The IFRA Standards set the maximum dose of a fragrance ingredient in finished consumer goods. They are primarily a tool for use by IFRA members in their daily work.
The typical user is a perfumer or someone else with a technical, regulatory or scientific background - and so the format and language of the Standards are written with this audience in mind.
However, we believe that it is an important part of our self-regulatory role to be transparent about the Standards we apply - which is why all of the Standards are available on this website.
Given their intended audience, some of the information presented can seem confusing or hard-to-understand for non-experts. We believe it is important to keep the information brief and relevant for a technical audience - but also to give a wider audience the chance to understand what information is in a Standard, and why.
Click here for a short explainer of the key information contained in a typical Standard.
The IFRA Standards-setting process principally involves IFRA, the Research Institute for Fragrance Materials (RIFM) and the independent Expert Panel on Fragrance Safety.
We also, through a consultation phase, involve our Members and stakeholders in the process.
Here's how it works:
IFRA sends RIFM information about a fragrance material, including exposure situation (usage concentration, variety of use, volume of use); chemical composition; olfactory profile; olfactory potential
RIFM prepares a comprehensive dossier on the material, including all available safety data. If necessary, RIFM initiates and organizes safety studies to fill gaps in knowledge about the material.
The independent Expert Panel evaluates the data. It checks whether the data supports current use levels in such a way that there is no risk to consumers. If the safety assessment does not support current use, the Panel instructs IFRA to issue a Standard.
IFRA prepares a Standard in line with its Standard-setting process
The draft Standard is sent to IFRA's members and stakeholders for consultation. The consultation period allows members and stakeholders to provide IFRA with additional data or scientific studies that may need to be considered in setting the final Standard.
If no additional information is received during the consultation phase, the final Standard is published as part of an 'Amendment to the IFRA Code of Practice'. Following publication, members have a specified period to change internal systems and apply the Standard.