The world’s first
AI‑powered
EDC specification &
configuration platform
Transform clinical trial setup from months to days with AI‑driven automation, ensuring 100% regulatory compliance across all major EDC systems.
Revolutionize your EDC Setup
Leova combines cutting-edge AI with deep clinical research expertise to deliver the most advanced EDC specification & configuration platform in the industry.
AI-Powered Specification Generation
Transform protocol documents into precise EDC specifications using advancedAI that understands clinical research requirements.
Intelligent Configuration Engine
Automatically configure your EDC system based on specifications with smart validation and compliance checks built-in.
Automated User Acceptance Testing
Run comprehensive UAT scenarios automatically to ensure your EDC system meets all study requirements before go-live.
Collaborative Workflow Management
Streamline team collaboration with role-based access, real-time updates, and integrated communication tools.
Real-Time Analytics & Reporting
Generate operational reports and submission-ready Biostats TLFs with real-time data insights and compliance tracking.
Regulatory Compliance Assurance
Maintain 100% regulatory compliance with built-in validation rules, audit trails, and FDA/EMA guideline adherence.
Rapid Deployment & Setup
Reduce EDC setup time by 90% with automated processes that typically take weeks, not months to complete.
Specification-Database Synchronization
Keep your database perfectly aligned with approved specifications through automated synchronization and change management.
Accelerated Study Timelines
Fast-track your clinical trials with streamlined processes that maintain quality while dramatically reducing setup time.
Streamline Your Clinical Trial Configuration
Leova simplifies and accelerates study setup by providing a complete, specification-driven platform for building, validating, and maintaining your clinical study database. From generating precise specifications to configuring your study space, running UAT, producing operational reports, and delivering submission-ready Biostats TLFs — Leova keeps your database fully in-sync with approved specifications. Leova ensures your studies stay compliant, adaptable, and always audit-ready.
Transparent Pricing for Study Setup, Testing and Reporting
Plan, configure and launch with complete control, with pricing tailored to your study phase and needs
Save up to 30% with multi-study purchases. Early adopters enjoy 30% off first-year purchases automatically
Select your study phase
Spec Starter
- Specification Generator
- Basic Support
- Standard Templates
Build Bundle
- Specification Generator
- Configurer
- Enhanced Support
- Custom Templates
Study-Ready Suite
- Spec Generator
- Configurer
- UAT
- Priority Support
- Advanced Analytics
Volume Discount Matrix
Discounts applied automatically when purchasing multiple study spaces upfront
Frequently Asked Questions
Get answers to common questions about our pricing and packages
About Us
Learn more about our mission, vision, and the values that drive us.
Our Mission
To revolutionize clinical trial management by providing an intelligent, automated platform that eliminates complexity, reduces timelines, and ensures regulatory compliance while empowering researchers to focus on what matters most - advancing medical science.
Our Vision
A world where clinical trials are accessible, efficient, and patient-centered, where breakthrough treatments reach those who need them faster, and where the burden of administrative complexity never stands in the way of medical innovation.