The technology at the heart of a global research network

Life Sciences

Real-time access to patients and data across the uMed network.

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Healthcare Providers

Deliver multiple research programmes without additional burden.

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Patients

Access to cutting edge research relevant to you.

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Life Sciences

By linking health record data to centrally managed patient engagement, uMed removes unnecessary manual process at the clinical site.

This foundational infrastructure enables rapid and highly cost efficient evidence creation across an international site network.

Find Patients

Rapid case finding & e-consent

Capture Data

Seamlessly integrate electronic medical record and patient generated data to 3rd party EDC tools

Manage Studies

Monitor patients and sites in real-time with the ability to connect to your CTMS

Healthcare Providers

uMed finds relevant research opportunities and then helps deliver these on behalf of providers in our network.

We do this by using electronic health record data to match patients to relevant opportunities, then with the approval of the site, uMed manages the communication of those patients for that study. This creates revenue-generating research capacity, without additional overhead or burden for the institution.

Uplift research capability

With uMed, healthcare providers can support multiple research studies without placing additional burden on frontline clinical staff. This ensures greater opportunity for patients whilst driving additional income for your organisation.

Retain full control

Providers in our network retain full control of their data and patients involvement in research programmes at all times. Practices are also free to engage in research outside of uMed.

Power internal research

Use the uMed platform to support internal research and quality improvement programs with no fee to your institution.

Patients

Get access to cutting edge clinical trials and enhanced support from your healthcare provider.

Making you aware of all the information and research that might be relevant to you can be a challenge for busy clinicians. uMed helps your healthcare provider to proactively communicate information about your care as well as research opportunities.

Bespoke research opportunities delivered to you

We make it easy for your healthcare provider to proactively send you opportunities to be part of medical research that is relevant to you.

Helping your healthcare provider to bring you better care

uMed makes it easier for your healthcare provider to send you tailored information, questionnaires and reminders, so they can deliver better care in a way that is convenient for you.

Greater transparency and control over your healthcare information

uMed will proactively inform you if an external organisation wishes to use your medical records. You can then choose if you want your information to be used in this way, and also opt into updates so you can see how your contribution has helped in the fight against disease.

How does it work?



							
								
							
							
								Step one, build a cohort
								Research organisations build a target patient cohort through our international database, derived from anonymised information contained in their electronic health records.



							
								
							
							
								Step two, create a research collaboration request?
								The research organisation creates a research collaboration request which is sent to the healthcare provider. This covers all the relevant information associated with this particular research study.  The healthcare provider is alerted to a pending collaboration request and, once approved, the patients will be engaged to participate in that study.



							
								
							
							
								Step three, patient engagement
								The specified patients will receive a text message, letter, or telephone call containing a request to take part in the research study from their recognised provider, facilitated by uMed. The accepted patients can be monitored & coordinated remotely without burden to the study site.



							
								
							
							
								Step four, study monitoring
								Both the research organisation and healthcare provider will have a full oversight over each study and the associated patient engagement and can continue to monitor through the study.