Let’s talk

Let’s discuss your regulatory toxicology project

A scientific question, a regulatory dossier to prepare, a study to launch? Our scientific team gets back to you within 48 working hours.

Why get in touch?

Request a quote

Budget scoping, study perimeter, indicative timeline. Detailed proposal within 5 working days.

Get in touch

A preliminary exchange with our scientific experts to qualify your need and inform your strategy.

Careers

Want to join a French CRO with 50 years of scientific heritage? Send us your application.

Lab visit

Discover our facilities in Porcheville (78, France). Visits organised by appointment for sponsors and partners.

Send us a message

Describe your need in a few lines — we’ll come back to you with a qualified scientific contact.

What to expect

First exchange within 48 working hours — a member of our scientific team picks up your request and qualifies it.
Qualified call with an expert — a technical discussion to frame the scope, the relevant methods and the regulatory context.
Detailed quote within 5 working days — a costed proposal covering methods, timeline, deliverables and terms.
Confidentiality preserved — option to sign an NDA from the very first exchange if the project requires it.

Frequently asked questions before a first contact

What documents should I prepare for a first exchange?

A brief description of your substance or product, the targeted regulatory context (REACH, cosmetics, biocides, ICH…) and any studies already conducted are enough for an initial qualification. No confidential document is required at this stage; we can sign an NDA upfront if needed.

Do you handle confidential studies?

All our services are conducted under a confidentiality agreement. Signing an NDA is systematic before any detailed exchange about the nature of the compound or product. Our facilities and teams are organised to ensure project segregation and traceability.

What are your standard turnaround times?

Lead times vary depending on the method and complexity of the file. As an indication: Ames test (4 to 6 weeks), in vitro micronucleus (6 to 8 weeks), chromosomal aberrations (8 to 10 weeks). Our quotes always include a detailed schedule with intermediate milestones.

Do you work internationally?

Yes. Our reports are written in English or French, on request, and comply with international standards (OECD, ICH, EMA, FDA). We regularly support sponsors based in Europe, North America and Asia.

Our laboratory