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 the study protocol and defines all activity schedules. Approvals are electronically documented; reviewers are notified by email and amendments to the 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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