myMedidata

myMedidata is a single patient portal developed by Medidata, built with patients and for patients. It consolidates all clinical trial activities — including eCOA, eConsent, sensors, and payments — into one connected experience, reducing friction for participants and simplifying coordination for sites and sponsors throughout the entire study lifecycle.

Designed to support both traditional and decentralized or hybrid trial models, myMedidata ensures that participation stays consistent as trials evolve. By eliminating the need for multiple apps, logins, and unnecessary steps, the platform helps improve patient engagement and supports retention across the study.

Core Capabilities

• Unified patient experience: One account and one destination for all clinical trial activities, removing the complexity of managing multiple platforms or credentials.
• eCOA: Patients can complete electronic clinical outcome assessments directly within the portal, on-site or remotely.
• eConsent: Patients can review and complete the informed consent process through the portal, streamlining a critical step in trial participation.
• Patient payments: Reimbursements and payments are managed within the same unified experience, reducing administrative burden for patients and sites.
• myMedidata Live: Telehealth and virtual visit capabilities are integrated, enabling remote site interactions and reducing travel burden for participants.
• Sensor integration: Connected sensor data is captured and managed within the platform alongside other trial activities.
• myMedidata Registries: Extends patient engagement beyond a single trial, enabling sponsors to educate and engage prospective participants before a trial begins and maintain contact with patients post-trial for future study opportunities.

Patient-Centric Design Principles

• Patient-centric by design: The portal is built around the needs and experience of trial participants, making engagement intuitive and accessible.
• Device agnostic: myMedidata is accessible via web browser as well as native iOS and Android applications, supporting both Bring Your Own Device (BYOD) models and provisioned devices.
• Trials without boundaries: The platform supports decentralized and hybrid trial participation, allowing patients to complete trial tasks from home or on-site.

Benefits for Sites, Sponsors, and CROs

• All data captured through myMedidata flows directly into Rave EDC, providing real-time visibility for study teams and supporting compliance monitoring.
• A unified source of patient data helps study teams maintain oversight across all patient-facing activities in one place.
• Simplified coordination for sites reduces administrative overhead and supports consistent patient engagement throughout the trial.
• Pre-qualified participant pools can be built ahead of trial start through myMedidata Registries, improving recruitment efficiency for sponsors.

Training and Support

• Medidata provides a range of training options for clients and partners, including self-paced and instructor-led courses available through the Medidata Global Education and Training section.

myMedidata integrates with the broader Medidata platform, connecting the patient experience with data and study management capabilities. Its support for decentralized and hybrid trial models makes it well-suited for sponsors seeking to reduce patient burden, improve retention, and maintain data quality across complex, evolving study designs.