Experts in design and development of digital products. Mobile and Web Applications.

A national medical association focused on hemostasis and thrombosis gathers hematologists, phlebologists, and lymphologists to advance research, diagnosis, and prevention of clot-related disorders. One of its strategic goals was to create a standardized data-collection system that would generate local evidence and inform more effective health policies.

Venous thromboembolism (VTE) is a leading cause of in-hospital complications, yet clinicians had no unified digital registry that reflected day-to-day reality. Without trustworthy local data, it was impossible to benchmark protocols, analyze outcomes, or design targeted prevention programs. The association needed an ethical, easy-to-use tool that blended naturally into routine practice and produced clean, research-grade information.

We built a web-and-mobile clinical registry tailored to physicians managing VTE cases. From UX to cloud infrastructure, every layer was crafted for speed, security, and scientific rigor.

• Secure, role-based access—only credentialed physicians can add or view cases.
• Built-in digital consent that anonymizes patient data and streamlines ethics compliance.
• Comprehensive clinical record—history, diagnostics, treatment, evolution, and complications.
• Longitudinal updates so physicians can reopen a case and add follow-up data, creating an evolving timeline.
• Private research dashboard ready for interactive analytics and future predictive models.
• Curated article library editable by the association, plus sponsor sections for anticoagulation partners.

Press releases:

• Montevideo Portal
• El Observador
• Telenoche
• El País

The registry is already driving multicenter studies, attracting reference hospitals and anticoagulant manufacturers, and seeding a real-world data set that simply did not exist before.