Labelling process

Step 01

Labelling request

Submission of the request and planning of the evaluations according to availability.

Step 02

Independent toxicological assessment

Complete analysis performed by an independent toxicology office. Targeted substances include:

Endocrine disruptors
Irritants
Allergens and sensitising substances
CMR substances (carcinogenic, mutagenic, reprotoxic)

Step 03

Comparison with international standards

The assessment results are compared against more than 60 international standards, taking into account:

Toxicological reference values (NOAEL)
Opinions from institutions such as the SCCS, CIR, NICNAS, NTP, IARC

Step 04

Score attribution (5 to 12 weeks)

The product receives a clear score from A+ to C based on the risks identified. A detailed report is provided, including substances that may become problematic in the future.

Step 05

Quality control and annual update

Each year:

Update

According to scientific and regulatory developments.

Control

Random quality control on a sample of labelled products.

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