Your partner in DMPK and in Agrosciences
Growing complexity, longer timelines, quality and confidentiality issues, high personnel turnover, continuous searching for expertise along with low costs: these are some of the most daunting pre-clinical and clinical research challenges you face today when outsourcing your priority studies. Eurofins ADME BIOANALYSES is a GLP compliant CRO founded in 1987. In recognition of the challenges you face, we offer you our expertise in the fields of pharmacokinetics, metabolism, bioanalysis and residue analysis.
A proven quality of services
Since the establishment of Eurofins ADME BIOANALYSES, we have been successfully inspected every 2 years by AFSSAPS[1].
Due to our expertise and comprehensive range of services which are compliant with EMEA and FDA regulatory requirements[2], we are well positioned to be your professional and valued partner.
The quality and reliability of our performance is best reflected by the numerous ongoing and long-lasting collaborations we maintain with leading international companies.
[1] AFSSAPS: Agence Française de Sécurité Sanitaire des Produits de Santé (French Agency for Health Products Safety)
[2] Successful FDA General Facility inspection July 2009
News
Eurofins ADME BIOANALYSES has worked on particular Bioanalytical methods such as Vitamins, Nicotine and Anti-Epileptic drugs