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          Australian Pesticides and Veterinary Medicines Authority
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            • Tailored guidance for applicants
              • Tailored 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
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              • 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
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                • 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
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                • Veterinary product
                  • Veterinary product
                  • That is similar and efficacy, safety, chemistry and manufacture data is required
                  • Closely similar and only chemistry data is required
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              • 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 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 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 submit a timeshift application
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            • Data guidelines
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                • Agricultural data guidelines
                • Adopted international technical guidance material
                • Chemistry and manufacture (Part 2)
                  • Chemistry and manufacture (Part 2)
                  • Specific guidelines
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                • Metabolism and kinetics (Part 4)
                • Residues (Part 5A)
                  • Residues (Part 5A)
                  • Specific guidelines
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                • 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
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              • Listing of labelling codes
            • Permits
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              • Before you apply
                • Before you apply
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                • Pre-application assistance
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                • What to include in your application
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                • What happens next
                • Requiring samples or further information
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              • Apply now
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            • Manufacturing
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              • COVID-19: advice for veterinary medicine manufacturers and holders
              • Manufacturing licences
                • Manufacturing licences
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                • Applying for a manufacturing licence
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                • After you apply
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                • 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
            • Import and export
              • Import and export
              • Importing agricultural chemicals or veterinary medicines
                • Importing agricultural chemicals or veterinary medicines
                • Responsibilities of importers
              • 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
                  • Information to be provided with applications for certificates of export
                • Apply now
            • 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
            • Making changes to veterinary products and actives—clarification for industry
            • Getting assistance from the APVMA
              • Getting assistance from the APVMA
              • General assistance
              • 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
              • How to apply 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
              • Manufacturing licences
            • Applications and decisions
              • Applications and decisions
              • Application summaries
              • Application summaries - Q&A
            • Transitional arrangements
              • Transitional arrangements
              • Applications
          • Chemicals and Products
            • Chemicals and Products
            • Search registered chemical products and permits
              • Search registered chemical products and permits
              • Search PubCRIS
              • Using PubCRIS
            • 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
              • Prioritisation of chemicals nominated for review
            • 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
              • Chemicals in the news
                • Chemicals in the news
                • Coronavirus (COVID-19)
                • Current review of chlorpyrifos
                • Information about glyphosate use
                • 2,4-D
                • Hendra virus vaccine
                • Current review of neonicotinoids
                • Pyrethrin and pyrethroid use on cats
                  • Pyrethrin and pyrethroid use on cats
                  • Registration of pyrethroid product
                  • Toxicity
                  • Guidance for cat owners
              • Spray drift
                • Spray drift
                • Drift reducing technology (DRT) incentives program
                • New registration application and label requirements in relation to spray drift management
                • New registration application and label requirements in relation to spray drift management – supplement 1
                • Priority list for spray drift label reviews
                • Protective No-Spray Zones
                • Spray Drift Data Guideline
                • Spray drift risk operating principles
                • Standard spray drift risk assessment scenarios
              • Pesticides and veterinary residues
            • Supplying chemicals
              • Supplying chemicals
              • Supply and sale of hormonal growth promotants
              • Hydroponic Product Sellers and agvet chemicals
              • Supply and sale of natural 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
              • Process for developing a standard for active constituents
              • Approval of active constituents
            • Health based guidance values
              • Health based guidance values
              • Acceptable daily intakes for agricultural and veterinary chemicals
              • Acute reference doses for agricultural and veterinary chemicals
            • FAISD handbook
          • Compliance and monitoring
            • Compliance and monitoring
            • Adverse Experience Reporting Program
              • Adverse Experience Reporting Program
              • The importance of the AERP
              • Scope of the AERP
              • Who can report an adverse experience?
              • Adverse Experience Reporting Program for veterinary medicines
              • Adverse Experience Reporting Program for agricultural chemicals
              • AERP: What happens after making a report
            • APVMA levy audit program
            • Compliance and monitoring function
              • Compliance and monitoring function
              • Analysts
                • Analysts
                • Criteria for Appointment as Approved Analyst
              • Evidential certificates
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              • Policy, strategy and disclosure
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            • Complying with the Agvet Code
              • Complying with the Agvet Code
              • Responsibilities of holders
                • Responsibilities of holders
                • Product stewardship
                • Evidential certificates
              • Complying with conditions
              • Maintaining particulars
              • Advertising agricultural and veterinary chemical products
            • Enforcement
              • Enforcement
              • APVMA's authority
              • Non-compliance risk
              • Formal warnings
              • Consent to import chemical products
              • Substantiation notices
              • Notice to attend, give information or produce documents or items
              • Enforcement outcomes
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              • Warrants
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              • Prosecution
            • Hormonal Growth Promotants (HGPs)
            • Monitoring
              • Monitoring
              • How we monitor compliance
                • How we monitor compliance
                • Audits and inspections frequently asked questions
                • Swimming Pool Sanitation and the Agricultural and Veterinary Chemicals Code 1994
              • Section 99 notices
            • Recalls
              • Recalls
              • Recall notices
            • Report a problem with a chemical or product
              • Report a problem with a chemical or product
              • Report suspected non-compliance
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          • Our science
            • Our science
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              • Collaboration
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          • About
            • About
            • The role of the APVMA
              • The role of the APVMA
              • A trusted regulator
                • A trusted regulator
                • Harmonisation
                • International participation
                • Other international bodies
                • The Rotterdam and Stockholm conventions
              • Access to safe and effective agricultural and veterinary chemicals
              • Ongoing compliance to ensure safety and efficacy
              • The Record and Register
            • Our structure
              • Our structure
              • Chief Executive Officer
            • APVMA basics
              • APVMA basics
              • What we regulate
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                • What we don't regulate
                • Products we don’t regulate
                • Product advice and competition
                • Use of chemicals
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                • Other information
                • Corporate governance
                • Our functions and powers
                • Communication, decision making and information
                  • Communication, decision making and information
                  • Communication between applicants and the APVMA
                    • Communication between applicants and the APVMA
                    • When we will notify applicants
                  • Consultation and collaboration
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                  • Data handling by the APVMA
                    • Data handling by the APVMA
                    • Approach to managing confidential commercial information (CCI)
                    • Applications without written consent for reference products
                  • External advice
                • Purpose and vision
            • Chemical regulation basics
              • Chemical regulation basics
              • Overview of agvet chemical regulation
              • The chemical and permit databases
              • Product regulation according to risk
              • Legislative framework
              • Administrative Practice Statement
              • CCI Practice Statement
              • Risk management
            • Service charter
            • How we make decisions
              • How we make decisions
              • Background to the reforms and the section 6A guidelines
              • Overarching principles and processes for the effective and efficient regulation of agricultural and veterinary chemical products
              • Approvals and registrations
              • Preliminary assessment
              • 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
              • International assessments
                • International assessments
                • Collaborative and international assessments
                • Guidance on veterinary drug joint reviews
                • Case Study–Brevis (metamitron) approved ahead of time
              • Formulation types
            • 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
            • Access, accountability and reporting
              • Access, accountability and reporting
              • Performance statistics
                • Performance statistics
                • Performance report: June 2020
                  • Performance report: June 2020
                  • Analysis by type of application
                  • Major and non-technical product applications
                  • Application by item number
                  • Average decision time
                  • 2019–20 year to date performance overview
                  • Glossary of terms
                • Performance report: March 2020
                  • Performance report: March 2020
                  • Analysis by type of application
                  • Major and non-technical product applications
                  • Applications by item number
                  • Average decision time
                  • 2019–20 year to date performance overview
                  • Glossary of terms
                • Performance report: December 2019
                  • Performance report: December 2019
                  • Analysis by type of application
                  • Major and non-technical product applications
                  • Applications by item number
                  • Average decision time
                  • 2019–20 year to date performance overview
                  • Glossary of terms
                • Statistics archive
                  • Statistics archive
                  • Quarterly report: April–June 2019
                    • Quarterly report: April–June 2019
                    • Analysis by type of application
                    • Major and non-technical product applications
                    • Applications by item number
                    • Average decision time
                    • 2018–19 year to date performance overview
                    • Glossary of terms
                  • Quarterly report: January–March 2019
                    • Quarterly report: January–March 2019
                    • Analysis by type of application
                    • Major and non-technical product applications
                    • Applications by item number
                    • Average decision time
                    • 2018–19 year to date performance overview
                    • Glossary of terms
                  • Quarterly report: October–December 2018
                    • Quarterly report: October–December 2018
                    • Analysis by type of application
                    • Major and non-technical product applications
                    • Applications by item number
                    • Average decision time
                    • Other regulatory functions
                    • 2018–19 year to date performance overview
                    • Glossary of terms
                  • Quarterly report: July–September 2018
                    • Quarterly report: July–September 2018
                    • Analysis by type of application
                    • Major and non-technical product applications
                    • Applications by item number
                    • Average decision time
                    • Other regulatory functions
                    • 2018–19 year to date performance overview
                    • Glossary of terms
                  • Quarterly report: April–June 2018
                    • Quarterly report: April–June 2018
                    • Analysis by type of application
                    • Major and non-technical product applications
                    • Applications by item number
                    • Average decision time
                    • Other regulatory functions
                    • 2017–18 year to date performance overview
                    • Glossary of terms
                  • Quarterly report: January–March 2018
                    • Quarterly report: January–March 2018
                    • Analysis by type of application
                    • Major and non-technical product applications
                    • Applications by item number
                    • Average decision time
                    • Other regulatory functions
                    • 2017–18 year to date performance overview
                    • Glossary of terms
                  • Quarterly report: October—December 2017
                    • Quarterly report: October—December 2017
                    • Analysis by type of application
                    • Major and non-technical product applications
                    • Applications by item number
                    • Average decision time
                    • Other regulatory functions
                    • 2017–18 year to date performance overview
                  • Quarterly report: July–September 2017
                    • Quarterly report: July–September 2017
                    • Analysis by type of application
                    • Major and non-technical product applications
                    • Applications by item number
                    • Average decision time
                    • Other regulatory functions
                    • 2017–18 year to date performance overview
                  • Quarterly report: April–June 2017
                    • Quarterly report: April–June 2017
                    • Analysis by type of application
                    • Major and non-technical product applications
                    • Applications by item number
                    • Average decision time
                    • Other regulatory functions
                    • 2016–17 year to date performance overview
                  • Quarterly report: January–March 2017
                    • Quarterly report: January–March 2017
                    • Analysis by type of application
                    • Major and non-technical product applications
                    • Application by item number
                    • Average decision time
                    • Other regulatory functions
                    • 2016–17 year to date performance overview
                  • Quarterly report: October–December 2016
                  • Quarterly report: July–September 2016
                    • Quarterly report: July–September 2016
                    • Part 1: Overview July–September 2016
                    • Part 2: Applications for products, actives and permits
                      • Part 2: Applications for products, actives and permits
                      • Performance statistics July–September 2016: Applications commenced
                      • Performance statistics July–September 2016: Applications finalised
                      • Performance statistics July–September 2016: Average decision time
                      • Performance statistics July–September 2016: Performance by assessment type
                      • Performance statistics July–September 2016: Preliminary assessment applications
                      • Performance statistics July–September 2016: Staffing considerations
                      • Performance statistics July–September 2016: Timeframe performance
                      • Performance statistics July–September 2016: Work-in-progress
                      • Performance statistics July–September 2016: Pre-application assistance
                    • Part 3: Other timeframe performance results July–September 2016
                  • Performance statistics July 2015–June 2016
                    • Performance statistics July 2015–June 2016
                    • Part 1: Overview
                    • Part 2: Applications for products, actives and permits
                      • Part 2: Applications for products, actives and permits
                      • Application types
                      • Applications commenced
                      • Applications finalised
                      • Average decision time
                        • Average decision time
                        • Interpreting average decision time
                      • Interpreting timeframe performance
                      • Performance by type of product assessment
                      • Pre-application assistance
                      • Preliminary assessment
                      • Staffing considerations
                      • Timeframe performance
                      • Work-in-progress
                    • Part 3: Other timeframe performance results
              • APVMA Regulator Performance Framework
                • APVMA Regulator Performance Framework
                • Regulator Performance Framework 2017–18
              • Analysis of time to complete a product application
              • Annual Procurement Plan
              • Audits
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                • Information Publication Scheme
                • Information publication scheme agency plan
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              • Gifts and benefits
            • Careers
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            • Social media
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              • APVMA Gazette
              • Annual Reports
                • Annual Reports
                • APVMA Annual Report 2018–19
                  • APVMA Annual Report 2018–19
                  • Annual Report 2018–19: Letter of transmittal
                  • Annual Report 2018–19: Vision and mission
                  • Annual Report 2018–19: Chapter 1—Summary and outlook
                  • Annual Report 2018–19: Chapter 2—Organisation overview
                  • Annual Report 2018–19: Chapter 3—Annual performance statement
                  • Annual Report 2018–19: Chapter 4—Corporate governance and management
                  • Annual Report 2018–19: Chapter 5—Financial performance
                  • Annual Report 2018–19: Acronyms and abbreviations
                  • Annual Report 2018–19: Glossary
                  • Annual Report 2018–19: Compliance index
                  • Annual Report 2018–19: Index
                • APVMA Annual Report 2017-18
                  • APVMA Annual Report 2017-18
                  • Letter of transmittal
                  • Vision and mission
                  • Chapter 1: Summary and outlook
                  • Chapter 2: Organisation overview
                  • Chapter 3: Annual performance statement
                  • Chapter 4: Corporate governance and management
                  • Chapter 5: Financial performance
                  • Acronyms and abbreviations
                  • Glossary
                  • Compliance index
                  • Index
                • APVMA Annual Report 2016–17
                  • APVMA Annual Report 2016–17
                  • Annual Report 2016–17—Letter of transmittal
                  • Annual Report 2016–17—Vision and mission
                  • Annual Report 2016–17—Chapter 1: Summary and outlook 2016–17
                  • Annual Report 2016–17—Chapter 2: Organisation overview
                  • Annual Report 2016–17—Chapter 3: Annual performance
                  • Annual Report 2016–17—Chapter 4: Corporate governance and management
                  • Annual Report 2016–17—Chapter 5: Financial performance
                  • Annual Report 2016–17—Acronyms and abbreviations
                  • Annual Report 2016–17—Glossary
                  • Annual Report 2016–17—Compliance index
                  • Annual Report 2016–17—Index
                • APVMA Annual Report 2015-16
                  • APVMA Annual Report 2015-16
                  • Annual Report 2015-16—Letter of transmittal
                  • Annual Report 2015-16—vision and mission
                  • Annual Report 2015-16—Chief Executive Officer's report and outlook
                  • Annual Report 2015-16—Chapter 1: Organisation overview
                  • Annual Report 2015-16—Chapter 2: Corporate governance and management
                  • Annual Report 2015-16—Chapter 3: Annual performance statement
                  • Annual Report 2015-16—Chapter 4: Financial performance
                  • Annual Report 2015-16—Appendix A: Progress against APVMA operational plan 2015-16 initiatives
                  • Annual Report 2015-16—Appendix B: Information on specific statutory provisions
                  • Annual Report 2015-16—Acronyms and abbreviations
                  • Annual Report 2015–16—Glossary
                  • Annual Report 2015-16—List of requirements (compliance index)
                  • Annual Report 2015-16—Index
                • APVMA Annual Report 2014–15
                  • APVMA Annual Report 2014–15
                  • Annual Report 2014–15—Letter of transmittal
                  • Annual Report 2014–15—Vision and mission
                  • Annual Report 2014–15—Chief Executive Officer's report and outlook
                  • Annual Report 2014–15—Chapter 1: Organisation overview
                  • Annual Report 2014–15—Chapter 2: Performance against strategies
                  • Annual Report 2014–15—Chapter 3: Management framework
                  • Chapter 4: Financial performance—Annual Report 2014–15
                  • Annual Report 2014–15—Chapter 5: Appendixes
                  • Annual Report 2014–15—Acronyms and abbreviations
                  • Annual Report 2014–15—Glossary
                  • Annual Report 2014–15—List of requirements
              • Corporate documents
              • Adverse Experience Reporting Program annual reports
            • Training and events
              • Training and events
              • Previous APVMA events
                • Previous APVMA events
                • APVMA Advisory Board Futures Forum 2014
                  • APVMA Advisory Board Futures Forum 2014
                  • APVMA Advisory Board Futures Forum 2014 - Summation
                • APVMA Nanotechnology Regulation Symposium 2014
                • Industry Information and Education Session in Sydney on 1 June 2015
                • Industry Information and Education Sessions in Melbourne on 17 August 2015
                • Industry Information and Education Session in Canberra 15 and 16 October 2015
                  • Industry Information and Education Session in Canberra 15 and 16 October 2015
                  • Program and speaker information—Canberra Industry Information and Education Session 15 and 16 October 2015
                  • Transcript for Andrew Negri, Australian Institute of Marine Science
                  • Transcript for Chris Lee-Steere
                  • Transcript for Distinguished Professor Jim Riviere
                  • Transcript for Distinguished Professor Nancy Monteiro-Riviere
                  • Transcript for Dr Jason Lutze, APVMA
                  • Transcript for Dr Phil Reeves
                  • Transcript for Dr Raj Bhula, APVMA
                  • Transcript for Ms Janis Baines, FSANZ
                  • Transcript for Professor Michael Roberts
                • Industry Information and Education Sessions in Canberra 8–9 November 2016
                  • Industry Information and Education Sessions in Canberra 8–9 November 2016
                  • Program and speaker information—Canberra Industry Information and Education Sessions 8–9 November 2016
                • Industry Information and Education Sessions in Melbourne on 9 May 2016
                • Industry information and education session in Canberra 13–14 September 2017
                  • Industry information and education session in Canberra 13–14 September 2017
                  • Day two - 14 September 2017
              • eLearning modules
                • eLearning modules
                • Permits eLearning module (text only)
                • Registrations eLearning module (text only)
            • Forms
            • Improving our business
              • Improving our business
              • Improved access to chemicals
                • Improved access to chemicals
                • The crop groupings project
                  • The crop groupings project
                  • Crop groupings project—consolidated responses to phase I consultation—March 2016
              • Contestability of the efficacy assessment
                • Contestability of the efficacy assessment
                • Agricultural scientific reviewers
                • Veterinary scientific reviewers
            • Online services update
          • Contact us
            • Contact us
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          This content is current only at the time of printing. This document was printed on 14 September 2020. A current copy is located at http://www.xlg888.com/node/32981

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          Content last updated: 
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          Content last reviewed: 
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          Data guidelines

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            • Chemistry and manufacture (Part 2)
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          The Australian Pesticides and Veterinary Medicines Authority acknowledges the traditional owners and custodians of country throughout Australia and acknowledges their continuing connection to land, sea and community. We pay our respects to the people, the cultures and the elders past, present and emerging.

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