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2. Types of assessment applications and information required

Introduction

This page explains the types of assessments certificates you can apply for, and the information you must have to support the assessment certificate type you choose.

There are 4 types of assessment certificates based on your categorisation outcome which you must have established by using our Guide to categorising your chemical importation and manufacture.

  1. Health and environment focus
  2. Health focus
  3. Environment focus
  4. Very low to low risk

Health and environment focus applications and information required

Choose this application if:

  • your introduction’s indicative human health risk is medium to high, and the indicative environment risk is medium to high, or
  • you do not have necessary data to demonstrate that the highest indicative risk of the introduction to both human health and the environment is low or very low.

Note: The numbers in brackets represent the document numbers in IUCLID6 Version 4.18.0.

IUCLID documentationMedium to high risk for health and environment
SectionsSubsections / DocumentsRequired / If available
1. General informationIdentification (1.1)Required
Composition (1.2)Required
Analytical information (1.4)Required
2. Classification, labellingGHS (2.1)Required
3. ManufactureEstimated quantities (3.2)Required
Site (3.3)Required for manufacture only
Manufacture (3.5.1)Required for manufacture only
Formulation or re-packing (3.5.2)If available – though at least one use must be provided in either 3.5.2, 3.5.3, 3.5.4 or 3.5.5.
Uses at industrial sites (3.5.3)
Widespread uses by professional workers (3.5.4)
Consumer uses (3.5.5)
Article service life (3.5.6)If available
4. Physical and chemical propertiesAppearance / physical state / colour (4.1)Required
Melting point / freezing point (4.2)Required
Boiling point (4.3)Required
Density (4.4)Required
Particle size distribution (Granulometry) (4.5)Required
Vapour pressure (4.6)Required
Partition coefficient (4.7)Required
Water solubility (4.8)Required
Solubility in organic solvents / fat solubility (4.9)If available
Surface tension (4.10)If available
Flash point (4.11)Required
Auto flammability (4.12)Required
Flammability (4.13)Required
Explosiveness (4.14)Required
Oxidising properties (4.15)Required
Oxidation reduction potential (4.16)If available
pH (4.20)If available
Dissociation constant (4.21)Required
Viscosity (4.22)If available
Self-reactive substances (4.23)If available
Additional physico-chemical information (4.27)If available
Nanomaterial agglomeration / aggregation (4.28.1)If available
Nanomaterial crystalline phase (4.28.2)If available
Nanomaterial crystallite and grain size (4.28.3)If available
Nanomaterial aspect ratio / shape (4.28.4)If available
Nanomaterial specific surface area (4.28.5)If available
Nanomaterial Zeta potential (4.28.6)If available
Nanomaterial surface chemistry (4.28.7)If available
Nanomaterial dustiness (4.28.8)If available
Nanomaterial porosity (4.28.9)If available
Nanomaterial pour density (4.28.10)If available
Nanomaterial photocatalytic activity (4.28.11)If available
Nanomaterial radical formation potential (4.28.12)If available
Nanomaterial catalytic activity (4.28.13)If available
Nanomaterial dispersion stability (4.28.14)If available
5. Environmental fate and pathwaysPhototransformation in air (5.1.1)If available
Hydrolysis (5.1.2)Required
Phototransformation in water (5.1.3)If available
Biodegradation in water: screening tests (5.2.1)Required
Biodegradation in soil (5.2.3)If available
Bioaccumulation: aquatic / sediment (5.3.1)Required (information on either 5.3.1 or 5.3.2)
Bioaccumulation: terrestrial (5.3.2)
Adsorption / desorption (5.4.1)Required
Henry’s Law constant (5.4.2)If available
Other distribution data (5.4.4)If available
Additional information on environmental fate and behaviour (5.6)If available
6. Ecotoxicological informationShort-term toxicity to fish (6.1.1)Required
Long-term toxicity to fish (6.1.2)If available
Short-term toxicity to aquatic invertebrates (6.1.3)Required
Long-term toxicity to aquatic invertebrates (6.1.4)If available
Toxicity to aquatic algae and cyanobacteria (6.1.5)Required
Toxicity to aquatic plants other than algae (6.1.6)If available
Toxicity to microorganisms (6.1.7)If available
Endocrine disruptor testing in aquatic vertebrates – in vivo (6.1.8)If available
Toxicity to other aquatic vertebrates (6.1.9)If available
Sediment toxicity (6.2)If available
Toxicity to soil macroorganisms except arthropods (6.3.1)If available
Toxicity to terrestrial arthropods (6.3.2)If available
Toxicity to terrestrial plants (6.3.3)If available
Toxicity to soil microorganisms (6.3.4)If available
Additional ecotoxicological information (6.6)If available
7. Toxicological informationBasic toxicokinetics (7.1.1)If available
Dermal absorption (7.1.2)If available
Acute toxicity: oral (7.2.1)Required (information on either 7.2.1, 7.2.2 or 7.2.3.)
Acute toxicity: inhalation (7.2.2)
Acute toxicity: dermal (7.2.3)
Acute toxicity: other routes (7.2.4)If available
Skin irritation / corrosion (7.3.1)Required
Eye irritation (7.3.2)Required
Skin sensitisation (7.4.1)Required
Respiratory sensitisation (7.4.2)If available
Repeated dose toxicity: oral (7.5.1)Required (information on either 7.5.1, 7.5.2 or 7.5.3)
Repeated dose toxicity: inhalation (7.5.2)
Repeated dose toxicity: dermal (7.5.3)
Repeated dose toxicity: other routes (7.5.4)If available
Genetic toxicity in vitro (7.6.1)Required. Information on point mutations (7.6.1 or 7.6.2) and chromosome damage (7.6.1 or 7.6.2)
Genetic toxicity in vivo (7.6.2)
Carcinogenicity (7.7)If available
Toxicity to reproduction (7.8.1)If available
Developmental toxicity / teratogenicity (7.8.2)If available
Toxicity to reproduction: other studies (7.8.3)If available
Neurotoxicity (7.9.1)If available
Immunotoxicity (7.9.2)If available
Specific investigations: other studies (7.9.4)If available
Health surveillance data (7.10.1)If available
Epidemiological data (7.10.2)If available
Direct observations: clinical cases, poisoning incidents and other (7.10.3)If available
Sensitisation data (humans) (7.10.4)If available
Exposure related observations in humans: other data (7.10.5)If available
Additional toxicological information (7.12)If available
9. Residues in food and feeding stuffIf available
11. Guidance on safe useRequired
13. Assessment report (attach SDS)Required

Health focus applications and information required

Choose this application if your introduction’s indicative human health risk is medium to high, and the indicative environment risk is very low to low.

You will need to be able to demonstrate that the highest indicative risk of the introduction to the environment is very low or low risk. If you can’t do this, choose ‘Health and environment focus’.

Note: The numbers in brackets represent the document numbers in IUCLID6 Version 4.18.0.

IUCLID documentationMedium to high risk for health and low to very low risk for environment
SectionsSubsections / DocumentsRequired / If available
1. General informationIdentification (1.1)Required
Composition (1.2)Required
Analytical information (1.4)Required
2. Classification, labellingGHS (2.1)Required
3. ManufactureEstimated quantities (3.2)Required
Site (3.3)Required for manufacture only
Manufacture (3.5.1)Required for manufacture only
Formulation or re-packing (3.5.2)If available – though at least one use (use name) must be provided in either 3.5.2, 3.5.3, 3.5.4 or 3.5.5.
Uses at industrial sites (3.5.3)
Widespread uses by professional workers (3.5.4)
Consumer uses (3.5.5)
Article service life (3.5.6)If available
4. Physical and chemical propertiesAppearance / physical state / colour (4.1)Required
Melting point / freezing point (4.2)Required
Boiling point (4.3)Required
Density (4.4)Required
Particle size distribution (Granulometry) (4.5)Required
Vapour pressure (4.6)Required
Partition coefficient (4.7)Required
Water solubility (4.8)Required
Solubility in organic solvents / fat solubility (4.9)If available
Surface tension (4.10)If available
Flash point (4.11)Required
Auto flammability (4.12)Required
Flammability (4.13)Required
Explosiveness (4.14)Required
Oxidising properties (4.15)Required
Oxidation reduction potential (4.16)If available
pH (4.20)If available
Dissociation constant (4.21)Required
Viscosity (4.22)If available
Self-reactive substances (4.23)If available
Additional physico-chemical information (4.27)If available
Nanomaterial agglomeration / aggregation (4.28.1)If available
Nanomaterial crystalline phase (4.28.2)If available
Nanomaterial crystallite and grain size (4.28.3)If available
Nanomaterial aspect ratio / shape (4.28.4)If available
Nanomaterial specific surface area (4.28.5)If available
Nanomaterial Zeta potential (4.28.6)If available
Nanomaterial surface chemistry (4.28.7)If available
Nanomaterial dustiness (4.28.8)If available
Nanomaterial porosity (4.28.9)If available
Nanomaterial pour density (4.28.10)If available
Nanomaterial photocatalytic activity (4.28.11)If available
Nanomaterial radical formation potential (4.28.12)If available
Nanomaterial catalytic activity (4.28.13)If available
Nanomaterial dispersion stability (4.28.14)If available
5. Environmental fate and pathwaysPhototransformation in air (5.1.1)If available
Hydrolysis (5.1.2)Required
Phototransformation in water (5.1.3)If available
Biodegradation in water: screening tests (5.2.1)If available
Biodegradation in soil (5.2.3)If available
Bioaccumulation: aquatic / sediment (5.3.1)If available
Bioaccumulation: terrestrial (5.3.2)If available
Adsorption / desorption (5.4.1)Required
Henry’s Law constant (5.4.2)If available
Other distribution data (5.4.4)If available
Additional information on environmental fate and behaviour (5.6)If available
6. Ecotoxicological informationShort-term toxicity to fish (6.1.1)If available
Long-term toxicity to fish (6.1.2)If available
Short-term toxicity to aquatic invertebrates (6.1.3)If available
Long-term toxicity to aquatic invertebrates (6.1.4)If available
Toxicity to aquatic algae and cyanobacteria (6.1.5)If available
Toxicity to aquatic plants other than algae (6.1.6)If available
Toxicity to microorganisms (6.1.7)If available
Endocrine disruptor testing in aquatic vertebrates – in vivo (6.1.8)If available
Toxicity to other aquatic vertebrates (6.1.9)If available
Sediment toxicity (6.2)If available
Toxicity to soil macroorganisms except arthropods (6.3.1)If available
Toxicity to terrestrial arthropods (6.3.2)If available
Toxicity to terrestrial plants (6.3.3)If available
Toxicity to soil microorganisms (6.3.4)If available
Additional ecotoxicological information (6.6)If available
7. Toxicological informationBasic toxicokinetics (7.1.1)If available
Dermal absorption (7.1.2)If available
Acute toxicity: oral (7.2.1)Required (information on either 7.2.1, 7.2.2 or 7.2.3)
Acute toxicity: inhalation (7.2.2)
Acute toxicity: dermal (7.2.3)
Acute toxicity: other routes (7.2.4)If available
Skin irritation / corrosion (7.3.1)Required
Eye irritation (7.3.2)Required
Skin sensitisation (7.4.1)Required
Respiratory sensitisation (7.4.2)If available
Repeated dose toxicity: oral (7.5.1)Required (information on either 7.5.1, 7.5.2 or 7.5.3)
Repeated dose toxicity: inhalation (7.5.2)
Repeated dose toxicity: dermal (7.5.3)
Repeated dose toxicity: other routes (7.5.4)If available
Genetic toxicity in vitro (7.6.1)Required. Information on point mutations (7.6.1 or 7.6.2) and chromosome damage (7.6.1 or 7.6.2)
Genetic toxicity in vivo (7.6.2)
Carcinogenicity (7.7)If available
Toxicity to reproduction (7.8.1)If available
Developmental toxicity / teratogenicity (7.8.2)If available
Toxicity to reproduction: other studies (7.8.3)If available
Neurotoxicity (7.9.1)If available
Immunotoxicity (7.9.2)If available
Specific investigations: other studies (7.9.4)If available
Health surveillance data (7.10.1)If available
Epidemiological data (7.10.2)If available
Direct observations: clinical cases, poisoning incidents and other (7.10.3)If available
Sensitisation data (humans) (7.10.4)If available
Exposure related observations in humans: other data (7.10.5)If available
Additional toxicological information (7.12)If available
9. Residues in food and feeding stuffIf available
11. Guidance on safe useRequired
13. Assessment report (attach SDS)Required

Environment focus applications and information required

Choose this application if your introduction’s indicative human health risk is very low to low, and the indicative environment risk is medium to high 

You will need to be able to demonstrate that the highest indicative human health risk of the introduction is very low or low risk. If you can’t do this, choose ‘Health and environment focus’.

Environment focus – information required

Note: The numbers in brackets represent the document numbers in IUCLID6 Version 4.18.0.

IUCLID documentationMedium to high risk for environment and low to very low risk for health
SectionsSubsections / DocumentsRequired / If available
1. General informationIdentification (1.1)Required
Composition (1.2)Required
Analytical information (1.4)Required
2. Classification, labellingGHS (2.1)Required
3. ManufactureEstimated quantities (3.2)Required
Site (3.3)Required for manufacture only
Manufacture (3.5.1)Required for manufacture only
Formulation or re-packing (3.5.2)If available – though at least one use (use name) must be provided in either 3.5.2, 3.5.3, 3.5.4 or 3.5.5.
Uses at industrial sites (3.5.3)
Widespread uses by professional workers (3.5.4)
Consumer uses (3.5.5)
Article service life (3.5.6)If available
4. Physical and chemical propertiesAppearance / physical state / colour (4.1)Required
Melting point / freezing point (4.2)Required
Boiling point (4.3)Required
Density (4.4)Required
Particle size distribution (Granulometry) (4.5)Required
Vapour pressure (4.6)Required
Partition coefficient (4.7)Required
Water solubility (4.8)Required
Solubility in organic solvents / fat solubility (4.9)If available
Surface tension (4.10)If available
Flash point (4.11)If available
Auto flammability (4.12)If available
Flammability (4.13)If available
Explosiveness (4.14)If available
Oxidising properties (4.15)If available
Oxidation reduction potential (4.16)If available
pH (4.20)If available
Dissociation constant (4.21)Required
Viscosity (4.22)If available
Self-reactive substances (4.23)If available
Additional physico-chemical information (4.27)If available
Nanomaterial agglomeration / aggregation (4.28.1)If available
Nanomaterial crystalline phase (4.28.2)If available
Nanomaterial crystallite and grain size (4.28.3)If available
Nanomaterial aspect ratio / shape (4.28.4)If available
Nanomaterial specific surface area (4.28.5)If available
Nanomaterial Zeta potential (4.28.6)If available
Nanomaterial surface chemistry (4.28.7)If available
Nanomaterial dustiness (4.28.8)If available
Nanomaterial porosity (4.28.9)If available
Nanomaterial pour density (4.28.10)If available
Nanomaterial photocatalytic activity (4.28.11)If available
Nanomaterial radical formation potential (4.28.12)If available
Nanomaterial catalytic activity (4.28.13)If available
Nanomaterial dispersion stability (4.28.14)If available
5. Environmental fate and pathwaysPhototransformation in air (5.1.1)If available
Hydrolysis (5.1.2)Required
Phototransformation in water (5.1.3)If available
Biodegradation in water: screening tests (5.2.1)Required
Biodegradation in soil (5.2.3)If available
Bioaccumulation: aquatic / sediment (5.3.1)Required (information on either 5.3.1 or 5.3.2)
Bioaccumulation: terrestrial (5.3.2)
Adsorption / desorption (5.4.1)Required
Henry’s Law constant (5.4.2)If available
Other distribution data (5.4.4)If available
Additional information on environmental fate and behaviour (5.6)If available
6. Ecotoxicological informationShort-term toxicity to fish (6.1.1)Required
Long-term toxicity to fish (6.1.2)If available
Short-term toxicity to aquatic invertebrates (6.1.3)Required
Long-term toxicity to aquatic invertebrates (6.1.4)If available
Toxicity to aquatic algae and cyanobacteria (6.1.5)Required
Toxicity to aquatic plants other than algae (6.1.6)If available
Toxicity to microorganisms (6.1.7)If available
Endocrine disruptor testing in aquatic vertebrates – in vivo (6.1.8)If available
Toxicity to other aquatic vertebrates (6.1.9)If available
Sediment toxicity (6.2)If available
Toxicity to soil macroorganisms except arthropods (6.3.1)If available
Toxicity to terrestrial arthropods (6.3.2)If available
Toxicity to terrestrial plants (6.3.3)If available
Toxicity to soil microorganisms (6.3.4)If available
Additional ecotoxicological information (6.6)If available
7. Toxicological informationBasic toxicokinetics (7.1.1)If available
Dermal absorption (7.1.2)If available
Acute toxicity: oral (7.2.1)If available
Acute toxicity: inhalation (7.2.2)If available
Acute toxicity: dermal (7.2.3)If available
Acute toxicity: other routes (7.2.4)If available
Skin irritation / corrosion (7.3.1)If available
Eye irritation (7.3.2)If available
Skin sensitisation (7.4.1)If available
Respiratory sensitisation (7.4.2)If available
Repeated dose toxicity: oral (7.5.1)If available
Repeated dose toxicity: inhalation (7.5.2)If available
Repeated dose toxicity: dermal (7.5.3)If available
Repeated dose toxicity: other routes (7.5.4)If available
Genetic toxicity in vitro (7.6.1)If available
Genetic toxicity in vivo (7.6.2)If available
Carcinogenicity (7.7)If available
Toxicity to reproduction (7.8.1)If available
Developmental toxicity / teratogenicity (7.8.2)If available
Toxicity to reproduction: other studies (7.8.3)If available
Neurotoxicity (7.9.1)If available
Immunotoxicity (7.9.2)If available
Specific investigations: other studies (7.9.4)If available
Health surveillance data (7.10.1)If available
Epidemiological data (7.10.2)If available
Direct observations: clinical cases, poisoning incidents and other (7.10.3)If available
Sensitisation data (humans) (7.10.4)If available
Exposure related observations in humans: other data (7.10.5)If available
Additional toxicological information (7.12)If available
9. Residues in food and feeding stuffIf available
11. Guidance on safe useRequired
13. Assessment report (attach SDS)Required

Very low to low risk applications and information required

You can select this if you have categorised your introduction as exempted or reported and you want your chemical to be added to the Inventory. If this is not the case, you do not need to apply for an assessment certificate for these categories.

Note: The numbers in brackets represent the document numbers in IUCLID6 Version 4.18.0.

IUCLID documentationVery low to low risk for health and environment risk
SectionsSubsections / DocumentsRequired / If available
1. General informationIdentification (1.1)Required
Composition (1.2)Required
Analytical information (1.4)Required
2. Classification, labellingGHS (2.1)Required
3. ManufactureEstimated quantities (3.2)Required
Site (3.3)Required for manufacture only
Manufacture (3.5.1)Required for manufacture only
Formulation or re-packing (3.5.2)

If available – though at least one use (use name) must be provided in either 3.5.2, 3.5.3, 3.5.4 or 3.5.5.

 

Uses at industrial sites (3.5.3)
Widespread uses by professional workers (3.5.4)
Consumer uses (3.5.5)
Article service life (3.5.6)If available
4. Physical and chemical propertiesAppearance / physical state / colour (4.1)Required
Melting point / freezing point (4.2)Required
Boiling point (4.3)Required
Density (4.4)Required
Particle size distribution (Granulometry) (4.5)Required
Vapour pressure (4.6)Required
Partition coefficient (4.7)Required
Water solubility (4.8)Required
Solubility in organic solvents / fat solubility (4.9)If available
Surface tension (4.10)If available
Flash point (4.11)If available
Auto flammability (4.12)If available
Flammability (4.13)If available
Explosiveness (4.14)If available
Oxidising properties (4.15)If available
Oxidation reduction potential (4.16)If available
pH (4.20)If available
Dissociation constant (4.21)Required
Viscosity (4.22)If available
Self-reactive substances (4.23)If available
Additional physico-chemical information (4.27)If available
Nanomaterial agglomeration / aggregation (4.28.1)If available
Nanomaterial crystalline phase (4.28.2)If available
Nanomaterial crystallite and grain size (4.28.3)If available
Nanomaterial aspect ratio / shape (4.28.4)If available
Nanomaterial specific surface area (4.28.5)If available
Nanomaterial Zeta potential (4.28.6)If available
Nanomaterial surface chemistry (4.28.7)If available
Nanomaterial dustiness (4.28.8)If available
Nanomaterial porosity (4.28.9)If available
Nanomaterial pour density (4.28.10)If available
Nanomaterial photocatalytic activity (4.28.11)If available
Nanomaterial radical formation potential (4.28.12)If available
Nanomaterial catalytic activity (4.28.13)If available
Nanomaterial dispersion stability (4.28.14)If available
5. Environmental fate and pathwaysPhototransformation in air (5.1.1)If available
Hydrolysis (5.1.2)Required
Phototransformation in water (5.1.3)If available
Biodegradation in water: screening tests (5.2.1)If available
Biodegradation in soil (5.2.3)If available
Bioaccumulation: aquatic / sediment (5.3.1)If available
Bioaccumulation: terrestrial (5.3.2)If available
Adsorption / desorption (5.4.1)Required
Henry’s Law constant (5.4.2)If available
Other distribution data (5.4.4)If available
Additional information on environmental fate and behaviour (5.6)If available
6. Ecotoxicological informationShort-term toxicity to fish (6.1.1)If available
Long-term toxicity to fish (6.1.2)If available
Short-term toxicity to aquatic invertebrates (6.1.3)If available
Long-term toxicity to aquatic invertebrates (6.1.4)If available
Toxicity to aquatic algae and cyanobacteria (6.1.5)If available
Toxicity to aquatic plants other than algae (6.1.6)If available
Toxicity to microorganisms (6.1.7)If available
Endocrine disruptor testing in aquatic vertebrates – in vivo (6.1.8)If available
Toxicity to other aquatic vertebrates (6.1.9)If available
Sediment toxicity (6.2)If available
Toxicity to soil macroorganisms except arthropods (6.3.1)If available
Toxicity to terrestrial arthropods (6.3.2)If available
Toxicity to terrestrial plants (6.3.3)If available
Toxicity to soil microorganisms (6.3.4)If available
Additional ecotoxicological information (6.6)If available
7. Toxicological informationBasic toxicokinetics (7.1.1)If available
Dermal absorption (7.1.2)If available
Acute toxicity: oral (7.2.1)If available
Acute toxicity: inhalation (7.2.2)If available
Acute toxicity: dermal (7.2.3)If available
Acute toxicity: other routes (7.2.4)If available
Skin irritation / corrosion (7.3.1)If available
Eye irritation (7.3.2)If available
Skin sensitisation (7.4.1)If available
Respiratory sensitisation (7.4.2)If available
Repeated dose toxicity: oral (7.5.1)If available
Repeated dose toxicity: inhalation (7.5.2)If available
Repeated dose toxicity: dermal (7.5.3)If available
Repeated dose toxicity: other routes (7.5.4)If available
Genetic toxicity in vitro (7.6.1)If available
Genetic toxicity in vivo (7.6.2)If available
Carcinogenicity (7.7)If available
Toxicity to reproduction (7.8.1)If available
Developmental toxicity / teratogenicity (7.8.2)If available
Toxicity to reproduction: other studies (7.8.3)If available
Neurotoxicity (7.9.1)If available
Immunotoxicity (7.9.2)If available
Specific investigations: other studies (7.9.4)If available
Health surveillance data (7.10.1)If available
Epidemiological data (7.10.2)If available
Direct observations: clinical cases, poisoning incidents and other (7.10.3)If available
Sensitisation data (humans) (7.10.4)If available
Exposure related observations in humans: other data (7.10.5)If available
Additional toxicological information (7.12)If available
9. Residues in food and feeding stuffIf available
11. Guidance on safe useRequired
13. Assessment report (attach SDS)Required

Reminder about the information you need to support the application type you've chosen

For all application types (except for health and environment focus), you must have sufficient supporting information to demonstrate the absence of hazard characteristics based on the ⁠acceptable test guidelines.

Additional application type - comparable hazard assessment 

A comparable hazard assessment is a type of assessment certificate application. In AICIS Business Services, we'll ask you if you are using an acceptable comparable hazard assessment. 

Choose this if your introduction has had a hazard assessment previously conducted by an acceptable overseas or Australian assessment body.

Assessment bodies we recognise

For assessment bodies, one of the following overseas or Australian assessment bodies must have already assessed your introduction. 

  • National Industrial Chemicals Notification and Assessment Scheme (NICNAS)
  • Australian Industrial Chemicals Introduction Scheme (AICIS)
  • Environment and Climate Change Canada (ECCC) / Health Canada (HC) – (certain Schedules)
  • United States Environmental Protection Agency (US EPA)
  • European Commission (EC) Scientific Committee on Consumer Safety (SCCS) or its equivalent former committees — the Scientific Committee on Consumer Products (SCCP) and the Scientific Committee on Cosmetic Products and Non-Food Products (SCCNFP)
  • Therapeutic Goods Administration (TGA)
  • Australian Pesticides and Veterinary Medicines Authority (APVMA)
  • Food Standards Australia New Zealand (FSANZ)
  • International parallel process assessments where Australia was involved as a secondary jurisdiction and Environment and Climate Change Canada (ECCC) / Health Canada (HC) or the United States Environmental Protection Agency (US EPA) performed the risk assessment
Contact us if you’d like to know more about eligible assessments and how to get permission to use them. 

How to apply for a comparable hazard assessment

Before you start your application, you will need to contact us for further guidance.  

Information for publication purposes

We may use information on the purity, volume and/or concentration in a defined scope of assessment for an assessment certificate.  

You need to agree with all participants the information that, for publication purposes, will be entered into AICIS Business Services about:

  • Purity – it must be a number between 0 and 100 with no more than 2 decimal digits
  • Volume – tonnes of the chemical to be introduced each year
  • Concentration – introduction and end use concentration.
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