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Study Design

Total Preclinical R&D Management Solution. The Most Integrated Study Design Module Available.

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Pristima XD Study Design Overview

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.

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Book a demo with us now to experience a tailored solution that specifically addresses your current business needs.

Reduce Compliance Risk

Implement an all-in-one digital cloud platform to be always ready to meet compliance needs.

Increase Efficiency​

Replace standalone applications and paper trails with fully customized digital solutions.

Reduce Cost by 30%

Compliance Embedded, Quality Engrained, Data Integrity Assured

Key Features of Pristima XD Study Design

Flexible protocol builder that supports a variety of study designs.

Full GLP and OECD compliance

Manages all reviews, approvals, and required amendments.

Scheduling of daily in-vivo measurements, aample collections, sample analyses, necropsy activities, and pathology requirements.

Support for a variety of workflows, including general toxicology, reproductive toxicology, safety pharmacology, and more.

Event scheduling at varying levels – for all animals, for individual animals, by group, by gender, by sub-group, or litter.

Pristima XD Software Modules

From subject acquisition through study submission, Pristima XD helps you manage the entire preclinical lifecycle.

Click a module to learn more about Pristima XD Core features and benefits:

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