Pristima™ is your single solution for toxicology and pathology data management.  It is the 21CFR part 11 compliant platform for the complete integration and automation of your preclinical research and development.  Pristima provides an unmatched set of capabilities for the Pharmaceutical Industry, Contract Research Organizations and Chemical Industries world wide. 

Our professional services team works with you to design, execute and document the validation, training and implementation of Xybion’s solutions as well as any other software system you may be considering. Xybion is experienced and knowledgeable in all areas of preclinical compliance to regulatory agencies worldwide. A team you can trust.