myMedidata Registries
Clinical trials are typically designed around one study at a time. That approach makes it difficult to maintain longitudinal patient engagement including pre-trial recruitment and post-trial follow-up.
myMedidata Registries is a unified patient registry and portal that supports ongoing patient engagement before, during, and after a study, enabling continuity beyond a single trial.
Give Patients One Place to Learn and Engage
Patients are more likely to participate and stay involved when they have a single, trusted place to explore clinical trial opportunities and remain connected over time. Registries makes it easy to support pre- and post-trial patient engagement.
Expand Patient Reach
Accelerate Recruitment Timelines
Build Research-ready Participant Groups
Support Long-term Patient Participation
Build Patient Relationships,
Not Just Data
Patients
Research-ready Patients before Studies Begin
Registries gives patients a single place to learn about clinical research opportunities, understand what participation involves, and stay connected over time.
By improving visibility and communication, it helps empower patients to engage on their terms.
Sites
The Right Patients for the Right Studies
Registries helps sites identify and engage patients who are more likely to be a fit for a given study.
By supporting early identification and pre-screening, it reduces screening burden and enables more efficient enrollment from the start.
Sponsors
A Patient Community Built for Long‑term Partnership
Registries helps sponsors maintain ongoing connections with patients who have expressed interest in research, supporting continuity across studies and reducing the need to rebuild engagement for each new trial.
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FAQ
Does myMedidata Registries support patient engagement beyond a single study?
Yes. myMedidata Registries is designed to expand patient participation from a single trial transaction to a pre-trial and post-trial engagement approach.This allows sponsors to engage and educate patients about their studies, build a pool of pre-qualified prospective participants before their trials start, and follow up post-trial with future trial opportunities.
How does the solution help facilitate patient recruitment?
myMedidata Registries helps accelerate recruitment by building a community of patients who have already expressed interest in participating in the sponsor’s trials before the trial begins. After the trial ends, by maintaining this pool of educated and empowered patients, sponsors can quickly match them to future clinical trial opportunities, significantly reducing the effort and resources needed to find eligible participants.
Does myMedidata Registries offer support for patient pre-screening?
Yes. myMedidata Registries can offer patients simple questionnaires, for which the responses can be used to assess their eligibility. Furthermore, myMedidata Registries offers MD Prescreen, a recruitment concierge service provided in partnership with Circuit Clinical. This enhancement provides additional patient pre-screening and trial matching conducted by qualified nurses and healthcare professionals, which improves the recruitment process for patients, sites, and sponsors.
Can myMedidata Registries assist with meeting diversity goals?
Yes. As part of the Medidata Diversity Program, myMedidata Registries helps sponsors recruit, engage, and retain underrepresented patient populations. By combining community engagement capabilities with site-level demographic data, the platform empowers clinical teams to meet diversity enrollment targets and comply with regulatory guidance.
Does Medidata offer training for its clients and partners?
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.