Address evidence gaps in days, not years
Using uMed’s cutting edge ACCESS Research Platform and master protocol embedded in a global network of healthcare institutions, uMed’s Cohort Studies allow researchers to build custom datasets that combine the power of electronic health records with clinical and patient generated data.
Gather Insights
Rapid access to appropriate patients allows short and long-term insight generation
R&D
Burden of disease
Patient profiling
Identification of unmet needs
Trial design support
Commercial
Market research
Patient preference
Unmet need
Pre-launch planning
Post-launch insights
Run a Study
Master protocol underpinned by uMed’s ACCESS Research Platform provides answers to multiple clinical questions through decentralized sub-studies.
Collect endpoints that aren't routinely collected in the health record or easy to find via secondary data sources
Access deeply characterized consented patient cohorts that exactly match your research requirements
Reach patients who are not normally included in research that better represent the total population
Answer new research questions at speed, without the cost and resource of setting up from scratch
Build new credible clinical evidence from IRB approved protocol programmes that will influence clinical practice & regulatory decisions
Access exclusive data with real-time integrated clinical outcomes that combine EMR, physician reported outcomes, and patient generated data
Hear directly from the patient’s perspective
“It's been 5 years since my diagnosis but this is my first time taking part in Parkinson's research because of my poor mobility. Being able to take part despite having no internet is a big positive and your nurses make this possible.”
AccessPD participant
