Created almost 20 years ago, 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.

Your regulatory & compliance dossiers in safe hands

what they say

Thanks to their expertise, CEHTRA consultants have become an indispensable partner for the regulatory activity of KEM ONE. I cannot emphasize enough how precious their support has been for all the complex REACH and Biocide dossiers that we have worked on together.

Patrick

Mise en oeuvre de REACH
Sans votre aide, votre efficacité, votre sens de l'écoute, on n'y serait probablement pas arrivé et bien sûr, à très bientôt car l'histoire ne fait que commencer.

REACH Manager

We greatly appreciate the efforts and expertise of everyone at CEHTRA involved on this project. It further validates that we definitely made the right choice when choosing a partner to help us.

M. Kersting, President at FedChem LLC

You saved us a considerable amount of money, and got the product's notification back on track.

Stephanie, Regulatory Specialist, Milliken Chemical

2 services you can trust CEHTRA with

Prioritisation / Anticipation REACH

More and more substances are listed on the ECHA Candidate List of substances of very high concern for Authorisation which comes with a business risk for a large number of industrial companies.
In order to predict the inclusion in this list, CEHTRA offers a Regulatory Watchdog service meaning that you will be informed of the probability of your substance being included in a 3, 5, or 10 year horizon. The service covers substances already commercialised and those currently being developed thus ensuring their mid-term use.
CEHTRA aims to build trust with our clients so you can feel your regulatory issues are safe in our hands.

Business Services

BIOCIDES

Are you required to renew an approval of an active substance, to submit a product authorisation or BPF dossier, to apply for Article 95 List inclusion or for Technical Equivalence?

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CHEMICALS

A solid, highly experienced team focused on helping you meet your compliance deadline. You're in safe hands.

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REACH AUTHORISATION

REACH Authorisation is a European risk management measure which aims to limit human and environmental exposure to substances considered of very high concern.

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COSMETICS

Demonstrate the safety of both your finished products and ingredients. Get the packaging safety tested. Shorten the time to market.

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FOOD & PACKAGING

Experienced, quality support in managing the complex and constantly evolving regulation on food and food packaging

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PHARMACEUTICALS

For the safety of your pharmaceutical substances & products CEHTRA can assist you in the development of your new drugs from early candidate safety profiling to marketing authorisation in the EU and the USA.

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PLANT PROTECTION

As a manufacturer or a distributor in the field of agriculture, you want to get your substances approved efficiently and get your Plant Protection Products on the market.

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MEDICAL DEVICES

A solid and comprehensive biological evaluation. From risk analysis, including physico-chemical and toxicological study monitoring through to the final biological evaluation report.

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News

25/04/2019

L’innovation est au cœur du développement international de Cehtra et de sa filiale Kreatis

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02/04/2019

Announcement. Launching a BIOCIDE CONSORTIUM

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20/03/2019

Publication in Speciality Chemical Magazine

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08/03/2019

Webinar - Chrome VI - Comment vous mettre en conformité avec les conditions d'autorisation du CTAC

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Events

14/06/2019

Cosmetic Valley - Congrès Consumer Safety & Cosmetics

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17/05/2019

SETAC Helisinki, Booth #23

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09/05/2019

Booth #26 - ECPA Regulatory Conference 2019 will be held in Ghent on 22nd and 23rd May, within the framework of the IUPAC Congress.

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04/04/2019

FREE WEBINAR - The 12 new Annex XIV substances: The keys to a successful application

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	Webinar Chemical Watch CEHTRA Stephane Pierre 12 new annex VIX substances. Dr. Stéphane Pierre explains in detail the 12 new substances which in the coming months will normally be included in Annex XIV. The market sectors impacted, the timeline, latest application dates and he gives his insight into what makes a sucessful application.
	CEHTRA Webinar Comment vous mettre en conformité avec les conditions autorisation. Un webinar en français présenté par Stéphane Pierre, notre expert en REACH Autorisation. Quelles mesures doivent mettre en place les utilisateurs de Chrome VI.
	CEHTRA Webinar ChromiumVI Prolongation 6 dec 2018 Un webinar en français présenté par Stéphane Pierre, notre expert en REACH Autorisation. Un zoom sur les demandes de prolongation d'utilisation de Chromium VI
	BPR Technical Equivalence A Practical Guide Webinar April 2018
	CEHTRA Partner of Your HSE Team
	CEHTRA Partenaire de Votre Equipe Reglementaire

2 services you can trust CEHTRA with

Prioritisation / Anticipation REACH

Business Services

BIOCIDES

CHEMICALS

REACH AUTHORISATION

COSMETICS

FOOD & PACKAGING

PHARMACEUTICALS

PLANT PROTECTION

MEDICAL DEVICES

News

L’innovation est au cœur du développement international de Cehtra et de sa filiale Kreatis

Announcement. Launching a BIOCIDE CONSORTIUM

Publication in Speciality Chemical Magazine

Webinar - Chrome VI - Comment vous mettre en conformité avec les conditions d'autorisation du CTAC

Events

Cosmetic Valley - Congrès Consumer Safety & Cosmetics

SETAC Helisinki, Booth #23

Booth #26 - ECPA Regulatory Conference 2019 will be held in Ghent on 22nd and 23rd May, within the framework of the IUPAC Congress.

FREE WEBINAR - The 12 new Annex XIV substances: The keys to a successful application

ALL ►

®CEHTRA