Pristima XD logo

Pristima XD

by Xybion · Since 1977
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ActiveAvailable globallyCloud
Quick facts
VendorXybion
Year launched1977
StatusActive
Location105 College Road East Princeton, New Jersey 08540
Countries servedGlobal
Languages9
Integrations1+
Free tier
Free trial
Contact salesYES

About Pristima XD

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Pristima XD by Xybion is a comprehensive Laboratory Information Management System (LIMS) designed to streamline data management processes in research laboratories and scientific institutions. One of its standout features is its ability to centralize and organize data from various sources, facilitating collaboration and efficient decision-making. The user interface of Pristima XD is intuitive and user-friendly, making it easy for users to navigate through the system. The design elements are clean and organized, enhancing the overall user experience. The software's dashboard provides a clear overview of key metrics and tasks, allowing users to quickly access the information they need. What sets Pristima XD apart from its competitors is its robust functionality. The software offers innovative features such as customizable workflows, advanced data visualization tools, and automated data analysis capabilities. These functionalities enable users to manage complex operations with ease and extract valuable insights from their data. In terms of performance, Pristima XD delivers excellent speed, efficiency, and reliability. It can handle large datasets with ease, allowing users to process and analyze data quickly and accurately.

Pros & Cons

What users like
  • +Comprehensive Platform
  • +Unifies all critical lab functions into a single platform, reducing data silos and improving study coordination.
  • +Regulatory Compliance Support
  • +Specifically designed to meet GLP and FDA requirements, including SEND data submission capabilities.
  • +Digital Pathology Integration
  • +Supports efficient, remote pathology review with compatibility across various slide scanners.
  • +Strong Data & Analytics Capabilities
  • +Centralized data management and built-in analytics support real-time monitoring and regulatory reporting.
  • +Enterprise Scalability
  • +Used by major pharmaceutical firms and contract research organizations for multi-site and global deployments.
What users flag
  • Primarily Suited for Preclinical Labs
  • Best optimized for preclinical and GLP-focused environments; less suitable for clinical or other types of labs.
  • Customization Requirements
  • Implementation may require configuration to match the unique workflows of each organization.
  • Ongoing Maintenance Needs
  • Regulatory updates, system upgrades, and integration changes require consistent attention and support.

Features

Key features

End-to-End Preclinical Lab Execution
Manages the full lifecycle of preclinical studies including study planning, execution, animal and resource management, toxicology, pathology, necropsy, histology, competency management, and CAPA in one unified platform.
Digital Pathology Integration
Supports scanner-agnostic whole-slide imaging, remote peer review, annotations, and metadata management in a secure and compliant environment.
Study Design, Protocol & Compliance Management
Enables centralized management of study protocols, audits, IACUC tracking, regulatory submissions, and non-conformance or CAPA processes.
Resource & Animal Colony Management
Handles animal housing, colony health records, veterinary care, and employee resource tracking for optimized lab management.

Additional features

Preclinical Module Suite
Includes modules for study design, costing, protocol execution, pathology, clinical pathology, necropsy, histology, and digital pathology workflows.
Veterinary & IACUC Compliance
Provides full veterinary oversight, animal health records, clinical observations, and institutional animal care compliance tracking.
Laboratory Logistics & Scheduling
Manages lab and study schedules, room and equipment allocation, staff assignments, and resource planning.
CAPA & Non-Conformance Tracking
Supports documentation and resolution workflows for deviations, non-conformances, and corrective or preventive actions.
SEND & Regulatory Submissions
Generates FDA-compliant SEND datasets for regulatory reporting and submission readiness.
Digital Pathology Workflow Tools
Enables viewing, annotating, and reviewing digital whole-slide images; compatible with multiple scanners.

Pricing

Free trial
Free version
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Countries & Languages

Global
Countries served
9
Interface languages
8
Billing currencies

Interface languages

EnglishSpanishFrenchGermanChineseJapaneseItalianPortugueseRussian.

Billing currencies

🇺🇸USD🇪🇺EUR🇬🇧GBP🇦🇺AUD🇨🇦CAD🇯🇵JPY🇨🇳CNY🇮🇳INR

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