Enabling patients to virtually participate in the industry’s most comprehensive patient-centric solution
The industry has begun to incorporate virtualizing technologies in trial design, often consisting of multiple point solutions.
myMedidata is a single-destination patient portal built on the industry’s leading Rave EDC, in use at more clinical research sites globally than any other system. With myMedidata, patients can use any online device to virtually learn, enroll and participate in clinical trial activities. This offers a streamlined and trusted approach to virtualizing clinical trials.
myMedidata encompasses all of the capabilities of Medidata’s patient-facing solutions for electronic consent and clinical outcomes assessment (eCOA) along with live video investigator/patient visits using myMedidata LIVE, all through one web-based intuitive interface.
Create a better patient experience and transform trials with myMedidata
See how myMedidata brings patient-facing solutions into one unified platform, giving sites the ability to streamline operations and maintain a consistent and traceable process, built using input from Medidata’s Patient Insights team of patient advocates.
Innovative, trusted, efficient, and scalable: our patient-centered solution is built to address the dilemma of accruing and retaining patients while navigating trial virtualization
To enroll in a new study virtually, patients are invited to create their myMedidata account, then are guided through an electronic consenting process, also 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.
Throughout the trial life cycle, patients access their myMedidata accounts to virtually complete any necessary electronic clinical outcome assessment. Study teams configure all patient data forms needed and the patient logs into myMedidata to complete the web-based forms.
During the COVID-19 pandemic, many clinical trials were paused in part due to the patient’s inability to travel to the trial site for scheduled clinic visits. myMedidata LIVE is a web-based, live video conferencing capability connecting patients with their clinical trial study staff, virtually. A myMedidata LIVE video visit between patients and sites can replace a scheduled site-based appointment and allow the study team to complete their data entry in Rave while the patient remains engaged offsite through myMedidata.
COVID-19 Symptom Tracker
COVID-19 Symptom Tracker
The COVID-19 Symptom Tracker is for sponsors and partners who want to track the impact of the disease on their studies as well as provide a database for researchers to analyze and possibly predict the course of the disease. Patients benefit by contributing to ongoing research about the impact of COVID-19.
Struggling with patient enrollment
and retention? Unsure how to enable virtualization in your clinical trials?
See how myMedidata can improve patient engagement and retention, accelerate clinical trial timelines, and mitigate risks with study virtualization.
Put patients at the forefront of your studies
Single clinical trial dashboard for life
Increase trial engagement before, during and after studies. myMedidata is accessible through any smart device and desktops/laptops which enables remote visits and encourages real-time data collection. myMedidata also eliminates the need for extra apps, logins and unnecessary provisioned devices.
Enables continuous clinical data capture
Put sites and patients on the same data platform and eliminate integrations. By reducing the need for provisioned devices and multiple vendors you can streamline operations significantly while decreasing study start up complexity.
Standardize on technology
Simplify clinical research obligations by putting patients on the same technology as the site staff. Remote visits and virtual patient engagement increases protocol adherence and compliance.