Drug Development Accelerated: AI That Designs Trials, Recruits Patients, and Ensures Compliance
Pharmaceutical Research Organization
We built a comprehensive clinical trial platform with AI-powered patient matching, automated regulatory compliance, real-time safety monitoring, and predictive analytics for trial success.
At a Glance
Key results and metrics from this project.
The Challenge
Drug development timelines are measured in years, with patient recruitment often being the biggest bottleneck. Regulatory compliance requires meticulous documentation, and trial data must be analyzed rapidly to identify safety signals.
The Solution
What we built to solve the challenge.
- Investigator portal with patient enrollment and visit tracking
- Sponsor dashboard with trial-wide analytics and site performance
- Patient portal for consent, diary entries, and appointment scheduling
- Regulatory affairs interface with submission tracking and document management
- Electronic data capture with real-time validation and query management
- Randomization and supply management ensuring treatment allocation
- Safety database with automated adverse event reporting
- Regulatory document management with version control and audit trails
- Patient matching analyzing EHR data to find eligible candidates
- Protocol optimization suggesting design improvements from historical data
- Safety signal detection identifying potential adverse event patterns
- Site performance prediction helping select optimal trial locations
Key Capabilities
Technology Stack
The Business Impact
Measurable results and transformation.
40% faster patient recruitment accelerating time to market. 35% reduction in trial costs through automation and efficiency. 95% regulatory compliance achievement eliminating audit findings.
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