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The most integrated study design module available
The Pristima XD study design module enables study directors to detail all aspects of study protocol and define all activity schedules. Approvals are electronically documented; reviewers are notified by email and amendments to protocol are effective immediately upon approval.
The Pristima XD study design enables quality data management by eliminating the need for data duplication or redundant workflows.
Key features of the Pristima XD Core Study Design module:
Flexible protocol builder, supporting a variety of study designs
Full GLP and OECD compliance
Manages all of the necessary reviews, approvals, and amendments required
Scheduling of daily in-vivo measurements, sample collections, sample analyses, necropsy activities, and pathology requirements
Support for a variety of workflows, including general toxicology, reproductive toxicology and safety pharmacology
Event scheduling at varying levels – for all animals, for individual animals, by group, by gender, by sub-group or litter
Pristima XD software modules provide full lifecycle automation and support
Learn more about other Pristima XD modules delivering full lifecycle automation and support for pharmacology and drug safety research study management, vivarium management, and veterinary care.
Click a module to learn more about Pristima XD core features and benefits:
