The technology at the heart of a global research network

What We Do

uMed is a technology platform embedded within a global network of healthcare providers that automates the process of building high quality prospective research registries

Why it is Unique

While others rely on aggregated data which blocks subject re-engagement, uMed can rapidly reach back to contact patients for clinical studies, engage in data collection from home, and to collect biomarker and genomics samples.

Life Sciences

Regulatory quality registries where patients can be compliantly re-engaged to support programmes from drug discovery to post-market.

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Healthcare Providers

Zero fee platform for providers to participate in many more studies without increasing overhead or burden on staff.

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Patients

Easy access to cutting edge research relevant to you and your health.

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Life Sciences

Build research-grade registry datasets, where patients within those datasets can be re-engaged with full regulatory compliance.

These can be used to support post-market regulatory submissions, payer negotiations and the creation of datasets enhanced with genomic & biomarker samples.

Protocol Driven Post Marketing Studies

Rapid creation of registries that combine health record data with patient reported outcomes based on a GCP compliant protocols

Collate Genomic & Biomarker Data

Re-target patients to enhance registry data with genomic and biomarker samples

Clinical Trial Recruitment

Rapidly Identify and remotely screen patients from across our site network

Healthcare Providers

uMed is secure, compliant and zero fee platform that uses EHR data to automate the clinical study process so providers can attract and deliver dozens more studies than is currently possible.

This creates additional revenue and research capacity for sites without increasing overhead or burden on staff.

Enhance Research Capacity

Support multiple research studies without placing additional burden on frontline clinical staff. This ensures greater opportunity for patients while driving additional income for your organisation.

Retain 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 an access 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, 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.