Pre Clinical Research Modules

We offer smart, streamlined tools to manage toxicology, pharmacokinetics, and safety studies—all before clinical trials begin. Accelerate discovery with organized data, compliance-ready reports, and seamless lab integration.

Study Management

Central hub for designing, planning, and tracking preclinical animal or analytical studies. It manages protocols, study timelines, dosing schedules, and regulatory compliance, ensuring each study aligns with predefined configurations.

Projects & Milestones

Enables oversight of multiple concurrent studies by organizing them into projects with defined milestones. Tracks progress, resource allocation, and timelines to ensure studies meet key deliverables and review checkpoints.

Laboratory & Analysis

Handles sample processing, test execution, and data collection for biological, chemical, or pathological analyses. Integrates with lab instruments and ensures traceability and standardization of data for GLP compliance.

Vivarium Management

Manages animal housing, breeding, health records, cage assignments, and environmental monitoring. Supports IAEC/IACUC compliance and ensures ethical treatment and traceability of all animals used in studies.

Facility Management

Oversees operational infrastructure such as equipment calibration, sanitation schedules, access control, and facility zoning to maintain a compliant and safe research environment.

Reports & Dashboards

Provides real-time insights into study performance, animal welfare metrics, lab results, and operational KPIs through customizable dashboards and regulatory-ready reports.

Efficient Data Storage

Centralized Animal Study Data

All data related to animal studies, such as dosing records, observations, and test results, are stored in a single, centralized system. This eliminates data silos, making it easier for research teams to access and analyze information quickly.

Stores dosing records, observations, and test results centrally.
Eliminates data silos for easier data access and quick analysis.
Seamlessly integrates toxicology reports, ensuring no data is lost.
Makes toxicology reports searchable for efficient data retrieval.
Improves data management for better research outcomes.

Regulatory Compliance

GLP Standards Adherence

The module is fully compliant with Good Laboratory Practices (GLP), which are essential for pre-clinical studies to ensure the integrity and reliability of data submitted to regulatory agencies like the FDA.

Ensures full compliance with Good Laboratory Practices (GLP).
Maintains data integrity for regulatory submissions.
Includes audit trails for tracking data changes.
Supports electronic signatures for secure authentication.
Provides detailed documentation to meet regulatory guidelines.

Seamless System Integration

LIMS Integration for Efficiency

The module integrates with existing Laboratory Information Management Systems (LIMS), enabling real-time data sharing between the pre-clinical ERP and laboratory operations for improved workflow efficiency.

Enables real-time data sharing with Laboratory Information Management Systems (LIMS).
Improves workflow efficiency through process automation.
Automates sample tracking, result logging, and reporting.
Reduces manual data entry, minimizing human errors.
Enhances data accuracy for reliable laboratory operations.

Features

Project Management:

Involves organizing and executing research projects, including creating, documenting, assigning teams, managing study plans, executing experiments, and preparing reports.