Preclinical Research
Preclinical LIMS
Purpose-built laboratory information management for preclinical research. Manage complex studies, track specimens, ensure GLP compliance, and accelerate your drug development pipeline with complete traceability.
18
Active Studies
3,240
Total Animals
100%
GLP Compliance
| Id | Title | Status | Value |
|---|---|---|---|
| GEN-TOX-2024-001 | General Toxicology | Active | 240 |
| ADME-SAF-2024-015 | ADME Study | Complete | 120 |
Designed for Preclinical Excellence
Key Features
Comprehensive tools for managing complex preclinical studies from protocol to final report.
Study Management
Complete study lifecycle management from protocol design through final reporting. Track milestones, timelines, and deliverables.
Subject Tracking
Comprehensive animal and subject management. Track housing, dosing schedules, observations, and clinical signs.
Specimen Management
Full specimen chain of custody from collection to analysis. Biobank integration and sample inventory management.
Bioanalytical Workflows
Integrated bioanalytical data management. Method validation, sample analysis, and concentration reporting.
Toxicology Support
Specialized workflows for toxicology studies including pathology integration, histology tracking, and organ weights.
PK/TK Analysis
Pharmacokinetic and toxicokinetic data management. Integration with PK modeling software and automated calculations.
Operations
Transform Your Laboratory
Streamline preclinical operations and get therapies to patients faster.
30% Faster Study Completion
Automated workflows and integrated data management reduce administrative overhead and accelerate study timelines.
Complete GLP Compliance
Built-in GLP workflows ensure every study meets regulatory requirements with full audit trails and electronic signatures.
Real-time Study Visibility
Live dashboards provide instant insight into study progress, resource utilization, and potential issues.
Seamless Data Integration
Connect with instruments, ELN, and downstream systems for end-to-end data flow without manual intervention.
Support for All Preclinical Studies
Pre-configured workflows for the full spectrum of preclinical research, easily customizable to your specific needs.
- General Toxicology
- Safety Pharmacology
- ADME Studies
- Carcinogenicity
- Reproductive Toxicology
- Genetic Toxicology
In Vivo Studies
Complete animal study management with dosing and observations
In Vitro Studies
Cell-based assays and in vitro toxicology workflows
Bioanalysis
Sample analysis with method validation support
Pathology
Histopathology and clinical pathology integration
Ready to Transform Your Preclinical Research?
See how Fiscal Ox Preclinical LIMS can accelerate your drug development pipeline. Schedule a personalized demo today.
Works Great With
Extend your preclinical research capabilities with these integrated solutions.
Lab Information Management System
Full-featured lab information management for analytical testing and compliance.
Quality Management System
Integrated quality processes for GLP compliance and regulatory requirements.
Document Management System
Centralized control for study protocols, SOPs, and regulatory documentation.