International Neuromodulation Registry

Our Ambition

We believe the International Neuromodulation Registry represents a transformative resource for manufacturers, clinicians, and researchers working to advance care in the neuromodulation field. By enabling structured, real-world data collection on device performance, long-term outcomes, and patient-reported impact across multiple indications and geographies, the registry will accelerate evidence generation that supports regulatory decisions, market access, and responsible innovation.

We are confident the INR will become a transformative evidence platform for the neuromodulation community – advancing clinical excellence, regulatory compliance, and patient outcomes.

International
Neuromodulation
Registry

Target Groups and Their Benefits

  • International Clinical Centres and Practitioners: Benefit from access to outcome benchmarks, peer comparisons, and decision-support analytics derived from aggregated international data.
  • Patients and Patient Organisations: Gain from more transparent, evidence-based care, and future inclusion in governance and Patient Reported Outcome Measures (PROMs) design.
  • Health Authorities and Policymakers: Use outputs to inform policy decisions, service planning, and registry-linked reimbursement models.
  • Researchers and Academics: Access harmonised datasets across geographies to conduct cross-national epidemiological studies.
  • Industry Stakeholders: Opportunity to engage via formal agreements to support post-market surveillance, health technology assessments, and real-world evidence generation support.