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Australian Pesticides and Veterinary Medicines Authority
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  • Registrations and permits
    • Search registered chemical products and permits
      • Search PubCRIS
      • Using PubCRIS
    • Chemical product registration
    • Guidance for applicants
    • Primary and secondary applications
    • Data guidelines
      • Agricultural data guidelines
      • Veterinary data guidelines
      • Crop groups
      • Risk assessment manuals
      • Module descriptors
    • Agricultural Labelling Code
    • Veterinary Labelling Code
    • Permits
    • Import and export
    • Holders and nominated agents
    • Getting assistance from the APVMA
    • Other Australian Government requirements
    • Limits on use and disclosure of information
    • Seek review of a decision
    • Applications and decisions
  • 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
    • FAISD Handbook
    • Health based guidance values
      • Acceptable daily intakes for agricultural and veterinary chemicals
      • Acute reference doses for agricultural and veterinary chemicals
    • Pesticides and veterinary residues
      • Export slaughter intervals – cattle
      • Export slaughter intervals – sheep
  • Regulatory operations
    • How we monitor compliance
    • Adverse Experience Reporting Program
    • Assessment, Investigation and Monitoring
    • Audits and inspections frequently asked questions
    • Chemical review
    • Enforcement
    • Hormonal growth promotants (HGPs)
    • Levy audit program
    • Manufacturing
    • Recalls
      • Agvet chemical recalls
    • Report a problem with a chemical or product
      • Report an adverse experience
      • Report suspected non-compliance
      • Holders to notify the APVMA of new information
  • Resources
    • Chemicals in the news
      • 1080
      • Bromadiolone and the mouse plague
      • Chlorpyrifos
      • Glyphosate
      • Neonicotinoids
    • Education
      • Presentations
      • Scheduled drugs and poisons
    • Importing chemicals
    • Supplying chemicals
      • Information for suppliers
    • Using chemicals
      • Information for farmers
      • Information for veterinarians
      • Choosing a chemical
      • Understanding pesticide chemical labels
      • Concerns about chemicals
      • Using chemicals correctly
      • Spray drift
      • Emerging technologies
  • Home
  • Registrations and permits
    • Registrations and permits
    • Search registered chemical products and permits
      • Search registered chemical products and permits
      • Search PubCRIS
      • Using PubCRIS
    • Chemical product registration
      • Chemical product registration
      • Agricultural Labelling Code
        • Agricultural Labelling Code
        • Data guidelines
        • Guidance for preparing information lists
        • Dossiers
        • Required information
        • Statutory criteria
          • Statutory criteria
          • Active constituent
          • Chemical product
            • Chemical product
            • Safety criteria
            • Efficacy criteria
            • Trade criteria
            • Labelling criteria
          • Satisfying the statutory criteria
        • Providing evidence of good manufacturing practice (GMP)
        • Guidance for applicants – submission of international data, standards and assessments
          • Guidance for applicants – submission of international data, standards and assessments
          • Accepted international data and standards
          • International and other national assessments
          • How to submit an international assessment
          • What happens once I submit my overseas/international assessment?
      • Applying for approvals, registrations and variations
      • Applying for a label approval
      • Which products/chemicals require registration
        • Which products/chemicals require registration
        • Does my veterinary product need to be registered?
          • Does my veterinary product need to be registered?
          • User guide: what is or isn't a veterinary product?
            • User guide: what is or isn't a veterinary product?
            • Animal cosmetic products
              • Animal cosmetic products
              • Excluded animal cosmetic products – acceptable cosmetic messages
            • Animal feed products
              • Animal feed products
              • Acceptable nutritional messages
              • Feed supplements – acceptable nutritional messages
              • Other requirements for whole unprocessed animal tissue
            • Devices, equipment and physical barrier products
            • Other products that don't require registration
          • Registration self-assessment tool (veterinary)
        • Does my agricultural product need to be registered?
        • Changes to stockfeed and petfood regulation
          • Changes to stockfeed and petfood regulation
          • END product FAQs
        • Novel products
        • Arrangements for products of low regulatory concern
          • Arrangements for products of low regulatory concern
          • Registration models
            • Registration models
            • Oral electrolyte products for the treatment of horses in exercise
          • Reserved chemical products
          • Listed chemical product
        • Exemptions
        • Substances not permitted for use on food-producing animals in Australia
        • Lures and attractants
      • Before you apply
        • Before you apply
        • About the approval and registration process
        • Who can apply
        • Restricted chemical products
        • Conditions of approval or registration and label approval
        • Minor variations
        • The risk analysis process
        • Timeframes and fees
        • Interchangeable Constituent Determination - Item 29
      • What to include in your application
      • Guide to completing an online application
        • Guide to completing an online application
        • Online Services Portal
        • Decision tree
        • Identification, applicant and nominated agent details
        • Data and information lists
          • Data and information lists
          • Using the information list editor
        • Access to information
        • Formulation
        • Manufacturing
        • Packaging and storage
        • Labels
        • Submitting an application
        • Submitting third party information
      • After you apply
        • After you apply
        • What happens next
        • Preliminary assessment process
        • Requiring samples or further information
          • Requiring samples or further information
          • Requiring additional information
          • Requiring samples to be given for analysis
          • Extended assessment period and maximum response period
      • Renew a registration
      • Technical policy
        • Technical policy
        • No-observed-effect level and no-observed-adverse effect level: use in animal health risk assessments
        • Worker health and safety risk assessments undertaken by the APVMA
      • After registration
        • After registration
        • Changes to products and actives
          • Changes to products and actives
          • Holders to notify the APVMA of new information
        • Annual returns
          • Annual returns
          • Annual reporting of actives–frequently asked questions
        • Levies charged on chemical products
          • Levies charged on chemical products
          • Declaration of leviable values
          • Notice of levy calculation
    • Guidance for applicants
      • Guidance for applicants
      • I want to register a new product with an existing active or new combination of approved actives
        • I want to register a new product with an existing active or new combination of approved actives
        • Agricultural product
        • Veterinary product
      • I want to register a new product which contains a new active constituent
        • I want to register a new product which contains a new active constituent
        • Agricultural product
          • Agricultural product
          • Requires a full assessment
          • Requires less than a full assessment
        • Veterinary product
      • I want to register a product that is based on an existing registered reference product
        • I want to register a product that is based on an existing registered reference product
        • Agricultural product
          • Agricultural product
          • Similar to a registered reference product and efficacy, safety, chemistry and manufacture data is required
          • Closely similar to a registered reference product and chemistry data is required
          • Closely similar to a registered reference product—no further data required
        • Veterinary product
          • Veterinary product
          • That is similar and efficacy, safety, chemistry and manufacture data is required
          • Closely similar and only chemistry data is required
          • Closely similar and data is not required
      • I want to register a product that is the same as a reference product
        • I want to register a product that is the same as a reference product
        • Agricultural product
          • Agricultural product
          • Uses my own product as the reference product and it has no protected data associated with it
          • Does not use my own product as the reference product and/or has protected data associated with the reference product
        • Veterinary product
          • Veterinary product
          • Uses my own product as the reference product and it has no protected data associated with it
          • Does not use my own product as the reference product and/or has protected data associated with the 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 an additional marketing name for my existing registered product
        • Agricultural product
        • Veterinary 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)
        • No technical assessment is required
        • Technical assessment is required
      • 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 product to alter the shelf life/expiry date, in-use shelf life and/or storage conditions
        • Agricultural product
          • Agricultural product
          • No technical assessment is required
          • Technical assessment is required
        • Veterinary product
          • Veterinary product
          • No technical assessment is required
          • Technical assessment is required
      • 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 product
        • Agricultural product
          • Agricultural product
          • No technical assessment is required
          • Technical assessment is required
        • Veterinary product
          • Veterinary product
          • No technical assessment is required
          • Technical assessment is required
      • I want to vary a withholding period and/or export interval
        • I want to vary a withholding period and/or export interval
        • Agricultural product
          • Agricultural product
          • I want to vary a withholding period and/or export interval for an agricultural product and no technical assessment is required
          • I want to vary a withholding period and/or export interval for an agricultural product and a technical assessment is required
        • Veterinary product
          • Veterinary product
          • I want to vary a withholding period and/or export interval for a veterinary product and no technical assessment is required
          • I want to vary a withholding period and/or export interval for a veterinary product and a technical assessment is required
      • I want to vary the use of my product to include a new crop, animal species or situation
        • I want to vary the use of my product to include a new crop, animal species or situation
        • Agricultural product
          • Agricultural product
          • To a new crop or situation and no technical assessment is required
          • To a food producing crop or situation
          • To a non-food producing crop or situation
        • Veterinary product
          • Veterinary product
          • To a new animal species or situation and no data of a technical nature is required
          • To a non-food species, including companion animals
          • To a food producing animal species
      • I want to vary the sites of product manufacture
        • I want to vary the sites of product manufacture
        • I want to vary the site of manufacture for my veterinary product and the variation involves the addition of an overseas site of manufacture that performs a primary step/s of manufacture
        • Guideline for the transfer of a manufacturing site for immunobiological products
      • 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 a product to include a new use, new application method, or new use instructions within an existing crop or situation (agricultural chemical products only)
        • No technical assessment is required
        • Technical assessment is required
      • I want to vary my product to make a change to the product formulation
        • I want to vary my product to make a change to the product formulation
        • Agricultural product
          • Agricultural product
          • A Prescribed Variation is required
          • No technical assessment is required
          • A technical assessment is required
        • Veterinary product
          • Veterinary product
          • A Prescribed Variation is required
          • No technical assessment is required
          • Technical assessment is required
      • I want to vary my product to include a new dose rate, frequency, route of administration or application method
        • I want to vary my product to include a new dose rate, frequency, route of administration or application method
        • No technical assessment is required
        • A technical assessment is required
      • I want to submit a timeshift application
    • Primary and secondary applications
    • Data guidelines
      • Data guidelines
      • Agricultural data guidelines
        • Agricultural data guidelines
        • Adopted international technical guidance material
        • Chemistry and manufacture (Part 2)
          • Chemistry and manufacture (Part 2)
          • Specific guidelines
        • Toxicology (Part 3)
        • Metabolism and kinetics (Part 4)
        • Residues (Part 5A)
          • Residues (Part 5A)
          • Specific guidelines
        • Overseas trade (Part 5B)
        • Occupational health and safety (Part 6)
        • Environment (Part 7)
          • Environment (Part 7)
          • Roadmap for insect pollinator risk assessments in Australia
        • Pesticides efficacy and crop safety general guideline (Part 8)
          • Pesticides efficacy and crop safety general guideline (Part 8)
          • Specific guidelines
        • 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
        • Veterinary data guidelines
        • Adopted international technical guidance material
        • Chemistry and manufacture (Part 2)
          • Chemistry and manufacture (Part 2)
          • Chemistry and manufacture of active constituents (Part 2)
            • Chemistry and manufacture of active constituents (Part 2)
            • Approval of active constituents for which information is not readily available
          • Chemistry and manufacture of products (Part 2)
          • Additional data guidelines for chemistry and manufacture (Part 2)
        • Toxicology (Part 3)
        • Metabolism and kinetics (Part 4)
          • Metabolism and kinetics (Part 4)
          • Comparative metabolism studies, selection of marker residues and ratios of marker residues to total residues
        • Residues (Part 5A)
          • Residues (Part 5A)
          • Specific guidelines
        • Overseas trade (Part 5B)
          • Overseas trade (Part 5B)
          • Veterinary drug residues in food commodities and overseas trade
        • 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
      • Crop groups
        • Crop groups
        • What is crop grouping?
        • Crop groupings project – consolidated responses to phase one consultation
          • Crop groupings project – consolidated responses to phase one consultation
          • NWPGP grain industry comments
      • Risk assessment manuals
      • Module descriptors
    • Agricultural Labelling Code
      • Agricultural Labelling Code
      • Globally harmonized system of classification and labelling
      • Agricultural Labelling Code
    • Veterinary Labelling Code
      • Veterinary Labelling Code
      • Specific labelling requirements
        • 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
        • 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
        • 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
    • Permits
      • Permits
      • Before you apply
        • Before you apply
        • About the application process
        • Types of permits
          • Types of permits
          • Export, research and miscellaneous permits
          • Minor use and emergency permits
            • Minor use and emergency permits
            • Guide for determining emergency uses or research purposes
            • Guide for determining minor uses
        • Who can apply
          • Who can apply
          • Fit and proper person test
        • Technical assessment
        • Timeframe and fees
        • Ability to comply with conditions
      • What to include in your application
        • What to include in your application
        • Required information
        • Statutory criteria
        • Labelling requirements
      • After you apply
        • After you apply
        • What happens next
        • Requiring samples or further information
      • Extend the duration of a permit
      • Search for a permit
    • Import and export
      • Import and export
      • Importing agricultural chemicals or veterinary medicines
      • Export permits
      • Export certificates
        • Export certificates
        • Before you apply
          • Before you apply
          • About the application process
          • Timeframe and fees
          • Who can apply
          • Common types of certificates
        • What to include in your application
          • What to include in your application
          • Information to be provided with a request for a section 70 certificate
      • Consent to import chemical products
    • Holders and nominated agents
      • Holders and nominated agents
      • Change a holder or nominated agent
        • Change a holder or nominated agent
        • Timeframe and fees for changing a holder or nominated agent
      • Definition of roles and actions for holders, nominated and authorised agents and authorising parties
    • Getting assistance from the APVMA
      • Getting assistance from the APVMA
      • Pre-application assistance
        • Pre-application assistance
        • Applying for pre-application assistance
        • Getting the most out of pre-application assistance
        • Pre-application assistance – timeframes and fees
        • How to withdraw a request for pre-application assistance
      • Technical assessment
    • Other Australian Government requirements
      • Other Australian Government requirements
      • Drinking water guidelines—pesticides
    • Limits on use and disclosure of information
      • Limits on use and disclosure of information
      • Information and the use of information
      • Limitation periods
      • Information lists
      • Authorising party
      • Exceptions
    • Seek review of a decision
      • Seek review of a decision
      • Reviewing decisions
      • Approval or variation of an active constituent or registration
      • Permits
      • Renewal of registration
      • Certificates for exporting agricultural and veterinary chemical product
      • Change the holder or nominated agent
    • Applications and decisions
      • Applications and decisions
      • Application summaries
      • Application summaries - Q&A
  • Chemicals and products
    • Chemicals and products
    • Active constituents
      • 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
    • FAISD Handbook
    • Health based guidance values
      • Health based guidance values
      • Acceptable daily intakes for agricultural and veterinary chemicals
      • Acute reference doses for agricultural and veterinary chemicals
    • Pesticides and veterinary residues
      • Pesticides and veterinary residues
      • Export slaughter intervals – cattle
      • Export slaughter intervals – sheep
  • Regulatory operations
    • Regulatory operations
    • How we monitor compliance
    • Adverse Experience Reporting Program
      • Adverse Experience Reporting Program
      • Adverse Experience Reporting Program annual reports
    • Assessment, Investigation and Monitoring
      • Assessment, Investigation and Monitoring
      • Responsibilities of holders
      • Analysts
        • Analysts
        • Criteria for Appointment as Approved Analyst
      • Maintaining particulars
      • Policy, strategy and disclosure
    • Audits and inspections frequently asked questions
    • Chemical review
      • Chemical review
      • Chemical review process
        • Chemical review process
        • Legislative basis
        • History of the chemical review program
        • The reconsideration process
        • Timeframes for chemical reviews
      • Listing of chemical reviews
        • Listing of chemical reviews
        • Chemicals nominated and prioritised for reconsideration
        • Label reviews
          • Label reviews
          • Anticoagulant rodenticides
          • 2,4-D
            • 2,4-D
            • Technical note on standards for the classification of nozzles in Australia
            • Technical note on aquatic regulatory acceptable level calculation
          • Bromoxynil
          • Mercury fungicides
      • 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
    • Enforcement
      • Enforcement
      • Formal warnings
      • Substantiation notices
      • Notice to attend, give information or produce documents or items
      • Enforceable Undertakings
      • Enforceable directions
      • Infringement notice penalty amounts
    • Hormonal growth promotants (HGPs)
      • Hormonal growth promotants (HGPs)
      • List of current HGP notification numbers
    • Levy audit program
    • Manufacturing
      • Manufacturing
      • COVID-19: advice for veterinary medicine manufacturers and holders
      • Manufacturing licences
        • Manufacturing licences
        • Manufacturers’ Licensing Scheme
        • Applying for a manufacturing licence
        • Who can apply
        • Manufacturing licence fees
        • Licence conditions
        • After you apply
        • Variation of a manufacturing licence
        • Audits to obtain and vary a licence
        • Apply now
      • Responsibilities of manufacturers
      • Exporting veterinary chemical products
      • Manufacturing overseas
        • Manufacturing overseas
        • GMP in overseas premises
        • Recognition of overseas GMP authorities
        • Overseas GMP documentation
        • Acceptable evidence of GMP compliance
        • APVMA audits of overseas manufacturers
      • Contract manufacture
        • Contract manufacture
        • Release for supply
        • Performing release for supply
        • Responsibilities in contract manufacture
      • Good Manufacturing Practice (GMP)
        • Good Manufacturing Practice (GMP)
        • The legislative basis for the APVMA’s role in manufacturing quality and licensing
        • Manufacturing Principles
      • Veterinary manufacturing permit
      • Audits
        • Audits
        • Arranging and undergoing an audit
        • Audit ratings and scores
        • Audits of Australian veterinary chemical product manufacturing sites
        • Audits of overseas manufacturing sites by APVMA-authorised auditors
        • Audit closure
        • The GMP audit cycle
        • Risk-based scheduling of GMP audits
      • Licensed manufacturers
    • Recalls
      • Recalls
      • Agvet chemical recalls
    • Report a problem with a chemical or product
      • Report a problem with a chemical or product
      • Report an adverse experience
      • Report suspected non-compliance
      • Holders to notify the APVMA of new information
  • Resources
    • Resources
    • Chemicals in the news
      • Chemicals in the news
      • 1080
      • Bromadiolone and the mouse plague
      • Chlorpyrifos
      • Glyphosate
      • Neonicotinoids
    • Education
      • Education
      • Presentations
      • Scheduled drugs and poisons
    • Importing chemicals
    • Supplying chemicals
      • Supplying chemicals
      • Information for suppliers
    • Using chemicals
      • Using chemicals
      • Information for farmers
        • Information for farmers
        • Chemicals and farming
        • Useful links for farmers
      • Information for veterinarians
      • Choosing a chemical
      • Understanding pesticide chemical labels
      • Concerns about chemicals
      • Using chemicals correctly
        • Using chemicals correctly
        • Workplace health and safety
        • Protective clothing
        • Spraying chemicals
        • Using veterinary medicines
        • Using pool chemicals
      • Spray drift
        • Spray drift
        • Spray drift definitions
        • Spray drift risk operating principles
      • Emerging technologies
  • About
    • About
    • About us
      • About us
      • APVMA basics
        • APVMA basics
        • What we regulate
        • Our functions and powers
        • Acronyms and glossary
          • Acronyms and glossary
          • Abbreviations and acronyms
          • Definition of terms
      • APVMA Board and Improvements Act
      • Audit and Risk Committee
      • Integrity
      • Our cost recovery arrangements
        • Our cost recovery arrangements
        • Cost recovery questions and answers
      • Our history
      • Our legislative framework
      • Our structure
        • Our structure
        • APVMA Chief Executive Officer
    • Access to information held by the APVMA
      • Access to information held by the APVMA
      • Agricultural and Veterinary Chemicals Code requests
      • Freedom of Information
        • Freedom of Information
        • Freedom of information disclosure log
    • Accountability and reporting
      • Accountability and reporting
      • Annual product sales data
        • Annual product sales data
        • Publication of annual product sales data: 2020–21
        • Publication of annual product sales data: 2019–20
      • APS Employee Census
      • Contracts over $100,000
      • Gifts and benefits
      • Indexed list of files
      • Information Publication Scheme
        • Information Publication Scheme
        • Information publication scheme agency plan
      • Legal expenditure
      • Performance statistics
        • Performance statistics
        • Performance report: September 2022
          • Performance report: September 2022
          • Analysis by type of application
          • Applications in detail
          • Applications by item number
          • Average decision time
        • Performance report: June 2022
          • Performance report: June 2022
          • Analysis by type of application
          • Applications in detail
          • Applications by item number
          • Average decision time
          • 2021–22 performance overview
        • Performance report: March 2022
          • Performance report: March 2022
          • Analysis by type of application
          • Applications in detail
          • Applications by item number
          • Average decision time
        • Performance report: December 2021
          • Performance report: December 2021
          • Analysis by type of application
          • Applications in detail
          • Applications by item number
          • Average decision time
        • Glossary of terms
        • Statistics archive
          • Statistics archive
          • Performance report: September 2021
            • Performance report: September 2021
            • Analysis by type of application
            • Applications in detail
            • Applications by item number
            • Average decision time
            • Updated format for performance reporting
          • Performance report: June 2021
            • Performance report: June 2021
            • Analysis by type of application
            • Major and non-technical product applications
            • Applications by item number
            • Average decision time
            • 2020–21 performance overview
          • Performance report: March 2021
            • Performance report: March 2021
            • Analysis by type of application
            • Major and non-technical product applications
            • Applications by item number
            • Average decision time
            • 2020–21 performance overview
          • Performance report: December 2020
            • Performance report: December 2020
            • Analysis by type of application
            • Major and non-technical product applications
            • Application by item number
            • Average decision time
            • 2020–21 performance overview
          • Performance report: September 2020
            • Performance report: September 2020
            • Analysis by type of application
            • Major and non-technical product applications
            • Application by item number
            • Average decision time
            • 2020–21 performance overview
      • Portfolio budget statements
      • Regulator Performance Framework
        • Regulator Performance Framework
        • Regulator Performance Framework 2017–18
      • Statutory appointments
    • Agvet chemical regulation
      • Agvet chemical regulation
      • Domestic collaboration
      • PubCRIS and Permits databases
      • Product regulation according to risk
      • Risk management
    • Careers
      • Careers
      • Benefits and conditions
      • Procedures for determining breaches of the APS Code of Conduct
    • Communication and decision making
      • Communication and decision making
      • How we make decisions
        • How we make decisions
        • Section 6A guidelines
        • Infringement Notice Guideline
        • Overarching principles and processes for the effective and efficient regulation of agricultural and veterinary chemical products
        • Approvals and registrations
        • Preliminary assessment guideline
        • Permits
        • Licences
        • Recategorising applications
        • Altering applications
        • Section 159 in the context of applications under the Agvet code
        • Limits on use of information
        • Reconsidering approvals and registrations
        • Varying relevant particulars and conditions
        • Module Descriptors
        • Formulation types
      • Communication between applicants and the APVMA
        • Communication between applicants and the APVMA
        • Service charter
      • Data handling by the APVMA
        • Data handling by the APVMA
        • Applications without written consent for reference products
        • CCI Practice Statement
      • External advice
      • Transparency
    • International
      • International
      • International activities
        • International activities
        • International chemical conventions
        • International participation
        • International standards and guidance
      • International engagement strategy
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This content is current only at the time of printing. This document was printed on 31 January 2023. A current copy is located at https://apvma.gov.au/node/32981

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  • Chemistry and manufacture (Part 2) - Veterinary

Chemistry and manufacture (Part 2) - Veterinary

  • Chemistry and manufacture of active constituents (Part 2)
  • Chemistry and manufacture of products (Part 2)

Specific guidelines

  • Additional data guidelines for chemistry and manufacture (Part 2)
  • Approval of active constituents for which information is not readily available
Content last updated: 
8 October 2018
Content last reviewed: 
13 April 2021
URL: 
https://apvma.gov.au/node/32981

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Data guidelines

  • Agricultural data guidelines
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    • Chemistry and manufacture (Part 2)
      • Chemistry and manufacture of active constituents (Part 2)
      • Chemistry and manufacture of products (Part 2)
      • Additional data guidelines for chemistry and manufacture (Part 2)
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The Australian Pesticides and Veterinary Medicines Authority (APVMA) is the Australian Government regulator of agricultural and veterinary (agvet) chemical products.

We acknowledge the traditional owners and custodians of country throughout Australia and acknowledge their continuing connection to land, sea and community. We pay our respects to the people, the cultures and the elders past, present and emerging.