Next Generation Registries
Dynamic real-world data driven registries providing a platform for researchers to reach directly to patients and address critical data gaps.
Bespoke Data and Samples
Participants can be rapidly recontacted to augment registry data with bespoke questionnaires and samples to answer key research questions and build specific clinical evidence pre and post launch
Granular Insights
Next Generation Registries offer researchers access to comprehensive datasets including health records, patient reported outcomes and DNA samples from consented participants
Clinical Trial Support
Next Generation Registry data helps to inform study site, sample size and endpoint criteria selection leading to faster, more efficient trials
We’re currently running two registries:
Parkinson’s Disease
Rapid insights & outcomes from a highly qualified cohort of PD patients
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Book a complimentary demonstration
For a clear picture of how uMed could work for you, book a free session with our team.