Medable provides a digital platform for decentralized clinical trials that utilizes patient-generated data to enhance participant recruitment and streamline data collection. By integrating tools for remote scheduling, consent management, and real-time reporting, the platform improves the efficiency and quality of clinical research across over 60 countries.
Funding
$304M raised to dateRaised to date based on public sources. This may differ from the amount the company actually raised and is based only on what is publicly available on the internet.
+2Founders
Product
Problem
Traditional clinical trials often suffer from limited participant reach, cumbersome data collection processes, and difficulties in maintaining participant engagement, leading to delays and increased costs. The reliance on clinic-based visits and manual data entry creates barriers to participation and hinders the collection of real-world data.
Solution
Medable offers a unified platform designed to streamline decentralized clinical trials (DCTs) by enhancing participant recruitment, simplifying data collection, and improving overall trial efficiency. The platform integrates tools for remote scheduling, electronic consent management (eConsent), telehealth visits, and real-time data reporting, enabling researchers to reach a broader patient population and gather high-quality evidence. By leveraging patient-generated data and facilitating remote interactions, Medable reduces the burden on participants and sites, while providing sponsors with greater control and visibility over trial progress. The platform's modular design and extensive integration capabilities allow for flexible deployment and seamless integration with existing clinical systems.
Target Audience
Medable's primary customers are pharmaceutical companies, biotech firms, and clinical research organizations (CROs) seeking to improve the efficiency, reach, and data quality of their clinical trials.
Features
- Remote scheduling and TeleVisit capabilities for convenient participant engagement
- Electronic consent management (eConsent) with compliant wet and dry signature options
- Remote data collection via mobile apps and connected devices
- Real-time data reporting and visualization dashboards for study oversight
- Integrated study notifications and participant reminders to improve adherence
- Support for over 120 languages to facilitate global trials
- Cloud-agnostic, single API platform for maximum reach and scalability
- Library of system integrations for seamless connectivity with existing clinical systems