Your Specialties, Our Expertise
CEHTRA stands for Consultancy for Environmental & Human Toxicology and Risk Assessment
Since 2001, we provide high quality scientific and innovative solutions ensuring regulatory compliance of chemicals to international obligations.
You are committed to the safety of your products.
We are committed to high quality regulatory services at optimized costs.
Our key services
Technical assistance & Expert advice
Dossier preparation and registration
Only Representative services
QSARs and Read-Across
Expert advice on critical roadblocks
Outsourcing & Régie
Our consultant at your site or at CEHTRA offices, with full access to CEHTRA expertise, tools and managers.
Full time/part time, dedicated to your needs.
Training & Mentoring
Wide catalog of regulatory and scientific trainings
Bespoke trainings to best suit clients' needs
Dedicated mentoring to meet your goals
Latest News
IUCLID dossier will be soon required for all new active substance applications
11 / 11 / 2020
Cyril DUROU from CEHTRA will be presenting at an upcoming Chemical Watch event on Biocides
17 / 10 / 2020
CEHTRA attending the Annual Biocontrol Industry Meeting 2020
1 / 7 / 2020
Introducing QuAC consortium
CEHTRA attending the Annual Biocontrol Industry Meeting 2020
Blandine Journel and Sylviane Gony from CEHTRA will be attending ABIM - Annual Biocontrol Industry Meeting, 19-21 October 2020 (ABIM 2020 – The virtual conference and exhibition). If you are attending this event, Blandine and Sylviane will be happy to answer any questions you may have regarding Plant Protection services at CEHTRA. Feel free to get in touch with them!
Introducing QuAC consortium
Introducing QuAC consortium – one umbrella to cover all Quaternary Ammonium Compounds.
If your company has interest in biocidal products containing QUATS (including specific ones as well as combinations of QUATs), this consortium is for you. Together, CEHTRA and Steptoe & Johnson LLP offer a unique combination of in-depth expertise and understanding of the regulatory and legal requirements to provide seamless support and maximise value for all consortium members. Besides cost reduction, this umbrella consortium will will provide answer to all your interests for QUATs.
Interested to know more? Attend one of our upcoming QuAC webinars where the team will present key aspects of this consortium – QuAC concept, strategy and costs. To register your interest, please get in touch with CEHTRA experts Nathalie Hanon, Cyril Durou and Annekathrin Faupel and Eléonore Mullier from Steptoe & Johnson LLP.
Cyril DUROU from CEHTRA will be presenting at an upcoming Chemical Watch event on Biocides
Are you attending the Chemical Watch event on Borderlines of the Biocidal Products Regulation (BPR) with other legislation on 18th November? Our Biocides expert and Executive Vice President Cyril Durou is one of the speakers at this event. His presentation will be focused on Regulatory overview between biocidal products, veterinary borderline products and veterinary medicines.
Please click on this link to have further information about this event:
IUCLID dossier will be soon required for all new active substance applications
In the framework of the implementation of the EC General Food Law and the Transparency Regulation, a IUCLID dossier will have to be submitted for every new active substance application from March 27th, 2021, and later in 2021 for renewal submissions. However, the CADDY dossier may not be immediately withdrawn and could still be required by some Member States. Therefore, applicants may be compelled to submit both IUCLID and CADDY dossiers.
CEHTRA has a long experience with both software systems: CADDY for the PPP regulation and IUCLID for REACh and Biocides regulations. Moreover, we can help you for the whole registration process, from data gap analysis to the final dossier submission and beyond, including IUCLID and CADDY dossiers.