Healthcare innovation study

Transforming clinical trial oversight with real-life evidence.

How global biomed leader Xeltis used Indeemo to bridge the gap between patient homes and clinical sites, ensuring Nobel Prize-winning technology delivers life-saving results.

Closing the oversight gap.

With breakthrough trials underway in the US, Xeltis faced a clinical blind spot. Traditional appointments left surgeons unable to monitor healing in real-time.

  • Proactive monitoring of life-threatening issues like pseudo-aneurysms.
  • Consistent oversight across 20 high-stakes US clinical sites.

Without Indeemo, we would be far behind. Problems often become critical before researchers have any idea of what is happening.

Nancy Foss | RN, CNN

Senior US Clinical Care Specialist, Xeltis

The clinical impact.

Indeemo redefined the standard of care for Xeltis patients by providing a continuous visual audit trail.

20

US trial sites

Consistent visibility across all primary US clinical locations.

Weekly

Safety checks

52 points of visibility per year, replacing sporadic clinic visits.

100%

Patient ownership

Empowering patients to monitor their own canulation rotation.

Zero

Missed criticals

Identifying issues early before they escalate to septic events.

Stories from the front line.

Hear Xeltis Senior US Clinical Care Specialist Nancy Foss | RN, CNN discuss the transformative potential of real-life evidence in healthcare.

Enhancing quality of care

"The core value is really enhancing the quality of patient care. It gives us eyes on access weekly."

Patient ownership

"Facilitates care by enabling the patient to take ownership and monitor rotation of sites."

Built for global clinical research.

The platform capabilities that allowed Xeltis to scale oversight efficiently across multiple clinical sites.

Global expansion ready

Deploy trials across borders with ease. Support for 34 languages ensures the platform is ready to scale from US trials to international markets seamlessly.

Longitudinal insight

Build a multi-year audit trail of real-world evidence. Track healing and device efficacy from initial implant through to full resorption over long-term study periods.

Regulatory-grade security

Protect sensitive PHI with enterprise-grade HIPAA compliance, facial blurring, and secure, encrypted data handling built for clinical research standards.

Empower your next clinical programme.

Learn how real-life evidence can transform your trial oversight. Complete the form below to book a demo with our team.