uromonitor

Progen Diagnostics · Technology Partner Solution
Cancer diagnostics

Uromonitor

A non-invasive, urine-based molecular test used in bladder cancer diagnosis and surveillance.

UK pathway
Live in the UK
01
Clinical need Understand where the technology fits in the bladder cancer pathway.
02
Pathway design Position Uromonitor alongside existing diagnostic and monitoring pathways.
03
Evidence & economics Build the clinical, operational and health-economic case for appropriate use.
04
UK adoption support Support evaluation, pilots, implementation and market development.

Bladder cancer surveillance can place a significant burden on patients and services.

Bladder cancer surveillance today typically relies on repeated cystoscopy — an invasive and resource-intensive procedure for patients and healthcare services.

Uromonitor is positioned around a different approach: a non-invasive, urine-based molecular test intended for use in bladder cancer diagnosis and surveillance.

The opportunity

Position molecular testing alongside existing diagnostic and monitoring pathways within bladder cancer services.

02 · The technology

A urine-based molecular approach to bladder cancer monitoring.

Uromonitor is a non-invasive molecular test based on a urine sample and intended for use within bladder cancer diagnosis and surveillance. Clinical performance, regulatory statements and adoption claims should remain based on approved evidence and current documentation.

01 Non-invasive sample
02 Molecular testing
03 Bladder cancer diagnostics
04 Surveillance pathway

Designed around the pathway, not simply the technology.

Uromonitor is positioned alongside existing diagnostic and monitoring pathways within bladder cancer services. The purpose of the UK proposition is not simply to introduce a test, but to understand where the technology fits, what clinical problem it addresses and what would be required for appropriate adoption.
01 Clinical pathway fit
02 Laboratory workflow
03 Patient pathway
04 Health economics
05 Implementation
04 · How the relationship works

Progen brings the technology. Lifecycle brings NHS market knowledge.

Progen Diagnostics

UK & Ireland route

Progen Diagnostics is the vehicle through which Uromonitor is brought to and developed in the UK and Ireland.

Uromonitor
From diagnostic technology to a practical UK proposition.
Lifecycle

Adoption support

Lifecycle holds a 50% share in Progen Diagnostics and contributes NHS market knowledge, pathway design, health-economic modelling, pilot development and adoption support.

Evidence first. Adoption second.

01

Evidence base

Clinical performance claims should be supported by approved evidence. The UK proposition is built around evidence relevant to the intended clinical use and pathway.

02

Clinical, economic & operational case

Lifecycle can assess the implications for patient pathways, service capacity, workforce, operational delivery and health economics when developing the UK case.

03

Regulatory & availability

Regulatory and availability statements should reflect current, approved documentation and should not be inferred from broader market activity or adoption.

06 · Pathway to UK adoption

More than distribution. A route into UK healthcare.

01 Identify the clinical need
02 Evaluate pathway fit
03 Build the evidence case
04 Develop evaluation or pilots
05 Support implementation
06 Support adoption & scale
Uromonitor · Progen Diagnostics

Want to discuss Uromonitor and its role in UK bladder cancer pathways?

Speak to the team about Uromonitor, the UK proposition and how Progen Diagnostics and Lifecycle support the route from technology to healthcare adoption.