Contract Research Organisations (CROs)
Purpose-built LIMS for preclinical and translational research. Study-centric workflows, tissue lifecycle tracking, GLP compliance, and sponsor reporting for contract research laboratories.
Built for Preclinical Research Excellence
CoreLIMS delivers comprehensive study management designed specifically for contract research organisations. Map cases to studies, track tissue lifecycles, and generate sponsor-ready reports with complete regulatory compliance.
From toxicology studies to translational research, our platform handles the unique requirements of CRO pathology services with GLP-friendly audit trails and document control.
- Study/project hierarchy above individual cases
- GLP-compliant audit trails and electronic signatures
- Sponsor portals for client access and reporting
- Regulatory data exports for submissions
From Study Setup to Final Report
Complete study lifecycle management with full traceability and sponsor visibility.
Study Setup
Configure study parameters, sponsor details, protocol requirements, and sampling schedules. Link SOPs and study plans.
Subject Management
Track test subjects across treatment groups. Manage dosing schedules, observations, and scheduled necropsy timepoints.
Tissue Collection
Systematic tissue collection with predefined organ lists. Track fresh, fixed, and frozen samples with complete chain of custody.
Histopathology Processing
Tissue processing, embedding, sectioning, and staining workflows. Track blocks and slides through to examination.
Pathology Evaluation
Peer review workflows, grading systems, and finding terminology. Image association and digital slide integration.
Sponsor Reporting
Generate study reports, data tables, and regulatory submission packages. Export data in sponsor-specified formats.
GLP-Ready from Day One
CoreLIMS is designed with Good Laboratory Practice requirements built in. Complete audit trails, electronic signatures, and document control support regulatory inspections and sponsor audits.
Training and competency records, SOP management, and deviation tracking ensure your pathology operations meet the highest compliance standards.
- 21 CFR Part 11 compliant electronic signatures
- Complete audit trails with reason-for-change logging
- Training records linked to system access
- SOP document control with version management
Purpose-Built for Contract Research
Comprehensive functionality designed for CRO pathology operations.
Study Hierarchy
Organise work by sponsor, study, and protocol. Map individual cases and samples to study timepoints and treatment groups.
Tissue Lifecycle Tracking
Complete traceability from collection through processing, examination, and archive. Track blocks, slides, and retained tissues.
Image Association
Link photomicrographs and digital slides to findings. Manage image libraries for reports and regulatory submissions.
Sponsor Portals
Secure client access for study monitoring, report review, and data downloads. Customisable visibility controls.
Data Exports
Export study data in multiple formats including SEND, Excel, and custom templates. Support regulatory submissions.
Peer Review Workflows
Structured pathology peer review with finding comparison, consensus workflows, and audit trail documentation.
Training & Competency
Maintain training records, track competency assessments, and link qualifications to system access permissions.
Document Control
Manage SOPs, study protocols, and work instructions with version control, approval workflows, and archiving.
Deviation Management
Log and track protocol deviations, corrective actions, and their impact on study integrity.
The CRO Advantage
Purpose-built for contract research with commercial buyers in mind.
Global Reach
Multi-language support, timezone handling, and international regulatory standards for global CRO operations.
Commercial Focus
Designed for commercial buyers with straightforward procurement, transparent pricing, and rapid deployment.
Less Friction
Faster implementation than healthcare systems. No complex NHS procurement or lengthy approval processes.
Trusted by Research Organisations
Ready to Streamline Your CRO Operations?
Book a demonstration and see how CoreLIMS can support your preclinical and translational research workflows.