All for successful registration of your compounds

At Eurofins Pharma services, our highly experienced staff provides a complete range of in vitro and in vivo toxicology activities. All of our services are performed in GLP facilities and can support all types of regulatory submissions.  This service is embedded in our network of drug development experts. For this reason we do not only provide you accurate and timely data of the highest scientific level, but also upfront a strategy and solution to your problem. That's why our clients are coming to us and are returning as partner. Depending on the specifics of the compounds and projects, we can propose innovative and flexible approaches to your preclinical drug development project. If you choose us to conduct your preclinical safety activities, you will get the best quality data and the famous Eurofins service.

Our services include:

• General toxicology - acute, sub-acute and chronic studies
• Safety Pharmacology
• Genetic Toxicology
• Reproductive Toxicology
• Immuno Toxicology
• In vitro Toxicology screens
• ADME screening and testing
• Bioanalysis
• Bioassays
• Biocompability and Medical device
• Histopathological preparation and read out

Eurofins Pharma Scandinavia, contact: