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.
Book a Demo
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.
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:
Necessary cookies are absolutely essential for the website to function properly. This category only includes cookies that ensures basic functionalities and security features of the website. These cookies do not store any personal information.
Any cookies that may not be particularly necessary for the website to function and is used specifically to collect user personal data via analytics, ads, other embedded contents are termed as non-necessary cookies. It is mandatory to procure user consent prior to running these cookies on your website.