The evaluation of substances for Endocrine Disruption (ED) potential is a growing concern from a regulatory perspective. This evaluation has been mandatory since 2018 under the Plant Protection Products and Biocide Products regulations. The year 2022 is expected to be a key turning point with the update of the regulation on Cosmetic Products and the addition of classification criteria for endocrine disruptors in the CLP regulation. Moreover, in the same year, REACH will be updated with new requirements to identify endocrine disruptors.
The evaluation of the ED potential of substances requires expertise and a good understanding of the state-of-the-art tools and available methods. CEHTRA can provide you with the necessary guidance to obtain reliable results using the most appropriate methods and to provide a balanced and independent ED assessment by experts of your active substances, chemicals, or ingredients.
Optimised assessment of ED properties
Generating new data
Data compilation for regulatory dossiers
Existing regulatory data
Targeted bibliographic search
Tailored testing strategies (based on in silico, in vitro and/or in vivo studies)
Study monitoring of ED specific studies
Robust study summaries
EFSA table and identification of lines of evidence
Reports on ED assessments of specific ingredients or formulations
Position papers on the relevance of ED potential of a substance for human health/environment
In silico screening by QSAR experts
Bespoke services adapted to many domains
(biocides, PPP, cosmetics, chemicals…)
Experienced in-house (eco)toxicologists
Interested to know more? Our key contact for Endocrine Disruption services, Julien LEGHAIT will be happy to answer all your queries. You can email him or simply drop your query into the chat window below.
Coordinator of Endocrine Disruption services