Choose from 5 options:
The manufacturing information you enter in IUCLID Section 3 is generally the same for all certificate application types
See Types of assessment applications and information required in the Guide to applying for an assessment certificate for a summary of information required for this section.
In this section, you must describe how your substance is manufactured, supplied and used, and identify where exposure to people and the environment may occur.
We recommend you first map the process (lifecycle) of the substance (for example, using a simple diagram) to understand how the substance is manufactured, handled and used.
In IUCLID, exposure scenarios are also called 'identified uses' or 'use descriptions'.
Assign exposure scenarios (use descriptions) for each stage of the substance’s lifecycle, including:
Although manufacture is not a ‘use’, you must still describe it as part of the substance's lifecycle.
You must allocate the total annual quantity of the substance across lifecycle stages and use scenarios (for example, manufacture, formulation and end use).
The total across all activities and uses must match your Section 3.2 estimates.
The following fields appear in most Section 3 documents:
Complete these fields consistently across all relevant sections.
You must report annual tonnage in Section 3.2 and allocate this across activities and uses in sections 3.5.1 to 3.5.5. The totals across all uses must match your Section 3.2 estimates.
In this section, you must report the total annual quantity of your substance for each year of the 5-year certificate period.
To report quantities:
You can flag CBI and restrict regulatory use (by jurisdiction).
Use Remarks to provide any extra information. For example, details of flagged CBI. Be specific on which tonnage you wish to flag (import, manufacture or both). Also provide:
For each site you have selected or created link to all applicable activities:
In this section, you must describe how the substance is manufactured.
Create one document per manufacturing activity.
Use a clear, descriptive name that distinguishes each manufacturing activity from others.
Provide a detailed technical description of the process. Include relevant operational steps, diagrams, tables, or other structured information, if useful.
You can link a composition created in Section 1.2 Composition, if relevant.
Enter the number of workers involved in the activity.
Select the option that best describes the conditions for this activity or use. Different/additional fields will display depending on your selection.
The fields required in this section are the same as those in Section 3.5.3 Uses at industrial sites, adapted for the relevant use type.
This section describes widespread use by professional workers.
Create one document for each type of widespread use.
The fields required in this section are the same as those in Section 3.5.2 Formulation or re-packing adapted for the relevant use type.
This section describes consumer uses of the substance.
Create one document for each type of consumer use.
Use this field to elaborate on the international regulatory status.
Select all functions that apply (multiple selections allowed).