Countries and Investigator Site Selection
Select lead enrolling countries and investigator sites using AI-powered data analytics
Company profile
Company profile
Phesi is a global provider of patient-centric data science solutions for clinical development, serving pharmaceutical and life sciences companies. The company's award-winning Trial Accelerator™ platform is powered by the world's largest clinical trials database, containing real-world data from over 325 million patients across 232 countries and territories, drawn from 719,183 clinical research projects and 22 global registries. Phesi's AI-driven solutions enable sponsors to optimize protocol design, create Digital Patient Profiles and Digital Twins, select high-performing investigator sites and countries, and generate Digital Trial Arms as external controls. By connecting real-world patient data with trial execution data, Phesi helps life sciences companies eliminate costly trial failures and protocol amendments, improve patient population accuracy and diversity, reduce trial timelines and patient burden across every stage of clinical development for any indication, including rare diseases. The company's proprietary integrated methodology and AI technologies analyze over 485,000 curated clinical trials, 4.2 million physicians, and 4,000+ disease indications. Phesi's approach transforms clinical development into a data-driven science, enabling predictive modeling across four key views: Patient Profile, Trial Performance, Country, and Investigator Site. The platform generates reliable evidence for drug development and commercialization without the expense or time required in traditional trials, helping pharmaceutical companies make more informed decisions and accelerate the path from research to market.
Company description Phesi official website
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01 · Operating footprint
Company-profile context for clinical focus, customers, deployment, integration, milestones, and partnerships.
Cloud Saas deployment with recorded integration context.
Company milestones
Won 2025 Clinical Trials Arena Excellence Award for Innovation (November 2025). Took leading position on Frost and Sullivan's Frost Radar™ for AI-enabled clinical trials (February 2026). Published major analysis of 600,000+ clinical trial protocols (May 2026).
Partnerships
02 · Flagship portfolio
Selected source-backed Company products and the available commercial context.
Select lead enrolling countries and investigator sites using AI-powered data analytics
Improve diversity, equity, and inclusion in clinical trial design and patient recruitment
Model diseases and patient outcomes using digital patient profiles and real-world data
Eliminate costly trial failures and protocol amendments using modal design value simulation
Plan clinical development programs using comprehensive data analytics and AI insights
AI-powered platform for patient-centric clinical trial design and execution using real-world data
Monitor and rescue underperforming clinical trials using real-time data analytics
03 · Research intelligence
Publications, preprints, clinical validation, and regulatory records in Evidence Position order.
Publications, clinical validation, and regulatory records connected to this Company appear here.
Research
Bone marrow transplantation · Sep 1, 2024
Clinical validation
No linked records are currently available.
Regulatory
No linked records are currently available.
04 · Company-reported outcomes
Company-reported outcomes and customer stories are distinct from linked Research Intelligence evidence.
Significantly quicker and cheaper development time through adaptive trial design optimization
Eliminate costly trial failures and protocol amendments using modal design value simulation
Improve patient population accuracy and diversity
Protocol design optimization and investigator site selection for C. difficile infection trial
Protocol optimization and study feasibility for Iron Overload Integrated Development Plan, Phase 1B Trial
Protocol design, country and investigator site selection for Non-Small Cell Lung Cancer trial
Protocol design and investigator site selection for Type 2 Diabetes Mellitus (T2DM) trial
Using Phesi's systematic analysis of clinical trial, protocol, and site space to inform new clinical programs and save existing ones
Phesi described as 'on the frontiers of defining clinical development as a science' by former SVP, Global Chief Medical Officer
Adaptive trial design optimization for priority asset development
Significantly quicker and cheaper development time achieved through optimized adaptive trial design
05 · Leadership
Leadership profiles and professional links from the current Company record.
Dr. Gen Li
Founder, President and CEO
06 · Company updates
Recent articles published on Phesi's official website.
No Company updates are currently listed.
07 · HAIC coverage
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No HAIC coverage is currently linked to this Company.
08 · Official presence
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09 · Market pathway
Other active Companies in the same market, selected alphabetically from the HAIC directory.
Market context
Companies using AI to optimize clinical trial design, accelerate patient recruitment, match patients to trials, predict trial outcomes, or improve clinical research efficiency. Includes patient enrollment and screening platforms, AI-powered trial matching, and tools that reduce the time and cost of bringing new treatments to market.
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