Australia New Zealand Food Standards Code—Schedule 20–maximum residue limits Variation Instrument No. APVMA 3, 2019

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Legislation au F2019L00670 Not in force Legislative Instrument

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EXPLANATORY STATEMENT

 

 

Australia New Zealand Food Standards Code—

Schedule 20—Maximum Residue Limits

Variation Instrument No. APVMA 3, 2019

 

 

Subsection 82(1) of the Food Standards Australia New Zealand Act 1991 provides that the Australian Pesticides and Veterinary Medicines Authority (APVMA) may vary the Maximum Residue Limits Standard to include or change a permitted maximum residue limit.  The Maximum Residue Limits Standard in the Australia New Zealand Food Standards Code (Food Standards Code) is Schedule 20 — Maximum Residue Limits. 

Schedule 20 is the Principal Instrument being amended by this Amendment Instrument.  It has existed in various forms since before the Food Standards Code was first published in 1997. 

Section 82 was part of amendments to the Food Standards Australia New Zealand Act 1991 (FSANZ Act), which were proclaimed to commence on 1 March 2011, that implemented a 2008 reform agreed to by the Council of Australian Governments (COAG) calling for the recognition by Food Standards Australia New Zealand (FSANZ) of the APVMA’s residue risk assessment and the promulgation of the resulting MRLs in the Food Standards Code, for domestically grown produce.  The reform was designed to streamline current regulatory processes and to eliminate duplication by allowing the APVMA to directly vary Schedule 20. 

The APVMA is an independent statutory authority of the Commonwealth.  Amongst other things, the APVMA is responsible for ensuring agricultural and veterinary (agvet) chemicals used in Australia are not harmful to public health due to residues in food. 

The Agreement between the Government of Australia and the Government of New Zealand concerning a Joint Food Standards System excludes MRLs for residues of agvet chemicals in food from the system setting joint food standards. Australia and New Zealand independently and separately develop MRLs for agvet chemicals in food. 

Assessment and Determination of MRLs

MRLs are regulatory standards which help to monitor that the agvet chemical product has been used in accordance with the approved label instructions.  If an MRL is exceeded, it usually indicates a misuse of the chemical but does not normally indicate a public health or safety concern.

In evaluating the safety and performance of agvet chemicals, the APVMA’s assessment also includes a determination of an MRL for the chemical in relation to relevant crops and animals.  The APVMA uses data from a series of residue trials and calculates whether the application of the minimum amount of chemical that is required to achieve effective pest or disease control will leave any residue in the plant or animal commodity.  In order to legitimise the presence of these residues, MRLs are established by the APVMA by entry into the APVMA’s MRL Standard (available at http://www.comlaw.gov.au).

If there are small amounts of chemical residue in produce, the APVMA uses the toxicological evaluation and the dietary exposure assessment to examine the potential occurrence of adverse effects on human health when the produce is consumed. 

Dietary exposure assessments undertaken by the APVMA as part of the registration of the relevant chemical products indicate that the MRL variations being made by the Amendment Instrument do not present any public health and safety concerns.

Schedule 20 of lists the maximum level of the residues of an agvet chemical that may occur in foods.  Including limits for residues of agvet chemicals in foods in the Food Standards Code has the effect of allowing the sale of food containing legitimate residues, where any residues do not exceed these limits.  Variations in MRLs reflect the changing use patterns of agvet chemicals available to chemical users including food producers.  These changes include both the development of new products and crop uses, and the withdrawal of older products following review by the APVMA. 

Regulatory Impact Assessment

The proposed changes to regulation are minor and machinery in nature involving necessary technical variations to the Food Standards Code.  In November 2010, the Office of Best Practice Regulation provided a standing exemption from the need to assess if a Regulatory Impact Statement is required for applications relating to variations to MRLs.

The proposed MRL amendments are an essential consequence of the decision by the APVMA to register agvet chemical products (or to vary and extend their approved label instructions); or to issue a permit in relation to an agvet chemical product; or an outcome of a review decision by the APVMA to withdraw or restrict older agvet chemical products.  The setting of an MRL and its incorporation in the Food Standards Code is a science-based outcome arising from these decisions and for which there is only very limited discretion on the part of the APVMA decision maker. 

The proposal to vary MRLs in the Food Standards Code is likely to have negligible impacts on business, individuals, regulatory agencies or the economy.  Primary producers understand the need to use only registered agvet chemical products and to use those products strictly in accordance with approved label instructions.  In doing so, produce grown will be within the MRL set by the APVMA and, with the incorporation of those MRLs into the Food Standards Code by this Amendment Instrument, the sale of the produce containing residues that do not exceed the MRL will be lawful.  To this extent, the incorporation of APVMA approved MRLs into Schedule 20   of the Food Standards Code benefits rather than burdens primary producers and consumers.

Consultations

The APVMA seeks the wider community’s involvement through public consultation as part of its evaluation process for the registration of new agvet chemical products or a major extension of the use of existing products to new crops and target animals.  During this consultation phase any person may comment or raise concerns about any relevant aspect of the intended registration, sale and use of the chemical product, including proposed MRLs and the dietary exposure assessment.  The APVMA addressed any concerns that were raised at the time as part of the registration and approval process. 

More specifically, by way of notice in the Agricultural and Veterinary Chemicals Gazette (No. APVMA 2) on 29 January 2019 the APVMA notified that it was proposing to incorporate these variations to MRLs into Schedule 20 and it invited public comment on the proposals. The APVMA did not receive any comments during this stage of the consultations.

A Sanitary and Phytosanitary notification to the World Trade Organization (WTO) was also made in relation to the variations to MRLs in Schedule 20 and comment was received in response to that notice consultations are continuing.

Variations to MRLs are Legislative Instruments

Pursuant to subsection 82(2) of the FSANZ Act, the variations to MRLs made by the Amendment Instrument is a legislative instrument for the purposes of the
Legislation Act 2003, but it is neither subject to the disallowance nor sunsetting provisions. 


NOTES ON ITEMS

Item 1 Name of Instrument

1. This item states that the full name of the Amendment Instrument is the Australia New Zealand Food Standards Code — Schedule 20 — Maximum Residue Limits Amendment Instrument No. APVMA 3, 2019.

Item 2 Commencement

2. Subsection 82(8) of the Food Standards Australia New Zealand Act 1991 has the effect that, despite the provisions in the Legislation Act 2003, a legislative instrument made by the APVMA varying Schedule 20 commences on the day a copy of the variation is published in the Gazette.

3. A Note to the item records that a copy of the variations made by the Amendment Instrument was published in the Commonwealth of Australia Agricultural and Veterinary Chemicals Gazette.

Item 3 Object

4. This item provides that the object of this Amendment Instrument is for the APVMA to vary Schedule 20 of the Food Standards Code to include or change MRLs pertaining to agricultural and veterinary chemical products.

Item 4 Interpretation

5. This item defines the APVMA and the Principal Instrument.

6. The APVMA is the Australian Pesticides and Veterinary Medicines Authority established by section 6 of the Agricultural and Veterinary Chemicals (Administration) Act 1992.

7. The Principal Instrument is Schedule 20 — Maximum Residue Limits of the Australia New Zealand Food Standard Code as defined in Section 4 of the Food Standards Australia New Zealand Act 1991 being the code published in Gazette
No. P 27 on 27 August 1987 together with any amendments of the standards in that code. 

8. The definition of Principal Instrument also notes that Schedule 20 was published in the Food Standards Gazette FSC 96 on Thursday 10 April 2015 and was registered as a legislative instrument on 1 April 2015 F2015L00468.

Item 5 Variations to Schedule 20

9. This item provides that the Schedule to this Amendment Instrument sets out the variations to Schedule 20 – Maximum Residue Limits of the Food Standards Code.

10. The variations to MRLs made by the Amendment Instrument include variations made by the APVMA to the MRL Standard for January 2019 comprising amendments numbered (Agricultural and Veterinary Chemicals Code Instrument No. 4 (MRL Standard) Amendment Instrument 2019 (No. 1)) inclusive.

 

By Authority:

Chief Executive Officer

Delegate of the APVMA

1 May 2019


STATEMENT OF COMPATIBILITY FOR A LEGISLATIVE INSTRUMENTTHAT DOES NOT RAISE ANY HUMAN RIGHTS ISSUES

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Overview

The Australia New Zealand Food Standards Code — Schedule 20 — Maximum Residue Limits Amendment Instrument No. APVMA 3, 2019, was enacted to streamline the process of varying maximum residue limits (MRLs) for agricultural and veterinary (agvet) chemicals in food. This legislative instrument, introduced under the Food Standards Australia New Zealand Act 1991, aims to eliminate duplication and ensure efficient regulatory processes. The Australian Pesticides and Veterinary Medicines Authority (APVMA) is responsible for varying MRLs in the Food Standards Code, reflecting the current use patterns of agvet chemicals. This authority allows the APVMA to directly amend the MRL Standard, which was established to monitor the safe use of agvet chemicals and to ensure that any residues in food do not exceed safe limits. The APVMA evaluates the safety of these chemicals and establishes MRLs accordingly, taking into account dietary exposure assessments to ensure public health is not compromised. The legislative instrument was enacted by the APVMA and is designed to benefit primary producers and consumers by allowing the lawful sale of produce with legitimate residues that do not exceed the established MRLs.

Scope and Application

The Australia New Zealand Food Standards Code—Schedule 20—Maximum Residue Limits Variation Instrument No. APVMA 3, 2019 applies to the Australian Pesticides and Veterinary Medicines Authority (APVMA) and governs the establishment and variation of maximum residue limits (MRLs) for agricultural and veterinary (agvet) chemicals in food within Australia. This legislation operates under the authority granted by subsection 82(1) of the Food Standards Australia New Zealand Act 1991, which empowers the APVMA to alter the MRLs in the Australia New Zealand Food Standards Code. The MRLs pertain to residues of agvet chemicals in food and are designed to ensure that any residues present do not pose a public health risk. The scope of this Act extends to all food products containing residues of agvet chemicals that are produced and sold within Australia. Notably, the Act does not cover MRLs for New Zealand, as Australia and New Zealand independently develop MRLs for agvet chemicals in food. The variations made to the MRLs by this Instrument are legislative instruments that do not fall under the disallowance or sunsetting provisions, and they commence on the day of publication in the Gazette.

Key Provisions

The primary operative sections of this legislation are sections 2 and 5. Section 2 outlines the object of the Amendment Instrument, which is for the APVMA to vary Schedule 20 of the Food Standards Code to include or change MRLs pertaining to agricultural and veterinary chemical products (Section 4). Section 5 provides the interpretation of key terms, such as the APVMA and the Principal Instrument (Schedule 20). The Schedule to this Amendment Instrument contains the specific variations to Schedule 20 – Maximum Residue Limits of the Food Standards Code (Section 9). The obligations and requirements imposed by this Act on the parties or entities it governs are primarily centred around the APVMA's role in assessing and determining MRLs for agricultural and veterinary chemical products. The APVMA is responsible for ensuring that these chemicals are not harmful to public health due to residues in food. This includes conducting residue trials, calculating MRLs, and incorporating them into the APVMA's MRL Standard. Additionally, the APVMA must consult with the wider community during the evaluation process for the registration of new chemical products or major extensions of the use of existing products to new crops and target animals. Failure to comply with the provisions of this legislation may result in civil or criminal consequences. However, the Explanatory Statement does not provide specific details on the offences, penalties, or consequences for breach. It is important to note that the APVMA is an independent statutory authority and is responsible for ensuring that agricultural and veterinary chemical products are safe for use in Australia. In summary, this legislation allows the APVMA to vary MRLs for agricultural and veterinary chemical products in the Food Standards Code. The APVMA is responsible for assessing and determining MRLs, and must consult with the wider community during the evaluation process. Failure to comply with the provisions of this legislation may result in civil or criminal consequences, although specific details on these consequences are not provided in the Explanatory Statement.

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