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Xybion Events – Eurotox 2015

Join Xybion Corproation as we showcase our industry leading preclinical software platform, Pristima, at this year’s Eurotox 2015 in Port, Portugal

Xybion is pleased to continue its support for EUROTOX which is the Federation of national societies of toxicology in Europe, which together have approximately 7,000 members. In addition, EUROTOX counts more than 200 individual members coming from 50 countries, mostly from Western Europe.

We will be showcasing a host of new, advanced software solutions for preclinical drug discovery at this year’s show.  We will be at booth #28. For information about scheduling a demonstration at our booth, please contact cfrade@xybion.com.

About the show

EUROTOX 2015 Congress will be held from 13-16 September 2015, at the Alfândega International Congress Center, Porto, Portugal. The topic of this congress, “Bridging Sciences for Safety”, upholds the important role of Toxicology in bridging the knowledge of sciences like Biology, Chemistry, Pharmacology, Physiology, and many others, for the desired path of humankind towards a safer world.

As such, the EUROTOX Annual Congress certainly represents a unique occasion to participate in the most important regular event of Toxicology in Europe and one of the most relevant in the world. It provides excellent opportunities for meeting delegates from all over the world, and is a privileged stage for exchanging ideas and experiences among colleagues and friends, establishing and reinforcing scientific networks, and learning the forefront scientific developments from distinguished scientists, opening minds for new concepts and paradigms in Toxicology and related sciences.

About Pristima

Pristima® is a fully integrated enterprise solution for preclinical data management that delivers complete life cycle automation and support for Pharmacology and Drug Safety Research Study Management, Vivarium Management, and Veterinary Care.  From breeding and ordering through the study submission process, the Pristima® Suite manages the planning and recording of data, controls authorized changes, and assembles the data for submission to regulatory agencies.