In Vitro Testing for Cosmetics: Alternative Methods for Product Safety (Reg. 1223/2009)
Cosmetic products marketed in Europe must comply with Regulation (EC) No. 1223/2009, which prohibits animal testing and requires the use of validated alternative methods, such as in vitro testing.
What the European Cosmetic Regulation Requires
Regulation 1223/2009 mandates a human safety assessment of the cosmetic product, which must be documented in the Product Information File (PIF).
Today, this assessment is based on a fully in vitro testing strategy, in accordance with SCCS guidelines.
In Vitro Testing Services Offered by Renolab
Renolab performs in vitro tests on:
- Individual ingredients
- Mixtures
- Final products
Using recognized methods for:
- Cytotoxicity Tests
- Skin irritation and corrosion
- Eye damage and irritation
- Skin sensitization
- Mutagenicity / Genotoxity
All tests are conducted in full compliance with Good Laboratory Practice (GLP) standards.
A Certified Laboratory for Cosmetics and Beyond
Renolab is a GLP-certified laboratory (certified by the Italian Ministry of Health) with extensive experience in the following sectors:
- Chemical substances (REACH)
- Biocides
- Cosmetics
- Medical devices
- Biopesticides
- Biostimulants
Renolab has also been recognized by the REACH Centre as one of the laboratories authorized to perform testing required under Reg. (EC) No. 1907/2006.
Contact
Want to know which tests your cosmetic product really needs?
Write to us at: info@renolab-glp.com