commonwealth of Australia Gazette requiring that specified goods be included in the part of the Register for listed goods. Such notices generally require that goods containing particular ingredients be included in that part of the Register. Once the notice is in effect, persons may apply for the listing on the Register of new therapeutic goods that contain ingredients or substances of the kind set out in the notice.

If Part 1 of Schedule 4 to the Regulations is amended to require goods that are the subject of a subsection 9A(5) notice to be included in the part of the Register for listed goods, the notice ceases to have effect (subsection 9A(6) of the Act).

A person can apply for a new ingredient or substance to be specified in a notice under subsection 9A(5). The TGA evaluates such applications, and the supporting data provided by the applicant, on the basis of safety and quality. The safety-focussed element determines whether the ingredient or substance is of sufficiently low risk to allow its inclusion in listed medicines, and the quality-focussed element characterises the precise and correct nature of the ingredient or substance.

‘Iron’ (Elemental iron)

‘Iron’ is a constituent of proteins such as haemoglobin and cytochromes, which are involved in essential processes in the body - such as the transportation of oxygen around the body, and the production of energy. Various degrees of iron deficiency can result from an inadequate iron intake and/or absorption, which can potentially lead to iron-deficiency anaemia.

‘Iron’, when a therapeutically active ingredient, consists of a very fine powder of elemental iron. This powder is often derived from pentacarbonyl iron and is usually referred to as carbonyl iron.

Currently, a number of iron compounds are permitted for use in listed medicines. These iron compounds include inorganic salts (e.g., ferrous sulphate) and organic salts (e.g., ferrous fumarate), and are predominantly used in the formulation of multi-vitamin/mineral supplements.

The Listing Notice for ‘iron’ (also known as elemental iron) also incorporates restrictions on the use of iron in listed medicines, which are based on the limits specified in the current Poisons Standard (also known as the Standard for the Uniform Scheduling of Medicines and Poisons) for ‘iron compounds’. These restrictions are designed to ensure the use of ‘iron’ in listed medicines within well-characterised safety limits.

In addition, in relation to quality requirements for listed medicines containing ‘iron’ as a therapeutically active ingredient, the United States Pharmacopeia-National Formulary includes a monograph for ‘iron, carbonyl’, which would constitute a standard for such goods under the Act (the British and European Pharmacopeias do not contain a monograph for this substance).

As such, ‘iron’ (also known as elemental iron) is considered to be safe for use as a therapeutically active ingredient in listed medicines, with the conditions noted in the Listing Notice.

To that end, the delegate of the Minister has determined that therapeutic goods containing elemental ‘iron’ as a therapeutically active ingredient be included in the part of the Register for listed goods, when the following conditions are met:

the preparations contain a daily dose of not more than 24 mg of iron; and

the primary pack contains not more than 750 mg of iron if the divided preparations contain more than 5 mg of iron per dosage unit; and

the preparations are for oral use only.

CONSULTATION

Consultation was not undertaken in relation to the making of the Listing Notice, as the notice is considered to be minor and machinery in nature, with low compliance costs for affected industry. The making of the Notice does not involve any new regulatory steps for industry, but rather provides a basis for products containing this ingredient to access the listing process rather than registration, a significant benefit for sponsors. The Office of Best Practice Regulation (OBPR) has advised that a regulatory impact statement is not required in relation to Listing Notices (OBPR Ref. 14416).

The effect of the Listing Notice is that sponsors wishing to use ‘iron’ (also known as elemental iron) in the formulation of a medicine can list the medicine on the Register rather than registering that medicine. Applications for new registered medicines are fully evaluated by the TGA for quality, safety and efficacy prior to inclusion on the Register, a process that is considerably more expensive and lengthy than the listing process.

In relation to compatibility with human rights, it is considered that the Listing Notice 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, and a Statement of Compatibility setting that out in further detail is set out below.

SUPPLEMENTARY MATERIAL – STATEMENT OF COMPATIBILITY FOR A LEGISLATIVE INSTRUMENT THAT DOES NOT RAISE ANY HUMAN RIGHTS ISSUES

Statement of Compatibility with Human Rights

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

Therapeutic Goods (Listing) Notice 2014 (No. 3) – iron (Elemental iron)

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 Bill/Legislative Instrument

Therapeutic Goods (Listing) Notice 2014 (No. 3) (the Notice) is a notice made by the delegate of the Minister for Health under subsection 9A(5) of the Therapeutic Goods Act 1989 (the Act). The effect of the Notice is to allow sponsors of orally ingested therapeutic goods containing elemental ‘iron’ as a therapeutically active ingredient to list, rather than register, those goods in the Australian Register of Therapeutic Goods (the Register) (registration being a considerably more expensive and lengthy process than listing). Once the Notice has commenced, persons can apply to list goods containing this ingredient on the Register.

Human rights implications

This legislative instrument does not engage any of the applicable rights or freedoms.

Conclusion

This legislative instrument is compatible with human rights as it does not raise any human rights issues.

Professor John Skerritt, delegate of the Minister for Health

Overview

The Therapeutic Goods (Listing) Notice 2014 (No. 3) was enacted to address the need for the inclusion of therapeutic goods containing elemental ‘iron’ as a therapeutically active ingredient in the Australian Register of Therapeutic Goods (ARTG). The notice was issued under subsection 9A(5) of the Therapeutic Goods Act 1989, with the intent to streamline the process for listing such goods in the ARTG, as opposed to the more rigorous and costly registration process. This measure aims to facilitate the timely availability of therapeutic goods that meet specific safety and quality standards, thereby ensuring the quality, safety, efficacy, and timely availability of therapeutic goods used or exported from Australia. The notice was issued by the delegate of the Minister for Health and took effect on the day after it was registered on the Federal Register of Legislative Instruments. The notice imposes certain conditions for the inclusion of these iron-containing goods in the ARTG, such as limiting the daily dose to not more than 24 mg of iron and ensuring that the primary pack contains no more than 750 mg of iron if the divided preparations contain more than 5 mg of iron per dosage unit. These conditions are intended to ensure the safe use of elemental iron in listed medicines. The notice also specifies that the preparations must be for oral use only. The Therapeutic Goods Administration (TGA) is responsible for evaluating the safety and quality of the applications for listing these goods, based on the data provided by the applicants.

Scope and Application

The Therapeutic Goods (Listing) Notice 2014 (No. 3) applies to therapeutic goods that contain elemental ‘iron’ as a therapeutically active ingredient and mandates their inclusion in the Australian Register of Therapeutic Goods for listed goods, provided specific conditions are met. This notice applies nationally across Australia and is applicable to any entities or individuals who manufacture, supply, import, or export such therapeutic goods within the country. The conditions under which these goods can be listed include a maximum daily dose of 24 mg of iron, a primary pack limit of 750 mg of iron for preparations exceeding 5 mg per dosage unit, and the restriction to oral use only. The scope of the Act is reinforced through the Therapeutic Goods Regulations 1990, which further detail the regulatory requirements for the quality, safety, and efficacy of therapeutic goods. Additionally, the notice ensures that the use of iron in listed medicines remains within well-characterised safety limits, as specified in the Poisons Standard. The notice does not extend or restrict its application through subordinate instruments but provides a streamlined process for listing rather than the more rigorous registration process, thereby reducing compliance costs and time for affected entities.

Key Provisions

The Therapeutic Goods (Listing) Notice 2014 (No. 3) (section 9A(5) of the Therapeutic Goods Act 1989) requires that therapeutic goods containing elemental ‘iron’ as a therapeutically active ingredient be included in the Australian Register of Therapeutic Goods (the Register) for listed goods, provided certain conditions are met. Specifically, the preparations must contain a daily dose of not more than 24 mg of iron (section 1(2)(a)), the primary pack must contain not more than 750 mg of iron if the divided preparations contain more than 5 mg of iron per dosage unit (section 1(2)(b)), and the preparations must be for oral use only (section 1(2)(c)). This notice allows for the listing of these goods on the Register, which is a less stringent process than the registration required for other types of medicines. The Act imposes several obligations on the parties and entities it governs. Manufacturers, importers, and sponsors of therapeutic goods containing elemental ‘iron’ must ensure that their products meet the conditions specified in the Listing Notice (sections 19B and 19D of the Therapeutic Goods Act 1989). This includes adhering to the maximum daily dose and primary pack limits for iron content, as well as ensuring that the goods are intended for oral use only. Failure to comply with these requirements can result in the goods not being listed on the Register, thereby preventing their supply in, import into, manufacture in, or export from Australia. The Therapeutic Goods (Listing) Notice 2014 (No. 3) does not create new offences or penalties by itself. However, failure to comply with the conditions specified in the notice can lead to civil or administrative consequences under the Therapeutic Goods Act 1989. For instance, supplying or importing therapeutic goods that do not meet the listing requirements can result in civil penalties (section 101 of the Act). Additionally, if the goods are deemed unsafe or substandard, the Therapeutic Goods Administration (TGA) may take enforcement action, which can include recalls, fines, and other administrative measures. Criminal penalties may also apply if the non-compliance is deemed to be intentional or reckless, potentially leading to prosecution under the Act.

Area of Law: Medical Law
Instrument: Notice
Concepts: Definitions & Interpretation; Regulatory Standards; Licensing & Registration

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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.

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