Xybion Pristima
The Gold Standard in Preclinical Software.
Overview
The Pristima Suite is a comprehensive, integrated platform specifically designed for preclinical research. It manages the entire lifecycle of pharmacology and drug safety studies, including study design, vivarium management, veterinary care, data collection, pathology, and generation of FDA SEND (Standard for Exchange of Nonclinical Data) datasets for submission. It aims to centralize data, ensure GLP compliance, and accelerate the drug development timeline.
✨ Key Features
- End-to-end preclinical study management
- Toxicology and Safety Pharmacology workflows
- Vivarium and animal colony management
- Veterinary care and clinical observations
- Pathology module
- FDA SEND dataset generation
- GLP and 21 CFR Part 11 compliance
🎯 Key Differentiators
- Comprehensive, all-in-one suite for the entire preclinical workflow
- Strong focus and deep functionality for in-vivo studies
- Integrated SEND dataset generation
Unique Value: Provides a single, unified environment to manage the entire preclinical study lifecycle, from subject acquisition through to final reporting and FDA SEND submission, ensuring compliance and reducing costs.
🎯 Use Cases (5)
✅ Best For
- Managing GLP-compliant toxicology studies
- Automating data collection for in-life study phases
- Preparing and assembling SEND-compliant datasets for FDA submission
💡 Check With Vendor
Verify these considerations match your specific requirements:
- Early-stage in-vitro research
- Clinical trial management
- Labs not conducting animal studies
🏆 Alternatives
Offers a more integrated and specialized solution for in-vivo studies compared to general-purpose LIMS or ELNs, which may require extensive customization to manage preclinical workflows.
💻 Platforms
🔌 Integrations
🛟 Support Options
- ✓ Email Support
- ✓ Phone Support
- ✓ Dedicated Support (Standard tier)
🔒 Compliance & Security
💰 Pricing
Free tier: NA
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