Screening Management Software for Population-Based Programmes

RADventure provides screening management software designed to support the delivery of population-based screening programmes across multiple disease areas. The platform, known as the Unified Screening Platform (USP), is built for real-world clinical delivery and is used in pilots, research settings, and large-scale national screening programmes.

One platform across multiple screening domains

RADventure supports screening programmes across different disease areas within a single, coherent platform architecture.

Breast cancer screening

RADventure supports organised breast cancer screening programmes with platforms covering invitation, imaging workflows, reporting, and follow-up. The iBOB system supports the Dutch National Breast Cancer Screening Programme, inviting over 1.1 million women per year with approximately 80 percent attendance. RADventure has also supported the MammoXL environment for sharing mammography images and reports across major Dutch hospitals, and implemented breast screening systems in Aruba, Curaçao, and the Canary Islands, enabling paperless end-to-end workflows.

Lung cancer screening

RADventure supports population-based lung cancer screening through Nelson+, enabling risk assessment, imaging workflows, AI integration, reporting, follow-up, and programme oversight in live clinical environments. Nelson+ provides end-to-end workflow management from invitation and risk assessment through to CT imaging, reporting, and outcomes tracking, and is designed for regional and national-scale deployment.

Clinical and population-based research

RADventure supports large-scale population-based research studies and emerging screening technologies by providing secure, auditable platforms for cohort selection, invitations, randomisation, and outcome tracking. Experience includes the ROBINSCA cardiovascular risk stratification study, the PROHTECT trial offering HPV self-sampling to screening non-responders, and the Dutch Chlamydia population screening programme, which invited approximately 600,000 participants using personalised portals and digital communications.

Cervical cancer screening

RADventure has designed and operated cervical cancer screening platforms in the Netherlands since the late 1990s, supporting large-scale organised screening programmes. The CIS (Cervix Information System) has supported the Dutch National Screening Programme since 1999, administering more than six million women over time. Earlier regional systems such as CERIS (1998–2011) were migrated into CIS. RADventure systems support call–recall, results tracking, treatment follow-up, registry synchronisation, and integration for HPV-based screening and self-sampling initiatives.

Colorectal cancer screening

RADventure provides end-to-end platform support for population-based colorectal cancer screening programmes, including invitation, test logistics, laboratory coordination, results handling, follow-up, and programme monitoring. Experience includes the Corero I and II trials evaluating gFOBT, FIT, and repeat FIT screening, the iColon 3 and iColon 4 trials comparing FIT strategies and participation behaviour, and the COCOS trial assessing colonoscopy versus CT-colonography screening. RADventure supported participant management, laboratory interfaces, reporting, and audit-ready data capture across these programmes.

Prostate and emerging screening programmes

RADventure supports prostate cancer screening within its multi-domain screening platform architecture, drawing on long-standing experience in delivering large-scale, organised cancer screening programmes. The platform provides configurable workflows for participant identification, invitation, risk assessment, test coordination, results management, and follow-up, and is designed to support pilot prostate screening initiatives as well as future population-level roll-out. This approach enables prostate cancer screening to be delivered using the same governance, auditability, and clinical safety principles proven across breast, cervical, colorectal, and lung cancer screening programmes.

Development of the Unified Screening Platform

The Unified Screening Platform (USP) did not originate as a generic software product. It was developed in direct response to real operational, governance, and clinical challenges encountered in population-based screening programmes. Since the late 1990s, USP has evolved through sustained collaboration with clinicians, screening organisations, public health bodies, and research consortia.

USP has developed in parallel with national screening programmes and large-scale research initiatives, including long-term involvement in cervical and breast cancer screening, population-based studies, and multi-domain screening delivery within a single programme architecture. This practice-driven evolution explains why USP is designed for governance, scale, and clinical safety, rather than for isolated case management.

Programme-level data management

RADventure USP is designed for programme management across screening domains, rather than isolated, single-case handling, enabling oversight and decision-making at scale within a unified platform.

Real-time programme oversight

RADventure USP provides continuous visibility into screening activity and outcomes across sites, providers, and screening domains, enabling programme teams to identify operational issues early and respond in a timely manner.

Participation and equity monitoring

The unified platform enables monitoring of participation, demographic coverage, and conversion between screening stages at programme level, supporting targeted interventions to improve uptake and equity across populations.

Longitudinal reporting and audit

RADventure USP supports structured, audit-ready data capture and longitudinal tracking across screening rounds and domains, enabling consistent reporting and evidence-based decision-making at programme, regional, and national level.

International delivery and collaboration

USP is deployed across multiple countries and healthcare systems and is designed to support international screening delivery. The platform enables multilingual use, including English, Dutch, Spanish and German, with additional languages configurable to meet local programme requirements.

Each USP implementation is delivered in close collaboration with screening providers and commissioners. Deployments are aligned with local clinical pathways, governance frameworks and reporting requirements to ensure safe, effective and compliant screening delivery.

Interested in working with the Unified Screening Platform?

If you are planning, piloting or delivering a population-based screening programme, we would be happy to explore how RADventure USP can support your objectives.