Clinical Trials
Fast-Track Clinical Trials: Streamline Contracts, Secure Compliance with AI
Challenge: Clinical trials are the engine of medical progress, but complex contracts slow you down. Manual processes lead to delays, regulatory compliance is a constant worry, and data-driven decision making is limited.
Solution: AI-powered Contract Lifecycle Management (CLM) empowers your research teams to
- Accelerate Approvals: Automate protocol review to expedite trial initiation. AI extracts key details, routes documents for faster approvals, and gets your research started sooner.
- Ensure Compliance: Maintain regulatory peace of mind. AI scans contracts for deviations from GCP, FDA regulations, and ethical standards, enabling proactive action to avoid costly delays.
- Optimize Site Selection: Make smarter decisions. AI analyzes historical data to identify factors that contribute to successful trials, helping you select high-performing sites and optimize contracts.
- Drive Strategic Research: Gain valuable insights from contract data. AI identifies trends, risks, and opportunities across your portfolio, allowing you to prioritize research initiatives and maximize impact.
Real-World Examples of AI in Action
Automated Protocol Review
Extract key information from protocols, like eligibility criteria and procedures, and route them for faster review and approval.
Real-Time Compliance Monitoring
AI scans contracts to identify potential compliance issues, such as missing informed consent language, enabling proactive measures to ensure regulatory adherence.
Predictive Analytics for Site Identification
Identify factors that contribute to successful trials, such as patient enrollment rates and protocol compliance, to make data-driven site selection decisions.
Contract Intelligence for Portfolio Management
Uncover trends in trial performance and costs to identify underperforming trials, highlight cost-saving opportunities, and strategically allocate resources for greater research impact.