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.
We can support you, the sponsors, to ensure proper execution of the non-clinical study protocols and successful regulatory filing.
Click on the image below to see our services.
ERA - Environmental Risk Assessment
In Silico Modelling & QSARs
Stéphane PIERRE Chemical Authorization Manager View CV ►
Maryse CORROLLER Expert Toxicologist View CV ►
Blandine JOURNEL Senior Ecotoxicologist View CV ►
Tick the services you are interested in
Send us your notification to be contacted ►
FOOD & PACKAGING
Meet the experts
CEHTRA near you
News & Events