Medable AI is an integrated suite of artificial intelligence capabilities within the Medable clinical trial platform, designed to accelerate and optimize digital and decentralized clinical research. The platform includes generative AI for rapid creation and digitization of clinical outcome assessments (eCOA), as well as Agent Studio—a no-code agent builder that enables clinical teams to configure custom AI agents for automating and streamlining complex trial workflows. Medable AI automates repetitive, time-intensive tasks, reduces study build times from days to minutes, and provides human-in-the-loop oversight for transparency and regulatory compliance. The system supports integration with enterprise tools and is built to remove operational bottlenecks, reduce costs, and accelerate the delivery of new therapies in life sciences.

## Key Features

Generative AI for eCOA Creation Automates the conversion and creation of digital clinical outcome assessments.

• Converts existing assessments into digital eCOAs in seconds
• ChatGPT-like interface for editing and scaling assessments

Agent Studio (No-Code Agent Builder) Enables rapid configuration of custom AI agents for clinical workflows.

• No coding required; clinical teams can build agents directly
• Supports protocol development, trial planning, and workflow optimization

CRA Agent (Clinical Research Associate Agent) Pre-built AI agent for clinical trial monitoring.

• Aggregates and condenses data across systems
• Automates routine monitoring and communication tasks

Human-in-the-Loop Oversight Ensures transparency and control in AI-driven processes.

• Supports regulatory compliance and auditability
• Allows for manual review and intervention

Enterprise Integration Seamless interoperability with major enterprise systems.

• Integrates with Salesforce, Microsoft, Gmail, and more
• Adheres to standard operating procedures and regulatory requirements

Real-Time Analytics and Benchmarking Provides actionable insights and performance benchmarking.

• Monitors trial progress and identifies bottlenecks
• Benchmarks against trusted industry sources

## Benefits

Accelerated Study Startup and Execution Reduces time to build and launch clinical trials.

• Study build times reduced from days to minutes
• Faster time to First Patient In (FPI)

Operational Efficiency and Cost Reduction Automates manual, repetitive tasks and streamlines workflows.

• Frees teams from legacy system bottlenecks
• Reduces operational costs and resource requirements

Enhanced Data Quality and Compliance Ensures transparency, auditability, and regulatory adherence.

• Human-in-the-loop oversight for critical processes
• Integrates standard operating procedures and compliance checks

Scalability and Flexibility Customizable AI agents adapt to diverse trial needs.

• No-code builder empowers clinical teams
• Supports a wide range of clinical development workflows