Pristima Suite®, the Total Preclinical Lab Management Solution, provides a module to facilitate the FDA SEND standards for preclinical submissions. The Standard for Exchange of Non-Clinical Data (SEND) is an implementation of the Study Data Tabulation Model for non-clinical studies. This standard was developed by the Clinical Data Interchange Standards Consortium’s (CDISC) SEND Team for non-clinical data collected from animal toxicology studies is the FIRST fully integrated end-to-end enterprise solution for tracking and http://npswu.org/levitra-online-50mg managing veterinary facilities and research subjects throughout the pre-clinical research process. From breeding and ordering through the order generic viagra study submission process, the Pristima Suite™ delivers essential capabilities across the entire drug discovery process to try it cheap levitra online facilitate your entire research program. For over 25 years, global pharma companies and CROs have relied on our flagship Pristima pre-clinical data management suite for effective, end-to-end processes. Pristima delivers quality, efficiency, and compliance assurance.
The Pristima Suite is a comprehensive Research and Safety Study Management application. The system offers advanced capabilities for toxicology and pathology data management. Pristima® VM delivers extensive capabilities for Vivarium Management and Veterinary Care. This unique solution delivers key features that effectively bridge the gap between the business, animal management and scientific aspects of research absent in many of today’s pre-clinical solutions. Pristima® VM’s rich graphical user interface and detailed reports and viagra online overnight visualizations deliver the most comprehensive animal facility solution.