- ContentsNotice under section 34AB of the Agricultural and Veterinary Chemicals Code scheduled to the Agricultural and Veterinary Chemicals Code Act 1994: anticoagulant rodenticides reconsideration - proposed decision to vary and affirm active…
Click on the tabs for more information about the status of each phase in the review process. For more information about how each phase is conducted, please read about the reconsideration process.
After a detailed review, the Australian Pesticides and Veterinary Medicines Authority (APVMA) has finalised its risk assessments on anticoagulant rodenticides and is proposing substantial changes to products in this category to protect the safety…
Details of current reconsiderations including published documents and details of previous review actions can be accessed from the listing of chemical review. The current forecast dates for publication of the proposed regulatory decisions, public…
Click on the tabs for more information about the status of each phase in the review process. For more information about how each phase is conducted, please read about the reconsideration process.
Click on the tabs for more information about the status of each phase in the review process. For more information about how each phase is conducted, please read about the reconsideration process.
The Agvet Code requires the APVMA to approve active constituent(s) contained in an agricultural chemical product intended for distribution, sale or use in Australia. This applies regardless of whether the product is formulated in Australia…
The Australian Pesticides and Veterinary Medicines Authority (APVMA) can issue a formal written warning if we have reasonable grounds to suspect that a person has contravened the Agvet Code, the Agricultural and Veterinary Chemicals…
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Application guidance
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I want to register a new product with an existing active or new combination of approved actives
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I want to register a new product that contains a new active constituent
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I want to register a product that is based on an existing registered reference product
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- I want to register a veterinary product that is based on an existing registered reference product and similar efficacy, safety, chemistry and manufacture data is required (Item 5)
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I want to vary my product to amend a restraint, contraindication, precaution or side effect statement (vet products only)
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- I want to vary my product to amend a restraint, contraindication, precaution or side effect statement (vet products only) and a technical assessment is required (Item 14)
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I want to vary my product to alter the shelf life/expiry date, in-use shelf life and/or storage conditions
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I want to vary my agricultural product to alter the shelf life/expiry date, in-use shelf life and/or storage conditions
- I want to vary my agricultural product to alter the shelf life/expiry date, in-use shelf life and/or storage conditions and no technical assessment is required (Item 12)
- I want to vary my agricultural product to alter the shelf life/expiry date, in-use shelf life and/or storage conditions and a technical assessment is required (Item 14)
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I want to vary my veterinary product to alter the shelf life/expiry date, in-use shelf life and/or storage conditions
- I want to vary my veterinary product to alter the shelf life/expiry date, in-use shelf life and/or storage conditions and no technical assessment is required (Item 12)
- I want to vary my veterinary product to alter the shelf life/expiry date, in-use shelf life and/or storage conditions and a technical assessment is required (Item 14)
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I want to vary my agricultural product to alter the shelf life/expiry date, in-use shelf life and/or storage conditions
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I want to vary a re-entry or handling instruction for my product
- I want to vary a re-entry or handling instruction for my agricultural product and no technical assessment is required (Item 12)
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I want to vary a withholding period and/or export interval
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- I want to vary a withholding period and/or export interval for a veterinary product and a technical assessment is required (Item 14)
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I want to vary the use of a product to include a new crop, animal species or situation
- I want to vary the use of an agricultural product to include a new crop or situation and no technical assessment is required (Item 12)
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- I want to vary the use of an agricultural product to include a food producing crop or situation (Item 14)
- I want to vary the use of a veterinary product to include a new animal species or situation and no data of a technical nature is required (Item 12)
- I want to vary the use of a veterinary product to include a non-food species, including companion animals (Item 14)
- I want to vary the use of a veterinary product to include a food producing animal species (Item 14)
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I want to vary the sites of product manufacture
- I want to vary the pack size of my registered product
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I want to vary the use of a product to include a new use, new application method, or new use instructions within an existing crop or situation (agricultural chemical products only)
- I want to vary the use of an agricultural product to include a new use, new application method, or new use instructions within an existing crop or situation and no technical assessment is required (Item 12)
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I want to vary the use of an agricultural product to include a new use, new application method, or new use instructions within an existing crop or situation and a technical assessment is required (Item 14)
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I want to vary my product to make a change to the product formulation
- I want to vary my agricultural product to make a change to the product formulation and a Prescribed Variation is required (Item 13A – only changes to non-active constituents in limited circumstances)
- I want to vary my agricultural product to make a change to the product formulation and no technical assessment is required (Item 12)
- I want to vary my agricultural product to make a change to the product formulation and a technical assessment is required (Item 14)
- I want to vary my veterinary product to make a change to the product formulation and a Prescribed Variation is required (Item 13A – only changes to non-active constituents in limited circumstances)
- I want to vary my veterinary product to make a change to the product formulation and no technical assessment is required (Item 12)
- I want to vary my veterinary product to make a change to the product formulation and a technical assessment is required (Item 14)
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I want to vary my product to include a new dose rate, frequency, route of administration or application method (vet products only)
- I want to vary my product to include a new dose rate, frequency, route of administration or application method (vet products only) No technical assessment is required (Item 12)
- I want to vary my veterinary product to include a new dose rate, frequency, route of administration or application method and a technical assessment is required (Item 14)
- I want to submit a timeshift application
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I want to register a new product with an existing active or new combination of approved actives
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