- Legislation Framework
The Agricultural and Veterinary Chemicals (Administration) Act 1992 establishes the APVMA as an independent statutory authority of the Commonwealth, responsible for the regulation and…
For a new agvet chemical product that contains a new active constituent, the APVMA must approve both the active constituent and register the product.
Registering a new product that contains a new active constituent is made via:
Item 1…A full assessment (Item 1) involves a comprehensive assessment of data for both the active constituent/s and the proposed chemical product is required for chemistry and manufacture, toxicology, poisons scheduling, residues and trade,…
A full assessment (Item 1) involves a comprehensive assessment of data for both the active constituent/s and the proposed chemical product is required for chemistry and manufacture, toxicology, poisons scheduling, residues and trade,…
Most applications to register new veterinary chemical products containing a new active constituent are submitted as a less than full assessment (Item 2) because one or more modules can be assessed below level 1. Examples include products…
Applications to register a new product based on that product being similar or closely similar to a registered reference product can be made via one of the following item numbers:
Item 5…
Schedule 6 of the Agvet Code Regulations provides statutory definitions of when a proposed product is similar or closely similar to a reference product. To determine the appropriate Item number…
Schedule 6 of the Agvet Code Regulations provides statutory definitions of when a proposed product is similar or closely similar to a reference product. To determine the appropriate Item number…
Schedule 6 of the Agvet Code Regulations provides statutory definitions of when a proposed product is similar or closely similar to a reference product. To determine the appropriate Item number…
Schedule 6 of the Agvet Code Regulations provides statutory definitions of when a proposed product is similar or closely similar to a reference product. To determine the appropriate Item number…
-
Registrations and permits
- Search products and permits
-
Chemical product registration
- Applying for approvals, registrations and variations
- Applying for a label approval
- Which products/chemicals require registration
- Before you apply
-
What to include in your application
-
Guide to completing an online application
-
After you apply
- Primary and secondary applications
- Renew a registration
- Technical policy
-
After registration
- APVMA Permit-to-label project
-
Applying for permits
-
Data guidelines
-
Agricultural data guidelines
- Adopted international technical guidance material
- Chemistry and manufacture (Part 2)
- Toxicology (Part 3)
- Metabolism and kinetics (Part 4)
- Residues (Part 5A)
- Overseas trade (Part 5B)
- Occupational health and safety (Part 6)
- Environment (Part 7)
- Pesticides efficacy and crop safety general guideline (Part 8)
- Special data (Part 10) - Products of gene technology
- Special data (Part 10) – Products of nanotechnology
- Guideline for the regulation of biological agricultural products
- Guidance on assessment and registration of anti-fouling paints
- Relevant data for module levels – agricultural chemical products
-
Veterinary data guidelines
- Adopted international technical guidance material
-
Chemistry and manufacture (Part 2)
- Toxicology (Part 3)
- Metabolism and kinetics (Part 4)
- Residues (Part 5A)
- Overseas trade (Part 5B)
- Occupational health and safety (Part 6)
- Environment (Part 7)
- Efficacy and target animal safety general guideline (Part 8)
- Special data (Part 10)
- Specific guidelines
- Relevant data for module levels – veterinary chemical products
- Guidelines for data to support efficacy and safety of teat disinfectants
- Crop Groups
- Module descriptors
- Risk assessment manuals
-
Agricultural data guidelines
-
Labelling Codes
- Agricultural Labelling Code
-
Veterinary Labelling Code
-
Specific labelling requirements
- Anthelmintics for dogs and cats
- Anthelmintics for horses
- Anthelmintics for sheep, goats and cattle
- Anti-inflammatories
- Antibiotics
- Complementary animal health products
- Ectoparasiticides for dogs and cats
- Ectoparasiticides for sheep and goats
- Euthanasiates
- Hormonal growth promotants
- Immunobiological products (veterinary vaccines, antisera, biologicals)
- Intramammary preparations
- Intraruminal products
- Non-prescription injectable products
- Products containing minerals
- Products for application to wounds
- Professional packs of oral non-prescription products
- Stomach tubing products
- Teat dips and sprays
- Therapeutic pet food products
- Preparing a label and approval process
-
Label content
- General labelling requirements
- Anthelmintics for dogs and cats
- Anthelmintics for horses
- Anthelmintics for sheep, goats and cattle
- Anti-inflammatories
- Antibiotics
- Complementary animal health products
- Ectoparasiticides for dogs and cats
- Ectoparasiticides for sheep and goats
- Euthanasiates
- Hormonal growth promotants
- Immunobiological products (veterinary vaccines, antisera, biologicals)
- Intramammary preparations
- Intraruminal products
- Non-prescription injectable products
- Products containing minerals
- Products for application to wounds
- Professional packs of oral non-prescription products
- Stomach tubing products
- Teat dips and sprays
- Therapeutic pet food products
- Label presentation and layout
-
Additional guidance
- Globally harmonized system of classification and labelling
- Promotional and display packs
- Individual, multi- and variable dose forms
- QR codes in the labelling and/or package leaflet
- Removable labels for small single-dose veterinary vaccines
- Professional packs of oral non-prescription veterinary products
-
Specific labelling requirements
- Globally harmonized system of classification and labelling
-
Import and export
- Holders and nominated agents
- Other government requirements
- Limits on use and disclosure of information
-
Application guidance
-
I want to register a new product with an existing active or new combination of approved actives
-
I want to register a new product that contains a new active constituent
- I want to register a new agricultural product that contains a new active constituent – full assessment (Item 1)
- I want to register a new agricultural product that contains a new active constituent – less than a full assessment (Item 2)
- I want to register a new veterinary product that contains a new active constituent (Item 2)
-
I want to register a product that is based on an existing registered reference product
- I want to register an agricultural product that is similar to a registered reference product and efficacy and safety and chemistry and manufacture data is required (Item 5)
- I want to register an agricultural product that is closely similar to a registered reference product and chemistry data is required (Item 6)
- I want to register an agricultural product that is closely similar to a registered reference product – no further data required (Item 7)
- 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)
- I want to register a veterinary product that is based on an existing registered reference product and is closely similar and only chemistry data is required (Item 6)
- I want to register a veterinary product that is based on an existing registered reference product and is closely similar and data is not required (Item 7)
- I want to register a product that is the same as a reference product
- I want to register a product and apply for the concurrent approval of a new source of active
- I want to register or vary a product and I need information on spray drift assessment and labelling
- I want an additional marketing name for my existing registered product
-
I want to vary my product to amend a restraint, contraindication, precaution or side effect statement (vet products only)
- I want to vary my product to amend a restraint, contraindication, precaution or side effect statement (vet products only) and no technical assessment is required (Item 12)
- 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)
-
I want to vary my 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
- 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)
-
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)
-
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 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)
- I want to vary a re-entry or handling instruction for my agricultural product and a technical assessment is required (Item 14)
- I want to vary a re-entry or handling instruction for my veterinary product and no technical assessment is required (Item 12)
- I want to vary a re-entry or handling instruction for my veterinary product and a technical assessment is required (Item 14)
-
I want to vary a withholding period and/or export interval
- I want to vary a withholding period and/or export interval for an agricultural product and no technical assessment is required (Item 12)
- I want to vary a withholding period and/or export interval for an agricultural product and a technical assessment is required (Item 14)
- I want to vary a withholding period and/or export interval for a veterinary product and no technical assessment is required (Item 12)
- I want to vary a withholding period and/or export interval for a veterinary product and a technical assessment is required (Item 14)
-
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)
- I want to vary the use of an agricultural product to include a non-food producing crop or situation (Item 14)
- 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)
-
I want to vary the sites of product manufacture
- I want to vary the pack size of my registered product
-
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)
-
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)
-
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)
-
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
- Active constituent applications guidance
- Training resources
-
I want to register a new product with an existing active or new combination of approved actives
- Get assistance
- Seek review of a decision
- Application summaries
-
Chemicals and products
-
Active constituents
- APVMA standards for active constituents for use in agricultural chemical products
- Active constituents exempt from the requirements of APVMA approval for use in agricultural or veterinary chemical products
- General list of impurities and classes of impurities of toxicological concern for agricultural active constituents
- Approval of active constituents
- Uniform expression of active constituents
- FAISD Handbook
- Health based guidance values
- Pesticides and veterinary residues
- Scheduled drugs and poisons
-
Active constituents
-
Regulation
- Adverse Experience Reporting Program
-
Chemical review
- Chemical review process
-
Listing of chemical reviews
- Reconsiderations listed in the Ministerial Direction
- List of voluntary cancellations at the request of the holder
- Voluntary suspensions at the request of the holder
- Prioritisation of chemicals nominated for review
- 2010 spray drift label review nominations
- Compliance and enforcement
- Hormonal growth promotants
- Levy audit program
-
Manufacturing
- Recalls
- Report a problem
- Resources
-
About
-
About us
- Agvet chemical regulation
- Use of agvet chemicals in Australia
- Access to information held by the APVMA
- Accountability and reporting
- Careers
-
Communication and decision making
-
Section 6A Guidelines
- Overarching principles and processes for the effective and efficient regulation of agricultural and veterinary chemical products
- Approvals and registrations
- Permits
- Remitting certain application fees under the Agvet Code
- Licences
- Recategorising applications
- Requesting information from applicants
- Limits on use of information
- Reconsidering approvals and registrations
- Varying relevant particulars and conditions
- Formulation types
- Previous s 6A Guidelines
- Communication between applicants and the APVMA
- Data handling by the APVMA
- External advice
- Transparency
-
Section 6A Guidelines
- Stakeholder engagement
-
International collaboration
- Our website and your privacy
-
About us
- Online Services Portal (Opens in a new tab/window)
- News, forms and publications
- Contact us
-
Registrations and permits
- Search products and permits
- Chemical product registration
- Applying for permits
- Data guidelines
- Labelling Codes
- Import and export
- Holders and nominated agents
- Other government requirements
- Limits on use and disclosure of information
- Application guidance
- Get assistance
- Seek review of a decision
- Application summaries
- Chemicals and products
- Regulation
- Resources