Servicio Navarro de Salud innovates genomics

• Fragmented genomic data sources and inadequate data segregation or user access controls
• Manual, non-standardized workflows slow down diagnosis
• Lack of interoperability with existing healthcare systems
• Absence of a centralized genetic variant knowledge base
• Difficulty navigating regulatory and legal compliance
• Growing volume and complexity of genomic information

• Implementation of TSuPreMe (T-Systems Suite for Precision Medicine), a digital platform for managing and analyzing genomic data
• Genomic and clinical data migration: including re-annotation, cataloging, and full traceability of genetic variants
• Seamless connection with the electronic health record, clinical systems, and the national SiGenES node
• A scalable, flexible architecture designed for growth, with built-in end-to-end security, traceability, and compliance tools
• Intuitive, user-centric interface for healthcare professionals
• Flexible deployment and ongoing support from T-Systems experts

• Faster, more accurate genetic diagnoses
• Significant operational efficiency and reduced costs
• Enhanced data traceability, sovereignty, and alignment with legal standards
• Streamlined collaboration across clinical and research teams and improved interoperability across systems and departments
• Strengthened the position of Navarre as a leader in personalized medicine

The Servicio Navarro de Salud – Osasunbidea (SNS-O) delivers universal public healthcare across Navarre, an autonomous region in northern Spain with around 670,000 residents and one of the highest life expectancies in Europe, averaging 85 years. Its network includes hospitals and primary care centers that ensure comprehensive health services for the population.