Optimized Trial Management
for Every Stage
Tailored SaaS Solutions with Scalable Automation and Customization
Essential Plan
Automation
High-level automation with minimal SME input, ideal for early-phase or smaller studies.
Focus
Provides foundational insights and streamlined trial management with quick, data-driven decision-making.
Key Features
Turnkey solutions for basic trial design, feature contributions, predictive outcomes, and competitor analysis.
Professional Plan
Automation & Customization
Balanced automation with moderate SME engagement, suitable for mid-level complexities (e.g., multi-site coordination, safety tracking).
Focus
Deeper analytics for managing more intricate trial operations, such as regulatory compliance and personalized recruitment.
Key Features
Adds regulatory readiness, emerging therapies, enrollment optimization, and risk management.
Enterprise Plan
Customization
Highly customizable with advanced AI/ML capabilities and significant SME involvement, designed for large-scale, complex, or global trials.
Focus
End-to-end, real-time monitoring and adaptation, advanced market positioning, and fast-tracking approvals for large, multi-country trials.
Key Features
Includes real-time risk-based monitoring, regulatory landscape alerts, automated protocol writing, and market trends benchmarking.
Optimized Trial Management
for Every Stage
Discover how the platform delivers dependable search results alongside success probability predictions with an accuracy exceeding 92%.
How Your Solution Works:
Unlocking Clinical Trial Success
How TrialKey’s AI-Driven Platform Tackles Your Clinical Trial Obstacles
Low Success Rates
Trials struggle to recruit and retain qualified patients, causing delays.
AI-Driven Validation
Up to 100,000 simulations refine trial design, boost enrollment, and cut risks.
Recruitment Roadblocks
Difficulty recruiting/retaining qualified patients delays trials.
Adaptive Inclusion/Exclusion
Optimizes recruitment criteria, site performance, and dropout risk.
Site Underperformance
Many sites fail to enroll enough patients, wasting resources and affecting timelines.
Advanced Site Analytics
Identifies high-performing sites to reduce costs and speed timelines.
Regulatory Delays
Prolonged contracting and approvals extend trial timelines unnecessarily.
Regulatory Simulation
Predictive modeling streamlines approvals and aligns with agency needs.
Protocol Complexity
Complex protocols lead to frequent amendments that disrupt trial progress.
Protocol Optimization
Simulates multiple scenarios, reducing costly amendments and delays.
Data Quality & Monitoring
Manual oversight consumes significant resources and slows trial progress.
AI-Powered Data Integrity
Minimizes manual monitoring, improving data quality and efficiency.
Lack of Diversity in Patient Populations
Trials often lack demographic representation, limiting generalizability.
Global Strategy
Tailored site selection and outreach to enhance diversity and patient pool.
How We Enhance Your Clinical Trial Designs
AI-Powered Trial Design: Utilising over 30 years of real-world trial data and advanced machine learning algorithms, we simulate every aspect of your trial to ensure optimal outcomes across various therapeutic areas and trial phases.
Enhanced Protocol Development: We help design precise inclusion and exclusion criteria, primary and secondary endpoints, and study structures that maximise your trial’s potential.
Resource Allocation & Site Selection: Gain insights into the most effective site locations, ideal patient pools, and the required number of sites to achieve statistically significant results.
Competitor Analysis & Benchmarking: Understand your trial’s positioning with in-depth competitor analysis and scenario simulations, allowing you to anticipate challenges and optimise your strategy.
