In vivo data to the highest scientific and technical standards
Scientific excellence for over 40 years
Since 1977 Scantox has been a trusted partner for in-vivo preclinical research services for the pharmaceutical and medical device industries. Our services and expertise enable clients to progress their drug or device development based on consistent, high-quality solid data to the highest technical and scientific standards.
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Why Scantox as your preferred CRO?
This enables clients to progress their development projects under one roof in a trustworthy collaborative matter based on the highest technical and scientific standards.
Questions?
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Regulatory toxicology is one of our core competences, and Scantox has for many years been a leading expert withinsafety studies using the Göttingen Minipig. We offer a full ull spectrum of preclinical toxicology studies, incl. GLP, and a wide species selection.
We offer formulation development and dose formulation manufactory including logistics for phase 1 and 2 clinical trials. Further, a full spectrum of bioanalysis with a comprehensive full package of LCMC/MS method development, validation
and sample analysis for both for exploratory, regulatory studies and clinical.
New Research Targets Tau Protein Abnormalities
Key Steps to Get Your IND Schedule on Track
Careers at Scantox
We are continuously looking for new talents to join our team. Check out our open positions or send us your CV and an unsolicited application.