- uMed identifies potential participants via health record data
- uMed has automated the process of patient outreach (after provider approval) through mobile messaging that comes from the patient’s recognized provider
- Additional automated pre-screening and consent improves enrollment rates dramatically, with a consistent conversion rate greater than 10%
The age of analog clinical studies is over. This is uMed.
We’ve pioneered the automation of the most time-consuming aspects of research: patient identification, enrollment and engagement.
- uMed supports interventional, observational and decentralised studies
- From initial outreach through consent and ongoing patient engagement, once you’ve approved your list of potential patients, uMed does the rest
- The uMed mobile engagement platform is free to use for your other sponsored or in-house studies
- uMed brings you a stream of sponsored studies pre-qualified for your patient population
- With a focus on non-interventional studies, uMed engagements are revenue-positive from day one
- Our sponsored studies and uMed international registries are ideal for every size provider, from community hospitals to large health systems and academic medical centers
We understand that GPs want to be more involved in clinical research but are already overstretched caring for patients.
uMed takes on the workload of engaging eligible patients for clinical studies, so that you can participate in more revenue-generating research without adding workload for your staff.
uMed processes data on behalf of your practice to support clinical studies. We will never utilise or share patient data without explicit permission from your practice.
Access more research opportunities for your practice.
uMed brings sponsored, revenue-generating studies to your health system from top-ten life
science and other research organizations.
uMed automates the traditionally manual processes of patient identification, outreach, and
consent, allowing your team to engage in far more studies than previously thought possible.
Once your team approves the study, uMed does the rest. Our automatic mobile platform handles the workload from patient outreach and consent through enrollment and collecting patient reported data.
uMed is the ideal solution for community hospitals with limited resources looking to expand your research footprint.
uMed brings you sponsored studies and international registries that match your patient population, and our intuitive user interface allows you to review and approve study documentation and relevant patient information quickly.
Once your team approves the study, uMed does the rest. Our automatic mobile platform handles the workload from patient outreach and consent through enrollment and collecting patient reported data. No clinic visits required.
Whether you’re an experienced Principal Investigator engaged in multiple clinical trials or a junior researcher looking for opportunities to build your experience, uMed’s sponsored studies and registries are an ideal addition to your portfolio.
We focus on remote, non-interventional studies which require minimal oversight from investigators. Once patients are approved for outreach, uMed handles the rest.
In addition to joining sponsored studies from our life science partners, uMed offers you the opportunity to participate in our international registries. We are currently looking for US-based PIs to support our COVID PASC and Parkinson’s Disease registries.
Find out more
For a clear picture of how uMed could work for you, book a free session with our team.