Decentralized Clinical Trials

Decentralized trials promise flexibility and speed—but delivering it without compromising safety, data quality, or site workflows is a real challenge.

Medidata’s integrated Decentralized Clinical Trials (DCT) program helps teams run hybrid and fully remote trials that work for patients, sites, and sponsors alike—using Medidata Consent, eCOA, and Sensors solutions designed for real-world execution.

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Run Your DCT
from
One Platform

Decentralized trials place new demands on patients and sites. From unfamiliar technology to coordinating drug delivery and lab collection, teams must still maintain compliance and data quality.

You need a solution that supports it all, simply and in one place.

Suite of Patient Engagement Solutions
Continuous Clinical Data Monitoring
Direct-to-patient (DtP) Investigational Product Delivery
Circuit Clinical Partnership for Turnkey Solution
Flexible, Custom Design
with Medidata’s Trial Dial™

Built to Ease Complexity for Everyone

Sponsors

For Sponsors:

Control and Confidence

Centralized oversight helps sponsors maintain compliance, data integrity, and patient safety—while scaling decentralized, hybrid, or fully remote trials with confidence.

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Resources


Explore deeper guidance and related materials.

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FAQ

Yes. The program is designed to be scalable and flexible, allowing you to virtualize as much or as little of a clinical trial as needed. It supports a hybrid approach through unified technologies like Medidata eConsent, eCOA, and Sensors solutions, ensuring high-quality data collection regardless of geography or trial complexity.

Yes. Through a partnership with Circuit Clinical, Medidata provides a turnkey solution that includes a national network of decentralized sites. These sites are already trained and certified on Medidata technology, which enhances patient access and inclusion while ensuring standardization across the study.

Medidata RTSM features robust DtP capabilities that offer high flexibility for decentralized and hybrid trials. It allows shipments to be triggered at the site, visit, or patient level, and enables patients to confirm incoming shipments directly through their myMedidata account.

Medidata addresses data quality challenges in DCTs through centralized, remote, and risk-based monitoring (RBQM) capabilities built on a unified platform. This allows study teams to shift from 100% on-site monitoring to remote oversight activities without sacrificing timelines or data integrity.

Yes. Medidata offers a variety of training options for our clients and partners, including both self-paced and instructor-led courses. To learn more about available courses and to access our resources, please visit the Medidata Global Education and Training section.