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Study Design

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

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.

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 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 Software Modules

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

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