Medable Studio is a no-code, AI-powered platform designed for sponsors and clinical research organizations (CROs) to build, deploy, and manage custom or pre-built agents that automate and optimize clinical trial workflows. The platform integrates generative AI to automate repetitive, time-intensive tasks such as digital outcome assessment creation, reducing study build times from days to minutes. Medable Studio supports seamless integration with over 13 clinical and enterprise systems, maintains human-in-the-loop oversight for transparency and regulatory compliance, and aligns with industry standards (GxP, ICH, HIPAA, GDPR, CDISC). The platform is purpose-built to eliminate operational bottlenecks, accelerate study startup, and enable rapid, scalable digital and decentralized clinical trials.

Key Features

No-Code Agent Builder Enables rapid creation and deployment of custom or pre-built AI agents for clinical workflows.

• No programming required; clinical teams configure agents directly
• Supports both bespoke and ready-to-go agent builds

Generative AI Integration Automates creation and digitization of clinical outcome assessments (eCOA).

• Converts existing assessments into digital eCOAs in seconds
• Integrated prompt interface for easy editing and scaling

System Integration Connects with 13+ clinical and enterprise platforms for unified data flow.

• Integrates with eCOA, Veeva EDC, IRT, CTMS, Salesforce, Microsoft, Gmail
• Eliminates manual data stitching and silos

Regulatory Compliance Built to meet life sciences standards and regulatory requirements.

• Supports GxP, ICH, HIPAA, GDPR, CDISC
• Incorporates SOPs, validation, and benchmarking

Human-in-the-Loop Oversight Allows teams to set automation guardrails and maintain control.

• Aligns agent actions with team workflows
• Ensures transparency and safety in critical processes

Multi-Study Participant App Enables patients to participate in multiple studies via a single app.

• Reduces app development and deployment time
• Available on major app stores

24/7 Support Provides continuous support for users and study teams.

• Ensures operational continuity and rapid issue resolution

Benefits

Accelerated Study Startup Reduces time to first patient in (FPI) and overall study timelines.

• Automates manual, repetitive tasks
• Enables rapid digital trial setup

Operational Efficiency Streamlines workflows and reduces administrative burden.

• Frees teams to focus on high-value activities
• Minimizes unproductive "white space" between trial phases

Enhanced Compliance and Transparency Ensures regulatory adherence and oversight.

• Human-in-the-loop controls for critical safety and compliance
• Transparent, auditable processes

Scalability and Flexibility Adapts to diverse trial requirements and organizational workflows.

• Supports both ready-to-go and custom agent builds
• Scales across sponsors, CROs, and global studies