
Provantis
GLP-compliant software for managing preclinical studies, optimizing workflows, ensuring data integrity, and accelerating regulatory submissions.
Overview
Provantis is a leading GLP-compliant software designed for managing preclinical studies, supporting every phase from design to reporting. It is trusted by study directors and lab managers worldwide to streamline workflows, ensure data integrity, and expedite regulatory submissions.
The software enhances data quality, reduces workloads, and offers significant cost savings. It is a fully integrated solution that optimizes study design, minimizes errors, and ensures compliance, providing a seamless user experience. Provantis simplifies the preclinical study process by integrating workflows across phases, improving data reliability, reducing costs, and accelerating submission times.
Provantis is suitable for both GLP and non-GLP environments and is scalable to meet the needs of individual scientists, research organizations, pharmaceutical companies, and universities. Its modular design allows for full customization to accommodate complex studies.
Key benefits of Provantis include:
- Reliable End-to-End Solution: A stable, feature-rich platform supporting various study designs and types.
- Seamless Data Integration: Integrates data across study phases, minimizing data loss.
- Enhanced Data Integrity: Reduces repetitive data entry and ensures audit-ready submissions.
- Cost Savings: Cuts costs by up to 18% by reducing errors and study durations.
- Boosts Collaboration: Facilitates real-time data sharing and streamlines peer review.
- Flexible and Modular: Adapts to evolving study needs with a customizable design.
- Faster Turnaround Times: Reduces reporting times by up to 50%.
Provantis offers a comprehensive list of feature-rich modules, including:
- General Toxicology: Supports toxicologists in conducting studies across species and administration routes.
- Study Setup: Streamlines study design with a powerful protocol creation tool.
- Pathology: Manages necropsy, histopathology, and organ weight data.
- Clinical Pathology: Provides instrument interfaces and handles sample data capture.
- Reproductive Toxicology: Supports studies including ICH protocols and developmental toxicity.
- Pharmacy Formulation: Tracks test item usage comprehensively.
- Data Exchanger: Securely imports external data into Provantis.
- Report Assembly: Simplifies preparation of study documentation.
- Tables & Statistics: Generates tabulated data and supports advanced statistical analysis.
Provantis is the preferred choice for many global labs, offering unmatched usability and flexibility. It integrates seamlessly across all study phases, eliminating data silos and ensuring a full chain of custody. Users achieve target timelines, reduce reporting workloads, and realize significant cost savings, maintaining compliance with regulatory standards.
