Preclinical Reporting

Pristima®, the Total Preclinical Solution, provides a complete business intelligence solution as part of its preclinical platform. The Pristima Report Compiler allows standard sets of tables, appendices, and graphs to be defined for automatic generation. These tables can come from anywhere in the system.

Your favorite groupings of tables are assembled into a “Set” which you name and each site may develop any number of these sets, each designed for a particular purpose such as the sponsor, study type, regulatory body that is receiving the final report, etc.

As a result, at any point in the study, depending on the characteristics of the study, you simply request a specific favorite set and all the reports in the set are generated at once. They are saved to a specific location on your network and subject to version control.

Pristima Reporting Module Features:

  • Design, generate, distribute and schedule reports
  • Tight Integration – All data stays under Pristima control. Robust embedded statistical analysis capabilities eliminate the need for third party applications
  • Filters to produce summarizations by study, animal, date, subgroup, and dose group upon demand
  • Reports may be displayed on screen, sent via email or printed
  • Visualization of data using graphs
  • Define format and content of output data tables produced in HTML, PDF, MS Office & CSV format Full GLP and OECD compliance

The Pristima Suite is a comprehensive Research and Safety Study Management application. The system offers advanced capabilities for toxicology and pathology data management.