myMedidata

Built for patients, by patients, myMedidata is a single destination patient portal, allowing patients to use any online device to virtually learn, enroll and engage in clinical trials. 

Only myMedidata enables the full range of tools to build scalable, flexible solutions at every level of decentralized and hybrid clinical trials and our expert teams help you tackle problems creatively to find the most effective level of decentralization.

myMedidata App

With this powerful native app, patients now have an additional option to easily access their myMedidata patient portal through any mobile device – integrating clinical trial activities seamlessly into daily life. 

The myMedidata App is built using Medidata Designer, our new platform configuration tool that builds rich patient experiences through easy to use screen templates, drastically reducing study start-up time.

myMedidata app is available on iOS and Android, and can be used both on the patients’ own devices (BYOD) or via a provisioned device.

Put Patients at the Forefront of Your Studies

Single Clinical Trial Dashboard for Life

Eliminate the need for extra apps, logins, and unnecessary provisioned devices by giving your patients one location for all of their clinical trial activities. myMedidata makes it simple and engaging for patients to participate in any clinical trial so your trials are easier, faster, and produce better results.

Enables Continuous Clinical Data Capture

Empower patients with choice in how they participate in research, so you can efficiently recruit the widest, most inclusive pool of participants, keep them engaged throughout your trial, and produce better study results. Only Medidata allows clinical trials to be more efficient with sites and patients on the same data platform, eliminating integrations and reducing burdens for patients and site staff.

Standardize on Technology

myMedidata is unified with the Medidata Platform – used by the majority of clinical trials worldwide – eliminating the need for multiple workflows, expediting timelines, mitigating risks, and reducing burdens. Only Medidata offers a scalable, end-to-end platform with easy configuration and multiple delivery models based on your specific trial needs.

Key Features of myMedidata

eConsent

Clearer Consenting Process

To virtually enroll in a new study, patients access their myMedidata account and are then guided through an electronic consenting process known as eConsent. Through myMedidata eConsent, patients watch the study’s eConsent video and review all relevant consent documents. Upon confirming full understanding of the consent, the patient virtually signs their web-based eConsent. myMedidata eConsent can be paired with myMedidata LIVE Video Visits to allow for additional communications and touchpoints between study site staff and patients.

Related Solutions

Learn More

The Value of Decentralized Clinical Trials

The world of clinical research has seen a pronounced shift in how clinical trials are conducted. Hear from Anthony Costello, CEO of Medidata, as he discusses with Harvard Business Review what DCTs mean for patients, doctors, and pharmaceutical companies.

Decentralized Clinical Trials: The Future of Clinical Research is Here

Download this white paper to read about the changing landscape around decentralized clinical trials, the types of solutions used to run DCTs, and how they benefit Patients, Sponsors, and Sites.

Site Perspectives on DCTs

In collaboration with SCRS, Medidata surveyed sites on their use of DCT solutions and technologies over the last two years. Read this whitepaper to see the results of that survey.

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