Study Design Module

Total Preclinical R&D Management Solution

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:

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